Memory and Learning Deficits Are Associated With Ca2+ Dyshomeostasis in Normal Aging

Neuronal intracellular Ca²⁺ homeostasis is critical to the normal physiological functions of neurons and neuronal Ca²⁺ dyshomeostasis has been associated with the age-related decline of cognitive functions. Accumulated evidence indicates that the underlying mechanism for this is that abnormal intracellular Ca²⁺ levels stimulate the dysregulation of intracellular signaling, which subsequently induces neuronal cell death. We examined intracellular Ca²⁺ homeostasis in cortical (in vivo) and hippocampal (in vitro) neurons from young (3-months), middle-age (12-months), and aged (24-months) wild type C57BL6J mice. We found a progressive age-related elevation of intracellular resting calcium ([Ca²⁺]_r) in cortical (in vivo) and hippocampal (in vitro) neurons associated with increased hippocampal neuronal calpain activity and reduced cell viability. In vitro, removal of extracellular Ca²⁺ or treatment with SAR7334 or dantrolene reduced [Ca²⁺]_r in all age groups and dantrolene treatment lowered calpain activity and increased cell viability. In vivo, both middle-aged and aged mice showed cognitive deficits compared to young mice, which improved after dantrolene treatment. These findings support the hypothesis that intracellular Ca²⁺ dyshomeostasis is a major mechanism underlying the cognitive deficits seen in both normal aging and degenerative neurologic diseases.

Introduction

Perturbations of intracellular Ca²⁺ concentration underlie the increased vulnerability of neurons to age-related processes like cognitive decline and degenerative neurological diseases including, Alzheimer’s and Parkinson’s disease (Disterhoft et al., 1994; Kirischuk and Verkhratsky, 1996; Lopez et al., 2008; Alzheimer’s Association Calcium Hypothesis, 2017; Kumar, 2020). The age-related cognitive decline includes impairment in retrieving intermediate-term memories, especially episodic memories that rely on spatial and temporal contexts (Tromp et al., 2015; Gollan and Goldrick, 2019). Emerging evidence supports the idea that a disruption of the mechanisms that normally regulate intracellular neuronal intracellular [Ca²⁺] plays a critical role in many of the neural dysfunctions underlying chronic brain disorders in aging (Thibault et al., 2007). Furthermore, the Ca²⁺ hypothesis states that intracellular Ca²⁺ dysfunction serves as a precursor and driver not only to aging-associated decrements in neuronal performance but also to the molecular mechanisms underlying neuronal degeneration.

Intracellular resting Ca²⁺ concentration ([Ca²⁺]_r) is maintained in neurons as a balance of the Ca²⁺ leak from the ryanodine receptor, the extrusion elicited by the plasma membrane Ca²⁺ pump, and sodium/calcium exchanger and plasmalemmal Ca²⁺ entry through the voltage-gated Ca²⁺ channels, transient receptor potential canonical (TRPC) channels, and the store-operated Ca²⁺ entry channels (Berridge et al., 2000; Eltit et al., 2010; Hill and Olson, 2012; Schwaller, 2012);(Wu et al., 2002; Tonkikh et al., 2006). For more than 35 years, evidence has been accumulating that brain aging is associated with dysregulation of intracellular calcium in neurons (Gibson and Peterson, 1987). Age-associated disruption in intracellular Ca²⁺ homeostasis has been related to several mechanisms that include enhanced L-type Ca²⁺ currents (Landfield, 1996; Thibault and Landfield, 1996), a decline in SERCA-mediated Ca²⁺ uptake by the endoplasmic reticulum (ER), oxidative modification of the inositol trisphosphate and ryanodine receptors (Kumar et al., 2018), a decreased expression of FKBP1b (Gant et al., 2015), and increased activity of calpains (Hinman et al., 2004), all of which might lead to an intracellular Ca²⁺ overload, protein degradation and neuronal death (Hinman et al., 2004).

However, the mechanisms governing this neuronal intracellular Ca²⁺ dysfunction and its potential link to cognitive impairment in aging are not fully understood, and consequently, this pathologic mechanism is not currently being targeted as a means of preventing or repairing cognitive dysfunction. Also, some of the potential pathways that could be involved in aging-mediated changes in intracellular [Ca²⁺] have not been fully studied. One of those Ca²⁺ pathways is the Ca²⁺ influx mediated by the transient receptor potential canonical (TRPC) channels (Liguori et al., 2018; Maria-Ferreira et al., 2020). TRPC proteins comprise nonselective cation channels in the sarcolemma that permit the permeability of Ca²⁺ and Na⁺ into the cells (Nilius and Szallasi, 2014). TRPC channels have been implicated in diverse neuronal physiological functions, but have also been linked with neurodegenerative processes (Bezprozvanny, 2009; Takada et al., 2013; Sukumaran et al., 2017; Maria-Ferreira et al., 2020). Another possible mechanism for increased intracellular [Ca²⁺] that may be involved in an increase in Ca²⁺ leak from the ER via ryanodine receptors (RyR; Lacampagne et al., 2017). Three mammalian isoforms of the RyR receptors have been described: RyR1, RyR2, and RyR3. Although all three isoforms can be found in the brain, the RyR2 isoform is the predominant isoform expressed in the cerebral cortex and the hippocampus (Giannini et al., 1995). An enhanced RyR Ca²⁺ leak has been postulated as contributing to Alzheimer pathogenesis, and pharmacological intervention to modify the leak normalized cognitive functions (Peng et al., 2012; Liang and Wei, 2015; Lacampagne et al., 2017).

The present study aimed to explore the involvement of ER Ca²⁺ leak via RyR receptors and the Ca²⁺ influx mediated by the TRPC channels on the resting intracellular Ca²⁺ dysregulation observed with aging. We hypothesized that: (i) aging is associated with a progressive increase in resting intracellular Ca²⁺ concentration ([Ca²⁺]_r) and Na⁺ ([Na⁺]_r); and (ii) pharmacological modification of either the ER-RyR1 leak or the Ca²⁺ influx mediated by TRPCs channels will reduce resting [Ca²⁺]_r and [Na⁺]_r and revert aging-related cognitive deficits.

Materials and Methods

Animals

Male and female 3–4-months (Young), 12–14-months (Middle Age), and 24–26-months (Aged) C57BL6J mice obtained from breeding colonies at the Mount Sinai Medical Center, from founders initially obtained from the Jackson Laboratory (Bar Harbor, ME, USA) were used as experimental models. The three mice ages: young, middle age, and aged were selected to be the equivalent to approximately 10, 40, and 80 human years based on the fact that one human year is equivalent to nine mice days (Dutta and Sengupta, 2016). Despite the vast differences in their lifespan, humans and mice show similar molecular mechanisms of aging (Demetrius, 2006). Mice were accommodated four per cage with food and water available ad libitum and were maintained on a 12 h light/dark cycle. All protocols used in the study were performed following the recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health and were approved by the institutional IACUCs were the animal experiments were performed.

Anesthesia

For in vivo experiments mice fasted (6 h), and water was withheld for 1 h before anesthesia. Mice were anesthetized with ketamine/xylazine (100/5 mg/kg body weight) and then placed on a temperature-controlled pad. Its nose was inserted into an anesthesia mask (Kent Scientific, Torrington, CT, USA) and all mice inhaled ultra-pure grade air (Airgas, Miami, FL, USA) and were allowed to breathe spontaneously. The vital signs (respiratory rate, heart rate, oxygen saturation, and rectal temperature) were monitored throughout the procedure. Tail and/or toe pinches were used to ensure the animal was fully anesthetized throughout the investigative procedures. Body temperatures were maintained between 36.9 and 37.3°C using a Peltier thermostatic low noise temperature controller ATC2000 (WPI, Sarasota, FL, USA) with feedback control from a rectal probe.

Surgical Procedures

Anesthetized mice were placed in a stereotaxic frame, and the head was firmly secured with the ear bars. Eye ointment was applied to prevent the animal’s eye from drying out. Dexamethasone (0.2 mg/Kg) was administered subcutaneously to prevent brain swelling. Pilot experiments show that dexamethasone at the dose used in the present study does not modify neuronal [Ca²⁺]_r (data not shown). After shaving and disinfection of the surgical site, the skin above the frontal-parietal temporal lobes was removed, and a mixture of lidocaine and epinephrine solution was injected into the periosteum to avoid bleeding and to reduce pain. A small circle of about 1 cm in diameter etched away with the aid of a pneumatic dental drill. The drilling was stopped when a very thin layer of bone was left. By pushing gently in the center of the draw circle, and the aid of small forceps, the remaining bone was removed from the skull. Gelfoam sponge was used in case of bleeding. Petrolatum was deposited around the craniotomy to create a “chamber,” which was filled and continuously perfused at a rate of 3–5 ml/min with warm sterile artificial cerebrospinal fluid (ACSF) equilibrated with a 95/5/% O₂/CO₂ mixture.

