Literature DB >> 7191299

[Effect of glucosidase inhibitor, Bay g 5421 (acarbose), on the blood glucose in obese diabetic patients ty pe 2 (NIDDM) (author's transl)].

H Laube, M Fouladfar, R Aubell, H Schmitz.   

Abstract

In a biometrically planned, randomised double blind crossover study the influence of a glucosidase inhibitor, acarbose, (Bay g 5421, pseudotetrasaccharide) on the blood glucose in a total of 10 dieting obese NIDDM patients was compared with placebo. There were no significant differences between the groups with regard to age, height, body weight and duration of diabetes. After a 2-week preliminary period 5 patients received Bay g 5421 for 4 weeks and then placebo for a further 4 weeks. After the same preliminary period the other 5 patients received placebo for 4 weeks and then Bay g 5421 for the second period of 4 weeks. On average, the blood glucose profiles were lower after Bay g 5421 than after placebo. This was statistically almost significant (p less than or equal to 0.09) for the area of the profiles, i.e., the average value of the 13 points of the daily profiles. The fraction of glycosylated hemoglobins (Hb A1a-c) was also lower during the period when the patients were treated with Bay g 5421 than with placebo. There was, however, no statistically significant difference. In contrast, the glucosuria-decrease during the Bay g 5421 period was significant. The serum cholesterol and serum triglycerides did not show any therapy-dependent difference. Thus it may be concluded that Bay g 5421 effectively reduces the blood glucose concentration, in particular, postprandial hyperglycemia in dieting diabetic patients type 2.

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Year:  1980        PMID: 7191299

Source DB:  PubMed          Journal:  Arzneimittelforschung        ISSN: 0004-4172


  6 in total

1.  Effect of acarbose on carbohydrate tolerance during administration of a fibre-free formula diet on healthy subjects.

Authors:  I E Walter-Sack; A Ittner-Holland; G Wolfram; N Zoellner
Journal:  Eur J Clin Pharmacol       Date:  1986       Impact factor: 2.953

2.  Effect of a long-term acarbose therapy on the metabolic control of sulphonylurea-treated diabetic patients.

Authors:  G Sachse; H Laube; E Mäser; K Federlin
Journal:  Diabetologia       Date:  1982-03       Impact factor: 10.122

3.  Complete biosynthetic pathway to the antidiabetic drug acarbose.

Authors:  Takeshi Tsunoda; Arash Samadi; Sachin Burade; Taifo Mahmud
Journal:  Nat Commun       Date:  2022-06-15       Impact factor: 17.694

4.  Long-term treatment of sulphonylurea-treated diabetics with the alpha-glucosidase inhibitor Bay g 5421 (acarbose)

Authors:  H Vierhapper; P Bratusch-Marrain; W Waldhäusl
Journal:  Diabetologia       Date:  1981-05       Impact factor: 10.122

5.  Improvement of metabolic control in insulin dependent diabetics treated with the alpha-glucosidase inhibitor acarbose for two months.

Authors:  J Gérard; A S Luyckx; P J Lefebvre
Journal:  Diabetologia       Date:  1981-11       Impact factor: 10.122

6.  Synthetic efforts for stereo structure determination of cytotoxic marine natural product pericosines as metabolites of Periconia sp. from sea hare.

Authors:  Yoshihide Usami; Hayato Ichikawa; Masao Arimoto
Journal:  Int J Mol Sci       Date:  2008-03-24       Impact factor: 6.208

  6 in total

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