Oliveira E, Fagundes A T S, Alves S B, Pazos-Moura C C, Moura E G, Passos M C F, Lisboa P C
Departamento de Ciências Fisiológicas, Instituto de Biologia Roberto Alcantara Gomes, Universidade do Estado do Rio de Janeiro, Brazil.
Horm Metab Res. 2007 Dec;39(12):867-70. doi: 10.1055/s-2007-992131. Epub 2007 Oct 31.
Leptin modulates the hypothalamus-pituitary-thyroid axis and peripheral metabolism of thyroid hormones (THs). We have studied the effect of acute and chronic leptin treatment upon liver mitochondrial glycerol phosphate dehydrogenase activity (mGPD), whose expression and activity are TH dependent. We performed 2 experiments: 1) acute leptin treatment - LepA: adult rats received a single leptin injection (8 microg/100 g BW); 2) chronic leptin treatment - LepC: adult rats received leptin (8 microg/100 g BW) daily, for 6 days. In both experiments, control groups were saline-treated. All rats were sacrificed 2 hours after the last dose. Liver mGPD activity was determined by colorimetric method. Liver D1 activity was measured by the release of (125)I from (125)I-rT3. Serum hormones were measured by RIA. LepA rats showed higher serum thyroid stimulating hormone (TSH) (+ 64%, p<0.05), free T4 (+ 34%, p<0.05), free T3 (+ 64%, p<0.05), and liver D1 activity (+ 85%, p<0.05), but no change in mGPD activity. Since THs increase mGPD activity, the unchanged level in the acute experiment is suggestive of an inhibitory role of leptin. LepC rats presented lower mGPD activity (-1.7-fold, p<0.05) and higher liver D1 activity (+ 32%, p<0.05), but no alteration in serum TSH and free THs. Our results show that leptin downregulates mGPD activity, mainly when hyperleptinemia is chronic.
瘦素调节下丘脑 - 垂体 - 甲状腺轴以及甲状腺激素(THs)的外周代谢。我们研究了急性和慢性瘦素处理对肝线粒体甘油磷酸脱氢酶活性(mGPD)的影响,其表达和活性依赖于THs。我们进行了2个实验:1)急性瘦素处理 - LepA:成年大鼠接受单次瘦素注射(8微克/100克体重);2)慢性瘦素处理 - LepC:成年大鼠每天接受瘦素(8微克/100克体重),共6天。在两个实验中,对照组接受生理盐水处理。所有大鼠在最后一剂后2小时处死。通过比色法测定肝mGPD活性。通过从(125)I - rT3释放(125)I来测量肝D1活性。通过放射免疫分析法测定血清激素。LepA组大鼠血清促甲状腺激素(TSH)升高(+ 64%,p<0.05)、游离T4升高(+ 34%,p<0.05)、游离T3升高(+ 64%,p<0.05)以及肝D1活性升高(+ 85%,p<0.05),但mGPD活性无变化。由于THs可增加mGPD活性,急性实验中该水平未改变提示瘦素有抑制作用。LepC组大鼠mGPD活性降低(-1.7倍,p<0.05)且肝D1活性升高(+ 32%,p<0.05),但血清TSH和游离THs无改变。我们的结果表明,瘦素下调mGPD活性,主要在慢性高瘦素血症时。