Ca²⁺-Selective Microelectrodes

Double-barreled Ca²⁺-selective microelectrodes were prepared and individually calibrated as described previously (Eltit et al., 2013). Ca²⁺ ionophore II (ETH 129; Fluka Sigma–Aldrich, St. Louis, MO, USA) was used to backfill the Ca²⁺-selective microelectrode. Resting membrane potential (Vm) and Ca²⁺ potentials were recorded via a high impedance amplifier (FD-223-WPI, Sarasota, FL, USA), as described previously (Lopez et al., 2018b). After obtaining measurements of resting [Ca²⁺]_r, all microelectrodes were recalibrated. If the initial and final calibration curves did not agree within 3 mV, data from that microelectrode were discarded.

Measurements and Recording of [Ca²⁺]_r in vivo

The pre-calibrated Ca²⁺-selective microelectrode was gently lowered to make contact with the artificial cerebrospinal fluid that filled the petrolatum chamber around the craniotomy using a three-axis micromanipulator. The microelectrode was then repositioned under direct visualization with the stereomicroscope. Neuron impalement was carried out under “blind conditions.” We were able to differentiate neurons from glial cells and astrocytes based on their resting membrane potential (Vm). Glial cells and astrocytes had a resting Vm in the vicinity of −58 mV while intact healthy neurons have a more polarized Vm which is equal to or more negative than −65 mV. Criteria for successful impalement included an abrupt drop to a steady level of Vm equal to or more negative than −65 mV, a stable recording of both Vm and Ca²⁺ potential for more than 1 min and an abrupt return to baseline on the exit of the microelectrode from the cell. Since encountering a cortical neuron was a random process, multiple attempts were conducted until a neuron that met the above criteria was found and remained quiescent (no spontaneous firing) during the recording. If the neuron was not quiescent the electrode was removed, and an alternative neuron found for the recording.

Preparation of Primary Hippocampal Pyramidal Neurons

Young, middle-aged, and aged mice were euthanized by cervical dislocation, and primary hippocampal pyramidal neurons were prepared as previously described (Robin et al., 2017). It is well established that most of the cognitive process depends upon proper hippocampal function, and that hippocampal function appears to be particularly age-sensitive(Foster, 1999). All experiments were conducted on neurons cultured for 7 days at 37°C, 5% CO₂, and room air.

Measurements and Recording of [Ca²⁺]_r and [Na⁺]_r in vitro

Resting intracellular Ca²⁺ and Na⁺ concentrations ([Ca²⁺]_r and [Na⁺]_r) were measured in isolated hippocampal pyramidal neurons from young, middle-aged, and aged mice using double/barreled Ca²⁺-and Na⁺-selective microelectrodes as previously described (Lopez et al., 2005; Eltit et al., 2013; Robin et al., 2017). Vm, Ca²⁺, and Na⁺ potentials were recorded via a high impedance amplifier (WPI FD-223; Word Precision Instruments, Sarasota, FL, USA) as described previously (Lopez et al., 2018b). All experiments were carried out at 37°C.

Calpain Activity

Calpain I and II activity were assessed in hippocampal neurons isolated from young, middle-aged, and aged mice using the Calpain-Glo protease assay (Promega, Madison, WI, USA). Neurons were incubated with the Calpain-Glo reagent for 10 min at 37°C, and luminescence was measured using a Synergy 2 plate reader (BioTek, Winooski, VT, USA). Intensity values for middle-aged and aged neurons are reported normalized to values from young neurons.

Neuronal Viability

Viability was determined in primary hippocampal neuron cultures using the 3-(4,5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide (MTT) assay according to the manufacturer’s protocol. After washing, neurons were incubated with 0.5 mg/ml MTT (Sigma–Aldrich, St. Louis, MO, USA) solution at 37 °C for 4 h. The medium was removed, and then 150 μl DMSO was added to each well and mixed thoroughly to dissolve the generated formazan. Data collected from young, middle-aged, and aged mice are represented as a reduction in MTT concentration relative to neurons from young mice.

Morris Water Maze

Cognitive function was determined using the Morris water maze (MWM) test (Morris, 1984; Sesay et al., 1996; Vaillend et al., 2004; Handattu et al., 2009; Faes et al., 2010; Lopez et al., 2018b). Young, middle-aged, and aged mice received three trials per day, with an inter-session interval of 30 min for four consecutive training days. After every trial, each mouse was towel-dried and kept warm with a heat lamp before being returned to its home cage, where it had free access to food and water. Mice were allowed to swim for 80 s or until the platform was reached. In the case where the mouse did not find the platform, it was guided to the platform and allow to stay there for a short period. Upon completion of the 4 days training period (TP) on day 5, the platform was removed to allow for probe testing. Three parameters were measured: (a) the escape latency time (ELT; time taken by each mouse to reach the site where the platform had been located), which was used as an index of acquisition or learning. The less time it took a mice to reach the site where the platform had been located, the better the learning ability; (b) the time spent by the mice in the target quadrant (TTQ)—in which was the platform previously located; and (c) the number of times the mouse crossed over the area where the platform was previously hidden (NETQ). The experiments were conducted in the morning between 9 am and 11 am. The behavior of the mice in the pool was recorded by a video tracking system (WatermazeScan, Reston, VA, USA) and stored for later analysis.

The Morris learning test was conducted in young, middle-aged and aged mice, which were divided randomly into two groups: Group 1: Testing the effect of aging on spatial learning and memory. Young (n_mice = 5), middle-aged (n_mice = 5), and aged mice (n_mice = 5) did not receive any treatment before or during the TP (TP) and/or probe trial (PT); Group 2: Testing the effect of dantrolene on cognitive abilities. All mice received dantrolene (DANT; 1 mg/kg, i.p.) for 5 days. before and every day during the TP and PT periods (n_mice = 5 mice per age group). The dantrolene dose used (1 mg/kg, i.p.) was chosen based on the fact that in preliminary studies we were able to show that this dose significantly reduced neuronal [Ca²⁺]_r but did not interfere with the ability of the mice to swim (unpublished observations).

Solutions

The sterile artificial cerebrospinal fluid (ACSF) used for in vivo studies contained in (mM) 135 NaCl, 1.8 KCl, 26 NaHCO₃, 1.25 NaH₂PO₄, 2 CaCl₂, 1 MgCl₂, and 5 glucose (pH 7.4; when bubbled with 95% O₂ and 5% CO₂). Ringer-Locke’s solution used for in vitro studies contained the following (in mM): 135 NaCl, 5 KCl, 2 CaCl₂, 1 MgCl₂, 5 glucose, tetrodotoxin (TTX 1.5 μM), 3.6 NaHCO₃ (pH 7.4). Ca²⁺ free solution was prepared by omitting Ca²⁺ and adding 1 mM EGTA. In all experiments, ACSF and the Ringer-Locke’s solution were aerated with a mixture of 95% O₂ and 5% CO₂. Dantrolene solution was prepared by dissolving the dantrolene powder in dimethyl sulfoxide and then adding the appropriate amount of dissolved dantrolene to the Ringer-Locke’s solution to make the desired concentration (20 μM). SAR7334 solutions (Tocris, Minneapolis, MN, USA) were prepared by adding concentrated stocks of the drug to the Ringer-Locke’s solution to a final concentration of 0.1 or 1 μM. We added TTX (1.5 μM; Abcam, Cambridge, MA, USA) to the Ringer-Locke’s solution to suppress Ca²⁺ oscillations because spontaneous Ca²⁺ oscillations interfered with the measurement of [Ca²⁺]_r. In previous experiments, we have demonstrated that TXX did not alter either the resting membrane potential or [Ca²⁺]_r in hippocampal neurons that were not firing spontaneously (Robin et al., 2017).

Statistical Analysis

Values are expressed as mean ± SD. The data were subjected to analysis of variance (one-way ANOVA) followed by Tukey’s post hoc comparisons tests to determine significance. p < 0.05 was considered as statistically significant. Analysis of these data failed to show sex differences; therefore, the data from male and female mice were combined for analysis. n_mice: indicates the number of mice used and n_cells: represents the number of successful measurements.

