Clarke Iain J, Scott Christopher J, Pereira Alda, Pompolo Sueli
Prince Henry's Institute of Medical Research, P.O. Box 5152, Clayton, Vic. 3168, Australia.
Domest Anim Endocrinol. 2006 May;30(4):260-75. doi: 10.1016/j.domaniend.2005.07.006. Epub 2005 Aug 11.
Increasing plasma estrogen (E) levels during the follicular phase of the estrous cycle trigger the pre-ovulatory surge of gonadotropin-releasing hormone (GnRH)/LH. Noradrenaline (NA)-producing cells of the brain stem are involved in regulating GnRH cells and project to the preoptic area (POA) and bed nucleus of stria terminalis (BnST). Input to GnRH cells may be direct or indirect, via relay neurons in the POA/BnST. To investigate this, we ascertained whether an alpha(1)-adrenergic antagonist would block/delay the LH surge in ovariectomised (OVX), E-treated ewes. E benzoate (EB) (50microg) was injected (i.m.) and Doxazosin (100nmol/h) or vehicle was infused into the third ventricle 2-26h after EB injection. Doxazosin reduced the magnitude of the LH surge, but did not affect timing. To determine if NA is released in the POA/BnST of cyclic ewes, we immunostained dopamine-beta-hydroxylase (DBH) in terminal fields. Reduced numbers of varicosities staining for DBH indicates release of NA. The number of varicosities immunostained for DBH was reduced in the dorsal and lateral BnST during the follicular phase and during the preovulatory LH surge compared to the luteal phase. These data suggest that noradrenergic mechanisms are involved in generation of the GnRH/LH surge via projections to the BnST and relay to GnRH cells. Since Doxasozin reduced the magnitude of the LH surge in the E-treated OVX ewe, and release of NA in cyclic ewes occurred during the follicular phase of the estrous cycle, we speculate that NA is a permissive factor in surge generation. Thus, increased noradrenergic activity is not a trigger mechanism for initiation of the surge.
在发情周期的卵泡期,血浆雌激素(E)水平升高会引发促性腺激素释放激素(GnRH)/促黄体生成素(LH)的排卵前激增。脑干中产生去甲肾上腺素(NA)的细胞参与调节GnRH细胞,并投射到视前区(POA)和终纹床核(BnST)。对GnRH细胞的输入可能是直接的,也可能是通过POA/BnST中的中继神经元间接进行的。为了对此进行研究,我们确定了α(1)-肾上腺素能拮抗剂是否会阻断/延迟卵巢切除(OVX)且经E处理的母羊的LH激增。注射苯甲酸雌二醇(EB)(50μg)(肌肉注射),并在EB注射后2 - 26小时将多沙唑嗪(100nmol/h)或溶剂注入第三脑室。多沙唑嗪降低了LH激增的幅度,但不影响时间。为了确定NA是否在周期性母羊的POA/BnST中释放,我们对终末区域的多巴胺-β-羟化酶(DBH)进行了免疫染色。DBH染色的曲张体数量减少表明NA已释放。与黄体期相比,在卵泡期和排卵前LH激增期间,背侧和外侧BnST中DBH免疫染色的曲张体数量减少。这些数据表明,去甲肾上腺素能机制通过投射到BnST并中继到GnRH细胞参与GnRH/LH激增的产生。由于多沙唑嗪降低了经E处理的OVX母羊的LH激增幅度,且周期性母羊的NA释放在发情周期的卵泡期发生,我们推测NA是激增产生中的一个允许因子。因此,去甲肾上腺素能活性增加不是激增起始的触发机制。