Kalra P S, Simpkins J W, Luttge W G, Kalra S P
Endocrinology. 1983 Dec;113(6):2065-71. doi: 10.1210/endo-113-6-2065.
We have earlier reported that dopamine (DA) activity in the preoptic anterior hypothalamic (POA-AH) region of castrated rats is inhibited by testosterone and accelerated by PRL. These results suggested that dopaminergic neurons may play an important role in male copulatory behavior, particularly in the attenuation of sex behavior reported to be associated with hyperprolactinemia. We have now examined the effects of severe hyperprolactinemia on the POA-AH DA activity in association with any modifications of copulatory behavior. Sexually experienced adult male rats were castrated and implanted sc with Silastic implants containing testosterone to maintain serum testosterone levels in the range found in intact rats. Hyperprolactinemia was induced by inoculation of minced MtTW15 PRL secreting pituitary tumor fragments. Copulatory behavior was assessed at weekly intervals in hyperprolactinemic and control rats. During the period of tumor growth serum PRL levels increased logarithmically. Whereas sexual activity continued to improve in control rats, there was a marked decrease in several important parameters of copulatory behavior in hyperprolactinemic rats. The most dramatic decrease occurred in the percentage of tumor-bearing rats ejaculating which decreased progressively to zero at 6 weeks after tumor inoculation. Ejaculation frequency decreased and ejaculation latency increased in tumor-bearing rats before the complete disappearance of ejaculatory behavior. The deficits in copulatory behavior of hyperprolactinemic rats were accompanied in parallel studies by significant depletions of DA concentrations in the POA-AH. Further, neuronal activity, as evidenced by the turnover rates measured by rate of loss of DA after tyrosine hydroxylase inhibition with alpha-methyl paratyrosine, was markedly augmented in the POA-AH of hyperprolactinemic rats as compared to control animals. These findings disclose a close association between the acceleration in POA-AH DA activity and the attenuation of copulatory behavior induced by hyperprolactinemia and suggest the probability of an underlying role of the POA-AH DA neurons in male sex behavior normally induced by testosterone.
我们之前报道过,去势大鼠视前区下丘脑前部(POA-AH)区域的多巴胺(DA)活性受睾酮抑制,受催乳素(PRL)促进。这些结果表明,多巴胺能神经元可能在雄性交配行为中起重要作用,尤其是在据报道与高催乳素血症相关的性行为减弱方面。我们现在研究了严重高催乳素血症对POA-AH区DA活性的影响以及与之相关的交配行为变化。将有性经验的成年雄性大鼠去势,并皮下植入含睾酮的硅橡胶植入物,以维持血清睾酮水平在完整大鼠的水平范围内。通过接种切碎的MtTW15催乳素分泌垂体肿瘤碎片诱导高催乳素血症。每周对高催乳素血症大鼠和对照大鼠的交配行为进行评估。在肿瘤生长期间,血清PRL水平呈对数增加。对照大鼠的性活动持续改善,而高催乳素血症大鼠的几个重要交配行为参数显著下降。最显著的下降发生在射精的荷瘤大鼠百分比上,在接种肿瘤后6周逐渐降至零。在射精行为完全消失之前,荷瘤大鼠的射精频率降低,射精潜伏期延长。在平行研究中,高催乳素血症大鼠交配行为的缺陷伴随着POA-AH区DA浓度的显著降低。此外,与对照动物相比,用α-甲基对酪氨酸抑制酪氨酸羟化酶后,通过DA损失率测量的周转率所证明的神经元活动在高催乳素血症大鼠的POA-AH区明显增强。这些发现揭示了POA-AH区DA活性加速与高催乳素血症诱导的交配行为减弱之间的密切关联,并提示POA-AH区DA神经元在正常由睾酮诱导的雄性性行为中可能起潜在作用。