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PMID: 19258492 Published · ppublish English Journal Article Review

Getting the message across: mechanisms of physiological cross talk by adipose tissue.

American journal of physiology. Endocrinology and metabolism ·Vol. 296 ·No. 6 ·2009-06-00 ·Pages E1210-29

Lee DE, Kehlenbrink S, Lee H, Hawkins M, Yudkin JS

Abstract

Obesity is associated with resistance of skeletal muscle to insulin-mediated glucose uptake, as well as resistance of different organs and tissues to other metabolic and vascular actions of insulin. In addition, the body is exquisitely sensitive to nutrient imbalance, with energy excess or a high-fat diet rapidly increasing insulin resistance, even before noticeable changes occur in fat mass. There is a growing acceptance of the fact that, as well as acting as a storage site for surplus energy, adipose tissue is an important source of signals relevant to, inter alia, energy homeostasis, fertility, and bone turnover. It has also been widely recognized that obesity is a state of low-grade inflammation, with adipose tissue generating substantial quantities of proinflammatory molecules. At a cellular level, the understanding of the signaling pathways responsible for such alterations has been intensively investigated. What is less clear, however, is how alterations of physiology, and of signaling, within one cell or one tissue are communicated to other parts of the body. The concepts of cell signals being disseminated systemically through a circulating "endocrine" signal have been complemented by the view that local signaling may similarly occur through autocrine or paracrine mechanisms. Yet, while much elegant work has focused on the alterations in signaling that are found in obesity or energy excess, there has been less attention paid to ways in which such signals may propagate to remote organs. This review of the integrative physiology of obesity critically appraises the data and outlines a series of hypotheses as to how interorgan cross talk takes place. The hypotheses presented include the "fatty acid hypothesis,", the "portal hypothesis,", the "endocrine hypothesis,", the "inflammatory hypothesis,", the "overflow hypothesis,", a novel "vasocrine hypothesis," and a "neural hypothesis," and the strengths and weaknesses of each hypothesis are discussed.

MeSH Terms
Adipose Tissue/immunology,metabolism Animals Endocrine System/immunology,metabolism Humans Insulin Resistance/physiology Obesity/immunology,metabolism Signal Transduction/physiology
Authors & Affiliations
5 authors, click to expand affiliations / ORCID
Lee Do-Eun
Department of Internal Medicine, Division of Endocrinology, Winthrop University Hospital, London, United Kingdom.
Kehlenbrink Sylvia
Lee Hanna
Hawkins Meredith
Yudkin John S
Article Info
Journal
American journal of physiology. Endocrinology and metabolism
Abbr.
Am J Physiol Endocrinol Metab
ISSN
0193-1849
Published
2009-06-00
Epub
2009-00-03
Pages
E1210-29
Language
English
Region
United States
NLM ID
100901226
Subset
IM
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