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L-linalool exerts a neuroprotective action on hemiparkinsonian rats
Linalool (LIN) is a monoterpene, responsible for the aroma of essential oils in some species. It presents a sedative and anxiolytic potential, enhancing GABAergic currents and behaving as a benzodiazepine-type of drug. The objectives of the present work were to study the neuroprotective effects of L...
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Published in: | Naunyn-Schmiedeberg's archives of pharmacology 2020-06, Vol.393 (6), p.1077-1088 |
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creator | de Lucena, Jalles Dantas Gadelha-Filho, Carlos Vinicius Jataí da Costa, Roberta Oliveira de Araújo, Dayane Pessoa Lima, Francisco Arnaldo Viana Neves, Kelly Rose Tavares de Barros Viana, Glauce Socorro |
description | Linalool (LIN) is a monoterpene, responsible for the aroma of essential oils in some species. It presents a sedative and anxiolytic potential, enhancing GABAergic currents and behaving as a benzodiazepine-type of drug. The objectives of the present work were to study the neuroprotective effects of LIN on a model of Parkinson’s disease. For that, male Wistar rats were divided into the following groups: sham-operated (SO), 6-OHDA-lesioned, and 6-OHDA-lesioned and treated with LIN (25, 50, and 100 mg/kg, p.o.) for 2 weeks. Afterwards, the animals were subjected to behavioral tests (apomorphine-induced rotations, open field, and forced swimming tests). Then, the animals were euthanized, and the striatum, hippocampus, and prefrontal cortex were processed for neurochemistry (nitrite and lipoperoxidation measurements) and immunohistochemistry (TH and DAT) assays. The results were analyzed by ANOVA and Tukey’s test for multiple comparisons and considered significant at
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doi_str_mv | 10.1007/s00210-019-01793-1 |
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p
< 0.05. LIN significantly improved the behavioral alterations of the 6-OHDA-lesioned group, as evaluated by the apomorphine-induced rotations, open field, and forced swimming tests. In addition, LIN partially reversed the decreased DA, DOPAC, and HVA contents observed in the 6-OHDA-lesioned striatum. The untreated 6-OHDA group presented increased nitrite contents and lipoperoxidation in all the brain areas studied, and these changes were completely reversed after LIN treatments. Finally, LIN significantly prevented the reduction in TH and DAT expressions demonstrated in the right 6-OHDA-lesioned striatum. All these data strongly suggest that LIN presents a neuroprotective action in hemiparkinsonian rats, probably related to the drug anti-inflammatory and antioxidant activities.</description><identifier>ISSN: 0028-1298</identifier><identifier>EISSN: 1432-1912</identifier><identifier>DOI: 10.1007/s00210-019-01793-1</identifier><identifier>PMID: 31938809</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Animal models ; Antioxidants ; Apomorphine ; Aroma ; Benzodiazepines ; Biomedical and Life Sciences ; Biomedicine ; Essential oils ; Immunohistochemistry ; Inflammation ; Linalool ; Movement disorders ; Neostriatum ; Neurodegenerative diseases ; Neuroprotection ; Neurosciences ; Original Article ; Parkinson's disease ; Pharmacology/Toxicology ; Prefrontal cortex ; Rodents ; γ-Aminobutyric acid</subject><ispartof>Naunyn-Schmiedeberg's archives of pharmacology, 2020-06, Vol.393 (6), p.1077-1088</ispartof><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2020</rights><rights>Springer-Verlag GmbH Germany, part of Springer Nature 2020.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c375t-a84ca57ddb70f6b06378e8277569d28518efa9b06dd32e833e03347391ae4e173</citedby><cites>FETCH-LOGICAL-c375t-a84ca57ddb70f6b06378e8277569d28518efa9b06dd32e833e03347391ae4e173</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31938809$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>de Lucena, Jalles Dantas</creatorcontrib><creatorcontrib>Gadelha-Filho, Carlos Vinicius Jataí</creatorcontrib><creatorcontrib>da Costa, Roberta Oliveira</creatorcontrib><creatorcontrib>de Araújo, Dayane Pessoa</creatorcontrib><creatorcontrib>Lima, Francisco Arnaldo Viana</creatorcontrib><creatorcontrib>Neves, Kelly Rose Tavares</creatorcontrib><creatorcontrib>de