Robert J. Richardson
Steven Petrou
Alexander Bryson- 1Florey Institute of Neuroscience and Mental Health, University of Melbourne, Melbourne, VIC, Australia
- 2Department of Neurology, Austin Health, Heidelberg, VIC, Australia
- 3Praxis Precision Medicines, Boston, MA, United States
- 4Department of Neurology, Eastern Health, Melbourne, VIC, Australia
Drugs that modulate the GABAA receptor are widely used in clinical practice for both the long-term management of epilepsy and emergency seizure control. In addition to older medications that have well-defined roles for the treatment of epilepsy, recent discoveries into the structure and function of the GABAA receptor have led to the development of newer compounds designed to maximise therapeutic benefit whilst minimising adverse effects, and whose position within the epilepsy pharmacologic armamentarium is still emerging. Drugs that modulate the GABAA receptor will remain a cornerstone of epilepsy management for the foreseeable future and, in this article, we provide an overview of the mechanisms and clinical efficacy of both established and emerging pharmacotherapies.
1 Introduction
Epilepsy is a common neurological disorder characterised by an excess of excitatory activity within neural circuits and a predisposition to seizures. GABA is the primary inhibitory neurotransmitter in the mammalian brain and therefore plays a central role in the maintenance of normal excitation-inhibition balance and the pathophysiology of epilepsy.
GABA exerts much of its inhibitory influence through GABAA receptors which comprise a diverse group of ligand-gated ion channels that serve as common targets for antiseizure medications (Perucca et al., 2023a; Perucca et al., 2023b; Bryson et al., 2023). Indeed, some of the earliest developed antiseizure medications such as potassium bromide and phenobarbital act primarily through positive allosteric modulation of the GABAA receptor and, more recently, there has been great interest in the development of novel compounds that precisely modulate inhibitory pathways through specific GABAA receptor subtypes (Engin et al., 2018; Owen et al., 2019; Jankovic et al., 2021; Cerne et al., 2022; Witkin et al., 2022). The development of these novel compounds has emerged from a growth in understanding of the structure and function of GABAA receptors and insights into complex inhibitory effects mediated by receptor subtypes exhibiting variation in cellular location and regional distribution.
In this mini review we will first provide a brief overview of key aspects of the GABAergic system most relevant to pharmacological modulation in epilepsy, and then discuss both long-standing and newer or emerging drugs whose primary mechanism of action is via modulation of GABAA receptor neurotransmission.
2 Background: GABAA receptor transmission and relevance in epilepsy
2.1 Structure and distribution of GABAA receptors
GABAA, GABAB and GABAC receptors have been well characterised and form the basis of GABAergic neurotransmission in the mammalian nervous system. Both GABAA and GABAC receptors are ligand gated ion channels, with the latter being largely confined to the retina and possessing no known role in the pathogenesis or pharmacological management of epilepsy (Enz and Cutting, 1999; Sieghart et al., 1999; Olsen and Sieghart, 2009; Sigel and Steinmann, 2012). GABAB receptors are G-protein coupled receptors that exert both post and pre-synaptic effects, in part through activation of inward-rectifying K+ channels and hyperpolarisation of the neuronal membrane (Bowery et al., 2002). No established antiseizure medications, and comparatively few drugs in wider clinical use, act primarily through modulation of the GABAB receptor. GABAA receptors, the focus of this review, are cys-loop heteropentameric ligand gated ion channels permeable to chloride and bicarbonate (Chuang and Reddy, 2018; Bryson et al., 2023). The subunits comprising the quaternary structure are denoted α-, β-, δ-, γ-, π-, θ-, ρ-, ε-, with genes encoding these subunits located on chromosomes 4, 5, 15, and X (Chuang and Reddy, 2018). To date, 19 subunits have been cloned termed α1-6, β1-3, δ1, γ1-3, π1, θ, ρ1-3 and ε1, which are assembled as heteropentamers within the endoplasmic reticulum before being trafficked to the neuronal cell membrane (Sieghart et al., 1999; Sigel and Steinmann, 2012; Chuang and Reddy, 2018). Given the number of possible subunit arrangements, there is potential for great diversity of GABAA receptors possessing a range of physiological and pharmacological properties. The majority of GABAA receptors in the mammalian brain are composed of α1β2γ2 subunits (50%–60%) with the next most prevalent (25%–35%) being composed of combinations of α1 or 2, β1,2 or 3 and γ2 (Olsen and Sieghart, 2008; 2009).
α1β2γ2 GABAA receptors are located within the synaptic cleft and possess rapid activation and desensitisation kinetics upon GABA binding which are ideal for fast neurotransmission (Gingrich et al., 1995). Although α2 and α3 containing receptors are also concentrated within the synaptic cleft they have differing regional and cellular distributions which carries relevance for subunit-specific drug development. GABAA receptors distributed within the extra-synaptic membrane tend to contain α4, α5 and α6 subunits and possess slower activation kinetics and incomplete desensitisation upon GABA binding (Glykys and Mody, 2007). α4 and α6 subunits preferentially co-assemble with δ-subunits, and these receptors are emerging as an important pharmacological target given their sensitivity to neurosteroids and their diverging physiological role compared to synaptic receptors (MacKenzie and Maguire, 2013).
Recently, a number of protein complexes that co-localise and interact with ligand-gated ion channels, including the GABAA receptor, have been identified (Maher et al., 2017). The auxillary subunits LHFPL4 (Davenport et al., 2017) and Cltpm1 (Ge et al., 2018) have been shown to regulate the stabilisation and trafficking of post-synaptic GABAA receptors, respectively, and Shisa7 interacts with α1, α2 and γ2 containing GABAA receptors to ehance trafficking and expression at synaptic and extrasynaptic sites (Han et al., 2019; Han et al., 2021). Shisa7 has also been shown to modulate GABAA receptor decay kinetics and, interestingly, enhance diazepam-potentiated inhibitory currents in hippocampal neurons. Although it is currently unknown if Shisa7 exerts a similar influence upon other compounds acting upon the GABAA receptor, is raises the intriguing possibility that auxiliary subunits may serve as future pharmacological targets.
2.2 Phasic and tonic GABAergic transmission
GABAA receptors mediate two main forms of neurotransmission which are subject to pharmacological modulation: phasic and tonic transmission. Phasic transmission occurs when GABA released from presynaptic axon terminals bind GABAA receptors clustered in the post-synaptic membrane. This results in a spatially precise and rapid change in chloride conductance which, due to higher postnatal expression of the potassium-chloride cotransporter, usually causes hyperpolarisation of the post-synaptic membrane in mature neurons (Farrant and Nusser, 2005; Farrant and Kaila, 2007; Kaila et al., 2014). At the cellular level phasic inhibition can exert multiple effects on neuronal function determined by the subcellular location of GABAA receptors and variation of the intracellular chloride gradient (Farrant and Nusser, 2005). For example, dendritic inhibitory inputs can suppress dendritic spikes and backpropagating action potentials and regulate coincidence detection of excitatory inputs (Tang et al., 2011; Groen et al., 2014). In contrast somatic and axonal inputs may co-ordinate spike timing and pyramidal cell synchronisation (Tremblay et al., 2016). The presence of GABAA receptor subunit variation across subcellular compartments raises the possibility of targeted pharmacological modulation of these physiological processes.
Tonic inhibition is a more persistent form of neurotransmission mediated by extracellular GABA activating extra-synaptic GABAA receptors. As such, tonic inhibition exerts a more non-specific inhibitory influence upon both neurons and glia and across subcellular regions including the axon, dendrites and cell body (Farrant and Nusser, 2005). Tonic inhibition plays a crucial role in normal brain development (Valeyev et al., 1993; LoTurco et al., 1995; Owens et al., 1999; Demarque et al., 2002) and, in the mature CNS, has been shown to exert an important modulatory role within the hippocampus (Semyanov et al., 2003), cerebral cortex (Vardya et al., 2008), thalamocortical relay networks (Porcello et al., 2003), midbrain (Tossell et al., 2021) and cerebellum (Hausser and Clark, 1997). Despite the diffuse actions of tonic inhibition more targeted effects may arise through localised extracellular GABA release from neurogliaform cells and cellular variation in extrasynaptic GABAA receptor subtype expression which may also be leveraged through pharmacologic manipulation (Olah et al., 2009; Tremblay et al., 2016).
2.3 GABAA receptor mutations and epilepsy
The relevance of GABAA neurotransmission in both the pathophysiology and treatment of epilepsy is underscored by the discovery of an expanding number of GABAA receptor mutations associated with forms of genetic epilepsy. These discoveries have also raised interesting pharmacotherapeutic issues. Mutations of the γ2 subunit (encoded by the GABRG2 gene) were the earliest identified and have since been comprehensively examined (Baulac et al., 2001; Wallace et al., 2001). These loss of function monogenic variants have been shown to cause developmental and epileptic encephalopathies (DEEs) including Dravet Syndrome and Lennox-Gastaut Syndrome, in addition to milder phenotypes such as Febrile Seizures and Genetic Generalized Epilepsies (Baulac et al., 2001; Wallace et al., 2001; Harkin et al., 2002; Kananura et al., 2002; Tian et al., 2013; Huang et al., 2014; Todd et al., 2014; Kang et al., 2015; Warner et al., 2019; Qu et al., 2021). Since the γ2 subunit contributes to the benzodiazepine binding site these variants may be associated with benzodiazepine insensitivity which carries implications for appropriate drug treatment (Fedi et al., 2006). Mutations of GABRA1/2/3/5, GABRB1/2/3 and GABRD, which encode the α1,2,3,5, β1,2,3 and δ subunits, respectively, have also been implicated in a spectrum of epilepsies, including severe DEEs, although variants of GABRA1 and GABRB2/3 mutations are most frequently encountered which likely reflects the prevalence of their expression in the CNS (Absalom et al., 2023). Interestingly, although most GABAA receptor variants show loss-of-function traits, characterization of several β3, δ and α4 variants revealed gain-of-function features including enhanced sensitivity to GABA and were associated with more severe early-onset phenotypes (Komulainen-Ebrahim et al., 2019; Mierzewska et al., 2021; Absalom et al., 2022; Ahring et al., 2022; Johannesen et al., 2022; Maillard et al., 2022) Importantly, the discovery of gain-of-function mutations carries treatment implications as drugs which enhanced GABAA receptor transmission tended to be more effective in loss-of-function variants.
