Protective mechanism of glucose against alloxan-induced beta-cell damage: pivotal role of ATP

Exp Mol Med. 2000 Mar 31;32(1):12-7. doi: 10.1038/emm.2000.3.

Abstract

Glucose prevents the development of diabetes induced by alloxan. In the present study, the protective mechanism of glucose against alloxan-induced beta-cell damage was investigated using HIT-T 15 cell, a Syrian hamster transformed beta-cell line. Alloxan caused beta-cell damages with DNA fragmentation, inhibition of glucose-stimulated insulin release, and decrease of cellular ATP level, but all of these beta-cell damages by alloxan were prevented by the presence of 20 mM glucose. Oligomycin, a specific inhibitor of ATP synthase, completely abolished the protective effects of glucose against alloxan-induced cell damage. Furthermore, treatment of nuclei isolated from HIT-T15 cells with ATP significantly prevented the DNA fragmentation induced by Ca2+. The results indicate that ATP produced during glucose metabolism plays a pivotal role in the protection of glucose against alloxan-induced beta-cell damage.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Adenosine Triphosphate / pharmacology
  • Alloxan / pharmacology*
  • Animals
  • B-Lymphocytes / cytology
  • B-Lymphocytes / drug effects*
  • B-Lymphocytes / metabolism
  • Calcium / pharmacology
  • Cell Line
  • Cell Nucleus / drug effects
  • Cell Nucleus / genetics
  • Cell Survival
  • DNA / drug effects
  • DNA / genetics
  • DNA / metabolism
  • DNA Fragmentation
  • Dose-Response Relationship, Drug
  • Egtazic Acid / pharmacology
  • Glucose / pharmacology*
  • Insulin / metabolism
  • Insulin Secretion
  • Oligomycins / pharmacology

Substances

  • Insulin
  • Oligomycins
  • Egtazic Acid
  • Alloxan
  • Adenosine Triphosphate
  • DNA
  • Glucose
  • Calcium