Ochedalski T, Subburaju S, Wynn P C, Aguilera G
Section on Endocrine Physiology, Developmental Endocrinology Branch, National Institutes of Child Health and Human Development, NIH, Bethesda, MD 20892, USA.
J Neuroendocrinol. 2007 Mar;19(3):189-97. doi: 10.1111/j.1365-2826.2006.01525.x.
In addition to its role in reproduction, oxytocin has central actions modulating behavioural and hypothalamic-pituitary-adrenal (HPA) axis responses during late pregnancy and lactation. The hypothesis that ovarian hormones modulate the effects of oxytocin on HPA axis activity was studied in 7-day ovariectomised rats receiving oestradiol with or without progesterone replacement and intracerebroventricular (i.c.v) minipump infusion of oxytocin (100 ng/h). In an initial experiment, i.c.v. oxytocin had no effect on basal or restraint-stimulated plasma adrenocorticotrophic hormone (ACTH) and corticosterone concentrations or hypothalamic corticotrophin-releasing factor (CRF) mRNA expression with low oestradiol replacement alone but it had a stimulatory effect in the presence of low oestradiol and progesterone. To investigate further whether oestradiol modulates central actions of oxytocin, rats received low dioestrous (low), pro-oestrous (medium) or pregnancy (high) oestradiol replacement levels, yielding plasma concentrations of < 5, 17.3 +/- 4.5 and 258 +/- 32 pg/ml, respectively, with or without i.c.v. oxytocin. Oestradiol caused dose-dependent increases in basal plasma ACTH and corticosterone concentrations but decreased the ACTH response to restraint stress. In parallel to the changes in basal plasma ACTH, high oestrogen increased basal CRF hnRNA, CRF mRNA in the paraventricular nucleus and pro-opiomelanocortin (POMC) mRNA in the pituitary gland, while decreasing restraint stress-stimulated levels. Intracerebroventricular administration of oxytocin reduced basal and stress-stimulated plasma ACTH, hypothalamic CRF hnRNA (30 min), CRF mRNA and pituitary POMC mRNA (4 h) levels parallel to the increases induced by elevating plasma oestradiol. The present study demonstrates the converse effects of oestradiol on basal and restraint stress-stimulated basal HPA axis activity, and that the ability of central oxytocin to inhibit HPA axis activity depends on the levels of circulating oestradiol.
除了在生殖过程中的作用外,催产素在妊娠晚期和哺乳期还具有调节行为及下丘脑-垂体-肾上腺(HPA)轴反应的中枢作用。本研究在7日龄去卵巢大鼠中进行,这些大鼠接受了有或无孕酮替代的雌二醇,并通过脑室内(i.c.v)微型泵输注催产素(100 ng/h),以探讨卵巢激素是否调节催产素对HPA轴活动的影响。在最初的实验中,单独给予低剂量雌二醇替代时,脑室内注射催产素对基础或束缚刺激后的血浆促肾上腺皮质激素(ACTH)和皮质酮浓度或下丘脑促肾上腺皮质激素释放因子(CRF)mRNA表达没有影响,但在低剂量雌二醇和孕酮存在的情况下具有刺激作用。为了进一步研究雌二醇是否调节催产素的中枢作用,大鼠接受了低动情期(低)、动情前期(中)或妊娠(高)雌二醇替代水平,血浆浓度分别为<5、17.3±4.5和258±32 pg/ml,同时有或无脑室内注射催产素。雌二醇导致基础血浆ACTH和皮质酮浓度呈剂量依赖性增加,但降低了ACTH对束缚应激的反应。与基础血浆ACTH的变化平行,高雌激素增加了基础CRF hnRNA、室旁核中的CRF mRNA以及垂体中的阿黑皮素原(POMC)mRNA,同时降低了束缚应激刺激后的水平。脑室内给予催产素可降低基础和应激刺激后的血浆ACTH、下丘脑CRF hnRNA(30分钟)、CRF mRNA和垂体POMC mRNA(4小时)水平,这与血浆雌二醇升高所诱导的增加情况相反。本研究证明了雌二醇对基础和束缚应激刺激后的基础HPA轴活动具有相反的作用,并且中枢催产素抑制HPA轴活动的能力取决于循环雌二醇的水平。