3 Established GABAA receptor pharmacotherapy in epilepsy.
Drugs that act on GABAA receptors have been used for the management of epilepsy for over a century and remain important treatment tools for acute and chronic seizure control (Rho and White, 2018).
3.1 Phenobarbital
Phenobarbital is a barbiturate and sedative-hypnotic agent, and one of the earliest discovered antiseizure medications introduced in 1912. Phenobarbital enhances both phasic and tonic inhibition through positive allosteric modulation of GABAA receptors and exhibits minimal subunit specificity. It has a long half-life of 75–120 h, is ∼25% renally excreted and is a broad hepatic enzyme inducer which is of relevance for administration in the intensive care setting in the context of status epilepticus and polypharmacy (Brodie and Kwan, 2012). Phenobarbital is used in both focal and generalised epilepsies and, in two meta-analyses, was found to have similar efficacy to both phenytoin and carbamazepine for time to 12-month seizure remission and first breakthrough seizure in these conditions, although carbamazepine was associated with lower rates of seizure recurrence and drug cessation (Nolan et al., 2013). Chronic use of phenobarbital is limited by concerns regarding sedation and cognitive adverse effects; however it retains an important role in resource-limited settings (Brodie and Kwan, 2012). Phenobarbital also has an established role in refractory status epilepticus (SE). In benzodiazepine-resistant SE, a systematic review and network meta-analyses suggested that phenobarbital was more effective for terminating seizures compared to phenytoin, lacosamide, valproate and levetiracetam (Brigo et al., 2022), and as first-line therapy it was found to have comparable efficacy to lorazepam (Treiman et al., 1998). Again, however, the use of phenobarbital in acute management is limited by adverse effects, including hypotension and respiratory depression, and a slow rate of administration, and it is often reserved as third-line therapy for SE in the intensive care setting.
3.2 Benzodiazepines
Benzodiazepines (BZDs) are widely prescribed for the acute management of seizures and status epilepticus. They are used less frequently as add-on therapy for the management of refractory chronic epilepsy. BZDs act as positive allosteric modulators of the GABAA receptor and bind at the interface of the γ2 and α1, α2, α3 or α5 subunits. Given the preferential localisation of γ2 subunit containing receptors at the post-synaptic membrane they augment phasic inhibition but have minimal effect on tonic inhibition (Benson et al., 1998).
The 1,4-benzodiazepines lorazepam, midazolam, and diazepam are used for a variety of clinical indications, including procedural sedation, anxiety, and alcohol withdrawal, and have established efficacy for the suppression of seizures (Kienitz et al., 2022). In addition to oral and intravenous formulations, midazolam and lorazepam are available as intranasal formulations, and midazolam as intramuscular and buccal formulations. Both lorazepam and diazepam have high oral bioavailability (over 90%) compared to midazolam (∼40–50%, due to metabolism in the intestinal epithelium) with peak concentrations reached between 30 and 120 min (Kienitz et al., 2022). Faster peak concentrations are achieved with buccal (∼30 min) and intranasal (7–15 min) midazolam, and so these routes have been investigated for the out-of-hospital management of seizures. Importantly, benzodiazepines have greatly varying half-lives with midazolam shortest (1.5–3 h) followed by lorazepam (8–25 h) and diazepam (24–48 h) (Kienitz et al., 2022). Comparative studies in the management of SE suggest that intravenous lorazepam is more effective than intravenous diazepam for pre-hospital termination of seizures (Alldredge et al., 2001) and a comparison of intravenous lorazepam to intramuscular midazolam found higher rates of seizure cessation on arrival to hospital with midazolam (Silbergleit et al., 2012) likely due to faster rates of administration. Finally, buccal midazolam has been associated with faster rates of out-of-hospital seizure termination compared to rectal diazepam in paediatric and residential care patients (Scott et al., 1999; Nakken and Lossius, 2011) and intranasal midazolam has been found to have comparable effectiveness to intravenous diazepam for terminating seizures in the paediatric population (Lahat et al., 2000; Mahmoudian and Zadeh, 2004).
Clobazam is a 1,5-benzodiazepine and possesses a different molecular structure to classical 1,4- benzodiazepines such as diazepam. This confers greater selectivity to GABAA receptors possessing the α2 subunit which may be implicated in the anticonvulsant effects of BZDs, and is associated with other favourable properties such as improved tolerability (Stephens et al., 2017; Engin, 2022). Consequently, clobazam has a more established role in the long-term management of epilepsy, with robust evidence in the treatment of the DEE Lennox-Gastaut Syndrome. In a randomised phase 2 trial clobazam exhibited a dose-dependent reduction in the frequency of atonic seizures with reductions of non-drop seizures also observed in the high-dose (1 mg/kg/day) group Kienitz et al., 2022 #292}and, in an open label extension, it was found that in over 80% of patients who had a favourable response this benefit was sustained by year three (Conry et al., 2014). Although trial evidence is limited, clobazam also appears to have efficacy as add-on therapy in the management of refractory focal epilepsy. The improved tolerability of clobazam has motivated the search for more targeted positive allosteric GABAA modulators to mitigate the side effects associated with classical benzodiazepine.
3.3 Vigabatrin
Vigabatrin is a structural analogue of GABA and was developed in 1974 using a rational drug design approach to inhibit GABA breakdown through the targeting of GABA-transaminase. This raises the intracellular concentration of GABA and leads indirectly to enhanced phasic and tonic GABAA receptor transmission by augmenting both vesicular release and extra-synaptic extrusion via GABA-transporters (GATs) (Ben-Menachem, 2011). Vigabatrin has a short half-life (5–7 h) and achieves low CSF concentrations, but, since it acts as an irreversible GABA-transaminase inhibitor, it is biological effect of increasing GABA levels within the brain can persist for over 1 week. Vigabatrin has efficacy in both infantile spasms and as add-on therapy for focal seizures in adults. It has been shown to rapidly decrease the frequency of infantile spasms within 5 days compared to placebo (Appleton and Montiel-Viesca, 1993; Appleton et al., 1999) and exhibits a dose-dependent increase in spasm cessation (Elterman et al., 2001; Elterman et al., 2010). Similar findings have been observed in adults with refractory focal seizures, with several randomised controlled trials showing a dose-dependent decrease in the number of median monthly seizures, and an increase in the proportion of subjects with over 50% seizure reduction (French et al., 1996; Dean et al., 1999). A particular concern with vigabatrin use is the development of an irreversible peripheral visual field defects. This occurs with a prevalence of 20%–25% in adults and approximately 15% in children, with onset observed within 9 months after commencement.
3.4 Tiagabine
Like vigabatrin, tiagabine indirectly enhances GABAA receptor transmission, and was strategically developed in the 1990s to act as a GAT blocker thereby enhancing the availability of GABA at the synaptic cleft. Tiagabine exhibits approximately 2.5-fold greater specificity for GAT1 which mediates glial and neuronal reuptake in the vicinity of the synaptic cleft which reflects its physiological impact of prolonging the duration of inhibitory post-synaptic currents. Tiagabine is metabolized through the CYP3A4 system and has a half-life of 5–9 h which is shortened with the concomitant use of hepatic enzyme inducing agents. Several studies have confirmed the benefit of tiagabine in refractory focal epilepsy in adults, including a placebo-controlled cross-over trial demonstrating a 54% response rate (over 50% reduction in seizure frequency) compared to 24% for placebo (Richens et al., 1995), and moderate-to-high doses of tiagabine (32 and 56 mg/day) showing greater response than low dose (16 mg/day) and placebo (Uthman et al., 1998). In the paediatric population there is also evidence for efficacy in focal epilepsy but there is the possibility of exacerbating certain generalised seizures types, including myoclonic seizures and primary generalised tonic-clonic convulsions (Uldall et al., 2000). Adverse effects, including fatigue and dizziness, and concerns raised about provoking seizures, in particular absence seizures associated with generalised spike-wave discharges, have limited its clinical use.
