TY - JOUR
T1 - Slow recovery of body fat lost during adenovirus-induced hyperleptinemia
AU - Higa, Moritake
AU - Kakuma, Tetsuya
AU - Pan, Wentong
AU - Wang, Zhuo Wei
AU - Babcock, Evelyn
AU - McCorkle, Kay
AU - Lee, Young
AU - Unger, Roger
N1 - Funding Information:
The authors thank Shirley Waggoner for outstanding technical contributions, Susan Kennedy for excellent secretarial services, and Yan-Ting Zhou, M.D., Ph.D., for important suggestions. We acknowledge the grant support of the Department of Veterans Affairs Institutional Support (SMI 821-109), The National Institutes of Health (DK02700-37), The National Institutes of Health/Juvenile Diabetes Foundation Diabetes Interdisciplinary Research Program, and Novo-Nordisk Corporation.
PY - 2000/12/29
Y1 - 2000/12/29
N2 - In normal rats, adenovirus-induced hyperleptinemia causes disappearance of visible body fat, down-regulation of lipogenic enzymes, and upregulation of oxidative enzymes and thermogenic proteins. In addition, preadipocyte markers replace mature adipocyte markers, suggesting dedifferentiation. In weight loss induced by caloric restriction, by contrast, the lipogenic machinery is essentially intact. To determine if the radical changes induced by leptin would slow the reappearance of body fat, we compared normal lean rats made hyperleptinemic by infusing an adenovirusleptin construct with diet-matched littermates. Initially, in plasma leptin the hyperleptinemic rats averaged @O50x the controls and, although it declined progressively, it was still slightly elevated at 150 days (P 〈 0.05). In the hyperleptinemics, body fat mass, quantified by magnetic resonance spectroscopy, remained below the pretreatment value for 60 days, while in diet-matched controls it exceeded the pretreatment value. Epididymal fat pad weight in hyperleptinemics was still 28% below paired controls at 150 days posttreatment. Histologic examination revealed adipocytes of hyperleptinemic animals to be smaller 60 days after treatment. At 60 days, adipose tissue UCP-2 gene expression in hyperleptinemics was still above controls, but expression of other lipogenic and oxidative enzymes had returned to baseline expression levels. We conclude that in normal rats recovery of body fat following adenovirus-induced hyperleptinemia is much slower than after caloric restriction, possibly because of persistent upregulation of adipocyte UCP-2.
AB - In normal rats, adenovirus-induced hyperleptinemia causes disappearance of visible body fat, down-regulation of lipogenic enzymes, and upregulation of oxidative enzymes and thermogenic proteins. In addition, preadipocyte markers replace mature adipocyte markers, suggesting dedifferentiation. In weight loss induced by caloric restriction, by contrast, the lipogenic machinery is essentially intact. To determine if the radical changes induced by leptin would slow the reappearance of body fat, we compared normal lean rats made hyperleptinemic by infusing an adenovirusleptin construct with diet-matched littermates. Initially, in plasma leptin the hyperleptinemic rats averaged @O50x the controls and, although it declined progressively, it was still slightly elevated at 150 days (P 〈 0.05). In the hyperleptinemics, body fat mass, quantified by magnetic resonance spectroscopy, remained below the pretreatment value for 60 days, while in diet-matched controls it exceeded the pretreatment value. Epididymal fat pad weight in hyperleptinemics was still 28% below paired controls at 150 days posttreatment. Histologic examination revealed adipocytes of hyperleptinemic animals to be smaller 60 days after treatment. At 60 days, adipose tissue UCP-2 gene expression in hyperleptinemics was still above controls, but expression of other lipogenic and oxidative enzymes had returned to baseline expression levels. We conclude that in normal rats recovery of body fat following adenovirus-induced hyperleptinemia is much slower than after caloric restriction, possibly because of persistent upregulation of adipocyte UCP-2.
KW - Caloric restriction
KW - Hyperleptinemia
KW - UCP-2
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U2 - 10.1006/bbrc.2000.4025
DO - 10.1006/bbrc.2000.4025
M3 - Article
C2 - 11162429
AN - SCOPUS:0034731408
SN - 0006-291X
VL - 279
SP - 786
EP - 791
JO - Biochemical and Biophysical Research Communications
JF - Biochemical and Biophysical Research Communications
IS - 3
ER -