Lipschitz D L, Crowley W R, Bealer S L
Department of Pharmacology and Toxicology, College of Pharmacy, University of Utah, Salt Lake City, UT 84112, USA.
J Neuroendocrinol. 2003 Aug;15(8):743-8. doi: 10.1046/j.1365-2826.2003.01052.x.
There is evidence that the central oxytocin system is activated and undergoes reorganization before parturition. The present study was designed to determine the effects of central oxytocin receptor blockade during late gestation on parturition, pup growth, and oxytocin release during suckling. Female Sprague-Dawley rats were implanted on gestation day 12-14 with Alzet osmotic minipumps containing an oxytocin receptor antagonist (d(CH2)5, Tyr(Me)(2), Orn(8)-vasotocin; OT-X) or artificial cerebrospinal fluid (VEH), which was infused into the third cerebral ventricle. Pumps were removed within 24 h of parturition. Daily maternal body weight and food intake were monitored during gestation and lactation. The length of gestation, duration of parturition, pup number, litter weight and interbirth interval were recorded. Subsequently, pup number and litter weights were recorded daily until lactation day 10 or 11, when maternal and pup behaviour, and plasma oxytocin concentration before and during suckling were measured. Central oxytocin blockade had no effect on the timing of parturition, maternal behaviour, litter size, still births, or litter weights at birth. However, beginning on day 3 of lactation, average weights of litters of OT-X females were significantly lower than litters of VEH-treated females. Furthermore, while basal plasma oxytocin concentrations, oxytocin increases in response to suckling and dam/pup interactions did not differ between groups, a significant delay in suckling-induced systemic oxytocin release was observed in OT-X females. Finally, OT-X dams weighed less than VEH dams during the postpartum observation period, although food intakes were similar. These data suggest that central actions of oxytocin during late gestation are necessary for the normal timing of systemic release of oxytocin during suckling, normal pup weight gain, and maintenance of maternal body weight.
有证据表明,中枢催产素系统在分娩前被激活并发生重组。本研究旨在确定妊娠后期中枢催产素受体阻断对分娩、幼崽生长以及哺乳期间催产素释放的影响。在妊娠第12至14天,给雌性Sprague-Dawley大鼠植入含有催产素受体拮抗剂(d(CH2)5, Tyr(Me)(2), Orn(8)-血管加压素;OT-X)或人工脑脊液(VEH)的Alzet渗透微型泵,将其注入第三脑室。在分娩后24小时内取出泵。在妊娠和哺乳期间监测母鼠的每日体重和食物摄入量。记录妊娠期长度、分娩持续时间、幼崽数量、窝仔重量和产仔间隔。随后,每天记录幼崽数量和窝仔重量,直到哺乳第10或11天,此时测量母鼠和幼崽的行为以及哺乳前后的血浆催产素浓度。中枢催产素阻断对分娩时间、母性行为、窝仔大小、死产或出生时的窝仔重量没有影响。然而,从哺乳第3天开始,OT-X组母鼠所产幼崽的平均体重显著低于VEH处理组母鼠所产幼崽。此外,虽然两组之间基础血浆催产素浓度、对哺乳和母鼠/幼崽互动的催产素增加没有差异,但在OT-X组母鼠中观察到哺乳诱导的全身催产素释放有显著延迟。最后,在产后观察期,OT-X组母鼠的体重低于VEH组母鼠,尽管食物摄入量相似。这些数据表明,妊娠后期催产素的中枢作用对于哺乳期间催产素的全身正常释放时间、幼崽正常体重增加以及母鼠体重维持是必要的。