3.5 Valproate
Although valproate possesses several mechanisms of action, including sodium channel blockade, modulation of excitatory neurotransmitters and inhibition of histone deacetylase, it is thought to achieve its anti-seizure effects at least in part through augmenting GABAA transmission (Davies, 1995), and so will be considered in further detail. Valproate does not appear to act directly on GABAA receptors but has shown to increase brain GABA levels through several pathways, including preferential inhibition of GABA-transaminase within neurons and enhancing glutamate decarboxylase (GAD) activity (Luder et al., 1990; Loscher, 1999). It is possible that valproate may also enhance GABA synaptic release and modulate metabolic pathways, such as the inhibition of alpha-ketoglutarate, to increase activity through the GABA shunt. Valproate has a half-life of 9–18 h and is metabolized through the hepatic CYP450 system and glucuronidation, and co-administration with hepatic enzyme inducers shorten its half-life. It is highly protein bound and inhibits hepatic metabolism, both of which can increase the levels of other antiseizure medications including lamotrigine, phenytoin, carbamazepine, and phenobarbital. Valproate has efficacy in both focal and generalised forms of epilepsy, and in the Standard and New Antiepileptic Drugs (SANAD) trial, which compared valproate to lamotrigine and topiramate in generalized and unclassified epilepsy, it was found to be more effective than lamotrigine for 12-month seizure remission, and superior to topiramate for time-to-treatment failure (Marson et al., 2007). The SANAD 2 trial compared valproate to levetiracetam as first-line treatment in patients with genetic/idiopathic generalised epilepsy, demonstrating superiority of valproate for both 12-month remission and time to first seizure (Marson et al., 2021). In patients with childhood absence epilepsy, valproate has been shown to have superior efficacy to lamotrigine, and is equivalent to ethosuximide, although was associated with higher rates of attentional deficits (Glauser et al., 2010). Despite its efficacy in a broad range of syndromes, a significant concern relates to teratogencitiy with high rates of congenital malformation and autism, and lower IQ in exposed infants necessitating careful counselling.
4 Emerging and novel GABAA receptor pharmacotherapy
4.1 Cenobomate
Cenobomate is a newer antiseizure medication that recently gained FDA and European Medicines Agency approvals for the treatment of refractory focal onset seizures in adults (Roberti et al., 2021). Cenobomate modulates both GABAA receptors (Sharma et al., 2020) and voltage gated sodium channels, with a preferential effect on channel inactivation leading to a reduction of the persistent sodium current (Nakamura et al., 2019). Cenobomate acts as a positive allosteric modulator of GABAA receptors through non-benzodiazepine binding sites. Although cenobomate acts upon both synaptic and extra-synaptic GABAA receptors, the half maximal effective concentration in a non-neuronal expression system was higher for α4, α5 and α6 containing GABAA receptor subtypes which are associated with extrasynaptic localisation, and in dissociated CA1 neurons cenobomate exerted a more pronounced effect on baseline GABA holding current than spontaneous inhibitory post synaptic currents. Together, these findings suggest that cenobomate preferentially modulates of tonic inhibition (Sharma et al., 2020).
In two randomised placebo-controlled Phase 2 trials in patients with refractory focal seizures, cenobomate at doses of 200 or 400 mg per day were associated with over 50% reduction in seizure frequency during treatment maintenance compared to placebo (Chung et al., 2020; Krauss et al., 2020; Rosenfeld et al., 2021). Notably, high rates (11%–26%) of seizure-freedom were also observed at these doses, and a post hoc analyses of two open-label phase 3 trials suggest that responder and seizure-free rates persist beyond 12 months (Aboumatar et al., 2022; Rosenfeld et al., 2021). A more recent cohort study in highly active (over 20 seizures/month) or ultra-refractory patients (over six anti-seizure medication failures), most of whom had undergone previous epilepsy surgery or vagal-stimulators insertion, showed clinically significant reductions seizure severity and frequency (Pena-Ceballos et al., 2023). Five percent of this cohort achieved seizure freedom and 70% of patients had a 50%–99% reduction in seizure frequency, most of whom were treated with over 250 mg of cenobomate (Pena-Ceballos et al., 2023).
Dose related adverse effects from cenobomate include somnolence, dizziness, fatigue, and coordination difficulties. Interestingly, adverse effects were more frequently reported in a patient cohort that was concurrently treated with a sodium channel blocking drug, perhaps due to the overlapping mechanism of action (Krauss et al., 2020). A rare severe side effect of Drug Rash with Eosinophilia and Systemic Symptoms (DRESS) was observed in one of the phase 2 trials (Krauss et al., 2020) but in studies using a slower dose titration no further cases were identified (Krauss et al., 2020; Lattanzi et al., 2020).
4.2 Darigabat
Darigabat is an imidazopyridine-related molecule that was developed to act selectively upon GABAA receptors containing α2,α3 and α5 subunits (Owen et al., 2019). Darigabat is a positive allosteric modulator and binds the benzodiazepine site of α1, α2, α3, and α5 subunit containing GABAA receptors, but its efficacy at α1-containing receptors is weak which may reduce unwanted side effects such as sedation and abuse potential whilst maintaining antiseizure and anti-anxiolytic properties which are be mediated primarily through α2 and α3-containing receptors (Engin et al., 2018; Nickolls et al., 2018; Owen et al., 2019; Cerne et al., 2022).
Darigabat has shown antiseizure efficacy in a range of preclinical epilepsy models in animals, including the kainic acid model of mesial temporal lobe epilepsy where it produced a statistically significant reduction in hippocampal paroxysmal discharges with comparable efficacy to diazepam (Owen et al., 2019; Bialer et al., 2020; Gurrell et al., 2022). Phase 1 clinical trials demonstrated safety and tolerance with only mild somnolence and dizziness reported in subjects (Nickolls et al., 2018; Bialer et al., 2022). In a small study of patients with photosensitive epilepsy, darigabat abolished the photoparoxysmal response in 6 of 7 patients following single doses between 17.5mg and 52 mg (Gurrell et al., 2019). There was no difference in suppression of photoparoxysmal responses between lower and higher doses of darigabat and efficacy was similar to that of lorazepam (Gurrell et al., 2019). Currently a large multicentred Phase 2 trial is underway (NCT04244175) to assess the safety and efficacy of darigabat as adjunctive therapy for refractory focal and generalised seizures, the results of which are unpublished (Cerne et al., 2022; Gurrell et al., 2022).
4.3 Padsenovil
Padsenovil was developed out of a rational drug discovery program to modulate both synaptic vesicle protein 2 (SV2) and GABAA receptors, thereby exerting an effect on both pre-synaptic and post-synaptic targets (Niespodziany et al., 2020). At the GABAA receptor, padsevonil binds at the benzodiazepine site and acts as a positive allosteric modulator and partial agonist which may reduce complications associated with full agonists (Leclercq et al., 2020). In vitro studies demonstrated greatest potency on α1 and α5 compared to α2 and α3 subunit containing receptors (Wood et al., 2020). Padsevonil showed promising results in several acute and chronic seizure models, including greater protection from seizures in the chronic 6 Hz seizure model compared to diazepam and the existing SV2 modulators levetiracetam and brivaracetam, and in a Phase 2 proof-of-concept trial showed significant reductions in weekly seizure frequency for treatment-resistant focal epilepsy. However, a randomised dose-finding trial and Phase 3 trial failed to observe a significant reduction in seizure frequency at any dose compared to placebo leading to discontinuation of drug development (Rademacher et al., 2022).
4.4 Alprazolam
Alprazolam is a short-acting and non-selective 1,4 benzodiazepine with an established role in the treatment of anxiety disorders. Despite animal studies showing potent antiseizure effects comparable to other benzodiazepines, alprazolam has historically not been used for the management of acute seizures (Jenck et al., 1992; De Sarro et al., 1996) and is unsuitable for the treatment of chronic epilepsy due to tolerance and drug dependence. However, alprazolam is being repurposed as an acute rescue medication for seizures in the outpatient setting via inhalation with the Staccato device as it achieves rapid onset of action combined with a relatively convenient administration route (French et al., 2019). In a proof-of-concept study, inhaled alprazolam supressed the photoparaxysmal response on electroencephalography within minutes and maintained its effects for up to 4 hours (French et al., 2019), and in a randomised trial of hospital inpatients Staccato alprazolam led to higher rates of seizure termination within 2 minutes compared to placebo (French et al., 2023). A phase 3 trial to test efficacy in the outpatient setting is now recruiting.
4.5 Stiripentol
Stiripentol is a structurally unique antiseizure medication that has been shown to modulate GABAA receptors in addition to several other secondary mechanisms, including inhibition of lactate dehydrogenase (LDH) (Nickels and Wirrell, 2017). Stiripentol acts independently of the benzodiazepine binding site, promotes increased GABAA receptor open time duration and its effects are blocked by phenobarbital, which together suggest a barbiturate-like effect (Quilichini et al., 2006). Stiripentol acts upon both synaptic and extrasynaptic GABAA receptor subtypes and has a propensity for α3 subunit-containing receptors which are expressed during embryonic and early post-natal development (Nickels and Wirrell, 2017). It enhances the delay constant of inhibitory post-synaptic potentials and augments tonic inhibition via activation of δ-containing receptors (Nickels and Wirrell, 2017). Stiripentol undergoes extensive hepatic metabolism and drug levels are reduced with co-administration of enzyme-inducing antiseizure medications such as phenytoin, carbamazepine and phenobarbital.
Stiripentol has efficacy in paediatric forms of epilepsy, in particular the severe developmental and epileptic encephalopathy Dravet Syndrome. Following promising results in an open-label adjunctive-therapy study, two placebo-controlled studies demonstrated impressive responder rates (over 50% reduction in seizure frequency) of 71% and 67% compared to placebo, and although the study sizes were small a significant proportion of participants achieved seizure freedom. In an open-label extension responder rates were maintained at over 50% (Chiron et al., 2000) although an important consideration is that clobazam, which also has benefit in Dravet syndrome, can increase stiripentol levels by inhibiting hepatic metabolism. Stirpentol also appears to carry benefit as adjunct therapy in childhood focal epilepsies and several case studies suggest a potential role as rescue therapy in refractory status epilepticus which may relate to modulation of extra-synaptic GABAA receptors (Nickels and Wirrell, 2017).
