Advertisement

Potential Role of Peroxisome Proliferator-Activated Receptor-α in the Modulation of Glucose-Stimulated Insulin Secretion

  1. Mary C. Sugden and
  2. Mark J. Holness
  1. From the Centre for Diabetes and Metabolic Medicine, Institute of Cell and Molecular Science, Barts and the London, Queen Mary’s School of Medicine and Dentistry, University of London, London, U.K
  1. Address correspondence and reprint requests to Professor M.C. Sugden, Centre for Diabetes and Metabolic Medicine, Medical Sciences Building, Queen Mary, University of London, Mile End Rd., London E1 4NS, U.K. E-mail: m.c.sugden{at}qmul.ac.uk

Abstract

In this review, we discuss the influence of peroxisome proliferator-activated receptor (PPAR)-α on islet insulin secretion and develop the hypothesis that modulation of PPAR-α function may be important for the regulation of compensatory insulin secretion. We have attempted to analyze the role of PPAR-α-linked fatty acid metabolism in islet function in health and in insulin-resistant states linked to lifestyle factors, in particular pregnancy and a diet inappropriately high in saturated fat. We have emphasized the potential for both actions of PPAR-α on insulin sensitivity that may be relayed systemically to the islet, leading to modulation of the insulin response in accordance with changes in insulin sensitivity, and direct effects of PPAR-α action on the islet itself. Finally, we have developed the concept that compensatory insulin secretion may have a function not only in glucoregulation but also in liporegulation. Thus, augmented insulin secretion may reflect a requirement for lipid lowering as well as for increased glucose disposal and is perceived to aim to compensate for impaired suppression of islet lipid delivery by insulin. This introduces the possibility of a continuum between liporegulation with islet compensation and lipodysregulation leading to islet decompensation in the development of type 2 diabetes.

Footnotes

  • This article is based on a presentation at a symposium. The symposium and the publication of this article were made possible by an unrestricted educational grant from Les Laboratoires Servier.

    • Accepted May 29, 2003.
    • Received March 17, 2003.
| Table of Contents
Advertisement