Schulz R, Wilhelm A, Pirke K M, Herz A
Life Sci. 1982;31(20-21):2167-70. doi: 10.1016/0024-3205(82)90110-2.
The effect of naloxone or clonidine, on serum levels of luteinizing hormone (LH) was investigated in immature male and female rats. After birth, naloxone progressively increased serum LH concentrations in females, reaching maximal effects on the 10th to the 16th day of life. Males failed to respond to naloxone during this period. Clonidine only moderately increased LH in immature female rats. However, immature males displayed a high sensitivity to this alpha 2-adrenoceptor agonist. The secretion pattern of LH caused by clonidine during the first two weeks of life resembled that evoked by naloxone in females. Thus, regulation of LH secretion of immature female rats involves endorphins, while in males control of LH-release is by adrenergic mechanisms.
在未成熟的雄性和雌性大鼠中研究了纳洛酮或可乐定对血清促黄体生成素(LH)水平的影响。出生后,纳洛酮使雌性大鼠血清LH浓度逐渐升高,在出生后第10至16天达到最大效应。在此期间,雄性大鼠对纳洛酮无反应。可乐定仅使未成熟雌性大鼠的LH适度增加。然而,未成熟雄性大鼠对这种α2肾上腺素能受体激动剂表现出高度敏感性。出生后前两周可乐定引起的LH分泌模式与雌性大鼠中纳洛酮引起的相似。因此,未成熟雌性大鼠LH分泌的调节涉及内啡肽,而雄性大鼠中LH释放的控制则是通过肾上腺素能机制。