Department of Agroforestry Sciences, University of Huelva, Palos de la Frontera, Carretera de Palos de la Frontera s/n, Palos de la Frontera, Huelva, Spain.
Biol Reprod. 2011 Mar;84(3):447-54. doi: 10.1095/biolreprod.110.086520. Epub 2010 Oct 27.
This study examined which neural mechanism (opioid, dopaminergic, or serotonergic system) is involved in the regulation of luteinizing hormone (LH) secretion, with and without nutritional modulation, at different times of the photoperiodic cycle. Goats were randomly distributed into two experimental groups that received either 1.1 (high group; n = 18) or 0.7 (low group; n = 18) times the nutritional maintenance requirements. The goats were exposed to alternations of 3 mo of long days and 3 mo of short days. Plasma LH concentrations were measured twice a week. The effects of intravenous injections of naloxone (endogenous opioid receptor antagonist), pimozide (dopaminergic(2) receptor antagonist), and cyproheptadine (serotonin 5-hydroxytryptamine(2) receptor antagonist) on LH secretion were assessed during challenges in three different photoperiodic situations: the onset of LH stimulation by short days (OnsetSD), the onset of LH inhibition by long days (OnsetLD), and during the LH inhibition by long days (LateLD). The role of the different neural systems was clearly modified by the level of nutrition. In the low-nutrition group, only naloxone increased LH concentrations during onsetLD (P < 0.05). However, in the high-nutrition group, naloxone increased the concentration and pulsatility of LH (P < 0.05) in onsetSD and onsetLD. Pimozide increased LH concentration and pulsatility (P < 0.05) in onsetLD and LH concentration in lateLD (P < 0.001). Finally, cyproheptadine significantly increased LH concentration at all three times (P < 0.001). These results provide evidence that all three systems are involved in the inhibition of LH release in onsetLD, and that the opioid and serotonin mechanisms are involved during the onsetSD that were enhanced by a high plane of nutrition.
这项研究旨在探讨在不同光周期时间点,黄体生成素(LH)分泌的调节涉及到哪些神经机制(阿片样物质、多巴胺能或 5-羟色胺能系统),以及营养调节的影响。将山羊随机分为两组进行实验,一组接受 1.1 倍(高营养组;n=18)或 0.7 倍(低营养组;n=18)的营养维持需求。山羊暴露在 3 个月的长日和 3 个月的短日交替中。每周两次测量血浆 LH 浓度。在三种不同光周期情况下进行静脉注射纳洛酮(内源性阿片受体拮抗剂)、匹莫齐特(多巴胺能(2)受体拮抗剂)和赛庚啶(5-羟色胺能 2 型受体拮抗剂)对 LH 分泌的影响评估:短日刺激 LH 的开始(短日刺激开始,OnsetSD)、长日抑制 LH 的开始(长日抑制开始,OnsetLD)和长日抑制期间的 LH(长日抑制后期,LateLD)。营养水平明显改变了不同神经系统的作用。在低营养组中,只有纳洛酮在长日刺激开始时增加了 LH 浓度(P<0.05)。然而,在高营养组中,纳洛酮增加了 OnsetSD 和 OnsetLD 中 LH 的浓度和脉冲性(P<0.05)。匹莫齐特增加了 OnsetLD 和 LateLD 中 LH 浓度和脉冲性(P<0.05)(P<0.001)。最后,赛庚啶显著增加了三个时间点的 LH 浓度(P<0.001)。这些结果表明,所有三个系统都参与了长日刺激开始时 LH 释放的抑制,而阿片样物质和 5-羟色胺能机制在高营养水平下增强了 OnsetSD 期间的参与。