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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" article-type="review-article">
<front>
<journal-meta>
<journal-id journal-id-type="nlm-ta">Explor Neurosci</journal-id>
<journal-id journal-id-type="publisher-id">EN</journal-id>
<journal-title-group>
<journal-title>Exploration of Neuroscience</journal-title>
</journal-title-group>
<issn pub-type="epub">2834-5347</issn>
<publisher>
<publisher-name>Open Exploration Publishing</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.37349/en.2023.00030</article-id>
<article-id pub-id-type="manuscript">100630</article-id>
<article-categories>
<subj-group>
<subject>Mini Review</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>Neuroprotective compounds from three common medicinal plants of West Bengal, India: a mini review</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<contrib-id contrib-id-type="orcid">https://orcid.org/0009-0009-8384-5984</contrib-id>
<name>
<surname>Ghosh</surname>
<given-names>Suvendu</given-names>
</name>
<role content-type="https://credit.niso.org/contributor-roles/writing-original-draft/">Writing—original draft</role>
<role content-type="https://credit.niso.org/contributor-roles/investigation/">Investigation</role>
<xref ref-type="aff" rid="I1">
<sup>1</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-8255-3271</contrib-id>
<name>
<surname>Singha</surname>
<given-names>Partha Sarathi</given-names>
</name>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/">Writing—review &amp; editing</role>
<role content-type="https://credit.niso.org/contributor-roles/investigation/">Investigation</role>
<xref ref-type="aff" rid="I2">
<sup>2</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<contrib-id contrib-id-type="orcid">https://orcid.org/0000-0002-4382-4283</contrib-id>
<name>
<surname>Ghosh</surname>
<given-names>Debosree</given-names>
</name>
<role content-type="https://credit.niso.org/contributor-roles/conceptualization/">Conceptualization</role>
<role content-type="https://credit.niso.org/contributor-roles/writing-original-draft/">Writing—original draft</role>
<role content-type="https://credit.niso.org/contributor-roles/writing-review-editing/">Writing—review &amp; editing</role>
<role content-type="https://credit.niso.org/contributor-roles/investigation/">Investigation</role>
<xref ref-type="aff" rid="I3">
<sup>3</sup>
</xref>
<xref ref-type="corresp" rid="cor1">
<sup>*</sup>
</xref>
</contrib>
<contrib contrib-type="editor">
<name>
<surname>Iriti</surname>
<given-names>Marcello</given-names>
</name>
<role>Academic Editor</role>
<aff>Milan State University, Italy</aff>
</contrib>
</contrib-group>
<aff id="I1">
<sup>1</sup>Department of Physiology, Hooghly Mohsin College, Chinsura, Hooghly Pin 712101, West Bengal, India</aff>
<aff id="I2">
<sup>2</sup>Department of Chemistry, Government General Degree College, Kharagpur II, Paschim Medinipur Pin 721149, West Bengal, India</aff>
<aff id="I3">
<sup>3</sup>Department of Physiology, Government General Degree College, Kharagpur II, Paschim Medinipur Pin 721149, West Bengal, India</aff>
<author-notes>
<corresp id="cor1">
<bold>
<sup>*</sup>Correspondence:</bold> Debosree Ghosh, Department of Physiology, Government General Degree College, Kharagpur II, Paschim Medinipur Pin 721149, West Bengal, India. <email>ghoshdebosree@gmail.com</email></corresp>
</author-notes>
<pub-date pub-type="ppub">
<year>2023</year>
</pub-date>
<pub-date pub-type="epub">
<day>26</day>
<month>12</month>
<year>2023</year>
</pub-date>
<volume>2</volume>
<issue>6</issue>
<fpage>307</fpage>
<lpage>317</lpage>
<history>
<date date-type="received">
<day>27</day>
<month>10</month>
<year>2023</year>
</date>
<date date-type="accepted">
<day>09</day>
<month>12</month>
<year>2023</year>
</date>
</history>
<permissions>
<copyright-statement>© The Author(s) 2023.</copyright-statement>
<license xlink:href="https://creativecommons.org/licenses/by/4.0/">
