Saleh, M. C., et al. “Uncoupling Protein-2: Evidence for Its Function As a Metabolic Regulator”. Diabetologia, vol. 45, no. 2, 2002, pp. 174-87, https://doi.org/10.1007/s00125-001-0737-x.

Genre

  • Journal Article
Contributors
Author: Saleh, M. C.
Author: Chan, Catherine B.
Author: Wheeler, M. B.
Date Issued
2002
Abstract

Uncoupling protein-2, discovered in 1997, belongs to a family of inner mitochondrial membrane proteins that, in general, function as carriers. The function(s) of uncoupling protein-2 have not yet been definitively described. However, mounting evidence suggests that uncoupling protein-2 could act in multiple tissues as a regulator of lipid metabolism. A role as a modulator of reactive oxygen species as a defence against infection is also postulated. In this review, a brief overview of the general and specific properties of uncoupling protein-2 is given and evidence for metabolic and immune regulatory functions is summarized. Uncoupling protein-2 could have particular importance in the regulation of lipid metabolism in adipose tissue and skeletal muscle. In addition, its ability to inhibit insulin secretion could also promote fat utilization over storage. Inhibition by uncoupling protein-2 of reactive oxygen species formation in macrophages and other tissues could have implications for regulation of immune function. The possibility of functions of uncoupling protein-2 in other tissues such as the brain are beginning to emerge.

Note

Department of Anatomy and Physiology, University of Prince Edward Island, Charlottetown, PE I, Canada.

Germany

LR: 20061115; PUBM: Print; JID: 0006777; 0 (Ion Channels); 0 (Membrane Transport Proteins); 0 (Mitochondrial Proteins); 0 (Proteins); 0 (Uncoupling Agents); 0 (mitochondrial uncoupling protein 2); CIN: Diabetologia. 2003 Jan;46(1):132-3; author reply 133-4. PMID: 12637992; RF: 149; ppublish

Source type: Electronic(1)

Language

  • English

Subjects

  • animals
  • Humans
  • Metabolic Diseases/metabolism
  • Uncoupling Agents/metabolism
  • Mitochondrial Proteins
  • Membrane Transport Proteins
  • Proteins/metabolism
  • Ion Channels
  • Homeostasis
Page range
174-187
Host Title
Diabetologia
Host Abbreviated Title
Diabetologia
Volume
45
Issue
2
ISSN
0012-186X

Department