Insulin clearance in obesity

Me Valera Mora, Antonino Scarfone, M Calvani, Av Greco, Geltrude Mingrone

Research output: Contribution to journalArticle

100 Citations (Scopus)

Abstract

Insulin uptake and degradation is a complex and not yet completely understood process involving not only insulin sensitive tissues. The most important degradative system is insulin degrading enzyme which is a highly conserved metalloendopeptidase requiring Zn(++) for its proteolytic action, although protein disulfide isomerase and cathepsin D are also involved in insulin metabolism. The liver and the kidney are the principal sites for insulin clearance. In obese subjects with hyperinsulinemia and high levels of free fatty acids, insulin hepatic clearance is impaired, while the glomerular filtration rate, renal plasma flow and albumin excretion are increased, suggesting a state of renal vasodilatation leading to an abnormally transmitted arterial pressure to the glomerular capillaries through a dilated afferent arteriole. Insulin can be cleared also by muscle, adipocytes, gastrointestinal cells, fibroblasts, monocytes and lymphocytes which contain insulin receptors and internalization and regulation mechanism for insulin metabolism.
Original languageEnglish
Pages (from-to)487-493
Number of pages7
JournalJournal of the American College of Nutrition
Volume22
Publication statusPublished - 2003

Keywords

  • Adipose Tissue
  • Animals
  • Blood Pressure
  • Cathepsin D
  • Diabetes Mellitus
  • Diabetes Mellitus, Type 2
  • Humans
  • Incidence
  • Insulin
  • Insulin Resistance
  • Insulysin
  • Kidney
  • Liver
  • Obesity
  • Protein Disulfide-Isomerases
  • Renal Plasma Flow
  • Vasodilation

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