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Bromocriptine in type 2 diabetes mellitus

Bromocriptine mesylate quick-release was approved by the Food and Drug Administration (FDA) in May 2009, for the treatment of type 2 diabetes. Bromocriptine is thought to act on the circadian neuronal activities in the hypothalamus, to reset an abnormally elevated hypothalamic drive for increased pl...

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Detalles Bibliográficos
Autores principales: Shivaprasad, C., Kalra, Sanjay
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3152192/
https://www.ncbi.nlm.nih.gov/pubmed/21847449
http://dx.doi.org/10.4103/2230-8210.83058
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author Shivaprasad, C.
Kalra, Sanjay
author_facet Shivaprasad, C.
Kalra, Sanjay
author_sort Shivaprasad, C.
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description Bromocriptine mesylate quick-release was approved by the Food and Drug Administration (FDA) in May 2009, for the treatment of type 2 diabetes. Bromocriptine is thought to act on the circadian neuronal activities in the hypothalamus, to reset an abnormally elevated hypothalamic drive for increased plasma glucose, free fatty acids, and triglycerides in insulin-resistant patients. Randomized controlled trials have shown that bromocriptine-QR lowers glycated hemoglobin by 0.4 – 0.8% either as monotherapy or in combination with other anti-diabetes medications. The doses used to treat diabetes (up to 4.8 mg daily) are much lower than those used to treat Parkinson's disease, and apart from nausea, the drug is well-tolerated. The novel mechanism of action, good side effect profile, and its effects to reduce cardiovascular event rates make it an attractive option for the treatment of type 2 diabetes.
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spelling pubmed-31521922011-08-16 Bromocriptine in type 2 diabetes mellitus Shivaprasad, C. Kalra, Sanjay Indian J Endocrinol Metab Review Article Bromocriptine mesylate quick-release was approved by the Food and Drug Administration (FDA) in May 2009, for the treatment of type 2 diabetes. Bromocriptine is thought to act on the circadian neuronal activities in the hypothalamus, to reset an abnormally elevated hypothalamic drive for increased plasma glucose, free fatty acids, and triglycerides in insulin-resistant patients. Randomized controlled trials have shown that bromocriptine-QR lowers glycated hemoglobin by 0.4 – 0.8% either as monotherapy or in combination with other anti-diabetes medications. The doses used to treat diabetes (up to 4.8 mg daily) are much lower than those used to treat Parkinson's disease, and apart from nausea, the drug is well-tolerated. The novel mechanism of action, good side effect profile, and its effects to reduce cardiovascular event rates make it an attractive option for the treatment of type 2 diabetes. Medknow Publications 2011-07 /pmc/articles/PMC3152192/ /pubmed/21847449 http://dx.doi.org/10.4103/2230-8210.83058 Text en © Indian Journal of Endocrinology and Metabolism 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 Review Article
Shivaprasad, C.
Kalra, Sanjay
Bromocriptine in type 2 diabetes mellitus
title Bromocriptine in type 2 diabetes mellitus
title_full Bromocriptine in type 2 diabetes mellitus
title_fullStr Bromocriptine in type 2 diabetes mellitus
title_full_unstemmed Bromocriptine in type 2 diabetes mellitus
title_short Bromocriptine in type 2 diabetes mellitus
title_sort bromocriptine in type 2 diabetes mellitus
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3152192/
https://www.ncbi.nlm.nih.gov/pubmed/21847449
http://dx.doi.org/10.4103/2230-8210.83058
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