Antidepressant activity of enicostemma littorale blume in shp2 (protein tyrosine phosphatase)-inhibited animal model of depression

Background: The objective of this study is to develop a new animal model based on signaling pathways to understand the pathophysiology, therapy of depression, and to investigate the antidepressant activity of Enicostemma littorale which is not yet established. Methods: Animal models of depression w...

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Main Authors: V A Doss, Dharaniyambigai Kuberapandian
Format: Article
Language:English
Published: Wolters Kluwer Medknow Publications 2016-01-01
Series:International Journal of Preventive Medicine
Subjects:
Online Access:http://www.ijpvmjournal.net/article.asp?issn=2008-7802;year=2016;volume=7;issue=1;spage=112;epage=112;aulast=
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author V A Doss
Dharaniyambigai Kuberapandian
author_facet V A Doss
Dharaniyambigai Kuberapandian
author_sort V A Doss
collection DOAJ
description Background: The objective of this study is to develop a new animal model based on signaling pathways to understand the pathophysiology, therapy of depression, and to investigate the antidepressant activity of Enicostemma littorale which is not yet established. Methods: Animal models of depression were raised by physical methods and administration of methyl isobutyl ketone (100 mg/kg b.w., i.p.,) and a protein tyrosine phosphatase inhibitor, sodium orthovanadate (30 mg/kg b.w., i.p.,) to young Wistar rats. E. littorale aqueous extract (100 mg/kg b.w., oral) was administered. Forced swimming test (FST), biochemical, and histopathological parameters were performed with reference to fluoxetine (20 mg/kg b.w., oral) treatment. Results: High-performance thin-layer chromatography confirmed the presence of swertiamarin, a unique glycoside present in the Gentianaceae family. FST indicated high rates of immobility in depressed groups and low rates in plant extract-administered group with reference to fluoxetine. Biochemical assays indicated significantly (P < 0.05) increased levels of total protein, superoxide dismutase, triglycerides, and total serum cholesterol, whereas significant reduction (P < 0.05) of glutathione peroxidase, catalase, and lipid peroxidation in plant extract-administered groups in comparison to the depressed groups. Histopathological analysis indicated disorganized neuronal architecture during depression whereas rejuvenation of neuronal patterns was observed during treatment with plant extract and fluoxetine. Conclusions: This study shows that sodium orthovanadate induces depression in animals and also establishes the antidepressant activity of E. littorale.
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spelling doaj.art-32c275a239be47a881ea4f744abd3f482022-12-21T21:47:26ZengWolters Kluwer Medknow PublicationsInternational Journal of Preventive Medicine2008-78022008-82132016-01-017111211210.4103/2008-7802.191187Antidepressant activity of enicostemma littorale blume in shp2 (protein tyrosine phosphatase)-inhibited animal model of depressionV A DossDharaniyambigai KuberapandianBackground: The objective of this study is to develop a new animal model based on signaling pathways to understand the pathophysiology, therapy of depression, and to investigate the antidepressant activity of Enicostemma littorale which is not yet established. Methods: Animal models of depression were raised by physical methods and administration of methyl isobutyl ketone (100 mg/kg b.w., i.p.,) and a protein tyrosine phosphatase inhibitor, sodium orthovanadate (30 mg/kg b.w., i.p.,) to young Wistar rats. E. littorale aqueous extract (100 mg/kg b.w., oral) was administered. Forced swimming test (FST), biochemical, and histopathological parameters were performed with reference to fluoxetine (20 mg/kg b.w., oral) treatment. Results: High-performance thin-layer chromatography confirmed the presence of swertiamarin, a unique glycoside present in the Gentianaceae family. FST indicated high rates of immobility in depressed groups and low rates in plant extract-administered group with reference to fluoxetine. Biochemical assays indicated significantly (P < 0.05) increased levels of total protein, superoxide dismutase, triglycerides, and total serum cholesterol, whereas significant reduction (P < 0.05) of glutathione peroxidase, catalase, and lipid peroxidation in plant extract-administered groups in comparison to the depressed groups. Histopathological analysis indicated disorganized neuronal architecture during depression whereas rejuvenation of neuronal patterns was observed during treatment with plant extract and fluoxetine. Conclusions: This study shows that sodium orthovanadate induces depression in animals and also establishes the antidepressant activity of E. littorale.http://www.ijpvmjournal.net/article.asp?issn=2008-7802;year=2016;volume=7;issue=1;spage=112;epage=112;aulast=DepressionEnicostemma littorale Blumesodium orthovanadate
spellingShingle V A Doss
Dharaniyambigai Kuberapandian
Antidepressant activity of enicostemma littorale blume in shp2 (protein tyrosine phosphatase)-inhibited animal model of depression
International Journal of Preventive Medicine
Depression
Enicostemma littorale Blume
sodium orthovanadate
title Antidepressant activity of enicostemma littorale blume in shp2 (protein tyrosine phosphatase)-inhibited animal model of depression
title_full Antidepressant activity of enicostemma littorale blume in shp2 (protein tyrosine phosphatase)-inhibited animal model of depression
title_fullStr Antidepressant activity of enicostemma littorale blume in shp2 (protein tyrosine phosphatase)-inhibited animal model of depression
title_full_unstemmed Antidepressant activity of enicostemma littorale blume in shp2 (protein tyrosine phosphatase)-inhibited animal model of depression
title_short Antidepressant activity of enicostemma littorale blume in shp2 (protein tyrosine phosphatase)-inhibited animal model of depression
title_sort antidepressant activity of enicostemma littorale blume in shp2 protein tyrosine phosphatase inhibited animal model of depression
topic Depression
Enicostemma littorale Blume
sodium orthovanadate
url http://www.ijpvmjournal.net/article.asp?issn=2008-7802;year=2016;volume=7;issue=1;spage=112;epage=112;aulast=
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