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Possible Modulation of the Anexiogenic Effects of Vitex Agnus-castus by the Serotonergic System

OBJECTIVE(S): There is well documented evidence for the increase in widespread use of complementary and alternative medicine in the treatment of physical and psychiatric symptoms and disorders within the populations. In the present study, we investigated the influence of Vitex agnus-castus (vitex) o...

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Autores principales: Yaghmaei, Parichehr, Oryan, Shahrbanoo, Fatehi Gharehlar, Laleh, Salari, Ali-Akbar, Solati, Jalal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3586884/
https://www.ncbi.nlm.nih.gov/pubmed/23493923
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author Yaghmaei, Parichehr
Oryan, Shahrbanoo
Fatehi Gharehlar, Laleh
Salari, Ali-Akbar
Solati, Jalal
author_facet Yaghmaei, Parichehr
Oryan, Shahrbanoo
Fatehi Gharehlar, Laleh
Salari, Ali-Akbar
Solati, Jalal
author_sort Yaghmaei, Parichehr
collection PubMed
description OBJECTIVE(S): There is well documented evidence for the increase in widespread use of complementary and alternative medicine in the treatment of physical and psychiatric symptoms and disorders within the populations. In the present study, we investigated the influence of Vitex agnus-castus (vitex) on anxiety-like behaviors of rats. MATERIALS AND METHODS: Elevated plus maze which is one of the methods used for testing anxiety is used in our present study. Rats were orally administrated with vitex for two week. The anxiety test was carried out after two weeks of oral administration of vitex. For evaluating interaction of vitex and serotonergic systems, rats were anaesthetized with ketamine and special cannulas were inserted stereotaxically into the third ventricle (TV) of brain. After 1 week recovery, the effects of serotonegic agents on anxiety were studied. RESULTS: Oral administration of vitex (100, 200, 300 mg/kg) for two weeks induced an anxiogenic-like effect which was shown through specific decreases in the percentages of open arm time (OAT %) and open arm entries (OAE %). Intra-TV infusion of 5HT(1A) receptor agonist, 8-OH-DPAT (5, 10 and 25 ng/rat) increased OAT% and OAE%, indicating anxiolytic–like behavior. However, injection of 5HT(1A) receptor antagonist NAN190 (0.25, 0.5 and 1 µg/rat) produced anxiogenic-like behavior. The most effective dose of 8-OH-DPAT (10 ng/rat), when co-administered with vitex (100, 200, 300 mg/kg), attenuated the anxiogenic-like effects of vitex significantly. Injection of the less effective dose of NAN190 (0.5 µg/rat), in combination with vitex (100, 200, 300 mg/kg), potentiate anxiogenic effects of vitex. CONCLUSIONS: These results illustrate that 5HT(1A) receptor is involved in the anxiogenic effects of vitex.
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spelling pubmed-35868842013-03-14 Possible Modulation of the Anexiogenic Effects of Vitex Agnus-castus by the Serotonergic System Yaghmaei, Parichehr Oryan, Shahrbanoo Fatehi Gharehlar, Laleh Salari, Ali-Akbar Solati, Jalal Iran J Basic Med Sci Original Article OBJECTIVE(S): There is well documented evidence for the increase in widespread use of complementary and alternative medicine in the treatment of physical and psychiatric symptoms and disorders within the populations. In the present study, we investigated the influence of Vitex agnus-castus (vitex) on anxiety-like behaviors of rats. MATERIALS AND METHODS: Elevated plus maze which is one of the methods used for testing anxiety is used in our present study. Rats were orally administrated with vitex for two week. The anxiety test was carried out after two weeks of oral administration of vitex. For evaluating interaction of vitex and serotonergic systems, rats were anaesthetized with ketamine and special cannulas were inserted stereotaxically into the third ventricle (TV) of brain. After 1 week recovery, the effects of serotonegic agents on anxiety were studied. RESULTS: Oral administration of vitex (100, 200, 300 mg/kg) for two weeks induced an anxiogenic-like effect which was shown through specific decreases in the percentages of open arm time (OAT %) and open arm entries (OAE %). Intra-TV infusion of 5HT(1A) receptor agonist, 8-OH-DPAT (5, 10 and 25 ng/rat) increased OAT% and OAE%, indicating anxiolytic–like behavior. However, injection of 5HT(1A) receptor antagonist NAN190 (0.25, 0.5 and 1 µg/rat) produced anxiogenic-like behavior. The most effective dose of 8-OH-DPAT (10 ng/rat), when co-administered with vitex (100, 200, 300 mg/kg), attenuated the anxiogenic-like effects of vitex significantly. Injection of the less effective dose of NAN190 (0.5 µg/rat), in combination with vitex (100, 200, 300 mg/kg), potentiate anxiogenic effects of vitex. CONCLUSIONS: These results illustrate that 5HT(1A) receptor is involved in the anxiogenic effects of vitex. Mashhad University of Medical Sciences 2012 /pmc/articles/PMC3586884/ /pubmed/23493923 Text en © 2012: Iranian Journal of Basic Medical Sciences This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Yaghmaei, Parichehr
Oryan, Shahrbanoo
Fatehi Gharehlar, Laleh
Salari, Ali-Akbar
Solati, Jalal
Possible Modulation of the Anexiogenic Effects of Vitex Agnus-castus by the Serotonergic System
title Possible Modulation of the Anexiogenic Effects of Vitex Agnus-castus by the Serotonergic System
title_full Possible Modulation of the Anexiogenic Effects of Vitex Agnus-castus by the Serotonergic System
title_fullStr Possible Modulation of the Anexiogenic Effects of Vitex Agnus-castus by the Serotonergic System
title_full_unstemmed Possible Modulation of the Anexiogenic Effects of Vitex Agnus-castus by the Serotonergic System
title_short Possible Modulation of the Anexiogenic Effects of Vitex Agnus-castus by the Serotonergic System
title_sort possible modulation of the anexiogenic effects of vitex agnus-castus by the serotonergic system
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3586884/
https://www.ncbi.nlm.nih.gov/pubmed/23493923
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