Forhead Alison J, Lamb Christopher A, Franko Kathryn L, O'Connor Deirdre M, Wooding F B Peter, Cripps Roselle L, Ozanne Susan, Blache Dominique, Shen Qingwu W, Du Min, Fowden Abigail L
Department of Physiology, Development and Neuroscience, University of Cambridge, Downing Street, Cambridge CB23EG, UK.
J Physiol. 2008 May 1;586(9):2393-403. doi: 10.1113/jphysiol.2007.149237. Epub 2008 Mar 6.
Leptin is an important regulator of appetite and energy expenditure in adulthood, although its role as a nutritional signal in the control of growth and metabolism before birth is poorly understood. This study investigated the effects of leptin on growth, carbohydrate metabolism and insulin signalling in fetal sheep. Crown-rump length-measuring devices and vascular catheters were implanted in 12 sheep fetuses at 105-110 days of gestation (term 145 +/- 2 days). The fetuses were infused i.v. either with saline (0.9% NaCl; n = 6) or recombinant ovine leptin (0.5-1.0 mg kg(-1) day(-1); n = 6) for 5 days from 125 to 130 days when they were humanely killed and tissues collected. Leptin receptor mRNA and protein were expressed in fetal liver, skeletal muscle and perirenal adipose tissue. Throughout infusion, plasma leptin in the leptin-infused fetuses was 3- to 5-fold higher than in the saline-infused fetuses, although plasma concentrations of insulin, glucose, lactate, cortisol, catecholamines and thyroid hormones did not differ between the groups. Leptin infusion did not affect linear skeletal growth or body, placental and organ weights in utero. Hepatic glycogen content and activities of the gluconeogenic enzymes glucose-6-phosphatase and phosphoenolpyruvate carboxykinase in the leptin-infused fetuses were lower than in the saline-infused fetuses by 44, 48 and 36%, respectively; however, there were no differences in hepatic glycogen synthase activity or insulin signalling protein levels. Therefore, before birth, leptin may inhibit endogenous glucose production by the fetal liver when adipose energy stores and transplacental nutrient delivery are sufficient for the metabolic needs of the fetus. These actions of leptin in utero may contribute to the development of neonatal hypoglycaemia in macrosomic babies of diabetic mothers.
瘦素是成年期食欲和能量消耗的重要调节因子,尽管其在出生前生长和代谢控制中作为营养信号的作用尚不清楚。本研究调查了瘦素对胎儿绵羊生长、碳水化合物代谢和胰岛素信号传导的影响。在妊娠105 - 110天(足月为145±2天)时,将顶臀长测量装置和血管导管植入12只绵羊胎儿体内。从妊娠125至130天起,给胎儿静脉输注生理盐水(0.9%氯化钠;n = 6)或重组羊瘦素(0.5 - 1.0 mg kg⁻¹天⁻¹;n = 6),持续5天,之后对其实施安乐死并收集组织。瘦素受体mRNA和蛋白在胎儿肝脏、骨骼肌和肾周脂肪组织中表达。在整个输注过程中,输注瘦素的胎儿血浆瘦素水平比输注生理盐水的胎儿高3至5倍,尽管两组之间胰岛素、葡萄糖、乳酸、皮质醇、儿茶酚胺和甲状腺激素的血浆浓度没有差异。瘦素输注不影响子宫内骨骼的线性生长或身体、胎盘和器官重量。输注瘦素的胎儿肝脏糖原含量以及糖异生酶葡萄糖-6-磷酸酶和磷酸烯醇式丙酮酸羧激酶的活性分别比输注生理盐水的胎儿低44%、48%和36%;然而,肝脏糖原合酶活性或胰岛素信号蛋白水平没有差异。因此,在出生前,当脂肪能量储备和经胎盘营养输送足以满足胎儿的代谢需求时,瘦素可能会抑制胎儿肝脏的内源性葡萄糖生成。瘦素在子宫内的这些作用可能导致糖尿病母亲巨大儿新生儿低血糖的发生。