Duplomb Laurence, Takaishi Kiyosumi, Park Byung-Hyun, Visser Theo J, Unger Roger H
Gifford Laboratories, Department of Internal Medicine, Center for Diabetes Research, University of Texas Southwestern Medical Center, 5323 Harry Hines Boulevard, Dallas, TX 75390, USA.
Biochem Biophys Res Commun. 2004 Oct 8;323(1):49-51. doi: 10.1016/j.bbrc.2004.08.057.
Sustained hyperleptinemia induced in normal rats causes the rapid disappearance of body fat. This is attributed to a marked increase in uncoupled fatty acid oxidation in the white adipocytes, which also occurs in hyperthyroidism. Because hyperleptinemic rats have normal plasma T3 or T4 levels, we tested the possibility of "localized hyperthyroidism" due to increased conversion of T4 to T3 in the adipose tissue. We therefore induced sustained hyperleptinemia in normal rats by intravenous injection of recombinant adenovirus containing the leptin cDNA (AdCMV-leptin) and measured the mRNA and the activity of enzymes involved in T4 metabolism in the disappearing fat. The epididymal fat pad remnants exhibited a decrease in mRNA of deiodinase 1 and a doubling of deiodinase 2 mRNA (p<0.05), but their enzyme activities did not differ from normoleptinemic controls. To determine if thyroid hormone was required for the fat-wasting action of hyperleptinemia, we infused AdCMV-leptin into rats made athyroid by total thyroidectomy or by methimazole therapy. The fat loss in hyperleptinemic athyroid rats was as great as in euthyroid controls. We conclude that the fat-wasting effect of sustained hyperleptinemia does not involve "local hyperthyroidism" in white adipose tissue and does not require thyroid hormone.
正常大鼠体内诱导产生的持续高瘦素血症会导致体脂迅速消失。这归因于白色脂肪细胞中解偶联脂肪酸氧化的显著增加,甲状腺功能亢进时也会出现这种情况。由于高瘦素血症大鼠的血浆T3或T4水平正常,我们测试了脂肪组织中T4向T3转化增加导致“局部甲状腺功能亢进”的可能性。因此,我们通过静脉注射含瘦素cDNA的重组腺病毒(AdCMV-瘦素)在正常大鼠中诱导持续高瘦素血症,并测量消失脂肪中参与T4代谢的酶的mRNA和活性。附睾脂肪垫残余物的脱碘酶1 mRNA减少,脱碘酶2 mRNA增加一倍(p<0.05),但其酶活性与正常瘦素血症对照组无差异。为了确定甲状腺激素是否是高瘦素血症消耗脂肪作用所必需的,我们将AdCMV-瘦素注入通过全甲状腺切除术或甲巯咪唑治疗造成甲状腺功能减退的大鼠体内。高瘦素血症甲状腺功能减退大鼠的脂肪损失与甲状腺功能正常的对照组一样大。我们得出结论,持续高瘦素血症的脂肪消耗作用不涉及白色脂肪组织中的“局部甲状腺功能亢进”,也不需要甲状腺激素。