Results

Effect of Aging and Dantrolene on [Ca²⁺]_r in Cortical Neurons in vivo

The impairment of intracellular Ca²⁺ homeostasis is considered to be a key pathological factor leading to aging-related neuronal dysfunction (Raza et al., 2007). Therefore, we measured [Ca²⁺]_r in vivo in polarized cortical neurons from young (3-months), middle-aged (12-months), and aged (24-months) mice to determine if there were any changes associated with normal aging in mice. In young mice, cortical neuronal [Ca²⁺]_r was 121 ± 2 nM. Interestingly in middle-aged WT mice neuronal [Ca²⁺]_r, increased 1.9-fold to 226 ± 27 nM, and in aged mice, it rose 2.7-fold to 334 ± 43 nM (Figure 1A). Dantrolene has been previously shown to reduce [Ca²⁺]_r in skeletal muscle and neurons (Lopez et al., 1987a,b; Robin et al., 2017). We found that pre-treatment of mice with Dantrolene (2 mg/kg IP) 60 min before measurements, decreased cortical neuronal [Ca²⁺]_r in all age-groups. However, the reduction of [Ca²⁺]_r in the middle-aged and aged cortical neurons was greater than in young neurons reaching levels that were the same or similar to those measured after dantrolene treatment in young mice (Figure 1A).

FIGURE 1

Figure 1. Increased [Ca²⁺]_r in aged neurons. Effect of dantrolene. [Ca²⁺]_r was measured in quiescent young, middle-aged, and aged cortical neurons in vivo (A) and hippocampal pyramidal neurons in vitro (B) using double-barreled ion-specific microelectrodes. [Ca²⁺]_r was significantly higher in the middle-aged and aged than young neurons in both conditions. Dantrolene (2 mg/Kg IP) in vivo (A) or (20 μM) in vitro (B) reduced [Ca²⁺]_r in all age-groups. The reduction of [Ca²⁺]_r greater in aged than young neurons. On the horizontal axis are indicated the experimental conditions used to measure [Ca²⁺]_r in vivo [Ca²⁺]_r measurements: n_mice = 3–5/age group, n_cell = 8–12/age group; in vitro [Ca²⁺]_r measurements: n_mice = 4–5/ per age group, n_cell = 11–17/age group. Values are expressed as means ± S.D. One-way ANOVA followed by Tukey’s post hoc comparisons, *p ≤ 0.05.

Effect of Aging and Dantrolene on [Ca²⁺]_r in Hippocampal Neurons in vitro

To allow a more mechanistic study of potential neuronal [Ca²⁺]_r dyshomeostasis in aging WT mice, we carried out measurements of [Ca²⁺]_r in isolated, polarized hippocampal pyramidal neurons from all three age groups. Similar to our in vivo findings from cortical neurons, day 7 cultured hippocampal neurons from middle-aged mice have a 1.7-fold higher [Ca²⁺]_r (199 ± 23 nM) and aged mice have a 2.4-fold higher [Ca²⁺]_r (286 ± 40 nM) than neurons from young mice (120 ± 2 nM; Figure 1B). Similar to our results in cortical neurons in vivo, when day 7 cultured hippocampal neurons were exposed to 20 μM dantrolene 15 min before recording [Ca²⁺]_r it reduced [Ca²⁺]_r all three age groups to levels that were below those in untreated young neurons (Figure 1B).

Increased Hippocampal Neuronal [Ca²⁺]_r is Mediated in Part by TRPC Channels

To determine how [Ca²⁺]_r is affected by extracellular sources of Ca²⁺, we incubated hippocampal neurons in Ca²⁺ free media for 15 min and found that this treatment reduced [Ca²⁺]_r in the two older age groups to levels similar to those in young neurons (Figure 2A). To determine the potential contributions TRPC3 and TRPC6 channels as a possible mechanism for the apparent increased extracellular Ca²⁺ entry observed in middle-aged and aged hippocampal neurons we incubated young, middle-age, and aged neurons with the TRPC3/TRPC6 channels blocker SAR7334 (Maier et al., 2015). SAR7334 reduced [Ca²⁺]_r in all age groups in a dose-dependent manner; however, the effect of SAR7334 was greater with increasing age (Figures 2B,C). Because TRPC channels are nonselective cation channels Sawamura et al., 2017; Samanta et al., 2018 and their increased activity might also allow significant Na⁺ entry, we also measured intracellular Na⁺ concentration ([Na⁺]_r). We found that [Na⁺]_r was 1.3-fold higher (10.6 ± 0.9 mM) in middle-aged neurons), and 1.8-fold higher in aged neurons (14.4 ± 0.9 mM) than in young neurons (8.0 ± 0.1 mM; Figure 2D). As was the case for [Ca²⁺]_r, SAR7334 (1 μM) significantly reduced [Na⁺]_r in neurons of all age groups, and like its effect on [Ca²⁺]_r, the reduction was more prominent in middle-aged (20%) and aged neurons (31%), compared to young neurons (6%) (Figure 2D).

FIGURE 2

Figure 2. Effects of Ca²⁺ free solution and SAR7334 on [Ca²⁺]_r and [Na⁺]_r in hippocampal pyramidal neurons. Panel (A) shows that removal of extracellular Ca²⁺ significantly lowered the [Ca²⁺]_r in all age-group; however, the magnitude of the reduction of [Ca²⁺]_r was more evident in aged than young neurons. Panels (B,C) illustrate SAR7334 elicited a dose-dependent reduction of [Ca²⁺]_r in the young, middle-aged and aged neurons, being more marked in aged neurons. Panel (D) exemplifies the reduction provoked by SAR7334 on [Na⁺]_r, which was greater in aged than young neurons. On the horizontal axis are indicated the experimental conditions used to measure [Ca²⁺]_r and [Na⁺]_r. For [Ca²⁺]_i measurements: n_mice = 3–5/age group, n_cell = 9–16/age group. For [Na⁺]_i measurements: n_mice = 4/per age group, n_cell = 12–15/age group. Values are expressed as means ± S.D. for each condition. One-way ANOVA followed by Tukey’s post hoc comparisons, *p ≤ 0.05.

Dantrolene Treatment Decreases Calpain Activity and Increases Hippocampal Cell Viability

Intracellular Ca²⁺ overload plays a major role in the development of cell injury (Cross et al., 2010). Activation of the Ca²⁺-dependent protease calpain is believed to be one mechanism by which increased [Ca²⁺]_r can cause damage (Hosfield et al., 1999; Cheng et al., 2018). Compared to young hippocampal neurons, calpain activity was significantly elevated in both middle-age (43%) and aged (113%) neurons (Figure 3A). Reducing neuronal [Ca²⁺]_r with 30 min of dantrolene (20 μM) pretreatment decreased the calpain activity by 26% in middle-aged and 37% in aged neurons compared to untreated controls (Figure 3A). In a direct measurement of hippocampal neuronal viability using the MMT assay, we found that the increased calpain activity in middle-aged and aged neurons was associated with a 28% and 53% decrease in viability respectively than young neurons (Figure 3B) and that the decrease of calpain with pretreatment with dantrolene was accompanied by a significant increase in neuronal viability, 31%, and 73%, respectively in middle-aged and aged neurons compared to untreated neurons (Figure 3B).

FIGURE 3

Figure 3. Effects of dantrolene on calpain activity and cell viability in aged hippocampal neurons. Calpain activity was higher in middle-aged and aged hippocampal neurons than young neurons (A), and these differences were accompanied by a decreased cell viability in middle-aged and aged hippocampal neurons compared to young neurons (B). Dantrolene (20 μM) reduced calpain activity, and increased cell viability in aged hippocampal neurons. On the horizontal axis are indicated the experimental conditions. For calpain: n_mice = 3/age group; for cell viability: n_mice = 4/per age group. Values are expressed as means ± S.D. for each condition. One-way ANOVA followed by Tukey’s post hoc comparisons, *p ≤ 0.05; NS, not significant.

Cognitive Impairment in Aged Mice and the Ability of Dantrolene to Attenuate Memory Deficits

As shown in Figure 4A, using the MWM as the method of assessing memory and learning, the ELT for middle-aged and aged mice was significantly longer compared to young mice during the whole TP and on the PT day. Dantrolene treatment (1 mg/kg/day, i.p.) for 5 days. before and during the TP and PT periods (10 days of treatment) significantly improved the escape latency in middle-aged and aged mice but had no significant effect in young mice (Figure 4B). In middle-aged mice, after the dantrolene treatment, the ELT values were not significantly different compared to young mice during the PT period (Figure 4B). However, in the aged group after the dantrolene treatment, the ELT values were significantly different (at any point during the PT period) compared to young mice. In assessments of memory retention, evaluated by the time spent in the quadrant and the number of times the mouse crossed over the area where the platform was previously hidden determined by the number of entries into the quadrant, both parameters showed an age-related deficit in untreated middle-aged and aged mice compared to young mice and dantrolene treatment significantly improved both of these deficits (Figures 4C,D).

