Yuen B S J, Owens P C, Symonds M E, Keisler D H, McFarlane J R, Kauter K G, McMillen I C
Department of Physiology, University of Adelaide, South Australia, Australia.
Biol Reprod. 2004 Jun;70(6):1650-7. doi: 10.1095/biolreprod.103.025254. Epub 2004 Feb 11.
We investigated whether leptin can suppress the prepartum activation of the fetal hypothalamus-pituitary-adrenal (HPA) axis and delay the timing of parturition in the sheep. First, we investigated the effects of a 4-day intravascular infusion of recombinant ovine leptin (n = 7) or saline (n = 6) on fetal plasma adrenocorticotropic hormone (ACTH) and cortisol concentrations, starting from 136 days gestation (i.e., at the onset of the prepartum activation of the fetal HPA axis. The effects of a continuous intrafetal infusion of leptin (n = 7) or saline (n = 5) from 144 days gestation on fetal plasma ACTH and cortisol concentrations and the timing of delivery were also determined in a separate study. There was an increase in fetal plasma ACTH (P < 0.01) and cortisol (P < 0.001) concentrations when saline was infused between 136-137 and 140-141 days gestation. Plasma ACTH and cortisol concentrations did not rise, however, when leptin was infused during this period of gestation. When leptin was infused after 144 days gestation, there was no effect of a 4- to 5-fold increase in circulating leptin on fetal ACTH concentrations. In contrast, leptin infusion from 144 days gestation suppressed (P < 0.05) fetal plasma cortisol concentrations by around 40% between 90 and 42 h before delivery. There was no difference, however, in the length of gestation between the saline- and leptin-infused groups (saline infused, 150.2 +/- 0.5 days; leptin infused, 149.8 +/- 1.0 days). In saline-infused fetuses, there was a significant negative relationship between the plasma concentrations of cortisol (y) and leptin (x) between 138 and 146 days gestation (y = 81.4 - 7.7x, r = 0.38, P < 0.005). This study provides evidence for an endocrine negative feedback loop between leptin and the HPA axis in fetal life.
我们研究了瘦素是否能抑制绵羊胎儿下丘脑-垂体-肾上腺(HPA)轴的产前激活并延迟分娩时间。首先,我们从妊娠136天(即胎儿HPA轴产前激活开始时)起,研究了连续4天血管内输注重组羊瘦素(n = 7)或生理盐水(n = 6)对胎儿血浆促肾上腺皮质激素(ACTH)和皮质醇浓度的影响。在另一项研究中,我们还确定了从妊娠144天起在胎儿体内连续输注瘦素(n = 7)或生理盐水(n = 5)对胎儿血浆ACTH和皮质醇浓度以及分娩时间的影响。在妊娠136 - 137天和140 - 141天之间输注生理盐水时,胎儿血浆ACTH(P < 0.01)和皮质醇(P < 0.001)浓度升高。然而,在这个妊娠期内输注瘦素时,血浆ACTH和皮质醇浓度并未升高。在妊娠144天后输注瘦素时,循环瘦素增加4至5倍对胎儿ACTH浓度没有影响。相比之下,从妊娠144天起输注瘦素在分娩前90至42小时之间使胎儿血浆皮质醇浓度降低了约40%(P < 0.05)。然而,输注生理盐水组和输注瘦素组之间的妊娠期长度没有差异(输注生理盐水组,150.2±0.5天;输注瘦素组,149.8±1.0天)。在输注生理盐水的胎儿中,妊娠138至146天期间,皮质醇(y)和瘦素(x)的血浆浓度之间存在显著负相关(y = 81.4 - 7.7x,r = 0.38,P < 0.005)。这项研究为胎儿期瘦素与HPA轴之间的内分泌负反馈回路提供了证据。