School of Veterinary Science, University of Liverpool, Leahurst Campus, Neston, Wirral CH64 7TE, UK.
Physiol Behav. 2013 Feb 17;110-111:158-68. doi: 10.1016/j.physbeh.2012.12.016. Epub 2013 Jan 8.
Increasing estradiol concentrations during the late follicular phase stimulate sexual behavior and the GnRH/LH surge, and it is known that kisspeptin signaling is essential for the latter. Administration of LPS can block these events, but the mechanism involved is unclear. We examined brain tissue from intact ewes to determine: i) which regions are activated with respect to sexual behavior, the LH surge and LPS administration, ii) the location and activation pattern of kisspeptin cells in control and LPS treated animals, and iii) whether CRFR type 2 is involved in such disruptive mechanisms. Follicular phases were synchronized with progesterone vaginal pessaries and control animals were killed at 0 h, 16 h, 31 h or 40 h (n=4-6/group) after progesterone withdrawal (time zero). At 28 h, other animals received endotoxin (LPS; 100 ng/kg) and were subsequently killed at 31 h or 40 h (n=5/group). LH surges only occurred in control ewes, during which there was a marked increase in c-Fos expression within the ventromedial nucleus (VMN), arcuate nucleus (ARC), and medial preoptic area (mPOA), as well as an increase in the percentage of kisspeptin cells co-expressing c-Fos in the ARC and mPOA compared to animals sacrificed at all other times. Expression of c-Fos also increased in the bed nucleus of the stria terminalis (BNST) in animals just before the expected onset of sexual behavior. However, LPS treatment increased c-Fos expression within the VMN, ARC, mPOA and diagonal band of broca (dBb), along with CRFR type 2 immunoreactivity in the lower part of the ARC and median eminence (ME), compared to controls. Furthermore, the percentage of kisspeptin cells co-expressing c-Fos was lower in the ARC and mPOA. Thus, we hypothesize that in intact ewes, the BNST is involved in the initiation of sexual behavior while the VMN, ARC, and mPOA as well as kisspeptin cells located in the latter two areas are involved in estradiol positive feedback only during the LH surge. By contrast, disruption of sexual behavior and the LH surge after LPS involves cells located in the VMN, ARC, mPOA and dBb, as well as cells containing CRFR type 2 in the lower part of the ARC and ME, and is accompanied by inhibition of kisspeptin cell activation in both the ARC and mPOA.
在卵泡晚期增加雌二醇浓度会刺激性行为和 GnRH/LH 激增,而众所周知,kisspeptin 信号对于后者是必不可少的。给予 LPS 可以阻断这些事件,但涉及的机制尚不清楚。我们检查了完整绵羊的脑组织,以确定:i)哪些区域与性行为、LH 激增和 LPS 给药有关,ii)在对照和 LPS 处理动物中 kisspeptin 细胞的位置和激活模式,以及 iii)CRFR 类型 2 是否参与这种破坏机制。通过孕激素阴道栓剂同步卵泡期,在孕激素撤退后 0 小时、16 小时、31 小时或 40 小时(每组 4-6 只)处死对照动物(时间为 0)。在 28 小时,其他动物接受内毒素(LPS;100ng/kg),并随后在 31 小时或 40 小时(每组 5 只)处死。只有在对照绵羊中才会发生 LH 激增,在此期间,腹内侧核(VMN)、弓状核(ARC)和内侧视前区(mPOA)中的 c-Fos 表达明显增加,并且与在所有其他时间处死的动物相比,ARC 和 mPOA 中共同表达 c-Fos 的 kisspeptin 细胞的百分比增加。在即将发生性行为之前,终纹床核(BNST)中的 c-Fos 表达也增加。然而,与对照相比,LPS 处理增加了 VMN、ARC、mPOA 和 Broca 斜角带(dBb)中的 c-Fos 表达,以及 ARC 下部和正中隆起(ME)中的 CRFR 类型 2 免疫反应性。此外,ARC 和 mPOA 中共同表达 c-Fos 的 kisspeptin 细胞的百分比较低。因此,我们假设在完整的绵羊中,BNST 参与性行为的启动,而 VMN、ARC 和 mPOA 以及位于后两个区域的 kisspeptin 细胞仅在 LH 激增期间参与雌二醇正反馈。相比之下,LPS 后性行为和 LH 激增的破坏涉及位于 VMN、ARC、mPOA 和 dBb 的细胞,以及位于 ARC 下部和 ME 的含有 CRFR 类型 2 的细胞,并伴有 ARC 和 mPOA 中 kisspeptin 细胞激活的抑制。