<license-p>This is an Open Access article licensed under a Creative Commons Attribution 4.0 International License (<ext-link ext-link-type="uri" xlink:href="https://creativecommons.org/licenses/by/4.0/">https://creativecommons.org/licenses/by/4.0/</ext-link>), which permits unrestricted use, sharing, adaptation, distribution and reproduction in any medium or format, for any purpose, even commercially, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.</license-p>
</license>
</permissions>
<abstract>
<p>Neural disorders refer to conditions of the nervous system due to infection or degeneration of the neurons leading to either neurodegenerative disorder or neuropsychiatric disorder. Some such disorders of the nervous system include Parkinsons’s disease, depression, amnesia, dementia, Alzheimer’s disease, schizophrenia, cerebrovascular impairment, epilepsy, seizure disorders, etc. In conventional medical system, some medicines belonging to the class of psychodelic drugs, sedatives, neurotransmitters, neuro-stimulants, etc. are in extensive use. Unfortunately, most of these drugs either delay the progression of the neural disorder or leave the patient with prominent adverse side effects. Several potent bioactive compounds with neuroprotective potential have been reported from medicinal plants and some of them have been found to be highly effective. Belonging from natural sources, mostly, the plant derived compounds exhibit minimum or no cytotoxicity at a prescribed standardised dose against a particular health ailment. Many such phytocompounds from plant sources with potent neuroprotective activities have been in use in Ayurvedacharya, Unani, and Chinese medicine for ages. The compounds if isolated chemically, modified to make more potent neuroprotective derivatives and utilised to make highly effective neuroprotective pharmaceutical formulations with minimum side effects, may open new revolutionary doorways in neuropharmacology. In this review, it has been briefly discussed about the neuroprotective compounds isolated from certain indigenous plants of West Bengal, India, and their mechanism of action.</p>
</abstract>
<kwd-group>
<kwd>Neuroprotection</kwd>
<kwd>phytocompounds</kwd>
<kwd>Ayurvedacharya</kwd>
<kwd>Alzheimer’s disease</kwd>
<kwd>Parkinsons’s disease</kwd>
</kwd-group>
</article-meta>
</front>
<body>
<sec id="s1">
<title>Introduction</title>
<p id="p-1">Plants are sources of myriads of potent bioactive compounds with medicinal properties [<xref ref-type="bibr" rid="B1">1</xref>, <xref ref-type="bibr" rid="B2">2</xref>]. Studies show that plants growing under the ocean are also a rich source of bioactive phytochemical and are of immense medicinal importance [<xref ref-type="bibr" rid="B3">3</xref>]. Plants have been medicinally important since the beginning of civilization and various medicines used in Ayurveda, Unani, etc. have their sources from plants. Many of the drugs of modern day owe their roots to plant origin. Potent bioactive compounds derived from plant sources are used as potent lead molecules for developing drugs with minimal side effects [<xref ref-type="bibr" rid="B4">4</xref>]. Plants of every region have their unique phytochemical. The composition of the phytochemicals is known to vary in quality and quantity depending on the geographic region and soil composition on which the plant grows [<xref ref-type="bibr" rid="B5">5</xref>]. Natural products have been in use as drug candidates since ages [<xref ref-type="bibr" rid="B6">6</xref>]. Plants growing in a particular region by default find their use in local folk medicine. Mother nature has gifted mankind with a vast reserve of different kinds of plants all around. Most of these plants are rich source of potent bioactive phytochemical. The plants like <italic>Murraya koenigii</italic>, <italic>Moringa olefera</italic>, <italic>Ocimum sanctum</italic>, <italic>Terminalia arjuna</italic>, <italic>Azadirachta indica</italic>, and <italic>Coriendrum sativum</italic> are some of the very common popular potent medicinal plants found in almost all regions of South-East Asia including India [<xref ref-type="bibr" rid="B7">7</xref>–<xref ref-type="bibr" rid="B11">11</xref>]. Several hundreds of medicinal plants growing in the Indian Sub-continent have been identified to have potent