Obesity and disturbed lipoprotein profile in estrogen receptor-α-deficient male mice

被引:260
作者
Ohlsson, C [1 ]
Hellberg, N
Parini, P
Vidal, O
Bohlooly, M
Rudling, M
Lindberg, MK
Warner, M
Angelin, B
Gustafsson, JÅ
机构
[1] Sahlgrens Univ Hosp, Dept Internal Med, Div Endocrinol, RCEM, S-41345 Gothenburg, Sweden
[2] Huddinge Univ Hosp, Karolinska Inst, Metab Unit, Ctr Endocrinol & Metab,Dept Med, S-14186 Huddinge, Sweden
[3] Huddinge Univ Hosp, Karolinska Inst, Mol Nutr Unit, Ctr Nutr & Toxicol, S-14186 Huddinge, Sweden
[4] Karolinska Inst, Novum, Dept Med Nutr, S-14157 Huddinge, Sweden
关键词
transgenic; cholesterol; leptin; lipoprotein profile; dual energy X-ray absorptiometry;
D O I
10.1006/bbrc.2000.3827
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Clinical case reports have documented disturbances of carbohydrate and lipid metabolism in aromatase deficient and estrogen resistant males. The aim of the present study was to explore the metabolic functions of estrogens in male mice and to dissect the estrogen receptor (ER) specificity of such effects. Total body fat content and serum levels of leptin were followed in ER alpha knockout (ERKO), ER beta knockout (BERKO), and ER alpha/beta double knockout (DERKO) mice. Neither the total body fat nor serum leptin levels were altered in any group before or during sexual maturation. However, after sexual maturation ERKO and DERKO, but not BERKO, demonstrated a clear increase in total body fat and enhanced serum leptin levels. Serum cholesterol was increased and a qualitative change in the Lipoprotein profile, including smaller LDL particles, was observed in ERKO and DERKO mice. In conclusion, ER alpha but not ER beta -inactivated male mice develop obesity after sexual maturation. (C) 2000 Academic Press.
引用
收藏
页码:640 / 645
页数:6
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