Brauer M M, Chávez-Genaro R, Richeri A, Viettro L, Frias A I, Burnstock G, Cowen T
Laboratorio de Biología Celular, Instituto de Investigaciones Biológicas Clemente Estable, Avenida Italia 3318, Montevideo 11600, Uruguay.
Auton Neurosci. 2002 Oct 31;101(1-2):13-22. doi: 10.1016/s1566-0702(02)00173-x.
Chronic administration of oestrogen to rats during the infantile/prepubertal period provokes, at 28 days of age, complete loss of noradrenaline-labelled intrauterine sympathetic nerves. It is not known whether oestrogen inhibits the growth or causes the degeneration of developing uterine sympathetic nerves, or whether the uterus recovers its innervation following cessation of infantile/prepubertal oestrogen treatment. In the present study, we analysed the time-course of the effects of oestrogen on the development of uterine sympathetic nerves in the rat, using histochemical methods. In addition, the pattern of sympathetic reinnervation of the uterus of intact and ovariectomised females was assessed 3 and 6 months after cessation of chronic oestrogen treatment. The ability of sympathetic nerves to reinnervate the oestrogenized uterine tissue was assessed in intraocular transplants of uterine myometrium into ovariectomised host rats. Early exposure to oestrogen did not inhibit the approach of sympathetic nerves to the uterus, but prevented the normal growth and maturation of intrauterine sympathetic fibres and abolished the innervation that reached the organ before initiation of treatment. Three or six months following cessation of oestrogen treatment, most of the sympathetic nerves were restricted to the mesometrium and mesometrial entrance, whereas intrauterine innervation remained persistently depressed as a consequence of a sustained oestrous-like state provoked by ovarian dysfunction (polycystic ovary). An organotypic regrowth of uterine sympathetic nerves was observed in ovariectomised infantile/prepubertal oestrogen-treated animals. After 5 weeks in oculo, the innervation of oestrogenized myometrial transplants was reduced by 50%, and substantial changes in the pattern of reinnervation were observed. In control transplants, 86% of the nerves were terminal varicose myometrial and perivascular nerve fibres, whereas 14% were preterminal nerve bundles. In oestrogenized myometrial transplants, 83% of the noradrenaline-labelled intercepting nerves were enlarged preterminal bundles and only 17% were terminal fibres. These results indicate that the oestrogenized myometrium is unattractive for sympathetic nerves and inhibits organotypic sympathetic reinnervation.
在幼年期/青春期前给大鼠长期施用雌激素,在28日龄时会导致去甲肾上腺素标记的子宫内交感神经完全丧失。目前尚不清楚雌激素是抑制发育中的子宫交感神经生长还是导致其退化,也不清楚在幼年期/青春期前雌激素治疗停止后子宫是否会恢复其神经支配。在本研究中,我们使用组织化学方法分析了雌激素对大鼠子宫交感神经发育影响的时间进程。此外,在慢性雌激素治疗停止3个月和6个月后,评估了完整和去卵巢雌性大鼠子宫交感神经再支配的模式。在将子宫肌层眼内移植到去卵巢宿主大鼠中,评估了交感神经对雌激素化子宫组织再支配的能力。早期接触雌激素并未抑制交感神经向子宫的靠近,但阻止了子宫内交感纤维的正常生长和成熟,并消除了在治疗开始前到达该器官的神经支配。雌激素治疗停止3或6个月后,大多数交感神经局限于子宫系膜和子宫系膜入口,而由于卵巢功能障碍(多囊卵巢)引发的持续发情样状态,子宫内神经支配持续受到抑制。在去卵巢的幼年期/青春期前接受雌激素治疗的动物中观察到子宫交感神经的器官型再生。眼内移植5周后,雌激素化肌层移植的神经支配减少了50%,并观察到再支配模式的实质性变化。在对照移植中,86%的神经是终末曲张的肌层和血管周围神经纤维,而14%是终末前神经束。在雌激素化肌层移植中,83%的去甲肾上腺素标记的拦截神经是增粗的终末前束,只有17%是终末纤维。这些结果表明,雌激素化的肌层对交感神经缺乏吸引力,并抑制器官型交感神经再支配。