McCracken J A, Custer E E, Eldering J A, Robinson A G
Worcester Foundation for Biomedical Research, Shrewsbury, MA 01545, USA.
Acta Neurobiol Exp (Wars). 1996;56(3):819-32. doi: 10.55782/ane-1996-1187.
During luteolysis in sheep, episodic pulses of oxytocin (OT), contributed by the neurohypophysis and the corpus luteum (CL), stimulate uterine luteolytic pulses of prostaglandin (PG) F2 alpha via endometrial OT receptors. To distinguish relative contributions of neurohypophysial and luteal OT, ovariectomized sheep were given estradiol-17 beta (E) and progesterone (P) to stimulate levels during the cycle. In intact sheep, luteectomy was performed to exclude the CL as a source of OT and to initiate P withdrawal. In ovariectomized sheep, E (1 microgram/h) for 12 to 36 h) superimposed on basal E(0.05 microgram/h), caused a series of 4 to 6 episodes of high frequency pulses of OT, each episode lasting 1 to 2 h at intervals of 3 h, and commencing at 24 h. Withdrawal of P (500 micrograms/h), superimposed on basal E in ovariectomized sheep, or luteectomy in intact sheep, evoked similar episodes of high frequency pulses of OT beginning at 24 h. We conclude that (1) an increase in E levels, or the return of E action following P withdrawal, causes intermittent increases in the frequency of the central OT pulse generator. (2) high frequency pulses of OT initiate subluteolytic levels of uterine PGF2 alpha which trigger a supplemental release of luteal OT; (3) luteal OT amplifies the secretion of uterine PGF2 alpha which initiates luteolysis and causes more luteal OT to be secreted; and (4) in addition to the established hypothalamic-anterior pituitary-gonadal axis for initiating the ovarian cycle (via the gonadotrophins), there is now evidence for a hypothalamic-posterior pituitary-gonadal axis for terminating the ovarian cycle (via OT).
在绵羊黄体溶解过程中,由神经垂体和黄体(CL)分泌的催产素(OT)的间歇性脉冲,通过子宫内膜OT受体刺激前列腺素(PG)F2α的子宫黄体溶解脉冲。为了区分神经垂体OT和黄体OT的相对贡献,对去卵巢绵羊给予雌二醇-17β(E)和孕酮(P)以刺激周期中的水平。在完整的绵羊中,进行黄体切除术以排除CL作为OT的来源并启动P的撤退。在去卵巢绵羊中,将E(1微克/小时)持续12至36小时叠加在基础E(0.05微克/小时)上,导致一系列4至6次高频OT脉冲发作,每次发作持续1至2小时,间隔3小时,并在24小时开始。在去卵巢绵羊中,将P(500微克/小时)的撤退叠加在基础E上,或在完整绵羊中进行黄体切除术,会引发从24小时开始的类似高频OT脉冲发作。我们得出结论:(1)E水平的升高,或P撤退后E作用的恢复,会导致中枢OT脉冲发生器频率的间歇性增加。(2)OT的高频脉冲引发子宫PGF2α的亚黄体溶解水平,从而触发黄体OT的补充释放;(3)黄体OT放大子宫PGF2α的分泌,从而启动黄体溶解并导致更多的黄体OT分泌;(4)除了已确立的用于启动卵巢周期(通过促性腺激素)的下丘脑 - 垂体前叶 - 性腺轴外,现在有证据表明存在用于终止卵巢周期(通过OT)的下丘脑 - 垂体后叶 - 性腺轴。