4.6 Neurosteroids
Neurosteroids such as allopregnanolone, allotetrahydrodeoxycorticosterone (THDOC) and androstanediol are endogenously produced metabolites of the steroid hormones progesterone and corticosterone (MacKenzie and Maguire, 2013). Neurosteroids are synthesised within the brain and fluctuations in their concentration are linked to physiological states such as the menstrual cycle, the postpartum period and increased stress states (Purdy et al., 1991; MacKenzie and Maguire, 2013; Reddy and Estes, 2016; Chen et al., 2019). There is also evidence that they play a pivotal role in several neuropsychiatric disorders including anxiety, pre-menstrual dysphoric disorder, anxiety (MacKenzie and Maguire, 2013; Sikes-Keilp and Rubinow, 2023) and epilepsy (Reddy, 2013).
Neurosteroids are potent GABAA receptor positive allosteric modulators and bind within the transmembrane domain of α and β subunits to activate both synaptic and extrasynaptic receptors (Hosie et al., 2007; Chen et al., 2019). δ-subunit containing receptors that mediate tonic inhibition are particularly sensitive to neurosteroids, and this mechanism of action has attracted significant interest for a potential role in refractory epilepsy and status epilepticus as there is evidence for synaptic receptor downregulation in these conditions (Belelli et al., 2002; Belelli et al., 2009; MacKenzie and Maguire, 2013).
Ganaxolone is an orally administered synthetic analogue of allopregnanolone and has been shown to supress seizure activity in numerous acute and chronic animal models (Carter et al., 1997; Kaminski et al., 2003; Reddy and Rogawski, 2009; 2010; Saporito et al., 2019). In humans, Ganaxolone has most robust evidence for the management of seizures associated with CDKL5 deficiency, a rare DEE associated with early-onset seizures and developmental impairment, and for which ganaxolone is approved in the US. Following encouraging results in a small open-label study, adjunctive ganaxolone was found to produce a 30.7% reduction in major seizures compared to 6.9% for placebo in a randomised placebo-controlled trial (Knight et al., 2022). Although ganaxolone has also been trialled in refractory adult focal epilepsy the observed benefits have been modest, and a phase 3 study did not show a significant reduction in seizure frequency compared to placebo (Meng et al., 2023). In a small dose-finding study for management of refractory status epilepticus, administration of intravenous ganaxolone as third-line therapy showed encouraging results with no subjects requiring intravenous anaesthesia within 24 h after treatment (Vaitkevicius et al., 2022). Although over 50% of cases comprised non-convulsive status epilepticus, a phase 3 randomised placebo-controlled trial is underway in light of these findings. Beyond ganaxolone, ETX155 is another candidate neurosteroid with efficacy for suppressing seizures in rodent models of epilepsy, and has recently commenced Phase 1 trials in photosensitive epilepsy (Perucca et al., 2023a).
4.7 Other subtype selective GABAA receptor modulators and exploratory therapies
The prospect of maximizing therapeutic effects associated with GABAA receptor modulation whilst minimizing drug dependence and sedation has led to the development of several subtype-selective compounds with promising pre-clinical characteristics, some of which are undergoing clinical development. ENX 101 is a α2, α3 and α5 subtype selective positive allosteric modulator that was well-tolerated by subjects in a Phase 1 study and is now undergoing Phase 2 testing for refractory focal epilepsy (Castellano et al., 2020; Jankovic et al., 2021; Perucca et al., 2023b). KRM-II-81 is an imidazodiazepine that is also highly selective for α2 and α3 subunit containing GABAA receptors. KRM-II-81 has shown efficacy that is comparable or superior to diazepam across both acute chemical and electrical seizure models, and chronic pharmaco-resistant rodent models, but has not yet undergone trials in humans (Witkin et al., 2022).
Beyond improved receptor selectivity, gene therapy looms as an important component of epilepsy therapy in the future, and several approaches in development are designed to augment GABAA receptor transmission. ETX101 is a recombinant adeno-associated viral (AAV) vector containing a GABA regulatory element designed to upregulate SCN1A (encoding the voltage-gated sodium channel NaV1.1) and restore interneuron function in patients with Dravet Syndrome.
Similar to ETX101, STK-001 is an antisense oligonucleotide designed to enhance the generation of wild-type SCN1A mRNA transcripts to restore inhibitory function in Dravet Syndrome (Bialer et al., 2020; Wengert et al., 2022). In mouse models, intraventricular administration of STK001 was associated with restoration of parvalbumin-positive interneuron firing, reduced seizures, and prolonged survival (Han et al., 2020). Following promising findings in Phase 1/2a studies in children with Dravet Syndrome, an open label extension is underway with interim results demonstrating reductions in seizure frequency and improvements in cognition and behaviour.
5 Conclusion
Modulation of the GABAA receptor has been a mainstay of the antiseizure pharmacological armamentarium for over a century, and older drugs such as barbiturates and classical benzodiazepines still retain their place in clinical practice in both resource-scarce settings and for the management of status epilepticus. The coming years will see the introduction of novel agents with subunit specificity and gene therapies (Table 1) that act to restore GABAA receptor transmission to correct inhibitory deficits. These developments build upon advances in our understanding of the complexities of the GABAergic system, and represent important steps toward precision epilepsy treatments that may improve efficacy whilst mitigating the adverse effects often associated with older drugs.
TABLE 1. Summary of established and emerging GABAA active medications used in epilepsy.
Author contributions
RR: Writing–original draft, Writing–review and editing. SP: Writing–review and editing. AB: Writing–review and editing.
Funding
The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.
Conflict of interest
SP is co-founder and equity holder in Praxis Precision Medicines and RogCon. SP is an employee of Praxis Precision Medicines. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
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References
Absalom, N. L., Liao, V. W. Y., Johannesen, K. M. H., Gardella, E., Jacobs, J., Lesca, G., et al. (2022). Gain-of-function and loss-of-function GABRB3 variants lead to distinct clinical phenotypes in patients with developmental and epileptic encephalopathies. Nat. Commun. 13, 1822. doi:10.1038/s41467-022-29280-x
Absalom, N. L., Lin, S. X. N., Liao, V. W. Y., Chua, H. C., Moller, R. S., Chebib, M., et al. (2023). GABAA receptors in epilepsy: elucidating phenotypic divergence through functional analysis of genetic variants. J. Neurochem. doi:10.1111/jnc.15932
Ahring, P. K., Liao, V. W. Y., Gardella, E., Johannesen, K. M., Krey, I., Selmer, K. K., et al. (2022). Gain-of-function variants in GABRD reveal a novel pathway for neurodevelopmental disorders and epilepsy. Brain 145, 1299–1309. doi:10.1093/brain/awab391
Alldredge, B. K., Gelb, A. M., Isaacs, S. M., Corry, M. D., Allen, F., Ulrich, S., et al. (2001). A comparison of lorazepam, diazepam, and placebo for the treatment of out-of-hospital status epilepticus. N. Engl. J. Med. 345, 631–637. doi:10.1056/NEJMoa002141
Aboumatar, S., Biton, V., Wechsler, R., Ferrari, L., Allen, F., and Rosenfeld, W. E. (2022). Post hoc analysis of a phase 3 study for treatment of uncontrolled focal seizures: Adjunctive cenobamate dose and seizure reduction by baseline seizure frequency. Epilepsy Res 186, 107014. doi:10.1016/j.eplepsyres.2022.107014
Appleton, R. E., and Montiel-Viesca, F. (1993). Vigabatrin in infantile spasms--why add on? Lancet 341, 962. doi:10.1016/0140-6736(93)91255-k
Appleton, R. E., Peters, A. C., Mumford, J. P., and Shaw, D. E. (1999). Randomised, placebo-controlled study of vigabatrin as first-line treatment of infantile spasms. Epilepsia 40, 1627–1633. doi:10.1111/j.1528-1157.1999.tb02049.x
Baulac, S., Huberfeld, G., Gourfinkel-An, I., Mitropoulou, G., Beranger, A., Prud'homme, J. F., et al. (2001). First genetic evidence of GABA(A) receptor dysfunction in epilepsy: a mutation in the gamma2-subunit gene. Nat. Genet. 28, 46–48. doi:10.1038/ng0501-46
Belelli, D., Casula, A., Ling, A., and Lambert, J. J. (2002). The influence of subunit composition on the interaction of neurosteroids with GABA(A) receptors. Neuropharmacology 43, 651–661. doi:10.1016/s0028-3908(02)00172-7
Belelli, D., Harrison, N. L., Maguire, J., Macdonald, R. L., Walker, M. C., and Cope, D. W. (2009). Extrasynaptic GABAA receptors: form, pharmacology, and function. J. Neurosci. 29, 12757–12763. doi:10.1523/JNEUROSCI.3340-09.2009
Ben-Menachem, E. (2011). Mechanism of action of vigabatrin: correcting misperceptions. Acta Neurol. Scand. Suppl, 5–15. doi:10.1111/j.1600-0404.2011.01596.x
Benson, J. A., Low, K., Keist, R., Mohler, H., and Rudolph, U. (1998). Pharmacology of recombinant gamma-aminobutyric acidA receptors rendered diazepam-insensitive by point-mutated alpha-subunits. FEBS Lett. 431, 400–404. doi:10.1016/s0014-5793(98)00803-5
Bialer, M., Johannessen, S. I., Koepp, M. J., Levy, R. H., Perucca, E., Perucca, P., et al. (2020). Progress report on new antiepileptic drugs: a summary of the Fifteenth Eilat Conference on New Antiepileptic Drugs and Devices (EILAT XV). II. Drugs in more advanced clinical development. Epilepsia 61, 2365–2385. doi:10.1111/epi.16726
Bialer, M., Johannessen, S. I., Koepp, M. J., Levy, R. H., Perucca, E., Perucca, P., et al. (2022). Progress report on new antiepileptic drugs: a summary of the Sixteenth Eilat Conference on New Antiepileptic Drugs and Devices (EILAT XVI): II. Drugs in more advanced clinical development. Epilepsia 63, 2883–2910. doi:10.1111/epi.17376
Bowery, N. G., Bettler, B., Froestl, W., Gallagher, J. P., Marshall, F., Raiteri, M., et al. (2002). International Union of Pharmacology. XXXIII. Mammalian gamma-aminobutyric acid(B) receptors: structure and function. Pharmacol. Rev. 54, 247–264. doi:10.1124/pr.54.2.247
Brigo, F., Igwe, S. C., Bragazzi, N. L., and Lattanzi, S. (2022). Clonazepam monotherapy for treating people with newly diagnosed epilepsy. Cochrane Database Syst. Rev. 2, CD013028. doi:10.1002/14651858.CD013028.pub2
Brodie, M. J., and Kwan, P. (2012). Current position of phenobarbital in epilepsy and its future. Epilepsia 53 (8), 40–46. doi:10.1111/epi.12027
Bryson, A., Reid, C., and Petrou, S. (2023). Fundamental Neurochemistry Review: GABA(A) receptor neurotransmission and epilepsy: principles, disease mechanisms and pharmacotherapy. J. Neurochem. 165, 6–28. doi:10.1111/jnc.15769
Carter, R. B., Wood, P. L., Wieland, S., Hawkinson, J. E., Belelli, D., Lambert, J. J., et al. (1997). Characterization of the anticonvulsant properties of ganaxolone (CCD 1042; 3alpha-hydroxy-3beta-methyl-5alpha-pregnan-20-one), a selective, high-affinity, steroid modulator of the gamma-aminobutyric acid(A) receptor. J. Pharmacol. Exp. Ther. 280, 1284–1295.
