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首页> 外文期刊>Proceedings of the Nutrition Society >The role of leptin in the transition from fetus to neonate
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The role of leptin in the transition from fetus to neonate

机译:瘦素在胎儿向新生儿过渡中的作用

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摘要

Leptin is a 16 kDa hormone which has been shown to have a major physiological role in the control of energy balance. Leptin is produced primarily in white adipose tissue, although there is evidence for its production in brown adipose tissue (BAT) and the placenta. BAT is critically important for the initiation of non-shivering thermogenesis in the newborn through the BAT-specific uncoupling protein (UCP), UCP1. This factor is particularly important in lambs in which levels of UCP1 peak at birth, concomitant with a rapid decline in plasma leptin levels. Our studies have examined the effect of acute and chronic administration of leptin to neonatal lambs, investigating effects on colonic temperature, UCP1 and thermogenic potential of BAT. Administration of leptin in sequential physiological doses of 10, 100 and 100 mug to neonatal lambs caused a modest increase in colonic temperature which was not observed in weight-matched vehicle-treated controls. This increase in colonic temperature was not mediated by an increase in either abundance or thermogenic potential of UCP1, as previously shown in adult rodents. UCP1 mRNA levels were 30 % lower in leptin-treated lambs, which is also contradictory to findings in adult rodents. Leptin treatment resulted in a dose-dependent rise in plasma leptin, with levels at the end of the study being almost twenty times greater in leptin-treated animals. To determine whether these findings in neonatal lambs were transient due to the complex milieu of hormones present after birth, we examined the effect of chronic leptin treatment over 6 d. Pairs of lambs were treated daily, from the second to seventh day of life with 100 mug leptin or vehicle. Colonic temperatures of leptin- and vehicle-treated animals remained similar throughout the study. UCP1 abundance was significantly lower in the leptin-treated animals, suggesting that the drop in UCP1 mRNA seen in the previous study had been translated to protein levels. In conclusion, the decline in plasma leptin levels at birth may be a signal to initiate enteral feeding. In lambs, the rapid loss of UCP1 mRNA, which occurs within the first few days of life, appears to be accelerated by leptin administration, possibly stimulating the development of white adipose tissue and generation of body heat through mechanisms other than non-shivering thermogenesis by UCP1 in BAT.
机译:瘦素是一种16 kDa的激素,已被证明在控制能量平衡方面具有重要的生理作用。瘦素主要在白色脂肪组织中产生,尽管有证据表明它在棕色脂肪组织(BAT)和胎盘中产生。 BAT对于通过BAT特异性解偶联蛋白(UCP)UCP1引发新生儿非颤动产热至关重要。这个因素在羔羊出生时UCP1水平达到峰值,同时血浆瘦素水平迅速下降的情况下尤为重要。我们的研究检查了急性和慢性瘦素对新生羔羊给药的作用,调查了对结肠温度,UCP1和BAT的产热潜力的影响。以10、100和100马克的连续生理剂量向新生儿羔羊施用瘦素会导致结肠温度的适度升高,这在体重匹配的媒介物治疗对照组中没有观察到。如先前在成年啮齿动物中所显示的,结肠温度的这种升高不是通过UCP1的丰度或产热潜力的升高来介导的。在瘦蛋白处理的羔羊中,UCP1 mRNA水平降低了30%,这也与成年啮齿动物的发现相矛盾。瘦素治疗导致血浆瘦素呈剂量依赖性上升,在研究结束时,瘦素治疗动物体内的水平几乎增加了二十倍。为了确定新生羔羊的这些发现是否是由于出生后荷尔蒙的复杂环境而短暂出现的,我们检查了长期瘦素治疗6 d的效果。从出生的第二天到第七天,每天用100杯瘦蛋白或溶媒治疗成对的羔羊。在整个研究过程中,瘦素和媒介物治疗动物的结肠温度保持相似。在瘦蛋白治疗的动物中,UCP1的丰度明显降低,这表明在先前的研究中看到的UCP1 mRNA的下降已转化为蛋白质水平。总之,出生时血浆瘦素水平的下降可能是启动肠内喂养的信号。在羔羊中,瘦素的施用似乎加速了UCP1 mRNA在生命的最初几天发生的快速丧失,这可能通过白色机制来刺激白色脂肪组织的发展和机体热量的产生,而不是通过热颤动来引起的。 BAT中的UCP1。

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