Javad Sharifi-Rad1*†
Amit Bahukhandi2†
Praveen Dhyani3†Priyanka Sati4†
Esra Capanoglu5†
Anca Oana Docea6†
Ahmed Al-Harrasi7*†
Abhijit Dey8†
Daniela Calina9*†- 1Phytochemistry Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran
- 2G.B Pant National Institute of Himalayan Environment, Almora, India
- 3Institute of Himalayan Bioresource Technology, Palampur, India
- 4Department of Biotechnology Graphic Era University, Dehradun, India
- 5Food Engineering Department, Faculty of Chemical and Metallurgical Engineering, Istanbul Technical University, Maslak, Turkey
- 6Department of Toxicology, University of Medicine and Pharmacy of Craiova, Craiova, Romania
- 7Natural and Medical Sciences Research Centre, University of Nizwa, Nizwa, Oman
- 8Department of Life Sciences, Presidency University, Kolkata, India
- 9Department of Clinical Pharmacy, University of Medicine and Pharmacy of Craiova, Craiova, Romania
Neoechinulins are diketopiperazine type indole alkaloids that demonstrate radical scavenging, anti-inflammatory, antiviral, anti-neurodegenerative, neurotrophic factor-like, anticancer, pro-apoptotic, and anti-apoptotic properties. An array of neoechinulins such as neoechinulins A-E, isoechinulins A-C, cryptoechunilin have been isolated from various fungal sources like Aspergillus sp., Xylaria euglossa, Eurotium cristatum, Microsporum sp., etc. Besides, neoechinulin derivatives or stereoisomers were also obtained from diverse non-fungal sources viz. Tinospora sagittata, Opuntia dillenii, Cyrtomium fortunei, Cannabis sativa, and so on. The main purpose of this review is to provide update information on neoechinulins and their analogues about the molecular mechanisms of the pharmacological action and possible future research. The recent data from this review can be used to create a basis for the discovery of new neoechinulin-based drugs and their analogues in the near future. The online databases PubMed, Science and Google scholar were researched for the selection and collection of data from the available literature on neoechinulins, their natural sources and their pharmacological properties. The published books on this topic were also analysed. In vitro and in vivo assays have established the potential of neoechinulin A as a promising anticancer and anti-neuroinflammatory lead molecule. Neoechinulin B was also identified as a potential antiviral drug against hepatitis C virus. Toxicological and clinical trials are needed in the future to improve the phyto-pharmacological profile of neoquinolines. From the analysis of the literature, we found that neoechinulins and their derivatives have special biological potential. Although some modern pharmacological analyzes have highlighted the molecular mechanisms of action and some signalling pathways, the correlation between these phytoconstituents and pharmacological activities must be validated in the future by preclinical toxicological and clinical studies.
Introduction
Neoechinulins are alkaloids and are consisted of three structural moieties viz. an indole, an isoprenyl and a diketopiperazine moiety. There are several neoechinulins and related metabolites including neoechinulins A-E, isoechinulins A-C, cryptoechunilin etc. (1). Neoechinulins have been isolated from Aspergillus sp. (2–5), ascomycete Xylaria euglossa (6), and some others (7, 8).
Echinulin, preechinulin, and neoechinulin E were also obtained as minor metabolites in the extracts of Eurotium amstelodami and E. rubrum cultures (9). Although rarely observed, neoechinulins and their derivatives or stereoisomers were also isolated from different sources. Stereoisomers of diketopiperazine indole alkaloids namely (12S, 22R)-Dihydroxyisoechinulin A, (12S, 22S)-Dihydroxyisoechinulin A, (12R)-Neoechinulin A, and (12S)-Neoechinulin A were isolated from hemp seed (10). Their presence in different plant sources including Tinosporae Radix (the roots of Tinospora sagittata) (11), Opuntia dillenii (12), Cyrtomium fortunei (13) etc. have also been reported. Table 1 presents the plant species as firstly reported natural sources of neoechinulins.
Table 1. The most important natural sources of neoechinulins.
Several therapeutic effects of neoechinulin A, B, and other derivatives have been reported in different studies including antioxidant, anti-inflammatory, antitumor effects, and neuroprotective activity (5, 16, 19–21).
In this paper, the aim is to review the therapeutic potential of neoechinulins together with their molecular mechanisms behind the biological activities, specifically focusing on preclinical pharmacological studies (Figure 1).