FIGURE 4

Figure 4. Effects of aging on cognitive function. Effects of dantrolene. The Morris water maze (MWM) was used to assess spatial learning and memory in young, middle-aged, and aged mice. Middle-aged and aged mice showed a reduced escape latency time (ELT; A), a time in the target quadrant (C), and the number of entries into the target quadrant (D) compared to young mice. Dantrolene (1 mg/kg, i.p) for 5 days. before and during the training period (TP), and probe trial (PT) periods improved all of the parameters studied (B–D). On the horizontal axis of panels (C,D) are indicated the experimental conditions. Values are expressed as mean ± SEM from n_mice = 10 per age group. One-way ANOVA followed by Tukey’s post hoc comparisons, *p ≤ 0.05; NS, not significant.

Discussion

This is the first study to directly examine changes in intracellular Ca²⁺ homeostasis using intracellular Ca²⁺ selective microelectrodes—in vivo—in cortical neurons and—in vitro—in hippocampal neurons associated with normal aging in WT mice. Mice were studied at three different ages, selected to be the equivalent to approximately 10 (young), 40 (middle-aged), and 80-year-old (aged) humans.

In young mice, neuronal intracellular [Ca²⁺] is maintained in the range of 100–120 nM in resting cells against a large extracellular concentration gradient (Lopez et al., 2008; Robin et al., 2017; Lopez et al., 2018a). Neuronal [Ca²⁺]_r is regulated by multifaceted mechanisms that balance Ca²⁺ influx and release from intracellular stores with intracellular sequestration and extracellular extrusion (Brini et al., 2014). Perturbations of any of the mechanisms involved in intracellular Ca²⁺ regulation will ultimately lead to a sustained rise of neuronal [Ca²⁺]_r. Several Ca²⁺-dependent regulatory processes undergo age-dependent changes, which correlate with cognitive decline (Gant et al., 2006; Bodhinathan et al., 2010); (Disterhoft et al., 1996). Also, studies have shown that reversal of the intracellular Ca²⁺ dyshomeostasis using Ca²⁺ channel antagonists (Disterhoft and Oh, 2006), antioxidants (Cartford et al., 2002), FKBP1b overexpression (Gant et al., 2015) and Ca²⁺ chelating agents as BAPTA (Tonkikh et al., 2006) improves aged-dependent cognoscitive deficits. We demonstrated in vivo that [Ca²⁺]_r in cortical neurons of middle-aged and aged mice is chronically elevated compared with young mice and that treatment with dantrolene can reduce [Ca²⁺]_r in middle aged and aged mice to levels near those of treated young mice. Similarly, [Ca²⁺]_r in isolated hippocampal pyramidal neurons after 7 days in culture show the same intracellular Ca²⁺ disturbances in middle-aged and aged neurons in vitro that we measured in cortical neurons in vivo and in these studies we were able to show that the changes in [Ca²⁺]_r were accompanied by a parallel increases in [Na⁺]_r. Like the in vivo experiments, treatment of cultured neurons with dantrolene lowers [Ca²⁺]_r in all age groups. Further research must be carried out to explore more in-depth the role of intracellular Ca²⁺ dysregulation observed with aging.

One important finding in this study is that our data show that intracellular Ca²⁺ dyshomeostasis occurs in mice at younger ages (12 months old) than those which are usually considered aged (24 months or older). This has important clinical implications since it demonstrates that alterations of neuronal [Ca²⁺]_r are progressive with age and begin at a much earlier age than has been previously assumed. Therefore, to be effective over the long term, therapies oriented to prevent cognitive decline might need to be initiated at a much earlier age. Our data showing an age-related increase in [Ca²⁺]_r with age are in agreement with the findings reported by Tonkikh et al. (2006) using hippocampal slices, and by Raza et al. (2007) and Hajieva et al. (2009) in hippocampal neurons who found that [Ca²⁺]_r, as determined by fluorescent dyes was elevated in aged (24 months old or older) neurons compared to young animals. However, other reports (Thibault et al., 2001; Lopez et al., 2008) found no differences in [Ca²⁺]_r between young and aged or middle-aged neurons. Diverse factors could account for this disagreement. Among them are differences in the methods used to isolate the neuronal preparations, the Ca²⁺ indicator employed to carry out the intracellular measurements, the age and type of neurons studied, neuronal viability status of the model studied, and the genetic strain of the animals. Our in vivo and in vitro studies were carried out in cortical and hippocampal pyramidal neurons that were proven viable because they had proven normal membrane potentials thus avoiding the potential for having included injured cells in our experimental groups. Additionally, [Ca²⁺]_r was measured directly with Ca²⁺ selective microelectrodes, to overcome the limitations imposed by the currently available fluorescent and metallochromic Ca²⁺ indicators (Alvarez-Leefmans et al., 1981; Hove-Madsen and Bers, 1992).

Ryanodine Receptor Leak and Neuronal Ca²⁺ Dysfunction

At normal physiological conditions, a fraction of ER Ca²⁺ leak occurs as uncoordinated openings of individual RyRs. This leak component can serve as an important protective mechanism against the ER Ca²⁺ overload in excitable tissues (Zima et al., 2010). However, changes in neuronal redox state, such as the increased oxidative condition exhibited by aged neurons, affect the resting RyR-leak and the RyR-mediated Ca²⁺ release (Paula-Lima et al., 2014), since RyR channels are highly redox-sensitive (Hidalgo and Donoso, 2008). ER depletion has been associated with activation of Ca²⁺ entry through store-operated Ca²⁺ channels proteins (SOCE) and TRPC channels to maintain the appropriate ER [Ca²⁺] that regulates neuronal functions (Sun et al., 2014). We found that dantrolene, a known blocker of the resting RyR-leak and RyRs-mediated Ca²⁺ release, reduced [Ca²⁺]_r and improved cognitive functions in middle-aged and aged-neurons. Dantrolene reduces intracellular [Ca²⁺] in the muscle (Lopez et al., 1987a,b, 1988) and neurons (Robin et al., 2017) and is currently used clinically to treat malignant hyperthermia (Harrison, 1988). Furthermore, dantrolene attenuates age-associated spatial memory deficits (Hopp et al., 2014) and has been previously shown to improve cognition deficits in a murine model of Alzheimer’s disease (Peng et al., 2012). Thus, the positive effects of dantrolene on [Ca²⁺]_r and cognitive functions in aged mice may be due to inhibition of excessive RyR-mediated Ca²⁺ leak.

Critical Role of TRPCs During Aging

TRPC channels are widely expressed in almost every mammalian cell. TRPC channels can be activated by diverse stimuli ranging from temperature, mechanical or osmotic stress, chemical compounds, and redox modification (Sawamura et al., 2017; Samanta et al., 2018). Increased TRPC expression has been associated with aging in the heart and aorta (Kaplan et al., 2007; Erac et al., 2010), and with neurodegenerative diseases (Selvaraj et al., 2010; Takada et al., 2013; Sukumaran et al., 2017). In our studies looking into the mechanisms behind the changes in [Ca²⁺]_r in aging hippocampal neurons, we found that if we incubated them with the TRPC3/TRPC6 blocker SAR7334 (Maier et al., 2015), [Ca²⁺]_r and [Na⁺]_r were lowered in neurons in all three age groups suggesting that that increased plasmalemmal Ca²⁺ influx through TRPC channels was at least in part responsible for the increased [Ca²⁺]_r and that lowering the activity of these TRPC channels could protect the neurons from the detrimental effects of excessive intracellular [Ca²⁺] and [Na⁺]. Thus, TRPC channels not only contribute to normal physiological processes but are also implicated in aging. It suggests that these channels could be used as potential therapeutic targets to prevent the neuronal changes observed during aging.

Calpain Activation and Cell Viability

Interestingly, the increased [Ca²⁺]_r in hippocampal neurons from middle-age and aged mice was associated with increased neuronal calpain activity, and reduced cell viability compared to young neurons. Calpain activation has previously been reported in aged neurons (Nixon, 2003) and proposed to be involved in age-associated neurodegenerative conditions such as Alzheimer’s disease (Battaglia et al., 2003; Nixon, 2003). Pretreatment with dantrolene, which reduces [Ca²⁺]_r, lowered calpain activity to or near to young neuron levels and improved cell viability in both middle-aged and aged neurons. This demonstrates that dantrolene has a neuroprotective effect, which is at least in part if not completely mediated by its ability to reduce [Ca²⁺]_r. This neuronal Ca²⁺ dyshomeostasis and decreased neuronal viability in middle-aged and aged mice was associated with significant age-related learning and cognitive memory deficits as measured by the MWM. As with the biochemical studies, these learning and memory deficits were significantly improved by dantrolene treatment.

