Mello N K, Mendelson J H, Bree M P, Ellingboe J, Skupny A S
J Pharmacol Exp Ther. 1985 Jun;233(3):588-96.
The effects of alcohol (2.5 and 3.5 g/kg) on luteinizing hormone (LH) and testosterone were studied in adult male macaque monkeys under both basal and naloxone-stimulated conditions. Integrated plasma samples were collected at 30-min intervals for 90 min before nasogastric intubation of alcohol (2.5 and 3.5 g/kg) or a sucrose control solution, isocalorically equivalent to 2.5 g/kg of alcohol. Under basal (non-naloxone-stimulated) conditions, alcohol (2.5 or 3.5 g/kg) did not change LH levels significantly from prealcohol control levels. When basal testosterone levels were normal (600-1300 ng/dl), alcohol significantly suppressed testosterone levels in a dose-dependent manner. Testosterone levels decreased by 52% (P less than .05) within 30 min after a 3.5 g/kg dose of alcohol. As average blood alcohol levels increased to 400 mg/dl and above, testosterone levels fell monotonically and remained over 70% below base-line levels (P less than .01). After administration of 2.5 g/kg alcohol, testosterone levels were significantly suppressed within 90 min (P less than .05) and remained 52 to 63% below control levels (P less than .02-.05) as average blood alcohol levels increased to 300 mg/dl. However, when basal testosterone levels were abnormally low (100-200 ng/dl), alcohol had no effect on testosterone or LH. Naloxone stimulation was used to circumvent the high incidence of abnormally low testosterone levels observed. Naloxone (0.5 mg/kg i.v.) administration 90 min after alcohol (2.5 and 3.5 g/kg) or sucrose control administration significantly increased LH levels in comparison to base line (P less than .02-.001). LH reached peak values within 60 min after naloxone administration. A significant increase in testosterone (P less than .001) was observed 90 min after naloxone administration as LH levels began to decline. Alcohol (2.5 and 3.5 g/kg) did not attenuate or delay naloxone-stimulated increases in LH and testosterone in comparison to sucrose control conditions.
研究了酒精(2.5克/千克和3.5克/千克)在基础状态和纳洛酮刺激状态下对成年雄性猕猴促黄体生成素(LH)和睾酮的影响。在经鼻胃管给予酒精(2.5克/千克和3.5克/千克)或等热量相当于2.5克/千克酒精的蔗糖对照溶液前90分钟,每隔30分钟采集一次血浆综合样本。在基础(非纳洛酮刺激)状态下,酒精(2.5克/千克或3.5克/千克)并未使LH水平与饮酒前对照水平相比发生显著变化。当基础睾酮水平正常(600 - 1300纳克/分升)时,酒精以剂量依赖方式显著抑制睾酮水平。给予3.5克/千克剂量酒精后30分钟内,睾酮水平下降了52%(P < 0.05)。随着平均血酒精水平升至400毫克/分升及以上,睾酮水平单调下降,且仍比基线水平低70%以上(P < 0.01)。给予2.5克/千克酒精后,随着平均血酒精水平升至300毫克/分升,睾酮水平在90分钟内显著受到抑制(P < 0.05),且仍比对照水平低52%至63%(P < 0.02 - 0.05)。然而,当基础睾酮水平异常低(100 - 200纳克/分升)时,酒精对睾酮或LH无影响。使用纳洛酮刺激来规避观察到的异常低睾酮水平的高发生率。在给予酒精(2.5克/千克和3.5克/千克)或蔗糖对照后90分钟静脉注射纳洛酮(0.5毫克/千克),与基线相比显著提高了LH水平(P < 0.02 - 0.001)。纳洛酮给药后60分钟内LH达到峰值。纳洛酮给药90分钟后,随着LH水平开始下降,观察到睾酮显著增加(P < 0.001)。与蔗糖对照情况相比,酒精(2.5克/千克和3.5克/千克)并未减弱或延迟纳洛酮刺激引起的LH和睾酮增加。