Barros Viana, Glauce Socorro</creatorcontrib><title>L-linalool exerts a neuroprotective action on hemiparkinsonian rats</title><title>Naunyn-Schmiedeberg's archives of pharmacology</title><addtitle>Naunyn-Schmiedeberg's Arch Pharmacol</addtitle><addtitle>Naunyn Schmiedebergs Arch Pharmacol</addtitle><description>Linalool (LIN) is a monoterpene, responsible for the aroma of essential oils in some species. It presents a sedative and anxiolytic potential, enhancing GABAergic currents and behaving as a benzodiazepine-type of drug. The objectives of the present work were to study the neuroprotective effects of LIN on a model of Parkinson’s disease. For that, male Wistar rats were divided into the following groups: sham-operated (SO), 6-OHDA-lesioned, and 6-OHDA-lesioned and treated with LIN (25, 50, and 100 mg/kg, p.o.) for 2 weeks. Afterwards, the animals were subjected to behavioral tests (apomorphine-induced rotations, open field, and forced swimming tests). Then, the animals were euthanized, and the striatum, hippocampus, and prefrontal cortex were processed for neurochemistry (nitrite and lipoperoxidation measurements) and immunohistochemistry (TH and DAT) assays. The results were analyzed by ANOVA and Tukey’s test for multiple comparisons and considered significant at
p
< 0.05. LIN significantly improved the behavioral alterations of the 6-OHDA-lesioned group, as evaluated by the apomorphine-induced rotations, open field, and forced swimming tests. In addition, LIN partially reversed the decreased DA, DOPAC, and HVA contents observed in the 6-OHDA-lesioned striatum. The untreated 6-OHDA group presented increased nitrite contents and lipoperoxidation in all the brain areas studied, and these changes were completely reversed after LIN treatments. Finally, LIN significantly prevented the reduction in TH and DAT expressions demonstrated in the right 6-OHDA-lesioned striatum. All these data strongly suggest that LIN presents a neuroprotective action in hemiparkinsonian rats, probably related to the drug anti-inflammatory and antioxidant activities.</description><subject>Animal models</subject><subject>Antioxidants</subject><subject>Apomorphine</subject><subject>Aroma</subject><subject>Benzodiazepines</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Essential oils</subject><subject>Immunohistochemistry</subject><subject>Inflammation</subject><subject>Linalool</subject><subject>Movement disorders</subject><subject>Neostriatum</subject><subject>Neurodegenerative diseases</subject><subject>Neuroprotection</subject><subject>Neurosciences</subject><subject>Original Article</subject><subject>Parkinson's disease</subject><subject>Pharmacology/Toxicology</subject><subject>Prefrontal cortex</subject><subject>Rodents</subject><subject>γ-Aminobutyric acid</subject><issn>0028-1298</issn><issn>1432-1912</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kE1LxDAQhoMoun78AQ9S8OKlOpNpN8lRFr9gwYueQ7ad1Wq3WZNW9N8b3VXBg5AwkHnmTfIIcYhwigDqLAJIhBzQpK0M5bghRliQzNGg3BSj1Nc5SqN3xG6MTwAwxrLcFjuEhrQGMxKTad42nWu9bzN-49DHzGUdD8Evg--56ptXzlwqvsvSeuRFs3Thuemi7xrXZcH1cV9szV0b-WBd98T95cXd5Dqf3l7dTM6neUWq7HOni8qVqq5nCubjGYxJadZSqXJsaqlL1Dx3Jp3XNUnWRAxEhSKDjgtGRXviZJWbnvYycOztookVt63r2A_RSiIDgJI-0eM_6JMfQvpnogogWUhdFImSK6oKPsbAc7sMzcKFd4tgPxXblWKbFNsvxRbT0NE6epgtuP4Z-XaaAFoBMbW6Bw6_d_8T-wEP0oVW</recordid><startdate>20200601</startdate><enddate>20200601</enddate><creator>de Lucena, Jalles Dantas</creator><creator>Gadelha-Filho, Carlos Vinicius Jataí</creator><creator>da Costa, Roberta Oliveira</creator><creator>de Araújo, Dayane Pessoa</creator><creator>Lima, Francisco Arnaldo Viana</creator><creator>Neves, Kelly Rose Tavares</creator><creator>de Barros Viana, Glauce Socorro</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20200601</creationdate><title>L-linalool exerts a neuroprotective action on hemiparkinsonian rats</title><author>de Lucena, Jalles Dantas ; Gadelha-Filho, Carlos Vinicius Jataí ; da Costa, Roberta Oliveira ; de Araújo, Dayane Pessoa ; Lima, Francisco Arnaldo Viana ; Neves, Kelly Rose Tavares ; de Barros Viana, Glauce Socorro</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c375t-a84ca57ddb70f6b06378e8277569d28518efa9b06dd32e833e03347391ae4e173</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Animal