Figure 1. A diagram with the relevant pharmacological properties of the most important neoechinulins and their potential mechanism of actions. NO, nitric oxide; PGE, prostaglandin E2; TNF-α, tumour necrosis alfa; IL-1β, interleukin-1β; NF-Kβ, Nuclear factor-κβ; MAPK, mitogen-activated protein kinase.
Purposes and Review Methodology
Search Strategy
A study was conducted on PubMed, ScienceDirect and Google scholar using various combinations of MESH terms and their synonyms: “neoechinulin,” “fungus,” “in vivo,” “in vitro,” “anti-inflammatory,” “anti-viral,” “anti- cancer ,” “neuroprotective.”
Inclusion Criteria
- extensive works with isolated neoechinulins with the evaluation of pharmacological activities
- pre-clinical experimental pharmacological studies with determining doses and mechanisms of action
- studies and articles written only in the English language
Exclusion Criteria
- studies that used in the experiment extracts from different parts of plants.
- studies in which neoechinulins have been associated with homoeopathic preparations or other nutritional supplements
- studies that included other substances, in silico studies, duplicates, abstracts
In this comprehensive review, we selected the best articles highlighting the possible molecular mechanisms of the pharmacological properties of neoechinulines. These data have been summarised in two figures and two tables.
Pharmacological Activities of Neoechinulins
Anti-inflammatory
Inflammation is an important defence mechanism of the body during acute inflammatory responses, maintaining tissue homeostasis (22, 23). However, sometimes uncontrolled acute inflammation might turn into chronic and lead to an array of medical conditions, including hepatitis, arthritis, and neurodegenerative ailments (24–26). In numerous inflammatory responses, macrophages reported to be activated by LPS 9 (lypopolisaccharides), produce pro-inflammatory mediators and cytokines viz. NO, interleukin-1β (IL-1β), PGE2 etc (27). These pro-inflammatory mediators and cytokines are induced by different enzymes like cyclooxygenase-2 (COX-2), iNOS (28, 29). Nuclear factor-kappa B (NF-κB) along with its inhibitory protein, IκB controls the transcription of pro-inflammatory mediators and cytokines such as NO (nitric oxide), iNOS (inducible isoform NO), COX-2 (ciclooxigenase 2), TNF-α (Tumour necrosis alfa), PGE2 (prostaglandin E2), and IL-1β (interleukin 1β) (30, 31) Besides, mitogen-activated protein kinases (MAPKs) are also known to induce production of cytokine and the expression of iNOS and COX-2 (32, 33).
Neoechinulin A exhibited anti-inflammatory activity (Table 1) on lipopolysaccharide (LPS)_-treated RAW264.7 macrophages which were implicated in the inhibition of NF-kB and p38 MAPK pathway (16). Besides, neoechinulin A induced reduction in the expression of iNOS catalyzes, COX-2 and MAPK pathway dose-dependently resulted in a dose-dependent decreased in the synthesis of nitric oxide (NO) and prostaglandin E2 (PGE2). This mechanism indicated that natural diketopiperazine-type indole alkaloids have anti-inflammatory properties, and their therapeutic potential can be used to treat inflammatory disorders (16). Moreover, neoechinulin A showed suppressive ability on Ab42-induced microglial activation and demonstrated capabilities to inhibit the production of neurotoxic inflammatory mediators (TNFα, IL-1β; IL-6; PGE2) in activated BV-2 cells through blocking the phosphorylation of MAPK. Therefore, results proved that neoechinulin A suppressed the production of reactive oxygen species (ROS) and reactive nitrogen species (RNS) remarkably and reduced the mRNA expressions and protein synthesis of various mediators of inflammation (34).
In another study, it has been reported that marine fungi produce natural metabolites that can reduce inflammation (35).
In another study, neoechinulins A and B were isolated from the marine fungus Eurotium sp. SF-5989, and their anti-inflammatory effects on lipopolysaccharide (LPS)-stimulated RAW264.7 macrophages were investigated. The results indicated that neoechinulin A inhibited the nitric oxide (NO) and prostaglandin E2 (PGE2) production as well as the inducible nitric oxide synthase (iNOS) and cyclooxygenase-2 (COX-2) expression, whereas neoechinulin B influenced the cell viability besides its similar suppressive effect on NO production at lower doses. Different mechanisms of action for neoechinulin A were also reported, indicating its potential as an anti-inflammatory agent (16).
