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产后早期营养过剩会改变幼年和成年大鼠下丘脑-垂体-甲状腺轴中的瘦素信号通路。

Postnatal early overnutrition changes the leptin signalling pathway in the hypothalamic-pituitary-thyroid axis of young and adult rats.

作者信息

Rodrigues Ananda Lages, de Moura Egberto Gaspar, Passos Magna Cottini Fonseca, Dutra Sheila Cristina Potente, Lisboa Patricia Cristina

机构信息

Departamento de Ciências Fisiológicas, Instituto de Biologia Roberto Alcantara Gomes, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, Brazil.

出版信息

J Physiol. 2009 Jun 1;587(Pt 11):2647-61. doi: 10.1113/jphysiol.2009.169045. Epub 2009 Apr 29.

Abstract

Postnatal early overnutrition (EO) is a risk factor for obesity in adult life. Rats raised in a small litter can develop hyperinsulinaemia, hyperphagia, hyperleptinaemia and hypertension as adults. Since leptin regulates the hypothalamic-pituitary-thyroid axis and the metabolism of thyroid hormones, we studied the leptin signalling pathway in pituitary and thyroid glands of the postnatal EO model. To induce EO, at the third day of lactation the litter size was reduced to three pups per litter (SL group). In control litters (NL group), the litter size was adjusted to 10 pups per litter. Body weight and food intake were monitored. Rat offspring were killed at 21 (weaning) and 180 days old (adulthood). Plasma thyroid hormones, thyroid-stimulating hormone (TSH) and leptin were measured by radioimmunoassay. Proteins of the leptin signalling pathway were analysed by Western blotting. Body weight of offspring in the SL group was higher from the seventh day of lactation (+33%, P < 0.05) until 180 days old (+18%, P < 0.05). Offspring in the SL group showed higher visceral fat mass at 21 and 180 days old (+176 and +52%, respectively, P < 0.05), but plasma leptin was higher only at 21 days (+88%, P < 0.05). The SL offspring showed higher plasma TSH, 3,5,3'-triiodothronine (T(3)) and thyroxine (T(4)) at 21 days (+60, +91 and +68%, respectively, P < 0.05), while the opposite was observed at 180 days regarding thyroid hormones (T(3), -10%; and T(4), -30%, P < 0.05), with no difference in TSH levels. In hypothalamus, no change was observed in the leptin signalling pathway at 21 days. However, lower janus thyrosine kinase 2 (JAK2) and phosphorilated-signal transducer and activator of transcription-3 (p-STAT3) content were detected in adulthood. In pituitary, the SL group presented higher leptin receptors (Ob-R), JAK2 and p-STAT3 content at 21 days and lower JAK2 and STAT3 content at 180 days old. In contrast, in thyroid, the Ob-R expression was lower in young SL rats, while the adult SL group presented higher Ob-R and JAK2 content. We showed that postnatal EO induces short- and long-term effects upon the hypothalamic-pituitary-thyroid axis. These changes may help to explain future development of metabolic and endocrine dysfunctions, such as metabolic syndrome and hypothyroidism.

摘要

产后早期营养过剩(EO)是成年后肥胖的一个风险因素。在小窝中饲养的大鼠成年后会出现高胰岛素血症、食欲亢进、高瘦素血症和高血压。由于瘦素调节下丘脑 - 垂体 - 甲状腺轴以及甲状腺激素的代谢,我们研究了产后EO模型的垂体和甲状腺中的瘦素信号通路。为诱导EO,在哺乳期第三天将每窝幼崽数量减少至3只(SL组)。在对照窝(NL组)中,每窝幼崽数量调整为10只。监测体重和食物摄入量。大鼠后代在21日龄(断奶)和180日龄(成年)时处死。通过放射免疫分析法测定血浆甲状腺激素、促甲状腺激素(TSH)和瘦素。通过蛋白质印迹法分析瘦素信号通路的蛋白质。SL组后代的体重从哺乳期第七天起更高(+33%,P < 0.05),直至180日龄(+18%,P < 0.05)。SL组后代在21日龄和180日龄时内脏脂肪量更高(分别为+176%和+52%,P < 0.05),但血浆瘦素仅在21日龄时更高(+88%,P < 0.05)。SL组后代在21日龄时血浆TSH、3,5,3'-三碘甲腺原氨酸(T(3))和甲状腺素(T(4))更高(分别为+60%、+91%和+68%,P < 0.05),而在180日龄时甲状腺激素情况相反(T(3),-10%;T(4),-30%,P < 0.05),TSH水平无差异。在21日龄时,下丘脑的瘦素信号通路未观察到变化。然而,成年期检测到janus酪氨酸激酶2(JAK2)和磷酸化信号转导及转录激活因子3(p-STAT3)含量较低。在垂体中,SL组在21日龄时瘦素受体(Ob-R)、JAK2和p-STAT3含量更高,在180日龄时JAK2和STAT3含量更低。相反,在甲状腺中,幼年SL大鼠Ob-R表达较低,而成年SL组Ob-R和JAK2含量更高。我们表明,产后EO对下丘脑 - 垂体 - 甲状腺轴有短期和长期影响。这些变化可能有助于解释未来代谢和内分泌功能障碍的发展,如代谢综合征和甲状腺功能减退。

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