Diabetes Research and Clinical Practice
Volume 77, Issue 3 , Pages 343-350, September 2007

Sulfonylurea and glinide reduce insulin content, functional expression of KATP channels, and accelerate apoptotic β-cell death in the chronic phase

  • Akira Takahashi

      Affiliations

    • Department of Diabetes and Clinical Nutrition, Graduate School of Medicine, Kyoto University, 54 Shogoin-Kawahara-cho, Sakyo-ku, Kyoto 606-8507, Japan
    • Nakamura Hospital, Osaka, Japan
  • ,
  • Kazuaki Nagashima

      Affiliations

    • Department of Diabetes and Clinical Nutrition, Graduate School of Medicine, Kyoto University, 54 Shogoin-Kawahara-cho, Sakyo-ku, Kyoto 606-8507, Japan
    • Corresponding Author InformationCorresponding author. Tel.: +81 75 751 3560; fax: +81 75 751 4244.
  • ,
  • Akihiro Hamasaki

      Affiliations

    • Department of Diabetes and Clinical Nutrition, Graduate School of Medicine, Kyoto University, 54 Shogoin-Kawahara-cho, Sakyo-ku, Kyoto 606-8507, Japan
  • ,
  • Naomitsu Kuwamura

      Affiliations

    • Department of Diabetes and Clinical Nutrition, Graduate School of Medicine, Kyoto University, 54 Shogoin-Kawahara-cho, Sakyo-ku, Kyoto 606-8507, Japan
  • ,
  • Yukiko Kawasaki

      Affiliations

    • Department of Diabetes and Clinical Nutrition, Graduate School of Medicine, Kyoto University, 54 Shogoin-Kawahara-cho, Sakyo-ku, Kyoto 606-8507, Japan
  • ,
  • Hiroki Ikeda

      Affiliations

    • Department of Diabetes and Clinical Nutrition, Graduate School of Medicine, Kyoto University, 54 Shogoin-Kawahara-cho, Sakyo-ku, Kyoto 606-8507, Japan
  • ,
  • Yuichiro Yamada

      Affiliations

    • Department of Diabetes and Clinical Nutrition, Graduate School of Medicine, Kyoto University, 54 Shogoin-Kawahara-cho, Sakyo-ku, Kyoto 606-8507, Japan
  • ,
  • Nobuya Inagaki

      Affiliations

    • Department of Diabetes and Clinical Nutrition, Graduate School of Medicine, Kyoto University, 54 Shogoin-Kawahara-cho, Sakyo-ku, Kyoto 606-8507, Japan
    • CREST of Japan Science and Technology Cooperation (JST), Kyoto, Japan
  • ,
  • Yutaka Seino

      Affiliations

    • Department of Diabetes and Clinical Nutrition, Graduate School of Medicine, Kyoto University, 54 Shogoin-Kawahara-cho, Sakyo-ku, Kyoto 606-8507, Japan
    • Kansai Denryoku Hospital, Osaka, Japan

Received 10 October 2006; received in revised form 24 November 2006; accepted 27 December 2006. published online 22 February 2007.

Abstract 

We previously found that chronic exposure to glibenclamide inhibits acute glibenclamide-induced insulin secretion by reducing the number of functional ATP-sensitive K+ (KATP) channels on the plasma membrane of pancreatic β-cells. In the present study, we compared sulfonylurea-induced and glinide-induced insulin secretion in pancreatic β-cells chronically exposed to these widely used oral hypoglycemic agents. Chronic exposure of pancreatic β-cells to sulfonylureas (glibenclamide or tolbutamide) and glinide (nateglinide) similarly impaired their acute effectiveness by reducing the insulin content and the number of functional KATP channels on the plasma membrane. Functional expression of the voltage-dependent Ca2+ channels (VDCCs), ion channels that play a critical role in the KATP channel dependent insulin secretory pathway, was similar to that in drug-untreated cells. Chronic exposure to each of the three agents similarly accelerated apoptotic β-cell death. Thus, reduction of the insulin content, reduction of the number of functional KATP channels on the plasma membrane, and acceleration of apoptotic β-cell death all are involved in impaired insulinotropic agent-induced acute insulin secretion in the chronic phase of sulfonylurea and glinide treatment. These findings help to clarify the mechanism of secondary failure after long-term therapy by these hypoglycemic agents, and should have important clinical implications regarding pharmacotherapy for type 2 diabetes.

Abbreviations: KATP, ATP-sensitive K+, VDCCs, voltage-dependent Ca2+ channels, DMEM, Dulbecco's modified Eagle's medium, KRBB, Krebs–Ringer bicarbonate buffer, RIA, radioimmunoassay, TUNEL, TdT-mediated dUTP nick end labeling, PBS, phosphate buffered saline, DMSO, dimethylsulfoxide

Keywords: Insulinotropic agents, Chronic exposure, KATP channel, Insulin secretion, Secondary sulfonylurea failure

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PII: S0168-8227(07)00042-3

doi:10.1016/j.diabres.2006.12.021

Diabetes Research and Clinical Practice
Volume 77, Issue 3 , Pages 343-350, September 2007