Anti-viral
Neoechinulin A, including emodin, emodin-8-O-β-D-glucoside, was isolated for the first time from the ethanolic root extract of Aconitum carmichaelii and was suggested for utilisation in discovering novel anti plant viral agents (14). Likewise, an aqueous extract of Portulaca oleracea showed the presence of neoechinulin D and possibilities for further utilisation for the treatment of diseases (15) (Table 1).
This information indicated that marine plants can produce neoechinulin and highlighted future gap area for further investigation.
Only ten diverse compounds viz., echinulin, neoechinulin A, neoechinulin D, dihydroauroglaucin, physcion, flavoglaucin, isodihydroauroglaucin, cinnalutein, asperflavin, and cyclo-L-Trp-L-Ala were isolated from Eurotium. chevalieri. Among these isolated compounds, neoechinulin D is reported with antiviral properties against herpes and inluenza viruses (17). Furthermore, neoechinulin B showed potency to inhibit the H1N1 virus-infected in MDCK cells (model mammalian cell line) and their ability to bind with influenza envelope hemagglutinin, breakdown of sialic acid receptor interaction and viral attachment to host cell. Therefore, neoechinulin B was cited as a potent inhibitor of the influenza virus (36) Similarly, in a study reporting neoechinulin B activity against HCV (hepatitis C virus) in the cell culture system, the compound was recorded as a novel suppressor of the LXR (liver X receptor). Neoechinulin B suppressed the induction of LXR-mediated transcription, disrupted double-membrane or multi membrane vesicles blocking the HCV replication and altered lipid metabolism. Thus, neoechinulin B can act as an anti-HCV agent without showing any type of cytotoxicity (18).
Neoechinulin B, a secondary metabolite of Aspergillus amstelodami was reported as a suppressor of the liver X receptor (LXR) in a cell culture system of the hepatitis C virus (HCV). The results of this study indicated that neoechinulin B suppresses LXR-mediated transcription, and interacts directly with LXRs (18).
In a recent study, a potent antiviral effect of neoechinulin B against H1N1 virus-infected in Madin-Darby canine kidney (MDCK) cells was also investigated. The authors reported that neoechinulin B was able to suppress influenza virus that included clinical isolates of amantadine- and oseltamivir-resistant strains. The mechanism was explained with the binding of neoechinulin B to influenza envelope hemagglutinin, disturbing its interaction with the sialic acid receptor and the virus attachment to host cells (37).
Anti-cancer
Neoechinulin A has the capabilities to act against different tumour cells (Figure 2) Most of the cancer cells block programmed cell death (apoptosis) through anti-apoptotic signalling pathways, thus disrupting the vital equilibrium between proliferation and death of the cells (38).
Figure 2. Summarised scheme of potential cytotoxic mechanisms of neochinulins to induce apoptosis in cancer cells. p53, p21, cellular tumour antigen; Bcl-2, B-cell lymphoma 2; Bax, Bcl-2-associated X Protein.
The expression of apoptosis-related proteins, in particular, anti-apoptotic proteins viz. Bcl-2, Bcl-xl, Mcl-1, and pro-apoptotic proteins viz. Bax, Bad, Bak is essential for apoptosis regulation (39). Study reported that neoechinulin A as an induced p53 tumour protein towards caspase-3 and thus enabled the HeLa cells to enter the apoptotic pathway. The results of this study showed that neoechinulins can down-regulate Bcl-2 protein expression and upregulate Bax protein expression, thus activating caspase-3 cascade and leading to the HeLa cells apoptosis. (40).
Anti-nitration, antioxidant activities and cytoprotection offered by neoechinulin A and its analogues against 3-morpholinosydnonimine (SIN-1)-induced phaeochromocytoma (PC12) cell death were measured to reveal the structure-activity relationships of these compounds (1) Z. The authors reported that the cytoprotective effect of an acyclic analogue was diminished while maintaining its antioxidant or anti-nitration properties. They have concluded that cytoprotective effect of neoechinulin A was provided by a mechanism not attributed to their antioxidant or anti-nitration properties (41).