models</topic><topic>Antioxidants</topic><topic>Apomorphine</topic><topic>Aroma</topic><topic>Benzodiazepines</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Essential oils</topic><topic>Immunohistochemistry</topic><topic>Inflammation</topic><topic>Linalool</topic><topic>Movement disorders</topic><topic>Neostriatum</topic><topic>Neurodegenerative diseases</topic><topic>Neuroprotection</topic><topic>Neurosciences</topic><topic>Original Article</topic><topic>Parkinson's disease</topic><topic>Pharmacology/Toxicology</topic><topic>Prefrontal cortex</topic><topic>Rodents</topic><topic>γ-Aminobutyric acid</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>de Lucena, Jalles Dantas</creatorcontrib><creatorcontrib>Gadelha-Filho, Carlos Vinicius Jataí</creatorcontrib><creatorcontrib>da Costa, Roberta Oliveira</creatorcontrib><creatorcontrib>de Araújo, Dayane Pessoa</creatorcontrib><creatorcontrib>Lima, Francisco Arnaldo Viana</creatorcontrib><creatorcontrib>Neves, Kelly Rose Tavares</creatorcontrib><creatorcontrib>de Barros Viana, Glauce Socorro</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Naunyn-Schmiedeberg's archives of pharmacology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>de Lucena, Jalles Dantas</au><au>Gadelha-Filho, Carlos Vinicius Jataí</au><au>da Costa, Roberta Oliveira</au><au>de Araújo, Dayane Pessoa</au><au>Lima, Francisco Arnaldo Viana</au><au>Neves, Kelly Rose Tavares</au><au>de Barros Viana, Glauce Socorro</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>L-linalool exerts a neuroprotective action on hemiparkinsonian rats</atitle><jtitle>Naunyn-Schmiedeberg's archives of pharmacology</jtitle><stitle>Naunyn-Schmiedeberg's Arch Pharmacol</stitle><addtitle>Naunyn Schmiedebergs Arch Pharmacol</addtitle><date>2020-06-01</date><risdate>2020</risdate><volume>393</volume><issue>6</issue><spage>1077</spage><epage>1088</epage><pages>1077-1088</pages><issn>0028-1298</issn><eissn>1432-1912</eissn><abstract>Linalool (LIN) is a monoterpene, responsible for the aroma of essential oils in some species. It presents a sedative and anxiolytic potential, enhancing GABAergic currents and behaving as a benzodiazepine-type of drug. The objectives of the present work were to study the neuroprotective effects of LIN on a model of Parkinson’s disease. For that, male Wistar rats were divided into the following groups: sham-operated (SO), 6-OHDA-lesioned, and 6-OHDA-lesioned and treated with LIN (25, 50, and 100 mg/kg, p.o.) for 2 weeks. Afterwards, the animals were subjected to behavioral tests (apomorphine-induced rotations, open field, and forced swimming tests). Then, the animals were euthanized, and the striatum, hippocampus, and prefrontal cortex were processed for neurochemistry (nitrite and lipoperoxidation measurements) and immunohistochemistry (TH and DAT) assays. The results were analyzed by ANOVA and Tukey’s test for multiple comparisons and considered significant at
p
< 0.05. LIN significantly improved the behavioral alterations of the 6-OHDA-lesioned group, as evaluated by the apomorphine-induced rotations, open field, and forced swimming tests. In addition, LIN partially reversed the decreased DA, DOPAC, and HVA contents observed in the 6-OHDA-lesioned striatum. The untreated 6-OHDA group presented increased nitrite contents and lipoperoxidation in all the brain areas studied, and these changes were completely reversed after LIN treatments. Finally, LIN significantly prevented the reduction in TH and DAT expressions demonstrated in the right 6-OHDA-lesioned striatum. All these data strongly suggest that LIN presents a neuroprotective action in hemiparkinsonian rats, probably related to the drug anti-inflammatory and antioxidant activities.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>31938809</pmid><doi>10.1007/s00210-019-01793-1</doi><tpages>12</tpages></addata></record> |
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subjects | Animal models Antioxidants Apomorphine Aroma Benzodiazepines Biomedical and Life Sciences Biomedicine Essential oils Immunohistochemistry Inflammation Linalool Movement disorders Neostriatum Neurodegenerative diseases Neuroprotection Neurosciences Original Article Parkinson's disease Pharmacology/Toxicology Prefrontal cortex Rodents γ-Aminobutyric acid |
title | L-linalool exerts a neuroprotective action on hemiparkinsonian rats |
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