Cognitive Function, Ca²⁺ Overload, and Aging

Using the MWM test (Morris, 1984), we assessed the learning and memory skills of spatial position and direction in young, middle-aged and aged mice. Escape latency was used to evaluate learning ability and memory retention and the number of platform crossings was used to evaluate spatial memory ability. Unexpectedly we found that these cognitive functions had already declined in middle-age compared with young mice as well as the expected decline in aged mice. Age-related cognitive decline has been associated with alterations of intracellular [Ca²⁺]_r (Wu et al., 2002) and degenerative neurological pathologies including Alzheimer’s and Parkinson’s disease (Disterhoft et al., 1994; Kirischuk and Verkhratsky, 1996; Lopez et al., 2008). Based on the present results, it is appealing to suggest that a neuronal intracellular Ca²⁺ dysregulation such as that observed in middle-aged and aged neurons predisposes to the development of age-related cognitive decline in mice but perhaps also in the pathophysiology of this phenomenon in humans as well.

Dantrolene Neuroprotection and Aging

Dantrolene is a hydantoin derivative which is currently the drug of choice for the treatment of patients suffering from malignant hyperthermia (Riazi et al., 2018). Dantrolene is also clinically useful for the treatment of symptoms associated with spasticity (Chou et al., 2004), and rhabdomyolysis induced by exercise (Edwards et al., 2003). Furthermore, dantrolene has been shown to have neuroprotective effects in multiple models of neurodegenerative disorders like Huntington’s disease (Chen et al., 2011) and Alzheimer’s disease (Wang et al., 2017; Liang and Wei, 2015). The muscle relaxant properties of dantrolene have been linked with its ability reduce [Ca²⁺]_r in humans (Lopez et al., 1992), swine (Lopez et al., 1987a) and mice (Yang et al., 2006; Cherednichenko et al., 2008; Eltit et al., 2013) although the exact mechanisms by which dantrolene exerts its therapeutic effects both in muscle and neurons are not fully understood. The predominant data supports the view that in skeletal muscle dantrolene acts selectively on the sarcoplasmic reticulum (SR) Ca²⁺ release channel (ryanodine receptor type 1, RyR1) to reduce SR leak and maintain normal SR Ca²⁺ stores (Fruen et al., 1997). In our model of normal aging, pretreatment with dantrolene appears to exert a neuroprotective effect on middle aged and aged neurons by reducing neuronal intracellular Ca²⁺ overload. When neuronal [Ca²⁺]_r is normalized elevated calpain activity, which is found in untreated neurons, is decreased and this decrease improves cell viability. In addition, we demonstrated that when dantrolene is given chronically for 10 days it is able to improve cognitive deficits observed in untreated middle aged and aged mice.

Study Limitations

Despite the originality of our study, some limitations should be acknowledged. First, we explored intracellular Ca²⁺ dysregulation as the only factor contributing to the pathogenesis of aging and not other hypotheses such as: (i) glial cell alterations (Popa-Wagner et al., 2019), (ii) blood-brain-barrier disruption (Fulop et al., 2019), (iii) alteration in circadian rhythms (Logan et al., 2018), and (iv) endothelial dysfunction (Tarantini et al., 2019). Second, we did not perform a dose-response curve on dantrolene and cognitive improvement. Third, we did not assess whether blocking TRPC channels or genetic manipulation TRPC and RyR channels can rescue or improve cognitive deficit in aged-mice. Finally, we also acknowledge the small number of mice used for behavioral testing.

Conclusions

In summary, the novel findings of the present study are: (i) the direct measurement of [Ca²⁺]_r in cortical neurons in vivo using Ca²⁺ selective microelectrodes; (ii) the demonstration of dysregulation of [Ca²⁺]_r in middle-aged as well as aged cortical and hippocampal neurons; (iii) the revelation that the elevation in [Ca²⁺]_r in middle-aged and aged neurons can be decreased or normalized by either dantrolene or SAR7374; (iv) that disruption of normal neuronal intracellular Ca²⁺ homeostasis leads to increases in calpain activity and a decrease in neuronal viability; (v) neuronal [Ca²⁺]_r dysregulation is associated with an age-related cognitive decline, as measured by MWM performance; and (vi) the reduction in [Ca²⁺]_r associated with dantrolene treatment in middle-aged and aged animals was accompanied with an improvement of cognition as measured by MWM.

Based on the above findings, it appears there is an interaction between cognitive decline observed in middle-aged and elderly mice and chronic intracellular Ca²⁺ dysregulation. Despite that alterations in ER-RyR Ca²⁺ leak and TRPC channels may not be the only pathogenic factors contributing to the pathogenesis of aging, the potential modification of those alterations is enough to enable expectations for new preventive or therapeutic strategies. Further research must be carried out to explore more in-depth the role of intracellular Ca²⁺ dysregulation and cognitive decline observed with aging.

Data Availability Statement

The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation, to any qualified researcher.

Ethics Statement

All protocols used in the study were performed following the recommendations in the Guide for the Care and Use of Laboratory Animals of the National Institutes of Health and approved by the IACUC of the Mount Sinai Medical Center.

Author Contributions

AU and VF: performed research and analyzed data. JA and PA: analyzed data and wrote the article. JL: designed research, performed research, analyzed data and wrote the article. All the authors contributed to manuscript revision, read and approved the submitted version.

Funding

This work was supported by the AFM-Téléthon-France (Grant no. 21543), Florida Heart Research Institute, and the NIH National Institute of Arthritis, Musculoskeletal, and Skin diseases 1R01AR068897-01A1.

Conflict of Interest

The 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.

Acknowledgments

We are grateful to Dr. Jose Kolster for his advice and suggestions on the in vivo experiments and his valuable comments.

References

Alvarez-Leefmans, F. J., Rink, T. J., and Tsien, R. Y. (1981). Free calcium ions in neurones of Helix aspersa measured with ion-selective micro-electrodes. J. Physiol. 315, 531–548. doi: 10.1113/jphysiol.1981.sp013762

PubMed Abstract | CrossRef Full Text | Google Scholar

Alzheimer’s Association Calcium Hypothesis, W. (2017). Calcium Hypothesis of Alzheimer’s disease and brain aging: A framework for integrating new evidence into a comprehensive theory of pathogenesis. Alzheimers Dement. 13, 178.e17–182.e17. doi: 10.1016/j.jalz.2016.12.006

PubMed Abstract | CrossRef Full Text | Google Scholar

Battaglia, F., Trinchese, F., Liu, S., Walter, S., Nixon, R. A., and Arancio, O. (2003). Calpain inhibitors, a treatment for Alzheimer’s disease: position paper. J. Mol. Neurosci. 20, 357–362. doi: 10.1385/jmn:20:3:357

PubMed Abstract | CrossRef Full Text | Google Scholar

Berridge, M. J., Lipp, P., and Bootman, M. D. (2000). The versatility and universality of calcium signalling. Nat. Rev. Mol. Cell Biol. 1, 11–21. doi: 10.1038/35036035

PubMed Abstract | CrossRef Full Text | Google Scholar

Bezprozvanny, I. (2009). Calcium signaling and neurodegenerative diseases. Trends Mol. Med. 15, 89–100. doi: 10.1016/j.molmed.2009.01.001

PubMed Abstract | CrossRef Full Text | Google Scholar

Bodhinathan, K., Kumar, A., and Foster, T. C. (2010). Redox sensitive calcium stores underlie enhanced after hyperpolarization of aged neurons: role for ryanodine receptor mediated calcium signaling. J. Neurophysiol. 104, 2586–2593. doi: 10.1152/jn.00577.2010

PubMed Abstract | CrossRef Full Text | Google Scholar

Brini, M., Cali, T., Ottolini, D., and Carafoli, E. (2014). Neuronal calcium signaling: function and dysfunction. Cell. Mol. Life Sci. 71, 2787–2814. doi: 10.1007/s00018-013-1550-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Cartford, M. C., Gemma, C., and Bickford, P. C. (2002). Eighteen-month-old Fischer 344 rats fed a spinach-enriched diet show improved delay classical eyeblink conditioning and reduced expression of tumor necrosis factor alpha (TNFalpha ) and TNFbeta in the cerebellum. J. Neurosci. 22, 5813–5816. doi: 10.1523/jneurosci.22-14-05813.2002

PubMed Abstract | CrossRef Full Text | Google Scholar

Chen, X., Wu, J., Lvovskaya, S., Herndon, E., Supnet, C., and Bezprozvanny, I. (2011). Dantrolene is neuroprotective in Huntington’s disease transgenic mouse model. Mol. Neurodegener. 6:81. doi: 10.14232/phd.644

