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Behavioral and Biochemical Evidences for Antidepressant-Like Activity of Celastrus Paniculatus Seed Oil in Mice
INTRODUCTION: Celastrus paniculatus seed oil, commonly known as Malkangni or Jyotishmati, was in use from time immemorial to treat brain related disorders. Celastrus paniculatus seed oil has significant antidepressant-like activity in chronic unpredictable stressed mice. The present study was undert...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Iranian Neuroscience Society
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892330/ https://www.ncbi.nlm.nih.gov/pubmed/27303599 |
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author | Valecha, Rekha Dhingra, Dinesh |
author_facet | Valecha, Rekha Dhingra, Dinesh |
author_sort | Valecha, Rekha |
collection | PubMed |
description | INTRODUCTION: Celastrus paniculatus seed oil, commonly known as Malkangni or Jyotishmati, was in use from time immemorial to treat brain related disorders. Celastrus paniculatus seed oil has significant antidepressant-like activity in chronic unpredictable stressed mice. The present study was undertaken to evaluate the antidepressant-like effect of Celastrus paniculatus seed oil in unstressed mice and to explore its mechanism of action. METHODS: The seed oil (50, 100, and 200 mg/kg, PO) and fluoxetine per se were administered for 14 successive days to Swiss young albino mice. On the 14(th) day, 60 min after drug administration, animals were subjected to Tail Suspension Test (TST) and Forced Swim Test (FST). The mechanism of action was also studied. RESULTS: The oil significantly decreased immobility period of mice in both tail suspension test and forced swim test, indicating its significant antidepressant-like activity. The efficacy was found to be comparable to fluoxetine (P<0.0001). ED(50) value of celastrus seed oil using FST and TST were 17.38 and 31.62 mg/kg, respectively. The oil did not show any significant effect on locomotor activity. It significantly inhibited brain MAO–A activity and decreased plasma corticosterone levels. Sulpiride (selective D(2)-receptor antagonist), p-CPA (tryptophan hydroxylase inhibitor), and baclofen (GABA(B) agonist) significantly attenuated the oil-induced antidepressant-like effect, when assessed during TST. DISCUSSION: Celastrus paniculatus seed oil produced significant antidepressant-like effect in mice possibly through interaction with dopamine D(2), serotonergic, and GABA(B) receptors; as well as inhibition of MAO–A activity and decrease in plasma corticosterone levels. |
format | Online Article Text |
id | pubmed-4892330 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Iranian Neuroscience Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-48923302016-06-14 Behavioral and Biochemical Evidences for Antidepressant-Like Activity of Celastrus Paniculatus Seed Oil in Mice Valecha, Rekha Dhingra, Dinesh Basic Clin Neurosci Research Papers INTRODUCTION: Celastrus paniculatus seed oil, commonly known as Malkangni or Jyotishmati, was in use from time immemorial to treat brain related disorders. Celastrus paniculatus seed oil has significant antidepressant-like activity in chronic unpredictable stressed mice. The present study was undertaken to evaluate the antidepressant-like effect of Celastrus paniculatus seed oil in unstressed mice and to explore its mechanism of action. METHODS: The seed oil (50, 100, and 200 mg/kg, PO) and fluoxetine per se were administered for 14 successive days to Swiss young albino mice. On the 14(th) day, 60 min after drug administration, animals were subjected to Tail Suspension Test (TST) and Forced Swim Test (FST). The mechanism of action was also studied. RESULTS: The oil significantly decreased immobility period of mice in both tail suspension test and forced swim test, indicating its significant antidepressant-like activity. The efficacy was found to be comparable to fluoxetine (P<0.0001). ED(50) value of celastrus seed oil using FST and TST were 17.38 and 31.62 mg/kg, respectively. The oil did not show any significant effect on locomotor activity. It significantly inhibited brain MAO–A activity and decreased plasma corticosterone levels. Sulpiride (selective D(2)-receptor antagonist), p-CPA (tryptophan hydroxylase inhibitor), and baclofen (GABA(B) agonist) significantly attenuated the oil-induced antidepressant-like effect, when assessed during TST. DISCUSSION: Celastrus paniculatus seed oil produced significant antidepressant-like effect in mice possibly through interaction with dopamine D(2), serotonergic, and GABA(B) receptors; as well as inhibition of MAO–A activity and decrease in plasma corticosterone levels. Iranian Neuroscience Society 2016-01 /pmc/articles/PMC4892330/ /pubmed/27303599 Text en Copyright© 2016 Iranian Neuroscience Society This work is licensed under a Creative Commons Attribution-NonCommercial 3.0 Unported License which allows users to read, copy, distribute and make derivative works for non-commercial purposes from the material, as long as the author of the original work is cited properly. |
spellingShingle | Research Papers Valecha, Rekha Dhingra, Dinesh Behavioral and Biochemical Evidences for Antidepressant-Like Activity of Celastrus Paniculatus Seed Oil in Mice |
title | Behavioral and Biochemical Evidences for Antidepressant-Like Activity of Celastrus Paniculatus Seed Oil in Mice |
title_full | Behavioral and Biochemical Evidences for Antidepressant-Like Activity of Celastrus Paniculatus Seed Oil in Mice |
title_fullStr | Behavioral and Biochemical Evidences for Antidepressant-Like Activity of Celastrus Paniculatus Seed Oil in Mice |
title_full_unstemmed | Behavioral and Biochemical Evidences for Antidepressant-Like Activity of Celastrus Paniculatus Seed Oil in Mice |
title_short | Behavioral and Biochemical Evidences for Antidepressant-Like Activity of Celastrus Paniculatus Seed Oil in Mice |
title_sort | behavioral and biochemical evidences for antidepressant-like activity of celastrus paniculatus seed oil in mice |
topic | Research Papers |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4892330/ https://www.ncbi.nlm.nih.gov/pubmed/27303599 |
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