Literature DB >> 6927727

Effect of acarbose on the 24-hour blood glucose profile and pattern of carbohydrate absorption.

R H Taylor, D J Jenkins, H M Barker, H Fielden, D V Goff, J J Misiewicz, D A Lee, H B Allen, G MacDonald, H Wallrabe.   

Abstract

Acarbose (Bay g 5421) is a powerful alpha-glucoside hydrolase inhibitor of potential value in the treatment of diabetes and hypoglycemic dumping syndrome after gastric surgery. The extent of its use may be limited by symptoms produced by carbohydrate malabsorption. To minimize these, the action of low doses of acarbose on 24-h blood glucose profiles and hydrogen evolution have been studied on four ambulant volunteers on control diets, after exclusion of sucrose and also after addition of guar in an attempt to enhance the therapeutic effect. Replacement of dietary sucrose by starch abolished significant hydrogen evolution in the morning after low doses of acarbose but did not reduce its effectiveness in decreasing the mean three-meal blood glucose area by 41% (P less than 0.002). Addition of hydrated guar to this diet reduced the mean three-meal glucose area after acarbose further by 72% (P less than 0.001) but increased hydrogen evolution. The results suggest that acarbose will be both effective and acceptable given at low dose when the dietary carbohydrate is starch.

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Year:  1982        PMID: 6927727     DOI: 10.2337/diacare.5.2.92

Source DB:  PubMed          Journal:  Diabetes Care        ISSN: 0149-5992            Impact factor:   19.112


  4 in total

Review 1.  Pharmacokinetic-pharmacodynamic relationships of Acarbose.

Authors:  T Salvatore; D Giugliano
Journal:  Clin Pharmacokinet       Date:  1996-02       Impact factor: 6.447

2.  Effects of acarbose on starch hydrolysis. Study in healthy subjects, ileostomy patients, and in vitro.

Authors:  M Hiele; Y Ghoos; P Rutgeerts; G Vantrappen
Journal:  Dig Dis Sci       Date:  1992-07       Impact factor: 3.199

Review 3.  Acarbose. A preliminary review of its pharmacodynamic and pharmacokinetic properties, and therapeutic potential.

Authors:  S P Clissold; C Edwards
Journal:  Drugs       Date:  1988-03       Impact factor: 9.546

4.  Inhibition of sucrose- and starch-induced glycaemic and hormonal responses by the alpha-glucosidase inhibitor emiglitate (BAY o 1248) in healthy volunteers.

Authors:  B Lembcke; U R Fölsch; W Gatzemeier; B Lücke; R Ebert; E Siegel; W Creutzfeldt
Journal:  Eur J Clin Pharmacol       Date:  1991       Impact factor: 2.953

  4 in total

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