The role of the renal kallikrein-kinin system in diabetic nephropathy

Curr Opin Nephrol Hypertens. 2007 Jan;16(1):22-6. doi: 10.1097/MNH.0b013e328011a20c.

Abstract

Purpose of review: Diabetic nephropathy is one of the most common complications in diabetes mellitus. Multiple pathogenic mechanisms are now believed to contribute to this disease, including inflammatory cytokines, autacoids and oxidative stress. Numerous studies have shown that the kallikrein-kinin system may be involved in these mechanisms. This review focuses on recent research advance on the potential role of the kallikrein-kinin system in the development of diabetic nephropathy, and its clinical relevance.

Recent findings: A collection of recent studies has shown that angiotensin-converting enzyme inhibitors, which inhibit angiotensin II formation and degradation of bradykinin, and vasopeptidase inhibitors attenuated the development of diabetic nephropathy in experimental animals and clinical settings. The role of the kallikrein-kinin system in diabetes is further supported by findings that diabetic nephropathy is worsened in diabetic mice lacking bradykinin B2 receptors. Although long-acting bradykinin B2 receptor agonists have been shown to have renal protective effects, their therapeutic benefits have not been well studied.

Summary: Current experimental investigations demonstrated that pharmacological intervention of the kallikrein-kinin system improved renal conditions in diabetes mellitus. These findings suggest that the kallikrein-kinin system may be a therapeutic target in preventing and treating diabetic nephropathy.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Bradykinin / agonists
  • Diabetes Mellitus / drug therapy
  • Diabetes Mellitus / enzymology
  • Diabetes Mellitus / etiology*
  • Heterocyclic Compounds, 3-Ring / therapeutic use
  • Humans
  • Kallikrein-Kinin System / drug effects
  • Kallikrein-Kinin System / physiology*
  • Kidney / enzymology*
  • Protease Inhibitors / therapeutic use
  • Rats
  • Renin-Angiotensin System / physiology

Substances

  • AVE 7688
  • Heterocyclic Compounds, 3-Ring
  • Protease Inhibitors
  • Bradykinin