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Effect of Alpinia calcarata on glucose uptake in diabetic rats-an in vitro and in vivo model
BACKGROUND: Diabetes mellitus is a heterogeneous metabolic disorders characterized by abnormally high levels of blood glucose The main objective of the present work is to study the effect of Alpinia calcarata on glucose uptake in streptozotocin (STZ) induced diabetic rats. METHODS: The diabetes was...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3946031/ https://www.ncbi.nlm.nih.gov/pubmed/24502532 http://dx.doi.org/10.1186/2251-6581-13-33 |
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author | Rajasekar, Ramya Manokaran, Kalaiselvi Rajasekaran, Narmadha Duraisamy, Gomathi Kanakasabapathi, Devaki |
author_facet | Rajasekar, Ramya Manokaran, Kalaiselvi Rajasekaran, Narmadha Duraisamy, Gomathi Kanakasabapathi, Devaki |
author_sort | Rajasekar, Ramya |
collection | PubMed |
description | BACKGROUND: Diabetes mellitus is a heterogeneous metabolic disorders characterized by abnormally high levels of blood glucose The main objective of the present work is to study the effect of Alpinia calcarata on glucose uptake in streptozotocin (STZ) induced diabetic rats. METHODS: The diabetes was induced by single dose of STZ (45 mg/kg) in citrate buffer, while the normal control group was given the vehicle (citrate buffer) only. After induction of diabetes, the diabetic animals were treated with ethanolic extract of Alpinia calcarata (200 mg/kg) and glibenclamide (2 mg/kg) for 30 days. Blood glucose estimation was performed every week of the study. At the end of study period, animals were sacrificed for biochemical studies. RESULTS: Streptozotocin induced diabetic rats shows the altered levels of various biochemical profiles. Those levels were brought back to near normal upon treatment with ethanolic extract of Alpinia calcarata and standard drug glibanclamide. No significant changes were observed on treatment with plant extract alone group indicated that there are no toxic substances present in Alpinia calcarata. The antidiabetic activity of plant extract was also further confirmed by histopathological studies. The ethanolic extract of Alpinia calcarata shows significant inhibition of alpha glucosidase activity and also enhancing the glucose uptake in rat hemidiaphragm. CONCLUSIONS: In conclusion, the ethanolic extract of Alpinia calcarata ameliorates the condition associated with diabetes. |
format | Online Article Text |
id | pubmed-3946031 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-39460312014-03-09 Effect of Alpinia calcarata on glucose uptake in diabetic rats-an in vitro and in vivo model Rajasekar, Ramya Manokaran, Kalaiselvi Rajasekaran, Narmadha Duraisamy, Gomathi Kanakasabapathi, Devaki J Diabetes Metab Disord Research Article BACKGROUND: Diabetes mellitus is a heterogeneous metabolic disorders characterized by abnormally high levels of blood glucose The main objective of the present work is to study the effect of Alpinia calcarata on glucose uptake in streptozotocin (STZ) induced diabetic rats. METHODS: The diabetes was induced by single dose of STZ (45 mg/kg) in citrate buffer, while the normal control group was given the vehicle (citrate buffer) only. After induction of diabetes, the diabetic animals were treated with ethanolic extract of Alpinia calcarata (200 mg/kg) and glibenclamide (2 mg/kg) for 30 days. Blood glucose estimation was performed every week of the study. At the end of study period, animals were sacrificed for biochemical studies. RESULTS: Streptozotocin induced diabetic rats shows the altered levels of various biochemical profiles. Those levels were brought back to near normal upon treatment with ethanolic extract of Alpinia calcarata and standard drug glibanclamide. No significant changes were observed on treatment with plant extract alone group indicated that there are no toxic substances present in Alpinia calcarata. The antidiabetic activity of plant extract was also further confirmed by histopathological studies. The ethanolic extract of Alpinia calcarata shows significant inhibition of alpha glucosidase activity and also enhancing the glucose uptake in rat hemidiaphragm. CONCLUSIONS: In conclusion, the ethanolic extract of Alpinia calcarata ameliorates the condition associated with diabetes. BioMed Central 2014-02-06 /pmc/articles/PMC3946031/ /pubmed/24502532 http://dx.doi.org/10.1186/2251-6581-13-33 Text en Copyright © 2014 Rajasekar et al.; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. 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 Rajasekar, Ramya Manokaran, Kalaiselvi Rajasekaran, Narmadha Duraisamy, Gomathi Kanakasabapathi, Devaki Effect of Alpinia calcarata on glucose uptake in diabetic rats-an in vitro and in vivo model |
title | Effect of Alpinia calcarata on glucose uptake in diabetic rats-an in vitro and in vivo model |
title_full | Effect of Alpinia calcarata on glucose uptake in diabetic rats-an in vitro and in vivo model |
title_fullStr | Effect of Alpinia calcarata on glucose uptake in diabetic rats-an in vitro and in vivo model |
title_full_unstemmed | Effect of Alpinia calcarata on glucose uptake in diabetic rats-an in vitro and in vivo model |
title_short | Effect of Alpinia calcarata on glucose uptake in diabetic rats-an in vitro and in vivo model |
title_sort | effect of alpinia calcarata on glucose uptake in diabetic rats-an in vitro and in vivo model |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3946031/ https://www.ncbi.nlm.nih.gov/pubmed/24502532 http://dx.doi.org/10.1186/2251-6581-13-33 |
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