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Laboratoire de Physiologie des Régulations Energétiques, Cellulaires et Moléculaires, Centre National de la Recherche Scientifique-Université Claude Bernard Lyon 1, Unité Mixte de Recherches 5123, F-69622 Villeurbanne Cedex, France
Thermogenic endurance and development
of metabolic cold adaptation in birds may critically depend on their
ability to synthesize and use fatty acids (FA) as fuel substrates.
Hepatic lipogenesis and the capacity to oxidize FA in thermogenic
tissues were measured in cold-acclimated (CA) ducklings (Cairina
moschata) showing original mechanisms of metabolic cold adaptation
in the absence of brown adipose tissue, the specialized thermogenic
tissue of rodents. The rate of FA synthesis from
[U-14C]glucose and from [1-14C]acetate,
measured in incubated hepatocytes isolated from 5-wk-old thermoneutral
(TN; 25°C) or CA (4°C) fed ducklings, was higher than in other
species. Hepatic de novo lipogenesis was further increased by cold
acclimation with both glucose (+194%) and acetate (+111%) as
precursor. Insulin slightly increased (+11-14%) hepatic lipogenesis from both precursors in CA ducklings, whereas glucagon was
clearly inhibitory (
29 to
51%). Enhanced de novo lipogenesis was
associated with higher (+171%) hepatocyte activity of glucose oxidation and larger capacity (+50 to +100%) of key lipogenic enzymes.
The potential for FA oxidation was higher in liver (+61%) and skeletal
muscle (+29 to +81%) homogenates from CA than from TN ducklings,
suggesting that the higher hepatic lipogenesis may fuel oxidation in
thermogenic tissues. Present data underline the high capacity to
synthesize lipids from glucose in species like muscovy ducks
susceptible to hepatic steatosis. Lipogenic capacity can be further
increased in the cold and may represent an important step in the
metabolic adaptation to cold of growing ducklings.
malic enzyme; glucose-6-phosphate-dehydrogenase; fatty acid synthase; acetyl-CoA carboxylase; glucagon; insulin; thermogenesis; fatty acid oxidation
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