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GLP-I secretion in healthy and diabetic Wistar rats in response to aqueous extract of Momordica charantia

BACKGROUND: Diabetes mellitus is one of the major global health disorders increasing at an alarming rate in both developed and developing countries. The objective of this study was to assess the effect of aqueous extract of Momordica charantia (AEMC) on fasting blood glucose (FBG), tissue glycogen,...

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Autores principales: Bhat, Gulzar Ahmad, Khan, Haseeb A., Alhomida, Abdullah S., Sharma, Poonam, Singh, Rambir, Paray, Bilal Ahmad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5960212/
https://www.ncbi.nlm.nih.gov/pubmed/29776414
http://dx.doi.org/10.1186/s12906-018-2227-4
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author Bhat, Gulzar Ahmad
Khan, Haseeb A.
Alhomida, Abdullah S.
Sharma, Poonam
Singh, Rambir
Paray, Bilal Ahmad
author_facet Bhat, Gulzar Ahmad
Khan, Haseeb A.
Alhomida, Abdullah S.
Sharma, Poonam
Singh, Rambir
Paray, Bilal Ahmad
author_sort Bhat, Gulzar Ahmad
collection PubMed
description BACKGROUND: Diabetes mellitus is one of the major global health disorders increasing at an alarming rate in both developed and developing countries. The objective of this study was to assess the effect of aqueous extract of Momordica charantia (AEMC) on fasting blood glucose (FBG), tissue glycogen, glycosylated haemoglobin, plasma concentrations of insulin and GLP-1 hormone (glucagon-like peptide 1) in healthy and diabetic wistar rats. METHODS: Male Wistar rats (both normal and diabetic) were treated with AEMC by gavaging (300 mg/kg body wt/day for 28 days). RESULTS: AEMC was found to increase tissue glycogen, serum insulin and GLP-1 non-significantly (P > 0.05) in normal, significantly (P < 0.01) in diabetic Wistar rats, whereas decrease in FBG and Glycosylated haemoglobin non-significantly (P > 0.05) in normal, significantly (P < 0.01) in diabetic Wistar rats. The elevation of GLP-1 level in normal and diabetic treated groups may be due to the L-cell regeneration and proliferation by binding with L-cell receptors and makes a conformational change, resulting in the activation of a series of signal transducers. The polar molecules of M. charantia also depolarize the L-cell through elevation of intracellular Ca(2+) concentration and which in turn releases GLP-1. GLP-1 in turn elevates beta-cell proliferation and insulin secretion. CONCLUSION: The findings tend to provide a possible explanation for the hypoglycemic action of M. charantia fruit extracts as alternative nutritional therapy in the management and treatment of diabetes.
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spelling pubmed-59602122018-05-24 GLP-I secretion in healthy and diabetic Wistar rats in response to aqueous extract of Momordica charantia Bhat, Gulzar Ahmad Khan, Haseeb A. Alhomida, Abdullah S. Sharma, Poonam Singh, Rambir Paray, Bilal Ahmad BMC Complement Altern Med Research Article BACKGROUND: Diabetes mellitus is one of the major global health disorders increasing at an alarming rate in both developed and developing countries. The objective of this study was to assess the effect of aqueous extract of Momordica charantia (AEMC) on fasting blood glucose (FBG), tissue glycogen, glycosylated haemoglobin, plasma concentrations of insulin and GLP-1 hormone (glucagon-like peptide 1) in healthy and diabetic wistar rats. METHODS: Male Wistar rats (both normal and diabetic) were treated with AEMC by gavaging (300 mg/kg body wt/day for 28 days). RESULTS: AEMC was found to increase tissue glycogen, serum insulin and GLP-1 non-significantly (P > 0.05) in normal, significantly (P < 0.01) in diabetic Wistar rats, whereas decrease in FBG and Glycosylated haemoglobin non-significantly (P > 0.05) in normal, significantly (P < 0.01) in diabetic Wistar rats. The elevation of GLP-1 level in normal and diabetic treated groups may be due to the L-cell regeneration and proliferation by binding with L-cell receptors and makes a conformational change, resulting in the activation of a series of signal transducers. The polar molecules of M. charantia also depolarize the L-cell through elevation of intracellular Ca(2+) concentration and which in turn releases GLP-1. GLP-1 in turn elevates beta-cell proliferation and insulin secretion. CONCLUSION: The findings tend to provide a possible explanation for the hypoglycemic action of M. charantia fruit extracts as alternative nutritional therapy in the management and treatment of diabetes. BioMed Central 2018-05-18 /pmc/articles/PMC5960212/ /pubmed/29776414 http://dx.doi.org/10.1186/s12906-018-2227-4 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Bhat, Gulzar Ahmad
Khan, Haseeb A.
Alhomida, Abdullah S.
Sharma, Poonam
Singh, Rambir
Paray, Bilal Ahmad
GLP-I secretion in healthy and diabetic Wistar rats in response to aqueous extract of Momordica charantia
title GLP-I secretion in healthy and diabetic Wistar rats in response to aqueous extract of Momordica charantia
title_full GLP-I secretion in healthy and diabetic Wistar rats in response to aqueous extract of Momordica charantia
title_fullStr GLP-I secretion in healthy and diabetic Wistar rats in response to aqueous extract of Momordica charantia
title_full_unstemmed GLP-I secretion in healthy and diabetic Wistar rats in response to aqueous extract of Momordica charantia
title_short GLP-I secretion in healthy and diabetic Wistar rats in response to aqueous extract of Momordica charantia
title_sort glp-i secretion in healthy and diabetic wistar rats in response to aqueous extract of momordica charantia
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5960212/
https://www.ncbi.nlm.nih.gov/pubmed/29776414
http://dx.doi.org/10.1186/s12906-018-2227-4
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