de Oliveira Elaine, Teixeira Silva Fagundes Aline, Teixeira Bonomo Isabela, Curty Flavio Henrique, Fonseca Passos Magna Cottini, de Moura Egberto Gaspar, Lisboa Patrícia Cristina
Department of Physiological Sciences, Roberto Alcantara Gomes Biology Institute, State University of Rio de Janeiro, Rio de Janeiro, Brazil.
Life Sci. 2007 Sep 22;81(15):1241-6. doi: 10.1016/j.lfs.2007.08.030. Epub 2007 Sep 9.
Leptin has stimulatory effects on the hypothalamic-pituitary-thyroid axis and on deiodinases activities. Here, we evaluated the effect of leptin injection upon in vivo and in vitro thyroid 125I uptake (RAIU). We designed two experiments: acute leptin (LepA) with a single dose of leptin (8 microg/100 g BW/sc), and chronic leptin (LepC), injected with the same dose of LepA, once a day, for 6 days. In parallel, control groups were saline-injected. For in vivo study, part of the animals were injected with 125I (3700 Bq) and killed after 15 or 120 min. In vivo thyroid RAIU was not changed in LepA animals. However, LepC animals showed higher in vivo thyroid RAIU (15 min:+130% and 120 min:+72%; p<0.05). For in vitro study, the other animals were killed and their thyroids were incubated with 125I. Thyroids explants from LepA and LepC groups presented lower thyroid 125I content (-32% and -29% p<0.05, respectively). The amount of our data suggest that, in vitro, leptin causes a direct inhibition of the rat thyroid RAIU, but in vivo, the effect of leptin was different according to the treatment period, which indicates that other indirect mechanisms are involved in the in vivo leptin chronic stimulation of the thyroid gland.
瘦素对下丘脑 - 垂体 - 甲状腺轴及脱碘酶活性具有刺激作用。在此,我们评估了注射瘦素对体内及体外甲状腺125I摄取(RAIU)的影响。我们设计了两个实验:急性瘦素实验(LepA),给予单剂量瘦素(8微克/100克体重/皮下注射);慢性瘦素实验(LepC),以相同剂量的瘦素A每天注射一次,持续6天。同时,对照组注射生理盐水。对于体内研究,部分动物注射125I(3700贝可),并在15或120分钟后处死。LepA组动物的体内甲状腺RAIU未发生变化。然而,LepC组动物的体内甲状腺RAIU较高(15分钟时:增加130%,120分钟时:增加72%;p<0.05)。对于体外研究,处死其他动物并将其甲状腺与125I一起孵育。LepA组和LepC组的甲状腺外植体甲状腺125I含量较低(分别降低32%和29%,p<0.05)。我们大量的数据表明,在体外,瘦素直接抑制大鼠甲状腺RAIU,但在体内,瘦素的作用根据处理时间不同而有所差异,这表明在体内瘦素对甲状腺的慢性刺激涉及其他间接机制。