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Calotropis procera: A potential cognition enhancer in scopolamine and electroconvulsive shock-induced amnesia in rats

OBJECTIVES: Present study evaluates the effect of Calotropis procera (Apocynaceae) dry latex on cognitive function in rats using scopolamine and electroconvulsive shock (ECS) induced amnesia model. MATERIALS AND METHODS: Male Wistar rats were pretreated with 200, 400 and 800 mg/kg of C. procera dry...

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Autores principales: Malabade, Rohit, Taranalli, Ashok D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4527065/
https://www.ncbi.nlm.nih.gov/pubmed/26288476
http://dx.doi.org/10.4103/0253-7613.161269
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author Malabade, Rohit
Taranalli, Ashok D.
author_facet Malabade, Rohit
Taranalli, Ashok D.
author_sort Malabade, Rohit
collection PubMed
description OBJECTIVES: Present study evaluates the effect of Calotropis procera (Apocynaceae) dry latex on cognitive function in rats using scopolamine and electroconvulsive shock (ECS) induced amnesia model. MATERIALS AND METHODS: Male Wistar rats were pretreated with 200, 400 and 800 mg/kg of C. procera dry latex in scopolamine-induced amnesia model. Dose showing maximum effect in cognitive performance was selected and further evaluated using scopolamine and ECS-induced amnesia model for its effect on neurochemical enzymes and cognitive performance. Acetylcholinesterase (AChE) activity, β amyloid(1-42), and dopamine level were analyzed, while the cognitive performance was assessed by elevated plus maze, step-through passive avoidance test, and Morris water maze. Simultaneously, C. procera dry latex (25, 50, 100, 250, 500, and 1000 μg/mL) was screened for in vitro AChE inhibition assay. RESULTS: Pretreatment with (200, 400 and 800 mg/kg) C. procera dry latex shows dose dependent increase in cognitive performance in scopolamine-induced amnesia. Further, pretreatment with the selected dose (800 mg/kg) showed significant improvement in transfer latency (P < 0.001, P < 0.01), escape latency (P < 0.05), time spent in target quadrant (P < 0.001) also significant decrease in AChE activity (P < 0.05), β amyloid(1-42) level (P < 0.001), and increase in dopamine level (P < 0.01) in rat brain homogenate when compared with scopolamine and ECS disease control groups. IC(50) for C. procera dry latex was found to be <1000 μg/mL. CONCLUSIONS: Pretreatment with C. procera dry latex (800 mg/kg) produced significant cognition enhancement by improving cognitive performance and decreasing the marker neurochemical enzyme activity in scopolamine and ECS-induced amnesia model.
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spelling pubmed-45270652015-08-18 Calotropis procera: A potential cognition enhancer in scopolamine and electroconvulsive shock-induced amnesia in rats Malabade, Rohit Taranalli, Ashok D. Indian J Pharmacol Research Article OBJECTIVES: Present study evaluates the effect of Calotropis procera (Apocynaceae) dry latex on cognitive function in rats using scopolamine and electroconvulsive shock (ECS) induced amnesia model. MATERIALS AND METHODS: Male Wistar rats were pretreated with 200, 400 and 800 mg/kg of C. procera dry latex in scopolamine-induced amnesia model. Dose showing maximum effect in cognitive performance was selected and further evaluated using scopolamine and ECS-induced amnesia model for its effect on neurochemical enzymes and cognitive performance. Acetylcholinesterase (AChE) activity, β amyloid(1-42), and dopamine level were analyzed, while the cognitive performance was assessed by elevated plus maze, step-through passive avoidance test, and Morris water maze. Simultaneously, C. procera dry latex (25, 50, 100, 250, 500, and 1000 μg/mL) was screened for in vitro AChE inhibition assay. RESULTS: Pretreatment with (200, 400 and 800 mg/kg) C. procera dry latex shows dose dependent increase in cognitive performance in scopolamine-induced amnesia. Further, pretreatment with the selected dose (800 mg/kg) showed significant improvement in transfer latency (P < 0.001, P < 0.01), escape latency (P < 0.05), time spent in target quadrant (P < 0.001) also significant decrease in AChE activity (P < 0.05), β amyloid(1-42) level (P < 0.001), and increase in dopamine level (P < 0.01) in rat brain homogenate when compared with scopolamine and ECS disease control groups. IC(50) for C. procera dry latex was found to be <1000 μg/mL. CONCLUSIONS: Pretreatment with C. procera dry latex (800 mg/kg) produced significant cognition enhancement by improving cognitive performance and decreasing the marker neurochemical enzyme activity in scopolamine and ECS-induced amnesia model. Medknow Publications & Media Pvt Ltd 2015 /pmc/articles/PMC4527065/ /pubmed/26288476 http://dx.doi.org/10.4103/0253-7613.161269 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
Malabade, Rohit
Taranalli, Ashok D.
Calotropis procera: A potential cognition enhancer in scopolamine and electroconvulsive shock-induced amnesia in rats
title Calotropis procera: A potential cognition enhancer in scopolamine and electroconvulsive shock-induced amnesia in rats
title_full Calotropis procera: A potential cognition enhancer in scopolamine and electroconvulsive shock-induced amnesia in rats
title_fullStr Calotropis procera: A potential cognition enhancer in scopolamine and electroconvulsive shock-induced amnesia in rats
title_full_unstemmed Calotropis procera: A potential cognition enhancer in scopolamine and electroconvulsive shock-induced amnesia in rats
title_short Calotropis procera: A potential cognition enhancer in scopolamine and electroconvulsive shock-induced amnesia in rats
title_sort calotropis procera: a potential cognition enhancer in scopolamine and electroconvulsive shock-induced amnesia in rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4527065/
https://www.ncbi.nlm.nih.gov/pubmed/26288476
http://dx.doi.org/10.4103/0253-7613.161269
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