Abstract
Annual Review of Nutrition
Vol. 20:
45-75
(Volume publication date July 2000)
(doi:10.1146/annurev.nutr.20.1.45)
LEPTIN—MUCH MORE THAN A SATIETY SIGNAL Ruth B. S. HarrisPennington Biomedical Research Center, Baton Rouge, Louisiana 70808; e-mail: harrisrb@pbrc.edu ▪ Abstract Much attention has focused on the effects of leptin as a central satiety agent. There is now a significant amount of evidence that leptin is active in the periphery. This review focuses on the ability of leptin to modify insulin sensitivity, tissue metabolism, stress responses, and reproductive function. Leptin's effect on several of these systems is mediated via the hypothalamic-pituitary axis. Therefore, although in vitro studies provide evidence for direct effects on specific tissues and metabolic pathways, it is essential to consider the interactions between leptin and other regulatory factors in vivo. Little is known about the regulation of peripheral receptor expression or the production of binding proteins. Both of these factors determine the bioactivity of circulating leptin and have the potential to induce a peripheral resistance to leptin, similar to the central “leptin resistance” observed in obese subjects. Future research will clarify which of the endocrine and metabolic actions of peripheral leptin are of physiological relevance and which should be considered a pharmacological manipulation. Most recent citing papers (via CrossRef)Leptin targets in the mouse brain The Journal of Comparative Neurology 514(5):518-532 (2009) Neuroendocrine and physiological regulation of intake with particular reference to domesticated ruminant animals Nutrition Research Reviews 21(02):207 (2009) Insulin counter-regulatory factors, fibrinogen and C-reactive protein during olanzapine administration: effects of the antidiabetic metformin International Clinical Psychopharmacology 22(2):69-76 (2007) Adipocyte biology Obesity Reviews 8(s1):41-44 (2007) Prostaglandin D2 and J2-series (PGJ2, Δ12-PGJ2) prostaglandins stimulate IL-6 and MCP-1, but inhibit leptin, expression and secretion by 3T3-L1 adipocytes Pflügers Archiv - European Journal of Physiology 453(2):177-187 (2006)
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