Castellano, D., Shepard, R. D., and Lu, W. (2020). Looking for novelty in an "old" receptor: recent advances toward our understanding of GABA(A)rs and their implications in receptor pharmacology. Front. Neurosci. 14, 616298. doi:10.3389/fnins.2020.616298
Cerne, R., Lippa, A., Poe, M. M., Smith, J. L., Jin, X., Ping, X., et al. (2022). GABAkines - advances in the discovery, development, and commercialization of positive allosteric modulators of GABA(A) receptors. Pharmacol. Ther. 234, 108035. doi:10.1016/j.pharmthera.2021.108035
Chen, Z. W., Bracamontes, J. R., Budelier, M. M., Germann, A. L., Shin, D. J., Kathiresan, K., et al. (2019). Multiple functional neurosteroid binding sites on GABAA receptors. PLoS Biol. 17, e3000157. doi:10.1371/journal.pbio.3000157
Chiron, C., Marchand, M. C., Tran, A., Rey, E., D'athis, P., Vincent, J., et al. (2000). Stiripentol in severe myoclonic epilepsy in infancy: a randomised placebo-controlled syndrome-dedicated trial. STICLO study group. Lancet 356, 1638–1642. doi:10.1016/s0140-6736(00)03157-3
Chuang, S. H., and Reddy, D. S. (2018). Genetic and molecular regulation of extrasynaptic GABA-A receptors in the brain: therapeutic insights for epilepsy. J. Pharmacol. Exp. Ther. 364, 180–197. doi:10.1124/jpet.117.244673
Chung, S. S., French, J. A., Kowalski, J., Krauss, G. L., Lee, S. K., Maciejowski, M., et al. (2020). Randomized phase 2 study of adjunctive cenobamate in patients with uncontrolled focal seizures. Neurology 94, e2311–e2322. doi:10.1212/WNL.0000000000009530
Colasante, G., Qiu, Y., Massimino, L., Di Berardino, C., Cornford, J. H., Snowball, A., et al. (2020). In vivo CRISPRa decreases seizures and rescues cognitive deficits in a rodent model of epilepsy. Brain 143, 891–905. doi:10.1093/brain/awaa045
Conry, J. A., Ng, Y. T., Kernitsky, L., Mitchell, W. G., Veidemanis, R., Drummond, R., et al. (2014). Stable dosages of clobazam for Lennox-Gastaut syndrome are associated with sustained drop-seizure and total-seizure improvements over 3 years. Epilepsia 55, 558–567. doi:10.1111/epi.12561
Davenport, E. C., Pendolino, V., Kontou, G., Mcgee, T. P., Sheehan, D. F., Lopez-Domenech, G., et al. (2017). An essential role for the tetraspanin LHFPL4 in the cell-type-specific targeting and clustering of synaptic GABA(A) receptors. Cell Rep. 21, 70–83. doi:10.1016/j.celrep.2017.09.025
Davies, J. A. (1995). Mechanisms of action of antiepileptic drugs. Seizure 4, 267–271. doi:10.1016/s1059-1311(95)80003-4
Dean, C., Mosier, M., and Penry, K. (1999). Dose-Response Study of Vigabatrin as add-on therapy in patients with uncontrolled complex partial seizures. Epilepsia 40, 74–82. doi:10.1111/j.1528-1157.1999.tb01991.x
Demarque, M., Represa, A., Becq, H., Khalilov, I., Ben-Ari, Y., and Aniksztejn, L. (2002). Paracrine intercellular communication by a Ca2+- and SNARE-independent release of GABA and glutamate prior to synapse formation. Neuron 36, 1051–1061. doi:10.1016/s0896-6273(02)01053-x
De Sarro, G., Gitto, R., Rizzo, M., Zappia, M., and De Sarro, A. (1996). 1,4-Benzodiazepine derivatives as anticonvulsant agents in DBA/2 mice. Gen. Pharmacol. 27, 935–941. doi:10.1016/0306-3623(95)02147-7
Elterman, R. D., Shields, W. D., Bittman, R. M., Torri, S. A., Sagar, S. M., and Collins, S. D. (2010). Vigabatrin for the treatment of infantile spasms: final report of a randomized trial. J. Child. Neurol. 25, 1340–1347. doi:10.1177/0883073810365103
Elterman, R. D., Shields, W. D., Mansfield, K. A., and Nakagawa, J.U.S.I.S.V.S. Group (2001). Randomized trial of vigabatrin in patients with infantile spasms. Neurology 57, 1416–1421. doi:10.1212/wnl.57.8.1416
Engin, E. (2022). GABA(A) receptor subtypes and benzodiazepine use, misuse, and abuse. Front. Psychiatry 13, 1060949. doi:10.3389/fpsyt.2022.1060949
Engin, E., Benham, R. S., and Rudolph, U. (2018). An emerging circuit pharmacology of GABA(A) receptors. Trends Pharmacol. Sci. 39, 710–732. doi:10.1016/j.tips.2018.04.003
Enz, R., and Cutting, G. R. (1999). GABAC receptor rho subunits are heterogeneously expressed in the human CNS and form homo- and heterooligomers with distinct physical properties. Eur. J. Neurosci. 11, 41–50. doi:10.1046/j.1460-9568.1999.00423.x
Farrant, M., and Kaila, K. (2007). The cellular, molecular and ionic basis of GABA(A) receptor signalling. Prog. Brain Res. 160, 59–87. doi:10.1016/S0079-6123(06)60005-8
Farrant, M., and Nusser, Z. (2005). Variations on an inhibitory theme: phasic and tonic activation of GABA(A) receptors. Nat. Rev. Neurosci. 6, 215–229. doi:10.1038/nrn1625
Fedi, M., Berkovic, S. F., Marini, C., Mulligan, R., Tochon-Danguy, H., and Reutens, D. C. (2006). A GABAA receptor mutation causing generalized epilepsy reduces benzodiazepine receptor binding. Neuroimage 32, 995–1000. doi:10.1016/j.neuroimage.2006.05.059
French, J., Biton, V., Dave, H., Detyniecki, K., Gelfand, M. A., Gong, H., et al. (2023). A randomized phase 2b efficacy study in patients with seizure episodes with a predictable pattern using Staccato® alprazolam for rapid seizure termination. Epilepsia 64, 374–385. doi:10.1111/epi.17441
French, J. A., Mosier, M., Walker, S., Sommerville, K., and Sussman, N. (1996). A double-blind, placebo-controlled study of vigabatrin three g/day in patients with uncontrolled complex partial seizures. Vigabatrin Protocol 024 Investigative Cohort. Neurology 46, 54–61. doi:10.1212/wnl.46.1.54
French, J. A., Wechsler, R., Gelfand, M. A., Pollard, J. R., Vazquez, B., Friedman, D., et al. (2019). Inhaled alprazolam rapidly suppresses epileptic activity in photosensitive participants. Epilepsia 60, 1602–1609. doi:10.1111/epi.16279
Ge, Y., Kang, Y., Cassidy, R. M., Moon, K. M., Lewis, R., Wong, R. O. L., et al. (2018). Clptm1 limits forward trafficking of GABA(A) receptors to scale inhibitory synaptic strength. Neuron 97, 596–610. doi:10.1016/j.neuron.2017.12.038
Gingrich, K. J., Roberts, W. A., and Kass, R. S. (1995). Dependence of the GABAA receptor gating kinetics on the alpha-subunit isoform: implications for structure-function relations and synaptic transmission. J. Physiol. 489 (2), 529–543. doi:10.1113/jphysiol.1995.sp021070
Glauser, T. A., Cnaan, A., Shinnar, S., Hirtz, D. G., Dlugos, D., Masur, D., et al. (2010). Ethosuximide, valproic acid, and lamotrigine in childhood absence epilepsy. N. Engl. J. Med. 362, 790–799. doi:10.1056/NEJMoa0902014
Glykys, J., and Mody, I. (2007). Activation of GABAA receptors: views from outside the synaptic cleft. Neuron 56, 763–770. doi:10.1016/j.neuron.2007.11.002
Groen, M. R., Paulsen, O., Perez-Garci, E., Nevian, T., Wortel, J., Dekker, M. P., et al. (2014). Development of dendritic tonic GABAergic inhibition regulates excitability and plasticity in CA1 pyramidal neurons. J. Neurophysiol. 112, 287–299. doi:10.1152/jn.00066.2014
Gurrell, R., Gorman, D., Whitlock, M., Ogden, A., Reynolds, D. S., Diventura, B., et al. (2019). Photosensitive epilepsy: robust clinical efficacy of a selective GABA potentiator. Neurology 92, e1786–e1795. doi:10.1212/WNL.0000000000007271
