Miglitol, a new α-glucosidase inhibitor
- 1 November 1999
- journal article
- review article
- Published by Taylor & Francis in Expert Opinion on Pharmacotherapy
- Vol. 1 (1) , 149-156
- https://doi.org/10.1517/14656566.1.1.149
Abstract
Miglitol (Bay m 1099, Bayer) is a second generation α-glucosidase inhibitor. It is a derivative of 1-desoxynojirimycin, and binds reversibly to the brushborder α-glucosidase enzymes. In contrast to its parent drug (acarbose, Bay g 5421, Bayer), miglitol is almost completely absorbed in the small intestine. It has to be taken with each main meal, and through its effect on carbohydrate digestion it blunts the postprandial blood glucose increase. Miglitol has no or a very small effect on fasting blood glucose levels. The blood-glucose lowering effects of miglitol in patients with Type 2 diabetes are lower than those of the frequently-used sulphonylurea compounds. Long-term studies show that a moderate average reduction of HbA1c of 0.3 - 0.7% point from baseline can be achieved. An advantage over sulphonylurea is the effect on serum insulin levels: miglitol therapy leads to slightly lower postprandial levels of serum insulin, whereas chronic sulphonylurea treatment usually increases serum insulin levels. This...Keywords
This publication has 35 references indexed in Scilit:
- In vitro study of the effect of miglitol on carbohydrate digestion and intestinal metabolism in normal and non-insulin-dependent diabetic ratsCanadian Journal of Physiology and Pharmacology, 1996
- Miglitol (Bay m 1099) has no extraintestinal effects on glucose control in healthy volunteersBritish Journal of Clinical Pharmacology, 1996
- The Effect of Intensive Treatment of Diabetes on the Development and Progression of Long-Term Complications in Insulin-Dependent Diabetes MellitusNew England Journal of Medicine, 1993
- α-Glucosidase Inhibition by Miglitol in NIDDM PatientsDiabetes Care, 1992
- Inhibition of Glycemic and Hormonal Responses after Repetitive Sucrose and Starch Loads by Different Doses of the α-Glucosidase Inhibitor Miglitol (BAY m 1099) in ManPharmacology, 1991
- The effects of the intestinal glucosidase inhibitor bay m 1099 (Miglitol) on glycemic status of obese ratsNutrition Research, 1989
- Effect of the alpha-glucosidase inhibitor N-hydroxyethyl-1-deoxynojirimycin (bay M 1099) on the biosynthesis of liver secretory glycoproteinsBiochemical Pharmacology, 1989
- Effects of N-hydroxyethyl-1-deoxynojirimycin (BAY m 1099) on the activity of neutral- and acid α-glucosidases in human fibroblasts and HepG2 cellsClinica Chimica Acta; International Journal of Clinical Chemistry, 1989
- 1-Deoxynojirimycin and related compounds inhibit glycogenolysis in the liver without affecting the concentration of phosphorylase aBiochemical Pharmacology, 1988
- The effect of newα-glucosidase inhibitors (BAY m 1099 and BAY o 1248) on meal-stimulated increases in glucose and insulin levels in manJournal of Molecular Medicine, 1986