neuroprotective activity. Some of these are <italic>Bacopa monnierae</italic>, <italic>Withania somnifera</italic>, <italic>Hypericum perforatum</italic>, <italic>Allium sativum</italic>, <italic>Centella asiatica</italic>, <italic>Nicotiana tabaccum</italic>, <italic>Celastrus paniculatus</italic>, <italic>Enhydra fluctuans</italic>, <italic>Ricinus communis</italic>, <italic>Ginkgo biloba</italic>, <italic>Angelica sinensis</italic>, <italic>Uncaria tomentosa</italic>, <italic>Terminalia chebula</italic>, <italic>Salvia officinalis</italic>, <italic>Physostigma venosum</italic>, <italic>Acorus calmus</italic>, <italic>Curcuma longa</italic>, <italic>Huperiza serrata</italic>, <italic>Glycyrrhiza glabra</italic>, <italic>Crocus sativus</italic>, and <italic>Valeriana wallichii</italic>, etc. [<xref ref-type="bibr" rid="B12">12</xref>].</p>
<p id="p-2">Neuroprotection refers to the mechanism of protection of neurons from injuries or degenerations and conserving their normal physiological functions [<xref ref-type="bibr" rid="B13">13</xref>, <xref ref-type="bibr" rid="B14">14</xref>]. Most common neurodegenerative diseases affect the aging population around the globe. Several plants derived traditional medication are there in use for ages for treating neurodegenerative situations, improving memory and learning as well as delaying the process of ageing [<xref ref-type="bibr" rid="B15">15</xref>, <xref ref-type="bibr" rid="B16">16</xref>].</p>
<p id="p-3">More than one hundred and twenty plants are known to be in use to address neurological ailments in the Asian countries [<xref ref-type="bibr" rid="B16">16</xref>]. These plants are rich sources of phytocompounds which have been studied to have potent neuroprotective activities [<xref ref-type="bibr" rid="B12">12</xref>]. Thus, the bioactive compounds and their derivatives with neuroprotective potential from these plants are used as lead compounds for developing neuro-psychopharmacological drug formulations. In this review, the neuroprotective compounds and their mechanism of action from four major indigenous plants grown in the state of West Bengal, India has been discussed.</p>
</sec>
<sec id="s2">
<title>Neuroprotective compounds from <italic>Withania somnifera</italic> (Aswagandha)</title>
<p id="p-4">
<italic>Withania somnifera</italic> (Ashwagandha) is a very common medicinal plant of India and has been in extensive use in Ayurveda for ages. The plant has several medicinal properties. Neuroprotective potential of Aswagandha is one of the most important and significant medicinal properties of the plant. It is known to be used as a nerve tonic in Ayurveda [<xref ref-type="bibr" rid="B17">17</xref>]. Studies show that <italic>Withania somnifera</italic> has cognition promoting impact [<xref ref-type="bibr" rid="B17">17</xref>]. It is reported to be effective in treating memory deficit in children and is also known to improve memory in aged people [<xref ref-type="bibr" rid="B17">17</xref>]. <italic>Withania somnifera</italic> is useful and effective in treating neurodegenerative diseases like Alzheimer’s, Parkinson’s and Huntington’s diseases [<xref ref-type="bibr" rid="B17">17</xref>]. <italic>Withania somnifera</italic> is commonly known as the “Indian Ginseng” and “Indian Winter Cherry” [<xref ref-type="bibr" rid="B18">18</xref>]. The plant is known to have γ-aminobutyric acid (GABA) mimetic effect and is reported to promote dendrites formation [<xref ref-type="bibr" rid="B19">19</xref>]. The plant is also known to improve energy levels. It has positive effects on mitochondrial health. The plant is also reported to have anxiolytic and antidepressant effects [<xref ref-type="bibr" rid="B20">20</xref>]. This effect of <italic>Withnia somnifera</italic> is reported to be by virtue of the glycowithanolides present in <italic>Withania somnifera</italic> [<xref ref-type="bibr" rid="B20">20</xref>]. Alkaloids like anaferine, isopelletierine, anahygrine, cuseohygrine have been reported to be present in <italic>Withania somnifera</italic> (<xref ref-type="table" rid="t1">Table 1</xref>). The plant has been known to be a source of saponins and steroidal lactones like withaferins, and withanolides [<xref ref-type="bibr" rid="B21">21</xref>]. Other bioactive compounds reported to be present in <italic>Withania somnifera</italic> are acylsterylglucosides, Withaferin A and sitoindosides (<xref ref-type="table" rid="t1">Table 1</xref>). These compounds have anti-stress effects [<xref ref-type="bibr" rid="B22">22</xref>]. Compounds like 5-dehydroxy withanolide-R and withasomniferin-A have been isolated from the aerial parts of the plant [<xref ref-type="bibr" rid="B23">23</xref>].</p>
