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Use of Dicarboxylic Acids in Type 2 Diabetes.
MedLine Citation:
PMID:  22242741     Owner:  NLM     Status:  Publisher    
Abstract/OtherAbstract:
Even number, medium chain dicarboxylic acids (DAs), naturally occurring in high plants, are a promising alternative energy substrate. Contrary to the homologous fatty acids, DAs are soluble in water as salts. They are β-oxidized providing Acetyl-CoAs and Succinyl-CoA, this latter an intermediate of the tricarboxylic acid cycle. Sebacic acid and dodecanedioic acid, DAs with 10 and 12 carbon atoms respectively, provide 6.6 kcal/g and 7.2 kcal/g each; therefore, their energy density is intermediate between glucose and fatty acids. DAs have been proved to be safe in both experimental animal and humans and their use has been recently proposed in diabetes. Studies in animals and humans with type 2 diabetes showed that oral administration of sebacic acid improved glycaemic control, probably by enhancing insulin sensitivity, and reduced hepatic gluconeogenesis and glucose output. Moreover, dodecanedioic acid intake reduced muscle fatigue during exercise in type-2 diabetes subjects, suggesting an improvement of energy utilization and "metabolic flexibility". In this article we will review the natural sources of DAs, their fate in animals and humans and their effect in improving glucose metabolism in type 2 diabetes. © 2012 The Authors. British Journal of Clinical Pharmacology © 2012 The British Pharmacological Society.
Authors:
Geltrude Mingrone; Lidia Castagneto-Gissey; Katherine Macé
Publication Detail:
Type:  JOURNAL ARTICLE     Date:  2012-1-13
Journal Detail:
Title:  British journal of clinical pharmacology     Volume:  -     ISSN:  1365-2125     ISO Abbreviation:  -     Publication Date:  2012 Jan 
Date Detail:
Created Date:  2012-1-16     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  7503323     Medline TA:  Br J Clin Pharmacol     Country:  -    
Other Details:
Languages:  ENG     Pagination:  -     Citation Subset:  -    
Copyright Information:
© 2012 The Authors. British Journal of Clinical Pharmacology © 2012 The British Pharmacological Society.
Affiliation:
Department of Internal Medicine, Catholic University of Rome, Rome, Italy; Nestlé Research Centre, Lausanne, Switzerland.
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