Neuroprotective
Neoechinulins displayed potent anti-neurodegenerative activities against neuro-inflammation, deposition of amyloid-β peptides in Alzheimer's disease, Parkinsonian-inducing neurotoxins and other cytotoxicity inducing neurotoxins (rotenone, MPP+, SIN-1, peroxynitrite) (Figure 2). Neoechinulin A showed cytoprotective properties in neuron-like PC12 cells subjected to a peroxynitrite-imposed oxidative injury (42). Besides, neoechinulin A protected PC12 cells from cytotoxic effects of 1-methyl-4-phenylpyridinium (MPP+), a potent neurotoxin provoking acute Parkinson's-like neurodegenerative symptoms in humans (43).
Several studies explored the biological potential of neoechinulin, in the treatment of neurodegenerative diseases (Table 2). Neurodegenerative diseases like Alzheimer's and Parkinson's diseases cause mortality and morbidity for millions of people across the globe (45). The predominant causative factors for these are mainly ageing and environmental (neurotoxins), apart from a small fraction of mutation related genes (46, 47). The main pathological changes related to these diseases are progressive and selective loss of dopaminergic neurons in the brain (48). This is mainly attributed to peroxynitrite, a potent oxidant generated in a biological system by the reaction of NO and superoxide anion (O2−) in vivo causing severe cell damage to neurons, by promoting the oxidation of various biomolecules (lipid, proteins and nucleic acids) (49–51) (Table 2).
Table 2. The most relevant pharmacological properties of neoechinulins, possible mechanisms, and signalling pathways.
Marine-derived natural products such as neoechinulins produce a variety of pharmacological effects for downstream amelioration of neurotoxins-induced cytotoxicity. Its pharmacological properties against various neurotoxins are generally attributed to the C8/C9 double bond, offering a conjugated system across the indole moiety to the diketopiperazine ring. Additionally, the antioxidant efficacy or electrophilic nature of the C-8 carbon may contribute to the cytoprotective ability of the alkaloid (19). However, diketopiperazine moiety is reported as a requisite for anti-nitration activity (38).
Neoechinulin A protects neuronal PC12 cells (cell line from rat adrenal medulla) against cell death imposed by peroxynitrite derived from SIN 1 [3-(4-morpholinyl) sydnonimine hydrochloride] (42). Neoechinulin A exhibited a strong affinity for specific binding to diverse proteins, namely chromogranin B and glutaredoxin 3. This high affinity of neoechinulin A might be responsible for the protection of PC12 cells from cytotoxicity by inducing S–morpholinosydnonimine (SIN-1). Neoechinulin, apart from its apparent antioxidant and anti-nitration activities, imparts cytoprotection to cells with neurotrophic factor-like and anti-apoptotic properties, probably via potentiation of NAD(P)H-producing ability of the cell (44). However, the NAD(P)H-generating dehydrogenase(s) involved in the process remain elusive (41).
Neoechinulin A treatment can be useful for the protection of PC12 cells against MPP++ neurotoxin cytotoxicity derived from prodrug 1-methyl-4-phenyl-1,2,3,6 tetrahydropyridine (MPTP) (52). The MPP++ which assembles in mitochondria and binds to electron transport chain's complex I, thus reducing ATP biosynthesis, leads to cell death; is ameliorated by an increase in the ability of cells to produce NADH (43). Furthermore, the increase in NADH or lowering of cellular ATP levels by Neoechinulin A is also found to be effective against Parkinsonian-inducing neurotoxins such as rotenone (a pesticide), targeting mitochondrial complex I in animal models such as rat pheochromocytoma cell line(38), thereby delaying the progression of neurodegenerative diseases. In another study, synthetic (–) and (+) neoechinulin A, displayed cytoprotection by preventing SIN-1-induced cytotoxicity in nerve growth factor (NGF)-differentiated PC12 cells. The structure-activity relationships explained that the C8/C9 double bond played a crucial role attributed to its anti-cytotoxic potential (21).
Neoechinulin A was also investigated for its efficacy on cognitive damage in mice treated with lipopolysaccharide (LPS) mice and its antidepressive properties in were also recorded. Neoechinulin A enhanced cognitive ability in LPS-insulted mice besides offering antidepressant-like properties (53) (Table 2).
