Metabolism - Clinical and Experimental
Volume 45, Issue 6 , Pages 731-737, June 1996

Improvement of insulin sensitivity and dyslipidemia with a new α-glucosidase inhibitor, voglibose, in nondiabetic hyperinsulinemic subjects

  • Kazuya Shinozaki

      Affiliations

    • Division of Atherosclerosis, Metabolism, and Clinical Nutrition, Department of Medicine, National Cardiovascular Center, Osaka Japan
    • Osaka Seamen's Insurance Hospital, Osaka, Japan
  • ,
  • Masaaki Suzuki

      Affiliations

    • Division of Atherosclerosis, Metabolism, and Clinical Nutrition, Department of Medicine, National Cardiovascular Center, Osaka Japan
    • Osaka Seamen's Insurance Hospital, Osaka, Japan
  • ,
  • Motoyoshi Ikebuchi

      Affiliations

    • Division of Atherosclerosis, Metabolism, and Clinical Nutrition, Department of Medicine, National Cardiovascular Center, Osaka Japan
    • Osaka Seamen's Insurance Hospital, Osaka, Japan
  • ,
  • Junya Hirose

      Affiliations

    • Division of Atherosclerosis, Metabolism, and Clinical Nutrition, Department of Medicine, National Cardiovascular Center, Osaka Japan
    • Osaka Seamen's Insurance Hospital, Osaka, Japan
  • ,
  • Yasushi Harano

      Affiliations

    • Division of Atherosclerosis, Metabolism, and Clinical Nutrition, Department of Medicine, National Cardiovascular Center, Osaka Japan
    • Osaka Seamen's Insurance Hospital, Osaka, Japan
  • ,
  • Yutaka Harano

      Affiliations

    • Corresponding Author InformationAddress reprint requests to Yutaka Harano, MD, Division of Atherosclerosis, Metabolism, and Clinical Nutrition, Department of Medicine, National Cardiovascular Center, 5-7-1, Fujishiro-dai, Suita, Osaka 565, Japan.
    • Division of Atherosclerosis, Metabolism, and Clinical Nutrition, Department of Medicine, National Cardiovascular Center, Osaka Japan
    • Osaka Seamen's Insurance Hospital, Osaka, Japan

Received 22 May 1995; accepted 4 December 1995.

Abstract 

This study was undertaken to investigate the effect of voglibose, a new α-glucosidase inhibitor, on glucose and lipid metabolism in nondiabetic hyperinsulinemic subjects. Sixteen nondiabetic subjects with hyperinsulinemia participated in the study. They were divided into two groups of eight subjects with normal (NGT) and impaired (IGT) glucose tolerance. A meal tolerance test and a 75-g oral glucose tolerance test (OGTT) were performed at the beginning (baseline phase) and end (treatment phase) of the 12-week treatment. Serum lipid levels were measured every 4 weeks throughout the treatment phase and follow-up phase (8 weeks). All patients received 10.2-mg tablet of voglibose before each test meal (3 tablets per day). We also measured insulin sensitivity using a steady-state plasma glucose (SSPG) method in eight normotensive hyperinsulinemic subjects and in eight age- and body mass index (BMI)-matched control subjects before and after the drug treatment. Voglibose significantly decreased the responses of plasma glucose and insulin on the meal tolerance test. The area under the curve for 2-hour insulin during the 75-g OGTT decreased after treatment, whereas that for 2-hour glucose did not change before and after treatment. SSPG was reduced after treatment, indicating improvement of insulin sensitivity. Moreover, treatment with voglibose resulted in a significant decline of triglyceride level and an elevation of high-density lipoprotein (HDL) cholesterol and apolipoprotein A-I. These values returned to near-baseline levels after the drug was discontinued. Consequently, we conclude that this agent not only has a direct hypoglycemic effect through decreased absorption of carbohydrate, but also a hypoinsulinemic and hypolipidemic effect via improved insulin sensitivity.

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 Supported by Special Coordination Funds for Promoting Science and Technology (Encouragement System of Center of Excellence) from the Science and Technology Agency of Japan, and by a grant for Scientific Research Expenses for Health and Welfare Programs (Clinical Treatment of Diabetes Mellitus, Akanuma).

PII: S0026-0495(96)90139-0

Metabolism - Clinical and Experimental
Volume 45, Issue 6 , Pages 731-737, June 1996