Fishman J, Norton B I, Hahn E F
Proc Natl Acad Sci U S A. 1980 May;77(5):2574-6. doi: 10.1073/pnas.77.5.2574.
Treatment of male rats with a single high dose of morphine (10 mg/kg, subcutaneously) results in a dramatic suppression of brain estradiol-2-hydroxylase activity. The suppression is blocked by naloxone and is decreased upon the development of tolerance. The injection of naloxone (0.4 mg/kg) alone produces a significant increase in brain estradiol-2-hydroxylase activity over control levels. The effects of the opiate agonists and antagonists on the activity of this brain enzyme coincide in degree and direction with their effects on plasma lutropin (luteinizing hormone) concentrations. Because the 2-hydroxyestrogens were shown to induce pituitary lutropin release, the present results indicate that the action of opiates, endogenous or exogenous, on pituitary gonadotropin release can be mediated by brain catechol estrogens.
给雄性大鼠单次皮下注射高剂量吗啡(10毫克/千克)会导致脑雌二醇-2-羟化酶活性显著受抑。这种抑制作用可被纳洛酮阻断,且随着耐受性的形成而减弱。单独注射纳洛酮(0.4毫克/千克)会使脑雌二醇-2-羟化酶活性显著高于对照水平。阿片类激动剂和拮抗剂对这种脑酶活性的影响在程度和方向上与其对血浆促黄体生成素浓度的影响一致。由于已表明2-羟基雌激素可诱导垂体促黄体生成素释放,因此目前的结果表明,内源性或外源性阿片类物质对垂体促性腺激素释放的作用可能由脑儿茶酚雌激素介导。