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Evaluation of sesamol and buspirone in stress induced anxiety in mice

OBJECTIVES: The present study was designed to elucidate the effects of sesamol, buspirone and their combination in immobilization stress induced behavioral and biochemical alterations in mice. MATERIALS AND METHODS: Male Laca mice (divided into 10 groups with 6 animals each) were pre-treated with se...

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Autores principales: Kumar, Anil, Kaur, Gurleen, Kalonia, Harikesh, Rinwa, Puneet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3608295/
https://www.ncbi.nlm.nih.gov/pubmed/23543858
http://dx.doi.org/10.4103/0253-7613.106435
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author Kumar, Anil
Kaur, Gurleen
Kalonia, Harikesh
Rinwa, Puneet
author_facet Kumar, Anil
Kaur, Gurleen
Kalonia, Harikesh
Rinwa, Puneet
author_sort Kumar, Anil
collection PubMed
description OBJECTIVES: The present study was designed to elucidate the effects of sesamol, buspirone and their combination in immobilization stress induced behavioral and biochemical alterations in mice. MATERIALS AND METHODS: Male Laca mice (divided into 10 groups with 6 animals each) were pre-treated with sesamol (5 and 10 mg/kg; p.o.), buspirone (5 and 10 mg/kg; p.o.) and combination of sesamol (5 and 10 mg/kg; p.o.) with buspirone (5 mg/kg; p.o.) for consecutive five days. On the 6(th) day, animals were immobilized for 6 h and various behavioral tests such as body weight, locomotor activity, mirror chamber test and elevated plus maze were carried out. Biochemical estimations such as lipid peroxidation and nitrite concentration, glutathione and catalase levels were done. Data was analyzed using One way ANOVA followed by Tukey's test (P < 0.05) was considered statistical significant. RESULTS: Immobilization stress significantly (P < 0.05) impaired body weight, locomotor activity, induced anxiety like behavioral and oxidative damage as compared to naοve animal. Pretreatment with sesamol (5 and 10 mg/kg; p.o.) and buspirone (5 and 10 mg/ kg; p.o.) significantly (P < 0.05) improved body weight, locomotor activity, and anxiety like behavior in mirror chamber as well as plus maze performance tasks and anti-oxidant like effect as evidenced by reduced lipid peroxidation, nitrite concentration and restoration of reduced glutathione and catalase activity as compared to control animals. Further, co- administration of sesamol (5 and 10 mg/kg) with buspirone (5 mg/kg) significantly (P < .05) potentiated the anti anxiety effects as compared to their effects alone. CONCLUSIONS: The present study suggests that combination of sesamol and buspirone potentiated the antianxiety effects against anxiety induced by immobilization stress and oxidative damage in mice.
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spelling pubmed-36082952013-03-29 Evaluation of sesamol and buspirone in stress induced anxiety in mice Kumar, Anil Kaur, Gurleen Kalonia, Harikesh Rinwa, Puneet Indian J Pharmacol Research Article OBJECTIVES: The present study was designed to elucidate the effects of sesamol, buspirone and their combination in immobilization stress induced behavioral and biochemical alterations in mice. MATERIALS AND METHODS: Male Laca mice (divided into 10 groups with 6 animals each) were pre-treated with sesamol (5 and 10 mg/kg; p.o.), buspirone (5 and 10 mg/kg; p.o.) and combination of sesamol (5 and 10 mg/kg; p.o.) with buspirone (5 mg/kg; p.o.) for consecutive five days. On the 6(th) day, animals were immobilized for 6 h and various behavioral tests such as body weight, locomotor activity, mirror chamber test and elevated plus maze were carried out. Biochemical estimations such as lipid peroxidation and nitrite concentration, glutathione and catalase levels were done. Data was analyzed using One way ANOVA followed by Tukey's test (P < 0.05) was considered statistical significant. RESULTS: Immobilization stress significantly (P < 0.05) impaired body weight, locomotor activity, induced anxiety like behavioral and oxidative damage as compared to naοve animal. Pretreatment with sesamol (5 and 10 mg/kg; p.o.) and buspirone (5 and 10 mg/ kg; p.o.) significantly (P < 0.05) improved body weight, locomotor activity, and anxiety like behavior in mirror chamber as well as plus maze performance tasks and anti-oxidant like effect as evidenced by reduced lipid peroxidation, nitrite concentration and restoration of reduced glutathione and catalase activity as compared to control animals. Further, co- administration of sesamol (5 and 10 mg/kg) with buspirone (5 mg/kg) significantly (P < .05) potentiated the anti anxiety effects as compared to their effects alone. CONCLUSIONS: The present study suggests that combination of sesamol and buspirone potentiated the antianxiety effects against anxiety induced by immobilization stress and oxidative damage in mice. Medknow Publications & Media Pvt Ltd 2013 /pmc/articles/PMC3608295/ /pubmed/23543858 http://dx.doi.org/10.4103/0253-7613.106435 Text en Copyright: © Indian Journal of Pharmacology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Kumar, Anil
Kaur, Gurleen
Kalonia, Harikesh
Rinwa, Puneet
Evaluation of sesamol and buspirone in stress induced anxiety in mice
title Evaluation of sesamol and buspirone in stress induced anxiety in mice
title_full Evaluation of sesamol and buspirone in stress induced anxiety in mice
title_fullStr Evaluation of sesamol and buspirone in stress induced anxiety in mice
title_full_unstemmed Evaluation of sesamol and buspirone in stress induced anxiety in mice
title_short Evaluation of sesamol and buspirone in stress induced anxiety in mice
title_sort evaluation of sesamol and buspirone in stress induced anxiety in mice
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3608295/
https://www.ncbi.nlm.nih.gov/pubmed/23543858
http://dx.doi.org/10.4103/0253-7613.106435
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