PubMed Abstract | CrossRef Full Text | Google Scholar

Cheng, S. Y., Wang, S. C., Lei, M., Wang, Z., and Xiong, K. (2018). Regulatory role of calpain in neuronal death. Neural Regen. Res. 13, 556–562. doi: 10.4103/1673-5374.228762

PubMed Abstract | CrossRef Full Text | Google Scholar

Cherednichenko, G., Ward, C. W., Feng, W., Cabrales, E., Michaelson, L., Samso, M., et al. (2008). Enhanced excitation-coupled calcium entry in myotubes expressing malignant hyperthermia mutation R163C is attenuated by dantrolene. Mol. Pharmacol. 73, 1203–1212. doi: 10.1124/mol.107.043299

PubMed Abstract | CrossRef Full Text | Google Scholar

Chou, R., Peterson, K., and Helfand, M. (2004). Comparative efficacy and safety of skeletal muscle relaxants for spasticity and musculoskeletal conditions: a systematic review. J. Pain Symptom Manage. 28, 140–175. doi: 10.1016/j.jpainsymman.2004.05.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Cross, J. L., Meloni, B. P., Bakker, A. J., Lee, S., and Knuckey, N. W. (2010). Modes of neuronal calcium entry and homeostasis following cerebral ischemia. Stroke Res. Treat. 2010:316862. doi: 10.4061/2010/316862

PubMed Abstract | CrossRef Full Text | Google Scholar

Demetrius, L. (2006). Aging in mouse and human systems: a comparative study. Ann. N Y Acad. Sci. 1067, 66–82. doi: 10.1196/annals.1354.010

PubMed Abstract | CrossRef Full Text | Google Scholar

Disterhoft, J. F., Moyer, J. R. Jr., and Thompson, L. T. (1994). The calcium rationale in aging and Alzheimer’s disease. Evidence from an animal model of normal aging. Ann. N Y Acad. Sci. 747, 382–406. doi: 10.1111/j.1749-6632.1994.tb44424.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Disterhoft, J. F., and Oh, M. M. (2006). Pharmacological and molecular enhancement of learning in aging and Alzheimer’s disease. J. Physiol. Paris 99, 180–192. doi: 10.1016/j.jphysparis.2005.12.079

PubMed Abstract | CrossRef Full Text | Google Scholar

Disterhoft, J. F., Thompson, L. T., Moyer, J. R. Jr., and Mogul, D. J. (1996). Calcium-dependent afterhyperpolarization and learning in young and aging hippocampus. Life Sci. 59, 413–420. doi: 10.1016/0024-3205(96)00320-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Dutta, S., and Sengupta, P. (2016). Men and mice: relating their ages. Life Sci. 152, 244–248. doi: 10.1016/j.lfs.2015.10.025

PubMed Abstract | CrossRef Full Text | Google Scholar

Edwards, J. G., Newtont, J. R., Ramzan, P. H., Pilsworth, R. C., and Shepherd, M. C. (2003). The efficacy of dantrolene sodium in controlling exertional rhabdomyolysis in the Thoroughbred racehorse. Equine Vet. J. 35, 707–711. doi: 10.2746/042516403775696221

PubMed Abstract | CrossRef Full Text | Google Scholar

Eltit, J. M., Ding, X., Pessah, I. N., Allen, P. D., and Lopez, J. R. (2013). Nonspecific sarcolemmal cation channels are critical for the pathogenesis of malignant hyperthermia. FASEB J. 27, 991–1000. doi: 10.1096/fj.12-218354

PubMed Abstract | CrossRef Full Text | Google Scholar

Eltit, J. M., Yang, T., Li, H., Molinski, T. F., Pessah, I. N., Allen, P. D., et al. (2010). RyR1-mediated Ca2+ leak and Ca2+ entry determine resting intracellular Ca2+ in skeletal myotubes. J. Biol. Chem. 285, 13781–13787. doi: 10.1074/jbc.m110.107300

PubMed Abstract | CrossRef Full Text | Google Scholar

Erac, Y., Selli, C., Kosova, B., Akcali, K. C., and Tosun, M. (2010). Expression levels of TRPC1 and TRPC6 ion channels are reciprocally altered in aging rat aorta: implications for age-related vasospastic disorders. Age 32, 223–230. doi: 10.1007/s11357-009-9126-z

PubMed Abstract | CrossRef Full Text | Google Scholar

Faes, C., Aerts, M., Geys, H., and De Schaepdrijver, L. (2010). Modeling spatial learning in rats based on Morris water maze experiments. Pharm. Stat. 9, 10–20. doi: 10.1002/pst.361

PubMed Abstract | CrossRef Full Text | Google Scholar

Foster, T. C. (1999). Involvement of hippocampal synaptic plasticity in age-related memory decline. Brain Res. Rev. 30, 236–249. doi: 10.1016/s0165-0173(99)00017-x

PubMed Abstract | CrossRef Full Text | Google Scholar

Fruen, B. R., Mickelson, J. R., and Louis, C. F. (1997). Dantrolene inhibition of sarcoplasmic reticulum Ca2+ release by direct and specific action at skeletal muscle ryanodine receptors. J. Biol. Chem. 272, 26965–26971. doi: 10.1074/jbc.272.43.26965

PubMed Abstract | CrossRef Full Text | Google Scholar

Fulop, G. A., Ahire, C., Csipo, T., Tarantini, S., Kiss, T., Balasubramanian, P., et al. (2019). Cerebral venous congestion promotes blood-brain barrier disruption and neuroinflammation, impairing cognitive function in mice. Geroscience 41, 575–589. doi: 10.1007/s11357-019-00110-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Gant, J. C., Chen, K. C., Kadish, I., Blalock, E. M., Thibault, O., Porter, N. M., et al. (2015). Reversal of aging-related neuronal Ca2+ dysregulation and cognitive impairment by delivery of a transgene encoding FK506-binding protein 12.6/1b to the hippocampus. J. Neurosci. 35, 10878–10887. doi: 10.1523/jneurosci.1248-15.2015

PubMed Abstract | CrossRef Full Text | Google Scholar

Gant, J. C., Sama, M. M., Landfield, P. W., and Thibault, O. (2006). Early and simultaneous emergence of multiple hippocampal biomarkers of aging is mediated by Ca2+-induced Ca2+ release. J. Neurosci. 26, 3482–3490. doi: 10.1523/jneurosci.4171-05.2006

PubMed Abstract | CrossRef Full Text | Google Scholar

Giannini, G., Conti, A., Mammarella, S., Scrobogna, M., and Sorrentino, V. (1995). The ryanodine receptor/calcium channel genes are widely and differentially expressed in murine brain and peripheral tissues. J. Cell Biol. 128, 893–904. doi: 10.1083/jcb.128.5.893

PubMed Abstract | CrossRef Full Text | Google Scholar

Gibson, G. E., and Peterson, C. (1987). Calcium and the aging nervous system. Neurobiol. Aging 8, 329–343. doi: 10.1016/0197-4580(87)90077-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Gollan, T. H., and Goldrick, M. (2019). Aging deficits in naturalistic speech production and monitoring revealed through reading aloud. Psychol. Aging 34, 25–42. doi: 10.1037/pag0000296.supp

PubMed Abstract | CrossRef Full Text | Google Scholar

Hajieva, P., Kuhlmann, C., Luhmann, H. J., and Behl, C. (2009). Impaired calcium homeostasis in aged hippocampal neurons. Neurosci. Lett. 451, 119–123. doi: 10.1016/j.neulet.2008.11.068

PubMed Abstract | CrossRef Full Text | Google Scholar

Handattu, S. P., Garber, D. W., Monroe, C. E., Van Groen, T., Kadish, I., Nayyar, G., et al. (2009). Oral apolipoprotein A-I mimetic peptide improves cognitive function and reduces amyloid burden in a mouse model of Alzheimer’s disease. Neurobiol. Dis. 34, 525–534. doi: 10.1016/j.nbd.2009.03.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Harrison, G. G. (1988). Malignant hyperthermia. Dantrolene–dynamics and kinetics. Br. J. Anaesth. 60, 279–286. doi: 10.1093/bja/60.3.279

PubMed Abstract | CrossRef Full Text | Google Scholar

Hidalgo, C., and Donoso, P. (2008). Crosstalk between calcium and redox signaling: from molecular mechanisms to health implications. Antioxid. Redox Signal. 10, 1275–1312. doi: 10.1089/ars.2007.1886

PubMed Abstract | CrossRef Full Text | Google Scholar

Hill, J. A., and Olson, E. N. (2012). Muscle: Fundamental Biology and Mechanisms of Disease. London, Waltham, MA: Academic Press.

