Pierroz D D, Catzeflis C, Aebi A C, Rivier J E, Aubert M L
Department of Pediatrics, University of Geneva School of Medicine, Switzerland.
Endocrinology. 1996 Jan;137(1):3-12. doi: 10.1210/endo.137.1.8536627.
Neuropeptide Y (NPY) is known to be involved in the central regulation of appetite, sexual behavior, and reproductive function. Whereas central administration of NPY strongly stimulates feeding in satiated animals, diet restriction or other unfavorable metabolic situations, such as diabetes, produce enhanced NPY gene expression and NPY release in the hypothalamus. Numerous studies have indicated that acute central administration of NPY results in various actions on LH secretion in the rat, either stimulatory or inhibitory. We recently demonstrated that chronic infusion of NPY into the lateral ventricle of adult intact female rats profoundly inhibited both the gonadotropic and somatotropic axes, with disruption of estrous cyclicity. Furthermore, we showed that central chronic infusion of NPY delayed sexual maturation in female rats. To analyze the effects of the same type of chronic NPY treatment on the pituitary-testicular axis, 45-day-old Sprague-Dawley male rats were implanted with stainless steel cannulas in the right lateral ventricle. Ten days later, Alzet osmotic minipumps were filled with different NPY solutions, adjusted to deliver 6, 18, or 36 micrograms/day, connected to the intracerebroventricular (icv) cannula, and sc implanted dorsally. The effects of these treatments were evaluated over 7 days. In one case, rats were castrated 5 days after initiation of NPY treatment, and the effect of castration was evaluated 2 days later. Chronic icv infusion of NPY produced the expected dose-related increases in food intake from 33.0 +/- 0.9 (basal) to 53.4 +/- 3.3 g/day (18 micrograms NPY/day) and body weight gain (5.7 +/- 0.7 to 10.5 +/- 1.2 d/day). As in female rats, this orexigenic action of NPY resulted in a significant dose-related decrease in pituitary weight, from 12.4 +/- 0.7 to 9.9 +/- 0.4 mg. The 7-day NPY infusion produced highly significant decreases in seminal vesicle weight (853 +/- 77 to 230 +/- 31 mg) and testis weight (3.82 +/- 0.09 to 3.18 +/- 0.15 g; P = 0.003). Plasma levels of testosterone (231 +/- 71 to 48 +/- 13 ng/dl), LH (20.7 +/- 3.7 to 9.1 +/- 1.2 ng/ml), and FSH (282 +/- 17 to 190 +/- 18 ng/ml) were markedly decreased at the 18 micrograms/day dosage, as also demonstrated for the 36 micrograms/day dosage. None of these effects was observed if vehicle was infused into the lateral ventricle instead of the NPY solution. When bilateral orchidectomy was performed 5 days after initiation of the NPY infusion (18 micrograms/day), the immediate LH and FSH rises usually seen after castration were seriously blunted.(ABSTRACT TRUNCATED AT 400 WORDS)
已知神经肽Y(NPY)参与食欲、性行为及生殖功能的中枢调节。虽然向饱足动物中枢给予NPY可强烈刺激进食,但节食或其他不利的代谢状况,如糖尿病,会使下丘脑NPY基因表达增强及NPY释放增加。大量研究表明,向大鼠中枢急性给予NPY会对促黄体生成素(LH)分泌产生多种作用,既有刺激作用,也有抑制作用。我们最近证明,向成年未受损雌性大鼠侧脑室慢性输注NPY会深刻抑制促性腺轴和促生长轴,并扰乱发情周期。此外,我们还表明,向雌性大鼠中枢慢性输注NPY会延迟其性成熟。为分析同一类型的慢性NPY处理对垂体 - 睾丸轴的影响,将45日龄的斯普拉格 - 道利雄性大鼠右侧侧脑室植入不锈钢套管。10天后,将Alzet渗透微型泵装满不同的NPY溶液,调整为每天输送6、18或36微克,连接到脑室内(icv)套管,并背侧皮下植入。在7天内评估这些处理的效果。在一个案例中,在NPY处理开始5天后对大鼠进行去势,并在2天后评估去势的效果。慢性脑室内输注NPY使食物摄入量按预期的剂量相关方式增加,从33.0±0.9(基础值)增加到53.4±3.3克/天(18微克NPY/天),体重增加(5.7±0.7到10.5±1.2克/天)。与雌性大鼠一样,NPY的这种促食欲作用导致垂体重量显著的剂量相关下降,从12.4±0.7毫克降至9.9±0.4毫克。7天的NPY输注使精囊重量(853±77降至230±31毫克)和睾丸重量(3.82±0.09降至3.18±0.15克;P = 0.003)显著降低。在18微克/天剂量时,血浆睾酮水平(231±71降至48±13纳克/分升)、LH水平(20.7±3.7降至9.1±1.2纳克/毫升)和促卵泡生成素(FSH)水平(282±17降至190±18纳克/毫升)明显降低,36微克/天剂量时也是如此。如果向侧脑室输注的是溶媒而非NPY溶液,则未观察到这些效应。在NPY输注(18微克/天)开始5天后进行双侧睾丸切除时,通常在去势后立即出现的LH和FSH升高受到严重抑制。(摘要截取自400字)