Gurrell, R., Iredale, P., Evrard, A., Duveau, V., Ruggiero, C., and Roucard, C. (2022). Pronounced antiseizure activity of the subtype-selective GABA(A) positive allosteric modulator darigabat in a mouse model of drug-resistant focal epilepsy. CNS Neurosci. Ther. 28, 1875–1882. doi:10.1111/cns.13927
Han, W., Li, J., Pelkey, K. A., Pandey, S., Chen, X., Wang, Y. X., et al. (2019). Shisa7 is a GABA(A) receptor auxiliary subunit controlling benzodiazepine actions. Science 366, 246–250. doi:10.1126/science.aax5719
Han, W., Shepard, R. D., and Lu, W. (2021). Regulation of GABA(A)rs by transmembrane accessory proteins. Trends Neurosci. 44, 152–165. doi:10.1016/j.tins.2020.10.011
Harkin, L. A., Bowser, D. N., Dibbens, L. M., Singh, R., Phillips, F., Wallace, R. H., et al. (2002). Truncation of the GABA(A)-receptor gamma2 subunit in a family with generalized epilepsy with febrile seizures plus. Am. J. Hum. Genet. 70, 530–536. doi:10.1086/338710
Hausser, M., and Clark, B. A. (1997). Tonic synaptic inhibition modulates neuronal output pattern and spatiotemporal synaptic integration. Neuron 19, 665–678. doi:10.1016/s0896-6273(00)80379-7
Hosie, A. M., Wilkins, M. E., and Smart, T. G. (2007). Neurosteroid binding sites on GABA(A) receptors. Pharmacol. Ther. 116, 7–19. doi:10.1016/j.pharmthera.2007.03.011
Huang, X., Hernandez, C. C., Hu, N., and Macdonald, R. L. (2014). Three epilepsy-associated GABRG2 missense mutations at the γ+/β-interface disrupt GABAA receptor assembly and trafficking by similar mechanisms but to different extents. Neurobiol. Dis. 68, 167–179. doi:10.1016/j.nbd.2014.04.015
Jankovic, S. M., Djesevic, M., and Jankovic, S. V. (2021). Experimental GABA A receptor agonists and allosteric modulators for the treatment of focal epilepsy. J. Exp. Pharmacol. 13, 235–244. doi:10.2147/JEP.S242964
Jenck, F., Moreau, J. L., Bonetti, E. P., Martin, J. R., and Haefely, W. E. (1992). Ro 19-8022, a nonbenzodiazepine partial agonist at benzodiazepine receptors: neuropharmacological profile of a potential anxiolytic. J. Pharmacol. Exp. Ther. 262, 1121–1127.
Johannesen, K. M., Iqbal, S., Guazzi, M., Mohammadi, N. A., Perez-Palma, E., Schaefer, E., et al. (2022). Structural mapping of GABRB3 variants reveals genotype-phenotype correlations. Genet. Med. 24, 681–693. doi:10.1016/j.gim.2021.11.004
Kaila, K., Ruusuvuori, E., Seja, P., Voipio, J., and Puskarjov, M. (2014). GABA actions and ionic plasticity in epilepsy. Curr. Opin. Neurobiol. 26, 34–41. doi:10.1016/j.conb.2013.11.004
Kaminski, R. M., Gasior, M., Carter, R. B., and Witkin, J. M. (2003). Protective efficacy of neuroactive steroids against cocaine kindled-seizures in mice. Eur. J. Pharmacol. 474, 217–222. doi:10.1016/s0014-2999(03)02086-7
Kananura, C., Haug, K., Sander, T., Runge, U., Gu, W., Hallmann, K., et al. (2002). A splice-site mutation in GABRG2 associated with childhood absence epilepsy and febrile convulsions. Arch. Neurol. 59, 1137–1141. doi:10.1001/archneur.59.7.1137
Kang, J. Q., Shen, W., Zhou, C., Xu, D., and Macdonald, R. L. (2015). The human epilepsy mutation GABRG2(Q390X) causes chronic subunit accumulation and neurodegeneration. Nat. Neurosci. 18, 988–996. doi:10.1038/nn.4024
Kienitz, R., Kay, L., Beuchat, I., Gelhard, S., Von Brauchitsch, S., Mann, C., et al. (2022). Benzodiazepines in the management of seizures and status epilepticus: a review of routes of delivery, pharmacokinetics, efficacy, and tolerability. CNS Drugs 36, 951–975. doi:10.1007/s40263-022-00940-2
Knight, E. M. P., Amin, S., Bahi-Buisson, N., Benke, T. A., Cross, J. H., Demarest, S. T., et al. (2022). Safety and efficacy of ganaxolone in patients with CDKL5 deficiency disorder: results from the double-blind phase of a randomised, placebo-controlled, phase 3 trial. Lancet Neurol. 21, 417–427. doi:10.1016/S1474-4422(22)00077-1
Komulainen-Ebrahim, J., Schreiber, J. M., Kangas, S. M., Pylkas, K., Suo-Palosaari, M., Rahikkala, E., et al. (2019). Novel variants and phenotypes widen the phenotypic spectrum of GABRG2-related disorders. Seizure 69, 99–104. doi:10.1016/j.seizure.2019.03.010
Krauss, G. L., Klein, P., Brandt, C., Lee, S. K., Milanov, I., Milovanovic, M., et al. (2020). Safety and efficacy of adjunctive cenobamate (YKP3089) in patients with uncontrolled focal seizures: a multicentre, double-blind, randomised, placebo-controlled, dose-response trial. Lancet Neurol. 19, 38–48. doi:10.1016/S1474-4422(19)30399-0
Lahat, E., Goldman, M., Barr, J., Bistritzer, T., and Berkovitch, M. (2000). Comparison of intranasal midazolam with intravenous diazepam for treating febrile seizures in children: prospective randomised study. BMJ 321, 83–86. doi:10.1136/bmj.321.7253.83
Lattanzi, S., Trinka, E., Zaccara, G., Striano, P., Del Giovane, C., Silvestrini, M., et al. (2020). Adjunctive cenobamate for focal-onset seizures in adults: a systematic review and meta-analysis. CNS Drugs 34, 1105–1120. doi:10.1007/s40263-020-00759-9
Leclercq, K., Matagne, A., Provins, L., Klitgaard, H., and Kaminski, R. M. (2020). Pharmacological profile of the novel antiepileptic drug candidate padsevonil: characterization in rodent seizure and epilepsy models. J. Pharmacol. Exp. Ther. 372, 11–20. doi:10.1124/jpet.119.261222
Loscher, W. (1999). Valproate: a reappraisal of its pharmacodynamic properties and mechanisms of action. Prog. Neurobiol. 58, 31–59. doi:10.1016/s0301-0082(98)00075-6
Loturco, J. J., Owens, D. F., Heath, M. J., Davis, M. B., and Kriegstein, A. R. (1995). GABA and glutamate depolarize cortical progenitor cells and inhibit DNA synthesis. Neuron 15, 1287–1298. doi:10.1016/0896-6273(95)90008-x
Luder, A. S., Parks, J. K., Frerman, F., and Parker, W. D. (1990). Inactivation of beef brain alpha-ketoglutarate dehydrogenase complex by valproic acid and valproic acid metabolites. Possible mechanism of anticonvulsant and toxic actions. J. Clin. Invest. 86, 1574–1581. doi:10.1172/JCI114877
Mackenzie, G., and Maguire, J. (2013). Neurosteroids and GABAergic signaling in health and disease. Biomol. Concepts 4, 29–42. doi:10.1515/bmc-2012-0033
Maher, M. P., Matta, J. A., Gu, S., Seierstad, M., and Bredt, D. S. (2017). Getting a handle on Neuropharmacology by targeting receptor-associated proteins. Neuron 96, 989–1001. doi:10.1016/j.neuron.2017.10.001
Mahmoudian, T., and Zadeh, M. M. (2004). Comparison of intranasal midazolam with intravenous diazepam for treating acute seizures in children. Epilepsy Behav. 5, 253–255. doi:10.1016/j.yebeh.2004.01.003
Maillard, P. Y., Baer, S., Schaefer, E., Desnous, B., Villeneuve, N., Lepine, A., et al. (2022). Molecular and clinical descriptions of patients with GABA(A) receptor gene variants (GABRA1, GABRB2, GABRB3, GABRG2): a cohort study, review of literature, and genotype-phenotype correlation. Epilepsia 63, 2519–2533. doi:10.1111/epi.17336
Marson, A., Burnside, G., Appleton, R., Smith, D., Leach, J. P., Sills, G., et al. (2021). The SANAD II study of the effectiveness and cost-effectiveness of levetiracetam, zonisamide, or lamotrigine for newly diagnosed focal epilepsy: an open-label, non-inferiority, multicentre, phase 4, randomised controlled trial. Lancet 397, 1363–1374. doi:10.1016/S0140-6736(21)00247-6
