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Anticonvulsant, Anxiolytic, and Sedative Activities of Verbena officinalis

We describe different neuropharmacological effects of Verbena officinalis crude extract (Vo.Cr). Pentylenetetrazole (PTZ)-induced seizures, elevated plus maze, light–dark box (LDB), open field and thiopental-induced sleeping test models were employed to evaluate Vo.Cr actions in mice. Vo.Cr dose-dep...

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Autores principales: Khan, Abdul Waheed, Khan, Arif-ullah, Ahmed, Touqeer
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5174135/
https://www.ncbi.nlm.nih.gov/pubmed/28066246
http://dx.doi.org/10.3389/fphar.2016.00499
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author Khan, Abdul Waheed
Khan, Arif-ullah
Ahmed, Touqeer
author_facet Khan, Abdul Waheed
Khan, Arif-ullah
Ahmed, Touqeer
author_sort Khan, Abdul Waheed
collection PubMed
description We describe different neuropharmacological effects of Verbena officinalis crude extract (Vo.Cr). Pentylenetetrazole (PTZ)-induced seizures, elevated plus maze, light–dark box (LDB), open field and thiopental-induced sleeping test models were employed to evaluate Vo.Cr actions in mice. Vo.Cr dose-dependently (100–500 mg/Kg) delayed onset time of myoclonic jerks and tonic-clonic seizures, while decreased duration of tonic-clonic seizures (P < 0.05, P < 0.001 vs. saline group). Vo.Cr at 100 and 300–500 mg/Kg doses reduced animals’ mortality in PTZ-induced seizures test to 75 and 0%, respectively. Vo.Cr (50–300 mg/Kg) significantly increased time spent and number of entries into open arms, while decreased time spent and number of entries into closed arms (P < 0.05, P < 0.01, P < 0.001 vs. saline group), measured in elevated plus maze. Vo.Cr (50–300 mg/Kg) increased time spent in light compartment, while decreased time spent in dark compartment (P < 0.01, P < 0.001 vs. saline group) in LDB, like caused by diazepam. In open field test, Vo.Cr decreased number of ambulations and rearings frequencies, while increased the number of central squares crossings. In thiopental-induced sleeping test, Vo.Cr (50–300 mg/Kg) decreased onset time of sleep, while increased the duration of sleep (P < 0.05, P < 0.01, P < 0.001 vs. saline group). These results indicate that Verbena officinalis possess anticonvulsant, anxiolytic and sedative activities, which provides scientific background for its medicinal application in various neurological ailments, such as epilepsy, anxiety, and insomnia.
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spelling pubmed-51741352017-01-06 Anticonvulsant, Anxiolytic, and Sedative Activities of Verbena officinalis Khan, Abdul Waheed Khan, Arif-ullah Ahmed, Touqeer Front Pharmacol Pharmacology We describe different neuropharmacological effects of Verbena officinalis crude extract (Vo.Cr). Pentylenetetrazole (PTZ)-induced seizures, elevated plus maze, light–dark box (LDB), open field and thiopental-induced sleeping test models were employed to evaluate Vo.Cr actions in mice. Vo.Cr dose-dependently (100–500 mg/Kg) delayed onset time of myoclonic jerks and tonic-clonic seizures, while decreased duration of tonic-clonic seizures (P < 0.05, P < 0.001 vs. saline group). Vo.Cr at 100 and 300–500 mg/Kg doses reduced animals’ mortality in PTZ-induced seizures test to 75 and 0%, respectively. Vo.Cr (50–300 mg/Kg) significantly increased time spent and number of entries into open arms, while decreased time spent and number of entries into closed arms (P < 0.05, P < 0.01, P < 0.001 vs. saline group), measured in elevated plus maze. Vo.Cr (50–300 mg/Kg) increased time spent in light compartment, while decreased time spent in dark compartment (P < 0.01, P < 0.001 vs. saline group) in LDB, like caused by diazepam. In open field test, Vo.Cr decreased number of ambulations and rearings frequencies, while increased the number of central squares crossings. In thiopental-induced sleeping test, Vo.Cr (50–300 mg/Kg) decreased onset time of sleep, while increased the duration of sleep (P < 0.05, P < 0.01, P < 0.001 vs. saline group). These results indicate that Verbena officinalis possess anticonvulsant, anxiolytic and sedative activities, which provides scientific background for its medicinal application in various neurological ailments, such as epilepsy, anxiety, and insomnia. Frontiers Media S.A. 2016-12-21 /pmc/articles/PMC5174135/ /pubmed/28066246 http://dx.doi.org/10.3389/fphar.2016.00499 Text en Copyright © 2016 Khan, Khan and Ahmed. http://creativecommons.org/licenses/by/4.0/ 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) or licensor 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.
spellingShingle Pharmacology
Khan, Abdul Waheed
Khan, Arif-ullah
Ahmed, Touqeer
Anticonvulsant, Anxiolytic, and Sedative Activities of Verbena officinalis
title Anticonvulsant, Anxiolytic, and Sedative Activities of Verbena officinalis
title_full Anticonvulsant, Anxiolytic, and Sedative Activities of Verbena officinalis
title_fullStr Anticonvulsant, Anxiolytic, and Sedative Activities of Verbena officinalis
title_full_unstemmed Anticonvulsant, Anxiolytic, and Sedative Activities of Verbena officinalis
title_short Anticonvulsant, Anxiolytic, and Sedative Activities of Verbena officinalis
title_sort anticonvulsant, anxiolytic, and sedative activities of verbena officinalis
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5174135/
https://www.ncbi.nlm.nih.gov/pubmed/28066246
http://dx.doi.org/10.3389/fphar.2016.00499
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