<table-wrap id="t1">
<label>Table 1</label>
<caption>
<p>Some neuroprotective phytochemicals from the medicinal plants <italic>Withania somnifera</italic>, <italic>Bacopa monnieri</italic>, and <italic>Centella asiatica</italic>, their actions and the mechanisms of their actions</p>
</caption>
<table frame="hsides" rules="groups">
<thead>
<tr>
<th rowspan="2">
<bold>Plant</bold>
</th>
<th colspan="2">
<bold>Neuroprotective phytochemicals</bold>
</th>
<th rowspan="2">
<bold>Neuroprpotective action</bold>
</th>
<th rowspan="2">
<bold>Mechanism of action</bold>
</th>
</tr>
<tr>
<th>
<bold>Phytochemicals</bold>
</th>
<th>
<bold>Chemical nature</bold>
</th>
</tr>
</thead>
<tbody>
<tr>
<td rowspan="9">
<italic>Withania somnifera</italic>
</td>
<td>Anaferine</td>
<td>Alkaloids</td>
<td rowspan="9">Protection against neurodegenerative diseases like Huntington’s disease, Parkinsonism, Alzheimer’s disease [<xref ref-type="bibr" rid="B24">24</xref>]</td>
<td rowspan="9">GABA mimetic action that promotes dendrites formation [<xref ref-type="bibr" rid="B19">19</xref>]</td>
</tr>
<tr>
<td>Withanolides</td>
<td>Steroidal lactones</td>
</tr>
<tr>
<td>Anahygrine</td>
<td>Alkaloids</td>
</tr>
<tr>
<td>Cuseohygrine</td>
<td>Alkaloids</td>
</tr>
<tr>
<td>Isopelletierine</td>
<td>Alkaloids</td>
</tr>
<tr>
<td>Withaferin A</td>
<td>Steroidal lactones</td>
</tr>
<tr>
<td>Sitoindosides</td>
<td>Acylsterylglucosides</td>
</tr>
<tr>
<td>5-Dehydroxy withanolide-R</td>
<td>Steroidal lactones</td>
</tr>
<tr>
<td>Withasomniferin-A</td>
<td>Steroidal lactones</td>
</tr>
<tr>
<td rowspan="15">
<italic>Bacopa monnieri</italic>
</td>
<td>Bacopaside III</td>
<td>Bascosides</td>
<td rowspan="15">Restoration of memory related disorders, restoration of nerve transmission, defensive role in schizophrenia [<xref ref-type="bibr" rid="B25">25</xref>]</td>
<td rowspan="15">NMDAR1 receptor turnover, stimulates certain kinases activity essential for normal neural transmission activity [<xref ref-type="bibr" rid="B26">26</xref>]</td>
</tr>
<tr>
<td>Bacopaside X</td>
<td>Bascosides</td>
</tr>
<tr>
<td>Bacoside A3</td>
<td>Bascosides</td>
</tr>
<tr>
<td>Bacopasaponin C</td>
<td>Bascosides</td>
</tr>
<tr>
<td>Apigenin</td>
<td>Flavonoid</td>
</tr>
<tr>
<td>Jujubogerin</td>
<td>Saponin glycosides</td>
</tr>
<tr>
<td>Pseudojujubogenin</td>
<td>Saponin glycosides</td>
</tr>
<tr>
<td>Cucurbitacin</td>
<td>Tetracyclic terpenes</td>
</tr>
<tr>
<td>Hersaponin</td>
<td>Alkaloids</td>
</tr>
<tr>
<td>Brahmine</td>
<td>Alkaloids</td>
</tr>
<tr>
<td>Monnierasides I–III</td>
<td>Phenylethanoid glycosides</td>
</tr>
<tr>
<td>D-Mannitol</td>
<td>Sugar alcohol</td>
</tr>
<tr>
<td>Nicotine</td>
<td>Alkaloids</td>
</tr>
<tr>
<td>Herpestine</td>
<td>Glycoside</td>
</tr>
<tr>
<td>Ebelin lactone</td>
<td>Lactone</td>
</tr>
<tr>
<td rowspan="7">
<italic>Centella asiatica</italic>
</td>
<td>Eugenol derivatives</td>
<td>Phenylpropanoid derivatives</td>
<td rowspan="7">Enhances cognition, improves memory. Anxiyolytic, anticonvulsant, protects against beta amyloid toxicity [<xref ref-type="bibr" rid="B27">27</xref>]</td>
<td rowspan="7">
<p>Improves antioxidative signaling pathways like Nrf2 and HO-1 pathways</p>
<p>Impacts other signal transduction pathways like ERK1/2 and PKB pathway [<xref ref-type="bibr" rid="B27">27</xref>]</p>
</td>
</tr>
<tr>
<td>Flavonoids</td>
<td>Phenylpropanoid derivatives</td>
</tr>
<tr>
<td>Caffeoylquinic acids</td>
<td>Phenylpropanoid derivatives</td>
</tr>
<tr>
<td>Plant sterols</td>
<td>Isoprenoids</td>
</tr>
<tr>
<td>Sesquiterpenes</td>
<td>Isoprenoids</td>
</tr>
<tr>
