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Antihyperglycemic action of rhodiola-aqeous extract in type1-like diabetic rats

BACKGROUND: Rhodiola rosea (Rhodiola) is a plant in the Crassulaceae family that grows in cold regions of the world. It is mainly used in clinics as an adaptogen. Recently, it has been mentioned that Rhodiola increases plasma β-endorphin to lower blood pressure. Thus, the present study aims to inves...

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Autores principales: Niu, Chiang-Shan, Chen, Li-Jen, Niu, Ho-Shan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3897963/
https://www.ncbi.nlm.nih.gov/pubmed/24417880
http://dx.doi.org/10.1186/1472-6882-14-20
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author Niu, Chiang-Shan
Chen, Li-Jen
Niu, Ho-Shan
author_facet Niu, Chiang-Shan
Chen, Li-Jen
Niu, Ho-Shan
author_sort Niu, Chiang-Shan
collection PubMed
description BACKGROUND: Rhodiola rosea (Rhodiola) is a plant in the Crassulaceae family that grows in cold regions of the world. It is mainly used in clinics as an adaptogen. Recently, it has been mentioned that Rhodiola increases plasma β-endorphin to lower blood pressure. Thus, the present study aims to investigate the antidiabetic action of Rhodiola in relation to opioids in streptozotocin-induced diabetic rats (STZ-diabetic rats). METHODS: In the present study, the plasma glucose was analyzed with glucose oxidase method, and the determination of plasma β-endorphin was carried out using a commercially available enzyme-linked immunosorbent assay. The adrenalectomy of STZ-diabetic rats was used to evaluate the role of β-endorphin. In addition, quantitative reverse transcription-polymerase chain reaction (qRT-PCR) and western blotting analysis were performed to investigate mRNA and protein expressions. RESULTS: Rhodiola-water extract dose-dependently lowered the plasma glucose in STZ-diabetic rats and this action was reversed by blockade of opioid μ-receptors using cyprodime. An increase of plasma β-endorphin by rhodiola-water extract was also observed in same manner. The plasma glucose lowering action of rhodiola-water extract was attenuated in bilateral adrenalectomized rats. In addition, continuous administration of rhodiola-water extract for 3 days in STZ-diabetic rats resulted in an increased expression of glucose transporter subtype 4 (GLUT 4) in skeletal muscle and a marked reduction of phosphoenolpyruvate carboxykinase (PEPCK) expression in liver. These effects were also reversed by blockade of opioid μ-receptors. CONCLUSIONS: Taken together, rhodiola-water extract improves hyperglycemia via an increase of β-endorphin secretion from adrenal gland to activate opioid μ-receptors in STZ-diabetic rats.
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spelling pubmed-38979632014-01-23 Antihyperglycemic action of rhodiola-aqeous extract in type1-like diabetic rats Niu, Chiang-Shan Chen, Li-Jen Niu, Ho-Shan BMC Complement Altern Med Research Article BACKGROUND: Rhodiola rosea (Rhodiola) is a plant in the Crassulaceae family that grows in cold regions of the world. It is mainly used in clinics as an adaptogen. Recently, it has been mentioned that Rhodiola increases plasma β-endorphin to lower blood pressure. Thus, the present study aims to investigate the antidiabetic action of Rhodiola in relation to opioids in streptozotocin-induced diabetic rats (STZ-diabetic rats). METHODS: In the present study, the plasma glucose was analyzed with glucose oxidase method, and the determination of plasma β-endorphin was carried out using a commercially available enzyme-linked immunosorbent assay. The adrenalectomy of STZ-diabetic rats was used to evaluate the role of β-endorphin. In addition, quantitative reverse transcription-polymerase chain reaction (qRT-PCR) and western blotting analysis were performed to investigate mRNA and protein expressions. RESULTS: Rhodiola-water extract dose-dependently lowered the plasma glucose in STZ-diabetic rats and this action was reversed by blockade of opioid μ-receptors using cyprodime. An increase of plasma β-endorphin by rhodiola-water extract was also observed in same manner. The plasma glucose lowering action of rhodiola-water extract was attenuated in bilateral adrenalectomized rats. In addition, continuous administration of rhodiola-water extract for 3 days in STZ-diabetic rats resulted in an increased expression of glucose transporter subtype 4 (GLUT 4) in skeletal muscle and a marked reduction of phosphoenolpyruvate carboxykinase (PEPCK) expression in liver. These effects were also reversed by blockade of opioid μ-receptors. CONCLUSIONS: Taken together, rhodiola-water extract improves hyperglycemia via an increase of β-endorphin secretion from adrenal gland to activate opioid μ-receptors in STZ-diabetic rats. BioMed Central 2014-01-13 /pmc/articles/PMC3897963/ /pubmed/24417880 http://dx.doi.org/10.1186/1472-6882-14-20 Text en Copyright © 2014 Niu 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 cited. 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
Niu, Chiang-Shan
Chen, Li-Jen
Niu, Ho-Shan
Antihyperglycemic action of rhodiola-aqeous extract in type1-like diabetic rats
title Antihyperglycemic action of rhodiola-aqeous extract in type1-like diabetic rats
title_full Antihyperglycemic action of rhodiola-aqeous extract in type1-like diabetic rats
title_fullStr Antihyperglycemic action of rhodiola-aqeous extract in type1-like diabetic rats
title_full_unstemmed Antihyperglycemic action of rhodiola-aqeous extract in type1-like diabetic rats
title_short Antihyperglycemic action of rhodiola-aqeous extract in type1-like diabetic rats
title_sort antihyperglycemic action of rhodiola-aqeous extract in type1-like diabetic rats
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3897963/
https://www.ncbi.nlm.nih.gov/pubmed/24417880
http://dx.doi.org/10.1186/1472-6882-14-20
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