Marson, A. G., Al-Kharusi, A. M., Alwaidh, M., Appleton, R., Baker, G. A., Chadwick, D. W., et al. (2007). The SANAD study of effectiveness of valproate, lamotrigine, or topiramate for generalised and unclassifiable epilepsy: an unblinded randomised controlled trial. Lancet 369, 1016–1026. doi:10.1016/S0140-6736(07)60461-9
Meng, J., Yan, Z., Tao, X., Wang, W., Wang, F., Xue, T., et al. (2023). The efficacy and safety of ganaxolone for the treatment of refractory epilepsy: a meta-analysis from randomized controlled trials. Epilepsia Open 8, 90–99. doi:10.1002/epi4.12669
Mierzewska, H., Laure-Kamionowska, M., Jezela-Stanek, A., Rydzanicz, M., Ploski, R., and Szczepanik, E. (2021). The neuropathological findings of developmental and epileptic encephalopathy-43 (DEE43) and delineation of a the molecular spectrum of novel case. Seizure 93, 75–80. doi:10.1016/j.seizure.2021.10.014
Nakamura, M., Cho, J. H., Shin, H., and Jang, I. S. (2019). Effects of cenobamate (YKP3089), a newly developed anti-epileptic drug, on voltage-gated sodium channels in rat hippocampal CA3 neurons. Eur. J. Pharmacol. 855, 175–182. doi:10.1016/j.ejphar.2019.05.007
Nakken, K. O., and Lossius, M. I. (2011). Buccal midazolam or rectal diazepam for treatment of residential adult patients with serial seizures or status epilepticus. Acta Neurol. Scand. 124, 99–103. doi:10.1111/j.1600-0404.2010.01474.x
Nickels, K. C., and Wirrell, E. C. (2017). Stiripentol in the management of epilepsy. CNS Drugs 31, 405–416. doi:10.1007/s40263-017-0432-1
Nickolls, S. A., Gurrell, R., Van Amerongen, G., Kammonen, J., Cao, L., Brown, A. R., et al. (2018). Pharmacology in translation: the preclinical and early clinical profile of the novel α2/3 functionally selective GABAA receptor positive allosteric modulator PF-06372865. Br. J. Pharmacol. 175, 708–725. doi:10.1111/bph.14119
Niespodziany, I., Ghisdal, P., Mullier, B., Wood, M., Provins, L., Kaminski, R. M., et al. (2020). Functional characterization of the antiepileptic drug candidate, padsevonil, on GABA(A) receptors. Epilepsia 61, 914–923. doi:10.1111/epi.16497
Nolan, S. J., Tudur Smith, C., Pulman, J., and Marson, A. G. (2013). Phenobarbitone versus phenytoin monotherapy for partial onset seizures and generalised onset tonic-clonic seizures. Cochrane Database Syst. Rev., CD002217. doi:10.1002/14651858.CD002217
Olah, S., Fule, M., Komlosi, G., Varga, C., Baldi, R., Barzo, P., et al. (2009). Regulation of cortical microcircuits by unitary GABA-mediated volume transmission. Nature 461, 1278–1281. doi:10.1038/nature08503
Olsen, R. W., and Sieghart, W. (2008). International Union of Pharmacology. LXX. Subtypes of gamma-aminobutyric acid(A) receptors: classification on the basis of subunit composition, pharmacology, and function. Update. Pharmacol. Rev. 60, 243–260. doi:10.1124/pr.108.00505
Olsen, R. W., and Sieghart, W. (2009). GABA A receptors: subtypes provide diversity of function and pharmacology. Neuropharmacology 56, 141–148. doi:10.1016/j.neuropharm.2008.07.045
Owen, R. M., Blakemore, D., Cao, L., Flanagan, N., Fish, R., Gibson, K. R., et al. (2019). Design and identification of a novel, functionally subtype selective GABA(A) positive allosteric modulator (PF-06372865). J. Med. Chem. 62, 5773–5796. doi:10.1021/acs.jmedchem.9b00322
Owens, D. F., Liu, X., and Kriegstein, A. R. (1999). Changing properties of GABA(A) receptor-mediated signaling during early neocortical development. J. Neurophysiol. 82, 570–583. doi:10.1152/jn.1999.82.2.570
Pena-Ceballos, J., Moloney, P. B., Munteanu, T., Doyle, M., Colleran, N., Liggan, B., et al. (2023). Adjunctive cenobamate in highly active and ultra-refractory focal epilepsy: a "real-world" retrospective study. Epilepsia 64, 1225–1235. doi:10.1111/epi.17549
Perucca, E., Bialer, M., and White, H. S. (2023a). New GABA-Targeting Therapies for the Treatment of Seizures and Epilepsy: I. Role of GABA as a Modulator of Seizure Activity and Recently Approved Medications Acting on the GABA System. CNS Drugs 37 (9), 755–779. doi:10.1007/s40263-023-01027-2
Perucca, E., White, H. S., and Bialer, M. (2023b). New GABA-Targeting Therapies for the Treatment of Seizures and Epilepsy: II. Treatments in Clinical Development. CNS Drugs 37 (9), 781–795. doi:10.1007/s40263-023-01025-4
Porcello, D. M., Huntsman, M. M., Mihalek, R. M., Homanics, G. E., and Huguenard, J. R. (2003). Intact synaptic GABAergic inhibition and altered neurosteroid modulation of thalamic relay neurons in mice lacking delta subunit. J. Neurophysiol. 89, 1378–1386. doi:10.1152/jn.00899.2002
Purdy, R. H., Morrow, A. L., Moore, P. H., and Paul, S. M. (1991). Stress-induced elevations of gamma-aminobutyric acid type A receptor-active steroids in the rat brain. Proc. Natl. Acad. Sci. U. S. A. 88, 4553–4557. doi:10.1073/pnas.88.10.4553
Qu, S., Zhou, C., Howe, R., Shen, W., Huang, X., Catron, M., et al. (2021). The K328M substitution in the human GABA(A) receptor gamma2 subunit causes GEFS+ and premature sudden death in knock-in mice. Neurobiol. Dis. 152, 105296. doi:10.1016/j.nbd.2021.105296
Quilichini, P. P., Chiron, C., Ben-Ari, Y., and Gozlan, H. (2006). Stiripentol, a putative antiepileptic drug, enhances the duration of opening of GABA-A receptor channels. Epilepsia 47, 704–716. doi:10.1111/j.1528-1167.2006.00497.x
Rademacher, M., Toledo, M., Van Paesschen, W., Liow, K. K., Milanov, I. G., Esch, M. L., et al. (2022). Efficacy and safety of adjunctive padsevonil in adults with drug-resistant focal epilepsy: results from two double-blind, randomized, placebo-controlled trials. Epilepsia Open 7, 758–770. doi:10.1002/epi4.12656
Reddy, D. S. (2013). Role of hormones and neurosteroids in epileptogenesis. Front. Cell Neurosci. 7, 115. doi:10.3389/fncel.2013.00115
Reddy, D. S., and Estes, W. A. (2016). Clinical potential of neurosteroids for CNS disorders. Trends Pharmacol. Sci. 37, 543–561. doi:10.1016/j.tips.2016.04.003
Reddy, D. S., and Rogawski, M. A. (2009). Neurosteroid replacement therapy for catamenial epilepsy. Neurotherapeutics 6, 392–401. doi:10.1016/j.nurt.2009.01.006
Reddy, D. S., and Rogawski, M. A. (2010). Ganaxolone suppression of behavioral and electrographic seizures in the mouse amygdala kindling model. Epilepsy Res. 89, 254–260. doi:10.1016/j.eplepsyres.2010.01.009
Rho, J. M., and White, H. S. (2018). Brief history of anti-seizure drug development. Epilepsia Open 3, 114–119. doi:10.1002/epi4.12268
Richens, A., Chadwick, D. W., Duncan, J. S., Dam, M., Gram, L., Mikkelsen, M., et al. (1995). Adjunctive treatment of partial seizures with tiagabine: a placebo-controlled trial. Epilepsy Res. 21, 37–42. doi:10.1016/0920-1211(95)00006-v
Roberti, R., De Caro, C., Iannone, L. F., Zaccara, G., Lattanzi, S., and Russo, E. (2021). Pharmacology of cenobamate: mechanism of action, pharmacokinetics, drug-drug interactions and tolerability. CNS Drugs 35, 609–618. doi:10.1007/s40263-021-00819-8
Rosenfeld, W. E., Nisman, A., and Ferrari, L. (2021). Efficacy of adjunctive cenobamate based on number of concomitant antiseizure medications, seizure frequency, and epilepsy duration at baseline: a post-hoc analysis of a randomized clinical study. Epilepsy Res. 172, 106592. doi:10.1016/j.eplepsyres.2021.106592