<td>Pentacyclic triterpenoids</td>
<td>Isoprenoids</td>
</tr>
<tr>
<td>Saponins</td>
<td>Glycoside compounds</td>
</tr>
</tbody>
</table>
<table-wrap-foot>
<fn>
<p>NMDAR1: <italic>N</italic>-methyl-<italic>D</italic>-aspartate receptor 1; Nrf2: nuclear factor erythroid 2-related factor 2; HO-1: heme oxygenase-1; ERK1/2: extracellular signal-regulated protein kinases 1 and 2; PKB: protein kinase B</p>
</fn>
</table-wrap-foot>
</table-wrap>
</sec>
<sec id="s3">
<title>Neuroprotective compounds from <italic>Bacopa monnieri</italic> (Brahmi)</title>
<p id="p-5">
<italic>Bacopa monnieri</italic> popularly known as Brahmi is a common medicinal herb grown abundantly in parts of West Bengal, India [<xref ref-type="bibr" rid="B28">28</xref>]. It is a small succulent herb grows naturally in wet soil. The herb was used by the ancient Vedic scholars to memorize lengthy scriptures and sacred hymns. A phytochemical namely Bacosides, is known to be present in Brahmi (<xref ref-type="table" rid="t1">Table 1</xref>), and causes an increase in the cerebral blood flow. This compound is extensively used as brain health supplement and is remarkably used in the treatment of Alzheimer’s disease [<xref ref-type="bibr" rid="B28">28</xref>]. The herb is primarily composed of bioactive compounds like dammarane-type triterpenoid saponins that are called Bacosides and they have jujubogenin or pseudo-jujubogenin moieties as their aglycone units [<xref ref-type="bibr" rid="B29">29</xref>]. Bacosides have been reported to promote nerve impulse transmission, repair damaged neurons by stimulating kinase activity and also stimulate neuronal synthesis [<xref ref-type="bibr" rid="B29">29</xref>]. Bacosides are also reported to restore nerve impulse transmission [<xref ref-type="bibr" rid="B29">29</xref>]. Studies conducted on murine model of schizophrenia reveals that administration of Brahmi resulted in restoration of the memory impairment by decreasing NMDAR1 in certain brain areas in the rats [<xref ref-type="bibr" rid="B30">30</xref>]. Another study shows that memory impairment induced by streptozoticin is restored by Brahmi in murine model [<xref ref-type="bibr" rid="B31">31</xref>]. Studies report that Brahmi has the ability to enhance the expression of 5-hydroxytryptamine type 3A (5-HT3A) receptors, the level of serotonin, and also the level of cyclic adenosine monophosphate response element binding protein (CREB) in hippocampus of postpartum rats and these facilitates the learning abilities of the experimental animals [<xref ref-type="bibr" rid="B32">32</xref>]. The fact that Brahmi has the potential to bring improvements in cognitive abilities, has now been well established with supporting experimental and clinical data [<xref ref-type="bibr" rid="B33">33</xref>, <xref ref-type="bibr" rid="B34">34</xref>]. Studies show that during clinical trials using Brahmi, there has not been any toxicity in the human subjects [<xref ref-type="bibr" rid="B34">34</xref>]. The studies reveal that Brahmi has the ability to improve nervousness, concentration and memory in adult subjects [<xref ref-type="bibr" rid="B34">34</xref>]. A study using 60 healthy human adults, reveals that Brahmi improves cognitive processing, attention, and working memory partly through the decrease in acetylcholinesterase (AChE) activity [<xref ref-type="bibr" rid="B35">35</xref>].</p>
<p id="p-6">Bacoside A (dammarane-type triterpenoid saponins), the primary neuroprotective compound group recognised from Brahmi is composed of bacopaside III, bacopaside X, Bacoside A3, and bacopasaponin C (<xref ref-type="table" rid="t1">Table 1</xref>) [<xref ref-type="bibr" rid="B33">33</xref>–<xref ref-type="bibr" rid="B35">35</xref>]. Through structural analysis, 12 analogues derived from the Bacosides have been reported, different saponin types have also been identified as essential ingredients which are known as bacopasides I–XII [<xref ref-type="bibr" rid="B36">36</xref>]. Other components of <italic>Bacopa</italic> are apigenin, monnierin, cucurbitacin, hersaponin, azlkaloids brahmine, monnierasides I–III, D-mannitol, nicotine and herpestine [<xref ref-type="bibr" rid="B37">37</xref>, <xref ref-type="bibr" rid="B38">38</xref>].</p>
