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Dioxins, the aryl hydrocarbon receptor and the central regulation of energy balance.
- Source :
-
Frontiers in neuroendocrinology [Front Neuroendocrinol] 2010 Oct; Vol. 31 (4), pp. 452-78. Date of Electronic Publication: 2010 Jul 17. - Publication Year :
- 2010
-
Abstract
- Dioxins are ubiquitous environmental contaminants that have attracted toxicological interest not only for the potential risk they pose to human health but also because of their unique mechanism of action. This mechanism involves a specific, phylogenetically old intracellular receptor (the aryl hydrocarbon receptor, AHR) which has recently proven to have an integral regulatory role in a number of physiological processes, but whose endogenous ligand is still elusive. A major acute impact of dioxins in laboratory animals is the wasting syndrome, which represents a puzzling and dramatic perturbation of the regulatory systems for energy balance. A single dose of the most potent dioxin, TCDD, can permanently readjust the defended body weight set-point level thus providing a potentially useful tool and model for physiological research. Recent evidence of response-selective modulation of AHR action by alternative ligands suggests further that even therapeutic implications might be possible in the future.<br /> (Copyright © 2010 Elsevier Inc. All rights reserved.)
- Subjects :
- Animals
Body Weight drug effects
Central Nervous System drug effects
Central Nervous System metabolism
Dioxins chemistry
Environmental Pollutants analysis
Environmental Pollutants metabolism
Female
Food Contamination analysis
Gene Expression Regulation drug effects
Humans
Male
Mice
Rats
Wasting Syndrome chemically induced
Wasting Syndrome metabolism
Dioxins metabolism
Dioxins toxicity
Energy Metabolism drug effects
Receptors, Aryl Hydrocarbon metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1095-6808
- Volume :
- 31
- Issue :
- 4
- Database :
- MEDLINE
- Journal :
- Frontiers in neuroendocrinology
- Publication Type :
- Academic Journal
- Accession number :
- 20624415
- Full Text :
- https://doi.org/10.1016/j.yfrne.2010.07.002