Toufexis D J, Thrivikraman K V, Plotsky P M, Morilak D A, Huang N, Walker C D
Douglas Hospital Research Center, Department of Psychiatry, Neurology & Neurosurgery, McGill University, Montreal, Quebec, Canada.
J Neuroendocrinol. 1998 Jun;10(6):417-27. doi: 10.1046/j.1365-2826.1998.00223.x.
Lactation in mammals is accompanied by a marked decrease in stress responsiveness that we previously attributed, in part, to a reduction in noradrenergic (NA) innervation of hypothalamic paraventricular nucleus (PVN) neurons controlling neuroendocrine stress responses. In the present study, we compared in-vivo PVN catecholamine secretion by microdialysis between nonlactating and lactating females and tested the effects of NA alpha-1 and alpha-2 receptor antagonists (corynanthine and idazoxan, respectively) on the acute stress response of lactating and virgin female rats. To determine if PVN alpha-adrenoreceptor density, affinity, or synthesis, changes as a function of lactation, we performed receptor autoradiography, Scatchard analysis and in situ hybridization of alpha-adrenoreceptors. Densitometric analysis of the alpha-adrenoreceptors in the supraoptic nucleus (SON) was used to evaluate changes in magnocellular neurons. Endogenous PVN norepinephrine release under basal conditions was lower in lactating females than in females who had their pups removed for 2 days, and microdialysate concentrations of adrenaline and MHPG were attenuated in lactating females. Alpha-2 adrenoreceptor density in the PVN showed a significant decrease from lactation day 3 to lactation days 10-12 and a reduction to 40% of virgin controls on days 10-20 of lactation. A similar pattern was observed for the SON. The affinity of hypothalamic alpha-2 adrenoreceptors was reduced as a function of lactation. Alpha-1 adrenoreceptor density in the PVN and in the hypothalamus rose as a function of lactation, although the affinity of these receptors was not altered. In contrast, alpha-1D adrenoreceptor subtype mRNA expression in the PVN decreased in middle lactating females (day 10) compared to virgins. Intracerebroventricular (i.c.v.) application of idazoxan, significantly increased the ACTH response to swim stress in virgin females, but had the opposite effect in lactating females. In contrast, i.c.v. corynanthine treatment significantly decreased the ACTH response in virgins, but not in lactating females. Overall, these data suggest that the secretion of NA in the PVN is reduced during lactation, and that the ability of PVN parvocellular neurons to respond to changes in synaptic NA levels (i.e. after stress) is also altered.
哺乳动物的泌乳伴随着应激反应性的显著降低,我们之前部分地将其归因于控制神经内分泌应激反应的下丘脑室旁核(PVN)神经元的去甲肾上腺素能(NA)神经支配减少。在本研究中,我们通过微透析比较了非泌乳和泌乳雌性动物体内PVN的儿茶酚胺分泌,并测试了NA α-1和α-2受体拮抗剂(分别为育亨宾碱和咪唑克生)对泌乳和未生育雌性大鼠急性应激反应的影响。为了确定PVN α-肾上腺素能受体的密度、亲和力或合成是否随泌乳而变化,我们进行了受体放射自显影、Scatchard分析以及α-肾上腺素能受体的原位杂交。对视上核(SON)中α-肾上腺素能受体进行光密度分析,以评估大细胞神经元的变化。泌乳雌性动物在基础条件下内源性PVN去甲肾上腺素释放低于幼崽被移除2天的雌性动物,并且泌乳雌性动物的微透析液中肾上腺素和3-甲氧基-4-羟基苯乙二醇(MHPG)浓度降低。PVN中α-2肾上腺素能受体密度从泌乳第3天到泌乳第10 - 12天显著降低,在泌乳第10 - 20天降至未生育对照组的40%。SON也观察到类似模式。下丘脑α-2肾上腺素能受体的亲和力随泌乳而降低。PVN和下丘脑中α-1肾上腺素能受体密度随泌乳增加,尽管这些受体的亲和力未改变。相反,与未生育动物相比,泌乳中期雌性动物(第10天)PVN中α-1D肾上腺素能受体亚型mRNA表达降低。脑室内(i.c.v.)注射咪唑克生显著增加未生育雌性动物对游泳应激的促肾上腺皮质激素(ACTH)反应,但对泌乳雌性动物有相反作用。相反,i.c.v.注射育亨宾碱处理显著降低未生育动物的ACTH反应,但对泌乳雌性动物无此作用。总体而言,这些数据表明泌乳期间PVN中NA分泌减少,并且PVN小细胞神经元对突触NA水平变化(即应激后)的反应能力也发生了改变。