<p id="p-7">Studies show that Bacosides have the potential to prevent amyloid beta peptide (Aβ) aggregation, and formation of fibrils [<xref ref-type="bibr" rid="B38">38</xref>] and also protect neurons from toxicity induced by Aβ [<xref ref-type="bibr" rid="B39">39</xref>]. The compounds are reported to directly interact with the neurotransmitter and thus bring changes in memory and learning [<xref ref-type="bibr" rid="B40">40</xref>, <xref ref-type="bibr" rid="B41">41</xref>]. Bacosides isolated from Brahmi, are non polar glycosides in nature and they easily cross the blood brain barrier [<xref ref-type="bibr" rid="B42">42</xref>–<xref ref-type="bibr" rid="B44">44</xref>]. This has been confirmed by radiopharmaceuticals biodistribution studies [<xref ref-type="bibr" rid="B45">45</xref>]. Thus, the Brahmi, rich in Bacosides have potent neuroprotective potentials and may be explored for utilizing the phytocompounds as lead molecules for developing more potent and effective neuroprotective drugs. Computational study predicts ebelin lactone as the most important compound from <italic>Bacopa monnieri</italic>. The study claims ebelin lactone as the most promising drug candidate and that it can be utilised to develop a drug against Alzheimer’s disease, post pre-clinical and clinical validations [<xref ref-type="bibr" rid="B46">46</xref>]. The herb has also been found to have potent neuroprotective and neurorescuing effects against neurodenerative disese like Parkinsons’s disease [<xref ref-type="bibr" rid="B47">47</xref>].</p>
</sec>
<sec id="s4">
<title>Neuroprotective compounds from <italic>Centella asiatica</italic></title>
<p id="p-8">
<italic>Centella asiatica</italic> is a small perennial plant that grows abundantly in hot humid tropical and sub-tropical regions around the globe. The plant grows extensively in West Bengal, India [<xref ref-type="bibr" rid="B48">48</xref>] (<xref ref-type="fig" rid="fig1">Figure 1</xref>). Some of the primary bioactive phytocompounds identified and reported from <italic>Centella asiatica</italic> are phenylpropanoid derivatives (eugenol derivatives, flavonoids, and caffeoylquinic acids) and isoprenoids (plant sterols, sesquiterpenes, saponins, and pentacyclic triterpenoids) (<xref ref-type="table" rid="t1">Table 1</xref>) [<xref ref-type="bibr" rid="B49">49</xref>].</p>
<fig id="fig1" position="float">
<label>Figure 1</label>
<caption>
<p>
<italic>Centella asiatica</italic>
</p>
</caption>
<graphic xmlns:xlink="http://www.w3.org/1999/xlink" xlink:href="en-02-100630-g001.tif" />
</fig>
<p id="p-9">Several studies have been conducted in rodent models and some in human models to investigate the neuroprotective potentials of <italic>Centella asiatica</italic> [<xref ref-type="bibr" rid="B49">49</xref>]. The medicinal plant <italic>Centella asiatica</italic> is traditionally known for enhancing the cognition and improving memories [<xref ref-type="bibr" rid="B50">50</xref>]. The plant is also known in folk medicine as an anxiolytic agent and anticonvulsant [<xref ref-type="bibr" rid="B51">51</xref>]. In Ayurveda the plant is known as “medhyarasayana” by virtue of its ability to improve memory and cognition [<xref ref-type="bibr" rid="B52">52</xref>]. <italic>Centella asiatica</italic> is reported to have neuroprotective effect and it has also been established in several <italic>in vitro</italic> models. Administration of <italic>Centella asiatica</italic> has been reported to improve antioxidant status, inhibit pro-inflammatory enzyme namely phospholipase A2 and protect against beta amyloid toxicity [<xref ref-type="bibr" rid="B49">49</xref>]. <italic>Centella asiatica</italic> is known to impose its neuroptropic effects by modulations of the signal transduction pathways including ERK1/2 and PKB pathway [<xref ref-type="bibr" rid="B53">53</xref>]. Increased dendritic arborization and synaptogenesis are the prime neuroptopic effects of <italic>Centella asiatica</italic> [<xref ref-type="bibr" rid="B53">53</xref>]. Most of these neurotropic and neuroprotective potentials of <italic>Centella asiatica</italic> are due to the potent phytocompounds present in the plant which include triterpene compounds asiaticoside, asiatic acid, and madecassoside [<xref ref-type="bibr" rid="B54">54</xref>]. The new group of compounds reported from <italic>Centella asiatica</italic> are caffeoylquinic acids and these have the potential of inducing the Nrf2-antioxidant response pathway and HO-1 signaling [<xref ref-type="bibr" rid="B55">55</xref>]. Studies show that by virtue of its ability to improve the antioxidative signaling pathway, the plant <italic>Centenella asciatica</italic> improves memories in experimental rats [<xref ref-type="bibr" rid="B55">55</xref>].</p>
</sec>
<sec id="s5">
<title>Other medicinal properties of <italic>Withania somnifera</italic>, <italic>Bacopa monnieri</italic> and <italic>Centella asiatica</italic></title>
<p id="p-10">All these three plants are known to possess several other medicinal properties besides that of neuroprotective actions. The plant <italic>Withania somnifera</italic>, popularly known as Aswagandha and the phytocompounds namely Withaferin A, withanolide A, withanolide D, and withaniamides are known to play significant pharmacological roles. Glycoproteins from <italic>Withania</italic> and lectin like-protein are reported to possess potent antimicrobial, anti-snake venom poison and antimicrobial therapeutic potentials [<xref ref-type="bibr" rid="B56">56</xref>]. In folk medicine, the plant <italic>Withania</italic> is known to be in use for treating ailments like hypothermia, diabetes, cancer, hepatitis, arthritis, asthma, ulcer, eyesores, heart problems, haemorrhoids, etc. The plant <italic>Withania</italic> is known to have anticancer, antimicrobial, and muscle strengthening activities. It is also reported to have potential in treating low back pain [<xref ref-type="bibr" rid="B57">57</xref>]. Several important secondary metabolites like steroids, alkaloids, phenolics, flavonoids, saponins, and glycosides have been reported from the <italic>Withania</italic> and these have potent medicinal properties [<xref ref-type="bibr" rid="B57">57</xref>]. Phytocompounds from different parts of the plant <italic>Withania</italic>, specially the roots have been extensively explored for their medicinal properties like treating male infertility, antianxiety, obsessive-compulsive disorder, etc., and several of these experimental studies have been evaluated successfully for clinical trials [<xref ref-type="bibr" rid="B56">56</xref>, <xref ref-type="bibr" rid="B57">57</xref>]. A bitter alkaloid named Somniferin has been isolated from <italic>Withania somnifera</italic> and is known to have hypnotic activity [<xref ref-type="bibr" rid="B58">58</xref>].</p>
<p id="p-11">The plant <italic>Bacopa monnieri</italic>, is also known to be a rich source of medicinal phytocompounds with various medicinal properties. Memory enhancing ability of the plant is well documented [<xref ref-type="bibr" rid="B59">59</xref>]. The plant is known to add years to life and also promotes rejuvenation [<xref ref-type="bibr" rid="B59">59</xref>]. Several potent medicinal phytochemicals namely triterpenoid saponins, monnierinalkaloids flavonoids, glycosides and other phytochemicals namely betulinic acid, betulic acid, oroxindin, wogonin, stigmasterol, beta-sitosterol, sapogenin, Brahmic acid, brahminoside, brahamoside, isobrahmic acid, etc., have been isolated from the leaves of the plant <italic>Bacopa monnieri</italic> [<xref ref-type="bibr" rid="B59">59</xref>]. Studies reveal broad therapeutic potentials of the <italic>Bacopa monnieri</italic> that include analgesic, anxiolytic, antioxidant, anti-inflammatory, anti-microbial, anti-depressant, anti-convulsant, adaptogenic, hepatoprotective, immunostimulatory, anti-ulcerative and anti-neoplastic, etc. [<xref ref-type="bibr" rid="B60">60</xref>–<xref ref-type="bibr" rid="B70">70</xref>]. Extracts of the plant <italic>Centella asiatica</italic> are reported to have extensive use in folk medicine in China and India and has potentials in boosting memory, preventing cognitive deficits and improving brain functions [<xref