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产前应激会降低雌二醇诱导的雄性和雌性大鼠催乳素释放。

Prenatal stress reduces estradiol-induced prolactin release in male and female rats.

作者信息

Kinsley C H, Bridges R S

机构信息

Harvard Medical School, Department of Anatomy and Cellular Biology, Boston, MA 02115.

出版信息

Physiol Behav. 1987;40(5):647-53. doi: 10.1016/0031-9384(87)90112-0.

Abstract

Prenatal stress is a potent disruptor of the normal course of sexual differentiation, affecting both males and females. In the present study, we wished to examine a sexually dimorphic endocrine response, estradiol (E2)-induced prolactin (Prl) release, in prenatally-stressed (P-S) males and females. Sprague-Dawley female rats were timed-mated (+ sperm = Day 1). From gestation days 15-22 one group of females was subjected to a thrice-daily regimen of heat and restraint stress (0830, 1230, and 1630 hr) consisting of placing the rats into a Plexiglas restraint tube over which were poised two 100 W floodlights. Control females remained undisturbed throughout pregnancy. At parturition all offspring were cross-fostered to untreated, recently-parturient dams and weaned at 25 days of age. Separate groups of P-S and Control males and females were gonadectomized and, for males, paired testes weights and body weights were recorded. Four days later the animals were implanted with Silastic capsules containing E2, and fitted with intra-atrial cannulae. The following day, blood samples were taken at 0900, 1300, 1500, and 1700 hr for a total of five days. Beginning with the 1700 hr sample on Day 2, and with the exception of the 1500 hr sample on Day 3, P-S males had significantly lower plasma Prl values than Control males through Day 4, and at the 1500 hr sample on Day 5. Moreover, at no point did P-S males exhibit a significant daily afternoon increase in Prl values, whereas Control males did so on Days 2 and 4.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

产前应激是正常性别分化过程的有力干扰因素,对雄性和雌性均有影响。在本研究中,我们希望检测产前应激(P-S)的雄性和雌性大鼠中一种性别特异性的内分泌反应,即雌二醇(E2)诱导的催乳素(Prl)释放。将斯普拉格-道利雌性大鼠定时交配(出现精子=第1天)。从妊娠第15至22天,一组雌性大鼠每天接受三次热应激和束缚应激(0830、1230和1630时),即将大鼠放入有机玻璃束缚管中,管上方放置两盏100瓦的泛光灯。对照雌性大鼠在整个孕期均不受干扰。分娩时,所有后代均交叉寄养至未经处理的、刚分娩的母鼠处,并在25日龄时断奶。将P-S组和对照组的雄性和雌性大鼠分别进行性腺切除,对于雄性大鼠,记录双侧睾丸重量和体重。四天后,给动物植入含E2的硅橡胶胶囊,并插入心房插管。次日,在0900、1300、1500和1700时采集血样,共采集五天。从第2天的1700时样本开始,除第3天的1500时样本外,直到第4天以及第5天的1500时样本,P-S组雄性大鼠的血浆Prl值均显著低于对照组雄性大鼠。此外,P-S组雄性大鼠在任何时间点的Prl值均未出现显著的每日下午升高,而对照组雄性大鼠在第2天和第4天出现了这种升高。(摘要截选至250字)

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