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Effect of CL-316,243, a thermogenic beta 3-agonist, on energy balance and brown and white adipose tissues in rats
Ist Teil von
American journal of physiology. Regulatory, integrative and comparative physiology, 1994-04, Vol.266 (4), p.1371-R1382
Ort / Verlag
United States
Erscheinungsjahr
1994
Quelle
MEDLINE
Beschreibungen/Notizen
J. Himms-Hagen, J. Cui, E. Danforth Jr, D. J. Taatjes, S. S. Lang, B. L. Waters and T. H. Claus
Department of Biochemistry, University of Ottawa, Ontario, Canada.
The objective was to assess the effect of a new, highly selective beta
3-adrenergic agonist, CL-316,243 (CL) (J. D. Bloom, M. D. Dutia, B. D.
Johnson, A. Wissner, M. G. Burns, E. E. Largis, J. A. Dolan, and T. H.
Claus., J. Med. Chem. 35: 3081, 1992), on energy balance and brown and
white adipose tissues (BAT and WAT, respectively) in young rats eating a
high-fat diet to induce obesity. Chronic treatment with CL increased body
temperature and 24-h energy expenditure, mainly by increasing resting
metabolic rate. Food intake was not altered but carcass fat was reduced.
Interscapular BAT was markedly hypertrophied, with three- to fourfold
increases in the content of uncoupling protein (UCP) and cytochrome
oxidase. Quantitative immunoelectron microscopy of interscapular BAT of
CL-treated rats showed smaller mitochondria with an unchanged total amount
of UCP per mitochondrion. The relative frequency of the four major cell
types in BAT (mature brown adipocytes, preadipocytes, interstitial cells,
endothelial cells) was not altered. The CL-induced hypertrophy differed
from that induced by chronic stimulation by endogenous norepinephrine (as
in cold-adaptation) in absence of hyperplasia (there was a slightly reduced
DNA content), absence of an increase in the thyroxine (T4) 5'-deiodinase
activity, and absence of a selective increase in UCP concentration. WAT
depots weighed less and had fewer cells (lower DNA content) in the
CL-treated rats. Some multilocular adipocytes appeared in these normally
almost exclusively unilocular WAT depots (mesenteric, inguinal, epididymal,
retroperitoneal). We conclude that CL not only promotes BAT mitochondrial
proliferation and thermogenesis and overall energy expenditure and
leanness, but also retards the development of WAT hyperplasia during the
early stage of diet-induced obesity.