ref-type="bibr" rid="B71">71</xref>]. Certain potent phytochemicals namely pentacyclic triterpenoid glycosides, madecassoside and asiaticoside have been reported from the plant. Corresponding aglycones, asiatic acid and madecassic acid of the mentioned compounds have also been reported to have potent medicinal properties. Asiaticoside and madecassoside are reported as marker compounds of <italic>Centella asiatica</italic> and are known to have wide pharmacological potentials. The triterpene compounds, asiaticoside and madecassoside have been reported to have anti-inflammatory, antioxidant, anti-allergic, wound healing, cardioprotective, hepatoprotective, neuroprotective, anxyiolytic, anti-fibrotic, antibacterial, anti-arthiritic, anti-tumor, anti-ulcerative properties. The compounds are also widely used for addressing issues of skin abnormalities and for treating burn injuries, asthma, lupus, psoriasis and scleroderma, etc. [<xref ref-type="bibr" rid="B71">71</xref>–<xref ref-type="bibr" rid="B76">76</xref>].</p>
</sec>
<sec id="s6">
<title>Conclusions</title>
<p id="p-12">Neurological diseases are usually long term disturbances that may occur in any stage of life. The common degenerative neural diseases includes Alzheimer’s disease, Parkinson’s disease, Huntington’s disease, insomnia, loss of cognitive ability, etc. The primary causes of these diseases are stress, ageing, inflammation, compromised immunity and neural injury. The chief neurotransmitter systems disabled in such illness are cholinergic, GABAergic, dopaminergic transmitter pathways. The plants discussed in this review work on several target molecules effecting these neurotransmitters, metabolism of the brain or checks oxidative stress mediated neural damage. The potent phytocompounds from these plants are also known to be affecting various signaling pathways and all together they have been found to be potent neuroprotective agents. There are extensive literature revealing <italic>in vitro</italic>, <italic>in vivo</italic>, and <italic>in silico</italic> studies and also successful clinical trials of some of the potent bioactive neuroprotective compounds from the plants namely <italic>Withania somnifera</italic>, <italic>Bacopa monnieri</italic> and <italic>Centella asiatica</italic>. These studies taken together, show that these indigenous West Bengal, India may be explored to utilise their rich source of bioactive neuroprotective compounds for developing new potent, effective and affordable neuropharmacological formulations and drugs which are expected to have minimum or no side effects.</p>
</sec>
</body>
<back>
<glossary>
<title>Abbreviations</title>
<def-list>
<def-item>
<term>ERK1/2</term>
<def>
<p>extracellular signal-regulated protein kinases 1 and 2</p>
</def>
</def-item>
<def-item>
<term>HO-1</term>
<def>
<p>heme oxygenase-1</p>
</def>
</def-item>
<def-item>
<term>NMDAR1</term>
<def>
<p>
<italic>N</italic>-methyl-<italic>D</italic>-aspartate receptor 1</p>
</def>
</def-item>
<def-item>
<term>Nrf2</term>
<def>
<p>nuclear factor erythroid 2-related factor 2</p>
</def>
</def-item>
<def-item>
<term>PKB</term>
<def>
<p>protein kinase B</p>
</def>
</def-item>
</def-list>
</glossary>
<sec id="s7">
<title>Declarations</title>
<sec>
<title>Author contributions</title>
<p>SG: Writing—original draft, Investigation. PSS: Writing—review &amp; editing, Investigation. DG: Conceptualization, Writing—original draft, Writing—review &amp; editing, Investigation.</p>
</sec>
<sec sec-type="COI-statement">
<title>Conflicts of interest</title>
<p>The authors declare that they have no conflicts of interest.</p>
</sec>
<sec>
<title>Ethical approval</title>
<p>Not applicable.</p>
</sec>
<sec>
<title>Consent to participate</title>
<p>Not applicable.</p>
</sec>
<sec>
<title>Consent to publication</title>
<p>Not applicable.</p>
</sec>
<sec sec-type="data-availability">
<title>Availability of data and materials</title>
<p>Not applicable.</p>
</sec>
<sec>
<title>Funding</title>
<p>Not applicable.</p>
</sec>
<sec>
<title>Copyright</title>
<p>© The Author(s) 2023.</p>
</sec>
</sec>
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