Google Scholar

Hinman, J. D., Duce, J. A., Siman, R. A., Hollander, W., and Abraham, C. R. (2004). Activation of calpain-1 in myelin and microglia in the white matter of the aged rhesus monkey. J. Neurochem. 89, 430–441. doi: 10.1046/j.1471-4159.2004.02348.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Hopp, S. C., D’angelo, H. M., Royer, S. E., Kaercher, R. M., Adzovic, L., and Wenk, G. L. (2014). Differential rescue of spatial memory deficits in aged rats by L-type voltage-dependent calcium channel and ryanodine receptor antagonism. Neuroscience 280, 10–18. doi: 10.1016/j.neuroscience.2014.09.007

PubMed Abstract | CrossRef Full Text | Google Scholar

Hosfield, C. M., Elce, J. S., Davies, P. L., and Jia, Z. (1999). Crystal structure of calpain reveals the structural basis for Ca(2+)-dependent protease activity and a novel mode of enzyme activation. EMBO J. 18, 6880–6889. doi: 10.1093/emboj/18.24.6880

PubMed Abstract | CrossRef Full Text | Google Scholar

Hove-Madsen, L., and Bers, D. M. (1992). Indo-1 binding to protein in permeabilized ventricular myocytes alters its spectral and Ca binding properties. Biophys. J. 63, 89–97. doi: 10.1016/s0006-3495(92)81597-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Kaplan, P., Jurkovicova, D., Babusikova, E., Hudecova, S., Racay, P., Sirova, M., et al. (2007). Effect of aging on the expression of intracellular Ca(2+) transport proteins in a rat heart. Mol. Cell. Biochem. 301, 219–226. doi: 10.1007/s11010-007-9414-9

PubMed Abstract | CrossRef Full Text | Google Scholar

Kirischuk, S., and Verkhratsky, A. (1996). Calcium homeostasis in aged neurones. Life Sci. 59, 451–459. doi: 10.1016/0024-3205(96)00324-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Kumar, A. (2020). Calcium signaling during brain aging and its influence on the hippocampal synaptic plasticity. Adv. Exp. Med. Biol. 1131, 985–1012. doi: 10.1007/978-3-030-12457-1_39

PubMed Abstract | CrossRef Full Text | Google Scholar

Kumar, A., Yegla, B., and Foster, T. C. (2018). Redox signaling in neurotransmission and cognition during aging. Antioxid. Redox Signal. 28, 1724–1745. doi: 10.1089/ars.2017.7111

PubMed Abstract | CrossRef Full Text | Google Scholar

Lacampagne, A., Liu, X., Reiken, S., Bussiere, R., Meli, A. C., Lauritzen, I., et al. (2017). Post-translational remodeling of ryanodine receptor induces calcium leak leading to Alzheimer’s disease-like pathologies and cognitive deficits. Acta Neuropathol. 134, 749–767. doi: 10.1007/s00401-017-1733-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Landfield, P. W. (1996). Aging-related increase in hippocampal calcium channels. Life Sci. 59, 399–404. doi: 10.1016/0024-3205(96)00318-9

PubMed Abstract | CrossRef Full Text | Google Scholar

Liang, L., and Wei, H. (2015). Dantrolene, a treatment for Alzheimer disease?. Alzheimer Dis. Assoc. Disord. 29, 1–5. doi: 10.1097/wad.0000000000000076

PubMed Abstract | CrossRef Full Text | Google Scholar

Liguori, I., Russo, G., Curcio, F., Bulli, G., Aran, L., Della-Morte, D., et al. (2018). Oxidative stress, aging and diseases. Clin. Interv. Aging 13, 757–772. doi: 10.2147/CIA.S158513

PubMed Abstract | CrossRef Full Text | Google Scholar

Logan, S., Owen, D., Chen, S., Chen, W. J., Ungvari, Z., Farley, J., et al. (2018). Simultaneous assessment of cognitive function, circadian rhythm and spontaneous activity in aging mice. Geroscience 40, 123–137. doi: 10.1007/s11357-018-0019-x

PubMed Abstract | CrossRef Full Text | Google Scholar

Lopez, J. R., Allen, P., Alamo, L., Ryan, J. F., Jones, D. E., and Sreter, F. (1987a). Dantrolene prevents the malignant hyperthermic syndrome by reducing free intracellular calcium concentration in skeletal muscle of susceptible swine. Cell Calcium 8, 385–396. doi: 10.1016/0143-4160(87)90013-3

PubMed Abstract | CrossRef Full Text | Google Scholar

Lopez, J. R., Medina, P., and Alamo, L. (1987b). Dantrolene sodium is able to reduce the resting ionic [Ca2+]i in muscle from humans with malignant hyperthermia. Muscle Nerve 10, 77–79. doi: 10.1002/mus.880100114

PubMed Abstract | CrossRef Full Text | Google Scholar

Lopez, J. R., Allen, P. D., Alamo, L., Jones, D., and Sreter, F. A. (1988). Myoplasmic free [Ca2+] during a malignant hyperthermia episode in swine. Muscle Nerve 11, 82–88. doi: 10.1002/mus.880110113

PubMed Abstract | CrossRef Full Text | Google Scholar

Lopez, J. R., Gerardi, A., Lopez, M. J., and Allen, P. D. (1992). Effects of dantrolene on myoplasmic free [Ca2+] measured in vivo in patients susceptible to malignant hyperthermia. Anesthesiology 76, 711–719. doi: 10.1097/00000542-199205000-00008

PubMed Abstract | CrossRef Full Text | Google Scholar

Lopez, J. R., Kolster, J., Uryash, A., Esteve, E., Altamirano, F., and Adams, J. A. (2018a). Dysregulation of Intracellular Ca(2+) in Dystrophic Cortical and Hippocampal Neurons. Mol. Neurobiol. 55, 603–618. doi: 10.1007/s12035-016-0311-7

PubMed Abstract | CrossRef Full Text | Google Scholar

Lopez, J. R., Uryash, A., Kolster, J., Esteve, E., Zhang, R., and Adams, J. A. (2018b). Enhancing endogenous nitric oxide by whole body periodic acceleration elicits neuroprotective effects in dystrophic neurons. Mol. Neurobiol. 55, 8680–8694. doi: 10.1007/s12035-018-1018-8

PubMed Abstract | CrossRef Full Text | Google Scholar

Lopez, J. R., Linares, N., Pessah, I. N., and Allen, P. D. (2005). Enhanced response to caffeine and 4-chloro-m-cresol in malignant hyperthermia-susceptible muscle is related in part to chronically elevated resting [Ca2+]i. Am. J. Physiol. Cell Physiol. 288, C606–C612. doi: 10.1152/ajpcell.00297.2004

PubMed Abstract | CrossRef Full Text | Google Scholar

Lopez, J. R., Lyckman, A., Oddo, S., Laferla, F. M., Querfurth, H. W., and Shtifman, A. (2008). Increased intraneuronal resting [Ca2+] in adult Alzheimer’s disease mice. J. Neurochem. 105, 262–271. doi: 10.1111/j.1471-4159.2007.05135.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Maier, T., Follmann, M., Hessler, G., Kleemann, H. W., Hachtel, S., Fuchs, B., et al. (2015). Discovery and pharmacological characterization of a novel potent inhibitor of diacylglycerol-sensitive TRPC cation channels. Br. J. Pharmacol. 172, 3650–3660. doi: 10.1111/bph.13151

PubMed Abstract | CrossRef Full Text | Google Scholar

Maria-Ferreira, D., De Oliveira, N. M. T., Da Silva, L. C. M., and Fernandes, E. S. (2020). Evidence of a role for the TRPC subfamily in mediating oxidative stress in Parkinson’s disease. Front. Physiol. 11:332. doi: 10.3389/fphys.2020.00332

PubMed Abstract | CrossRef Full Text | Google Scholar

Morris, R. (1984). Developments of a water-maze procedure for studying spatial learning in the rat. J. Neurosci. Methods 11, 47–60. doi: 10.1016/0165-0270(84)90007-4

PubMed Abstract | CrossRef Full Text | Google Scholar

Nilius, B., and Szallasi, A. (2014). Transient receptor potential channels as drug targets: from the science of basic research to the art of medicine. Pharmacol. Rev. 66, 676–814. doi: 10.1124/pr.113.008268

PubMed Abstract | CrossRef Full Text | Google Scholar

Nixon, R. A. (2003). The calpains in aging and aging-related diseases. Ageing Res. Rev. 2, 407–418. doi: 10.1016/s1568-1637(03)00029-1

