Literature DB >> 8112483

Effect of an alpha-glucosidase inhibitor on intestinal fermentation and faecal lipids in diabetic patients.

T Nakamura1, K Takebe, K Kudoh, A Terada, Y Tandoh, Y Arai, N Yamada, M Ishii, H Kikuchi.   

Abstract

Eight non-insulin-dependent diabetes mellitus patients, in whom oral hypoglycaemic agents were not effective, were treated with an alpha-glucosidase inhibitor, AO-128 (0.9 mg/day) for 6 months. After 6 months of treatment there was a statistically significant decrease in the blood glucose level 1 and 2 h postprandially. The 2 h blood glucose level was also significantly reduced after 2 months' treatment. The insulin and HbA1c levels after 2 and 6 months' treatment were lower than those before administration. Faecal weight, the frequency of bowel movements, the ratio of hydroxy fatty acids to total fatty acids, and faecal short-chain carboxylic acid content were all increased significantly during treatment. The initially hard stools became normal or soft, although no actual diarrhoea developed. Both faecal bile-acid excretion and the ratio of primary bile acids to total bile acids were increased significantly after 2 months, but they showed some recovery towards the pretreatment levels after 6 months' treatment. There was no distinct change in neutral sterol and fatty acid excretion. Breath hydrogen excretion showed a slight increase after treatment. These results suggest that intestinal fermentation was promoted and the intestinal transit time was shortened by AO-128 administration.

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Year:  1993        PMID: 8112483     DOI: 10.1177/030006059302100504

Source DB:  PubMed          Journal:  J Int Med Res        ISSN: 0300-0605            Impact factor:   1.671


  2 in total

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Authors:  H Luo; T Imoto; Y Hiji
Journal:  World J Gastroenterol       Date:  2001-04       Impact factor: 5.742

2.  Impact of voglibose on the pharmacokinetics of dapagliflozin in Japanese patients with type 2 diabetes.

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Journal:  Diabetes Ther       Date:  2013-01-10       Impact factor: 2.945

  2 in total

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