Saporito, M. S., Gruner, J. A., Dicamillo, A., Hinchliffe, R., Barker-Haliski, M., and White, H. S. (2019). Intravenously administered ganaxolone blocks diazepam-resistant lithium-pilocarpine-induced status epilepticus in rats: comparison with allopregnanolone. J. Pharmacol. Exp. Ther. 368, 326–337. doi:10.1124/jpet.118.252155
Scott, R. C., Besag, F. M., and Neville, B. G. (1999). Buccal midazolam and rectal diazepam for treatment of prolonged seizures in childhood and adolescence: a randomised trial. Lancet 353, 623–626. doi:10.1016/S0140-6736(98)06425-3
Semyanov, A., Walker, M. C., and Kullmann, D. M. (2003). GABA uptake regulates cortical excitability via cell type-specific tonic inhibition. Nat. Neurosci. 6, 484–490. doi:10.1038/nn1043
Sharma, R., Nakamura, M., Neupane, C., Jeon, B. H., Shin, H., Melnick, S. M., et al. (2020). Positive allosteric modulation of GABA(A) receptors by a novel antiepileptic drug cenobamate. Eur. J. Pharmacol. 879, 173117. doi:10.1016/j.ejphar.2020.173117
Sieghart, W., Fuchs, K., Tretter, V., Ebert, V., Jechlinger, M., Hoger, H., et al. (1999). Structure and subunit composition of GABA(A) receptors. Neurochem. Int. 34, 379–385. doi:10.1016/s0197-0186(99)00045-5
Sigel, E., and Steinmann, M. E. (2012). Structure, function, and modulation of GABA(A) receptors. J. Biol. Chem. 287, 40224–40231. doi:10.1074/jbc.R112.386664
Sikes-Keilp, C., and Rubinow, D. R. (2023). GABA-Ergic modulators: new therapeutic approaches to premenstrual dysphoric disorder. CNS Drugs 37, 679–693. doi:10.1007/s40263-023-01030-7
Silbergleit, R., Durkalski, V., Lowenstein, D., Conwit, R., Pancioli, A., Palesch, Y., et al. (2012). Intramuscular versus intravenous therapy for prehospital status epilepticus. N. Engl. J. Med. 366, 591–600. doi:10.1056/NEJMoa1107494
Stephens, D. N., King, S. L., Lambert, J. J., Belelli, D., and Duka, T. (2017). GABA(A) receptor subtype involvement in addictive behaviour. Genes Brain Behav. 16, 149–184. doi:10.1111/gbb.12321
Street, J. S., Qiu, Y., and Lignani, G. (2023). Are genetic therapies for epilepsy ready for the clinic? Epilepsy Curr. 23, 245–250. doi:10.1177/15357597231176234
Tanenhaus, A., Stowe, T., Young, A., Mclaughlin, J., Aeran, R., Lin, I. W., et al. (2022). Cell-selective adeno-associated virus-mediated SCN1A gene regulation therapy rescues mortality and seizure phenotypes in a Dravet syndrome mouse model and is well tolerated in nonhuman primates. Hum. Gene Ther. 33, 579–597. doi:10.1089/hum.2022.037
Tang, Z. Q., Dinh, E. H., Shi, W., and Lu, Y. (2011). Ambient GABA-activated tonic inhibition sharpens auditory coincidence detection via a depolarizing shunting mechanism. J. Neurosci. 31, 6121–6131. doi:10.1523/JNEUROSCI.4733-10.2011
Tian, M., Mei, D., Freri, E., Hernandez, C. C., Granata, T., Shen, W., et al. (2013). Impaired surface αβγ GABA(A) receptor expression in familial epilepsy due to a GABRG2 frameshift mutation. Neurobiol. Dis. 50, 135–141. doi:10.1016/j.nbd.2012.10.008
Todd, E., Gurba, K. N., Botzolakis, E. J., Stanic, A. K., and Macdonald, R. L. (2014). GABAA receptor biogenesis is impaired by the γ2 subunit febrile seizure-associated mutation, GABRG2(R177G). Neurobiol. Dis. 69, 215–224. doi:10.1016/j.nbd.2014.05.013
Tossell, K., Dodhia, R. A., Galet, B., Tkachuk, O., and Ungless, M. A. (2021). Tonic GABAergic inhibition, via GABAA receptors containing αβƐ subunits, regulates excitability of ventral tegmental area dopamine neurons. Eur. J. Neurosci. 53, 1722–1737. doi:10.1111/ejn.15133
Treiman, D. M., Meyers, P. D., Walton, N. Y., Collins, J. F., Colling, C., Rowan, A. J., et al. (1998). A comparison of four treatments for generalized convulsive status epilepticus. Veterans Affairs Status Epilepticus Cooperative Study Group. N. Engl. J. Med. 339, 792–798. doi:10.1056/NEJM199809173391202
Tremblay, R., Lee, S., and Rudy, B. (2016). GABAergic interneurons in the neocortex: from cellular properties to circuits. Neuron 91, 260–292. doi:10.1016/j.neuron.2016.06.033
Uldall, P., Bulteau, C., Pedersen, S. A., Dulac, O., and Lyby, K. (2000). Tiagabine adjunctive therapy in children with refractory epilepsy: a single-blind dose escalating study. Epilepsy Res. 42, 159–168. doi:10.1016/s0920-1211(00)00173-x
Uthman, B. M., Rowan, A. J., Ahmann, P. A., Leppik, I. E., Schachter, S. C., Sommerville, K. W., et al. (1998). Tiagabine for complex partial seizures: a randomized, add-on, dose-response trial. Arch. Neurol. 55, 56–62. doi:10.1001/archneur.55.1.56
Vaitkevicius, H., Ramsay, R. E., Swisher, C. B., Husain, A. M., Aimetti, A., and Gasior, M. (2022). Intravenous ganaxolone for the treatment of refractory status epilepticus: results from an open-label, dose-finding, phase 2 trial. Epilepsia 63, 2381–2391. doi:10.1111/epi.17343
Valeyev, A. Y., Cruciani, R. A., Lange, G. D., Smallwood, V. S., and Barker, J. L. (1993). Cl-channels are randomly activated by continuous GABA secretion in cultured embryonic rat hippocampal neurons. Neurosci. Lett. 155, 199–203. doi:10.1016/0304-3940(93)90707-r
Vardya, I., Drasbek, K. R., Dosa, Z., and Jensen, K. (2008). Cell type-specific GABA A receptor-mediated tonic inhibition in mouse neocortex. J. Neurophysiol. 100, 526–532. doi:10.1152/jn.01224.2007
Wallace, R. H., Marini, C., Petrou, S., Harkin, L. A., Bowser, D. N., Panchal, R. G., et al. (2001). Mutant GABA(A) receptor gamma2-subunit in childhood absence epilepsy and febrile seizures. Nat. Genet. 28, 49–52. doi:10.1038/ng0501-49
Warner, T. A., Smith, N. K., and Kang, J. Q. (2019). The therapeutic effect of stiripentol in Gabrg2(+/Q390X) mice associated with epileptic encephalopathy. Epilepsy Res. 154, 8–12. doi:10.1016/j.eplepsyres.2019.04.006
Witkin, J. M., Lippa, A., Smith, J. L., Jin, X., Ping, X., Biggerstaff, A., et al. (2022). The imidazodiazepine, KRM-II-81: an example of a newly emerging generation of GABAkines for neurological and psychiatric disorders. Pharmacol. Biochem. Behav. 213, 173321. doi:10.1016/j.pbb.2021.173321
Wood, M., Daniels, V., Provins, L., Wolff, C., Kaminski, R. M., and Gillard, M. (2020). Pharmacological profile of the novel antiepileptic drug candidate padsevonil: interactions with synaptic vesicle 2 proteins and the GABA(A) receptor. J. Pharmacol. Exp. Ther. 372, 1–10. doi:10.1124/jpet.119.261149
Keywords: benzodiazepines, epilepsy, GABA A receptor, GABA allosteric modulators a, neurosteriod, antisense, oligonucleotide-drug conjugates
Citation: Richardson RJ, Petrou S and Bryson A (2024) Established and emerging GABAA receptor pharmacotherapy for epilepsy. Front. Pharmacol. 15:1341472. doi: 10.3389/fphar.2024.1341472
Received: 20 November 2023; Accepted: 07 February 2024;
Published: 21 February 2024.
Edited by:
Wei Lu, National Institute of Neurological Disorders and Stroke (NIH), United StatesReviewed by:
Kinga Aurelia Gawel, Medical University of Lublin, PolandCopyright © 2024 Richardson, Petrou and Bryson. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Alexander Bryson, cm9iZXJ0LnJpY2hhcmRzb25AZmxvcmV5LmVkdS5hdQ==, YWxleGFuZGVyLmJyeXNvbkBmbG9yZXkuZWR1LmF1