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Neuroprotective Effects of Myrtenal in an Experimental Model of Dementia Induced in Rats
There is growing attention on natural substances capable of stimulating the cholinergic system and of exerting antioxidant effects, as potential therapeutic agents in Alzheimer's disease (AD). The aim of the present study is to evaluate the expected neuroprotective mechanisms of myrtenal (M) in...
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Published in: | Antioxidants 2022-02, Vol.11 (2), p.374 |
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creator | Dragomanova, Stela Pavlov, Stoyan Marinova, Desislava Hodzev, Yordan Petralia, Maria Cristina Fagone, Paolo Nicoletti, Ferdinando Lazarova, Maria Tzvetanova, Elina Alexandrova, Albena Kalfin, Reni Tancheva, Lyubka |
description | There is growing attention on natural substances capable of stimulating the cholinergic system and of exerting antioxidant effects, as potential therapeutic agents in Alzheimer's disease (AD). The aim of the present study is to evaluate the expected neuroprotective mechanisms of myrtenal (M) in an experimental model of dementia in rats. Dementia was induced in male Wistar rats by scopolamine (Sc) administration (0.1 mg/kg for 8 days and 20.0 mg/kg on day 9). The animals were divided into 5 groups (1) Controls; (2) Sc; (3) Sc + Myrtenal (40 mg/kg), (4) Sc + Galantamine (1 mg/kg); (5) Sc + Lipoic acid (30 mg/kg). Changes in recognition memory and habituation were evaluated via the Novel Object Recognition and Open Field tests. Acetylcholinesterase (AChE) activity, ACh levels, and changes in oxidative status of the brain were measured biochemically. The histological changes in two brain regions-cortex and hippocampus, were evaluated qualitatively and quantitatively. Myrtenal improved recognition memory and habituation, exerted antioxidant effects and significantly increased ACh brain levels. Histologically, the neuroprotective capacity of myrtenal was also confirmed. For the first time, we have demonstrated the neuroprotective potential of myrtenal in an experimental model of dementia. Our study provides proof-of-concept for the testing of myrtenal, in association with standard of care treatments, in patients affected by cognitive decline. |
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The aim of the present study is to evaluate the expected neuroprotective mechanisms of myrtenal (M) in an experimental model of dementia in rats. Dementia was induced in male Wistar rats by scopolamine (Sc) administration (0.1 mg/kg for 8 days and 20.0 mg/kg on day 9). The animals were divided into 5 groups (1) Controls; (2) Sc; (3) Sc + Myrtenal (40 mg/kg), (4) Sc + Galantamine (1 mg/kg); (5) Sc + Lipoic acid (30 mg/kg). Changes in recognition memory and habituation were evaluated via the Novel Object Recognition and Open Field tests. Acetylcholinesterase (AChE) activity, ACh levels, and changes in oxidative status of the brain were measured biochemically. The histological changes in two brain regions-cortex and hippocampus, were evaluated qualitatively and quantitatively. Myrtenal improved recognition memory and habituation, exerted antioxidant effects and significantly increased ACh brain levels. Histologically, the neuroprotective capacity of myrtenal was also confirmed. For the first time, we have demonstrated the neuroprotective potential of myrtenal in an experimental model of dementia. Our study provides proof-of-concept for the testing of myrtenal, in association with standard of care treatments, in patients affected by cognitive decline.</description><identifier>ISSN: 2076-3921</identifier><identifier>EISSN: 2076-3921</identifier><identifier>DOI: 10.3390/antiox11020374</identifier><identifier>PMID: 35204256</identifier><language>eng</language><publisher>Switzerland: MDPI AG</publisher><subject>acetylcholine ; Acetylcholinesterase ; Acids ; Alzheimer's disease ; Animal models ; antioxidant ; Antioxidants ; Binding sites ; Cholinergic transmission ; Cognitive ability ; Dementia ; Dementia disorders ; experimental dementia ; Galantamine ; Habituation ; Laboratory animals ; Lipoic acid ; Memory ; myrtenal ; Neurodegenerative diseases ; Neuroprotection ; Neurosciences ; Oxidative stress ; Pattern recognition ; Proteins ; Scopolamine</subject><ispartof>Antioxidants, 2022-02, Vol.11 (2), p.374</ispartof><rights>2022 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><rights>2022 by the authors. 2022</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c484t-7a86a6e1692ef7928566a700057dde544900a35b8fe5843b1671bb31b56ab34f3</citedby><cites>FETCH-LOGICAL-c484t-7a86a6e1692ef7928566a700057dde544900a35b8fe5843b1671bb31b56ab34f3</cites><orcidid>0000-0002-6694-1992 ; 0000-0002-7764-3640 ; 0000-0002-4570-8462 ; 0000-0002-7770-3316 ; 0000-0003-1845-2753</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2632219944/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2632219944?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27901,27902,36989,36990,44566,53766,53768,74869</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/35204256$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Dragomanova, Stela</creatorcontrib><creatorcontrib>Pavlov, Stoyan</creatorcontrib><creatorcontrib>Marinova, Desislava</creatorcontrib><creatorcontrib>Hodzev, Yordan</creatorcontrib><creatorcontrib>Petralia, Maria Cristina</creatorcontrib><creatorcontrib>Fagone, Paolo</creatorcontrib><creatorcontrib>Nicoletti, Ferdinando</creatorcontrib><creatorcontrib>Lazarova, Maria</creatorcontrib><creatorcontrib>Tzvetanova, Elina</creatorcontrib><creatorcontrib>Alexandrova, Albena</creatorcontrib><creatorcontrib>Kalfin, Reni</creatorcontrib><creatorcontrib>Tancheva, Lyubka</creatorcontrib><title>Neuroprotective Effects of Myrtenal in an Experimental Model of Dementia Induced in Rats</title><title>Antioxidants</title><addtitle>Antioxidants (Basel)</addtitle><description>There is growing attention on natural substances capable of stimulating the cholinergic system and of exerting antioxidant effects, as potential therapeutic agents in Alzheimer's disease (AD). The aim of the present study is to evaluate the expected neuroprotective mechanisms of myrtenal (M) in an experimental model of dementia in rats. Dementia was induced in male Wistar rats by scopolamine (Sc) administration (0.1 mg/kg for 8 days and 20.0 mg/kg on day 9). The animals were divided into 5 groups (1) Controls; (2) Sc; (3) Sc + Myrtenal (40 mg/kg), (4) Sc + Galantamine (1 mg/kg); (5) Sc + Lipoic acid (30 mg/kg). Changes in recognition memory and habituation were evaluated via the Novel Object Recognition and Open Field tests. Acetylcholinesterase (AChE) activity, ACh levels, and changes in oxidative status of the brain were measured biochemically. The histological changes in two brain regions-cortex and hippocampus, were evaluated qualitatively and quantitatively. Myrtenal improved recognition memory and habituation, exerted antioxidant effects and significantly increased ACh brain levels. Histologically, the neuroprotective capacity of myrtenal was also confirmed. 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subjects | acetylcholine Acetylcholinesterase Acids Alzheimer's disease Animal models antioxidant Antioxidants Binding sites Cholinergic transmission Cognitive ability Dementia Dementia disorders experimental dementia Galantamine Habituation Laboratory animals Lipoic acid Memory myrtenal Neurodegenerative diseases Neuroprotection Neurosciences Oxidative stress Pattern recognition Proteins Scopolamine |
title | Neuroprotective Effects of Myrtenal in an Experimental Model of Dementia Induced in Rats |
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