Overall Conclusion and Future Perspectives
Neoechinulins and their analogues, derived from marine fungi, with proven pharmacological benefits for human health, can be prolific therapeutic agents for many existing diseases. Due to these positive pharmacological effects, neoquinolines derived from marine fungi can be considered in the future as potential functional and integrative nutrition, as part of functional and integrative medicine, with a major role in preventing, reducing causes, manifestations of diseases through a diet appropriate to each patient. In the future, neoquinolines may be introduced into functional foods or dietary compounds (nutraceuticals) that benefit human health by preventing or treating diseases, or by correcting metabolic disorders, or by preventing the progression or recurrence of a pathological situation.
The therapeutic applications of neoechinulins and their natural and synthetic analogues and derivatives are needed to be explored by more animal models via analysing their structure-activity relationships and elucidating their underlying mechanisms of action specific to various biosynthesis and signalling pathways and possible cross-talks through high throughout techniques. Although primarily obtained from fungal sources, such compounds have also been discovered in higher plants. Numerous researches have demonstrated their potential as anti-inflammatory, anti-viral, anti-cancerous and anti-Parkinson's properties. Besides, they exhibited potent anti-neurodegenerative efficacy against neuroinflammation and neurotoxicity. Structure-activity relationships of neoechinulins and their analogues with their reported bioactivities are in their nascent stage and are needed to be elucidated. The reported antioxidant or electrophilic property of the C-8 carbon, both of which are contributed by the double bond in C-8/C-9, is probably attributed to the cytoprotective nature of this alkaloid. Besides, diketopiperazine moiety was reported as a requisite for anti-nitration activity. However, this potential, along with ever-expanding microbial resistance to conventional drugs and quest for the search for novel natural compounds of pharmacological importance, is to be complemented by an investigation of the specific biosynthesis pathway, signalling pathway through high throughput techniques.
Author Contributions
JS-R, ADe, EC, AB, PD, PS, and ADo contributed significantly to analysis and manuscript preparation. ADe, JS-R, AA-H, and DC assistance to the revision of the manuscript. ADe, AA-H, JS-R, and ADo supported valuable discussion. JS-R, ADo, and DC revised the whole manuscript. All authors collated documents, wrote the manuscript, read, and approved the final manuscript.
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.
Abbreviations
COX-2, cyclooxygenase-2; HCV, hepatitis C virus; 5-HT, 5-hydroxytryptamine; iNOS, inducible nitric oxide synthase; IκB, inhibitor of nuclear factor-kappa B; IL-1β, interleukin-1β; i.c.v., intracerebroventricular; LPS, lipopolysaccharide; LXR, liver X receptor; MDCK, Madin-Darby canine kidney; MAPKs, mitogen-activated protein kinases; MPTP, 1-methyl-4-phenyl-1,2,3,6 tetrahydropyridine; MPP+, 1-methyl-4-phenylpyridinium; NGF, nerve growth factor; NO, nitric oxide; NF-κB, nuclear factor-kappa B; O2−, superoxide anion; PC12, phaeochromocytoma; PGE2, prostaglandin E2; RNS, reactive nitrogen species; ROS, reactive oxygen species; SIN-1, 3-morpholinosydnonimine.
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Keywords: neoechinulins, alkaloid, fungus, in vitro, in vivo, anticancer, antiviral, anti-inflammatory
Citation: Sharifi-Rad J, Bahukhandi A, Dhyani P, Sati P, Capanoglu E, Docea AO, Al-Harrasi A, Dey A and Calina D (2021) Therapeutic Potential of Neoechinulins and Their Derivatives: An Overview of the Molecular Mechanisms Behind Pharmacological Activities. Front. Nutr. 8:664197. doi: 10.3389/fnut.2021.664197
Received: 04 February 2021; Accepted: 22 June 2021;
Published: 16 July 2021.
Edited by:
Zhenzhou Zhu, Wuhan Polytechnic University, ChinaReviewed by:
Tânia Rodrigues Dias, University of Aveiro, PortugalDenis Baranenko, ITMO University, Russia
Copyright © 2021 Sharifi-Rad, Bahukhandi, Dhyani, Sati, Capanoglu, Docea, Al-Harrasi, Dey and Calina. 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: Javad Sharifi-Rad, javad.sharifirad@gmail.com; Ahmed Al-Harrasi, aharrasi@unizwa.edu.om; Daniela Calina, calinadaniela@gmail.com
†These authors have contributed equally to this work and share first authorship