PubMed Abstract | CrossRef Full Text | Google Scholar

Paula-Lima, A. C., Adasme, T., and Hidalgo, C. (2014). Contribution of Ca2+ release channels to hippocampal synaptic plasticity and spatial memory: potential redox modulation. Antioxid. Redox Signal. 21, 892–914. doi: 10.1089/ars.2013.5796

PubMed Abstract | CrossRef Full Text | Google Scholar

Peng, J., Liang, G., Inan, S., Wu, Z., Joseph, D. J., Meng, Q., et al. (2012). Dantrolene ameliorates cognitive decline and neuropathology in Alzheimer triple transgenic mice. Neurosci. Lett. 516, 274–279. doi: 10.1016/j.neulet.2012.04.008

PubMed Abstract | CrossRef Full Text | Google Scholar

Popa-Wagner, A., Hermann, D., and Gresita, A. (2019). Genetic conversion of proliferative astroglia into neurons after cerebral ischemia: a new therapeutic tool for the aged brain?. Geroscience 41, 363–368. doi: 10.1007/s11357-019-00084-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Raza, M., Deshpande, L. S., Blair, R. E., Carter, D. S., Sombati, S., and Delorenzo, R. J. (2007). Aging is associated with elevated intracellular calcium levels and altered calcium homeostatic mechanisms in hippocampal neurons. Neurosci. Lett. 418, 77–81. doi: 10.1016/j.neulet.2007.03.005

PubMed Abstract | CrossRef Full Text | Google Scholar

Riazi, S., Kraeva, N., and Hopkins, P. M. (2018). Updated guide for the management of malignant hyperthermia. Can. J. Anaesth. 65, 709–721. doi: 10.1007/s12630-018-1108-0

PubMed Abstract | CrossRef Full Text | Google Scholar

Robin, G., Lopez, J. R., Espinal, G. M., Hulsizer, S., Hagerman, P. J., and Pessah, I. N. (2017). Calcium dysregulation and Cdk5-ATM pathway involved in a mouse model of fragile X-associated tremor/ataxia syndrome. Hum. Mol. Genet. 26, 2649–2666. doi: 10.1093/hmg/ddx148

PubMed Abstract | CrossRef Full Text | Google Scholar

Samanta, A., Hughes, T. E. T., and Moiseenkova-Bell, V. Y. (2018). Transient receptor potential (TRP) channels. Subcell. Biochem. 87, 141–165. doi: 10.1007/978-981-10-7757-9_6

PubMed Abstract | CrossRef Full Text | Google Scholar

Sawamura, S., Shirakawa, H., Nakagawa, T., Mori, Y., and Kaneko, S. (2017). “TRP channels in the brain: what are they there for?,” in Neurobiology of TRP Channels, ed. T. L. R. Emir. (Boca Raton, FL: CRC Press/Taylor & Francis), 295–322.

Google Scholar

Schwaller, B. (2012). The regulation of a cell’s Ca(2+) signaling toolkit: the Ca (2+) homeostasome. Adv. Exp. Med. Biol. 740, 1–25. doi: 10.1007/978-94-007-2888-2_1

PubMed Abstract | CrossRef Full Text | Google Scholar

Selvaraj, S., Sun, Y., and Singh, B. B. (2010). TRPC channels and their implication in neurological diseases. CNS Neurol. Disord. Drug Targets 9, 94–104. doi: 10.2174/187152710790966650

PubMed Abstract | CrossRef Full Text | Google Scholar

Sesay, A. K., Errington, M. L., Levita, L., and Bliss, T. V. (1996). Spatial learning and hippocampal long-term potentiation are not impaired in mdx mice. Neurosci. Lett. 211, 207–210. doi: 10.1016/0304-3940(96)12747-6

PubMed Abstract | CrossRef Full Text | Google Scholar

Sukumaran, P., Sun, Y., Schaar, A., Selvaraj, S., and Singh, B. B. (2017). TRPC channels and Parkinson’s disease. Adv. Exp. Med. Biol. 976, 85–94. doi: 10.1007/978-94-024-1088-4_8

PubMed Abstract | CrossRef Full Text | Google Scholar

Sun, Y., Sukumaran, P., Bandyopadhyay, B. C., and Singh, B. B. (2014). Physiological function and characterization of TRPCs in neurons. Cells 3, 455–475. doi: 10.3390/cells3020455

PubMed Abstract | CrossRef Full Text | Google Scholar

Takada, Y., Numata, T., and Mori, Y. (2013). Targeting TRPs in neurodegenerative disorders. Curr. Top. Med. Chem. 13, 322–334. doi: 10.2174/1568026611313030009

PubMed Abstract | CrossRef Full Text | Google Scholar

Tarantini, S., Yabluchanskiy, A., Csipo, T., Fulop, G., Kiss, T., Balasubramanian, P., et al. (2019). Treatment with the poly(ADP-ribose) polymerase inhibitor PJ-34 improves cerebromicrovascular endothelial function, neurovascular coupling responses and cognitive performance in aged mice, supporting the NAD+ depletion hypothesis of neurovascular aging. Geroscience 41, 533–542. doi: 10.1007/s11357-019-00101-2

PubMed Abstract | CrossRef Full Text | Google Scholar

Thibault, O., Gant, J. C., and Landfield, P. W. (2007). Expansion of the calcium hypothesis of brain aging and Alzheimer’s disease: minding the store. Aging Cell 6, 307–317. doi: 10.1111/j.1474-9726.2007.00295.x

PubMed Abstract | CrossRef Full Text | Google Scholar

Thibault, O., Hadley, R., and Landfield, P. W. (2001). Elevated postsynaptic [Ca2+]i and L-type calcium channel activity in aged hippocampal neurons: relationship to impaired synaptic plasticity. J. Neurosci. 21, 9744–9756. doi: 10.1523/jneurosci.21-24-09744.2001

PubMed Abstract | CrossRef Full Text | Google Scholar

Thibault, O., and Landfield, P. W. (1996). Increase in single L-type calcium channels in hippocampal neurons during aging. Science 272, 1017–1020. doi: 10.1126/science.272.5264.1017

PubMed Abstract | CrossRef Full Text | Google Scholar

Tonkikh, A., Janus, C., El-Beheiry, H., Pennefather, P. S., Samoilova, M., Mcdonald, P., et al. (2006). Calcium chelation improves spatial learning and synaptic plasticity in aged rats. Exp. Neurol. 197, 291–300. doi: 10.1016/j.expneurol.2005.06.014

PubMed Abstract | CrossRef Full Text | Google Scholar

Tromp, D., Dufour, A., Lithfous, S., Pebayle, T., and Despres, O. (2015). Episodic memory in normal aging and Alzheimer disease: insights from imaging and behavioral studies. Ageing Res. Rev. 24, 232–262. doi: 10.1016/j.arr.2015.08.006

PubMed Abstract | CrossRef Full Text | Google Scholar

Vaillend, C., Billard, J. M., and Laroche, S. (2004). Impaired long-term spatial and recognition memory and enhanced CA1 hippocampal LTP in the dystrophin-deficient Dmd(mdx) mouse. Neurobiol. Dis. 17, 10–20. doi: 10.1016/j.nbd.2004.05.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Wang, Y., Shi, Y., and Wei, H. (2017). Calcium dysregulation in Alzheimer’s disease: a target for new drug development. J. Alzheimers Dis. Parkinsonism 7:374. doi: 10.4172/2161-0460.1000374

PubMed Abstract | CrossRef Full Text | Google Scholar

Wu, W. W., Oh, M. M., and Disterhoft, J. F. (2002). Age-related biophysical alterations of hippocampal pyramidal neurons: implications for learning and memory. Ageing Res. Rev. 1, 181–207. doi: 10.1016/s1568-1637(01)00009-5

PubMed Abstract | CrossRef Full Text | Google Scholar

Yang, T., Riehl, J., Esteve, E., Matthaei, K. I., Goth, S., Allen, P. D., et al. (2006). Pharmacologic and functional characterization of malignant hyperthermia in the R163C RyR1 knock-in mouse. Anesthesiology 105, 1164–1175. doi: 10.1097/00000542-200612000-00016

PubMed Abstract | CrossRef Full Text | Google Scholar

Zima, A. V., Bovo, E., Bers, D. M., and Blatter, L. A. (2010). Ca(2)+ spark-dependent and -independent sarcoplasmic reticulum Ca(2)+ leak in normal and failing rabbit ventricular myocytes. J. Physiol. 588, 4743–4757. doi: 10.1113/jphysiol.2010.197913

PubMed Abstract | CrossRef Full Text | Google Scholar