Mello N K, Mendelson J H, Kelly M, Diaz-Migoyo N, Sholar J W
Alcohol and Drug Abuse Research Center, McLean Hospital-Harvard Medical School, Belmont, MA 02178, USA.
J Pharmacol Exp Ther. 1997 Apr;281(1):70-83.
Clinical studies suggest that cocaine disrupts reproductive function, but because cocaine abusers often abuse opiates and alcohol, it has been difficult to determine the contribution of cocaine alone. The effects of chronic cocaine self-administration on menstrual cycle duration and basal levels of progesterone were examined in eight female rhesus monkeys and compared with the effects of occasional administration of single cocaine doses (0.4 or 0.8 mg/kg) in six otherwise drug-free controls. All monkeys had normal ovulatory menstrual cycles before cocaine exposure. Monkeys self-administered cocaine (0.10 mg/kg/injection) and food (1 gm banana pellets) in 4 daily sessions on a second-order schedule (fixed ratio 2 [variable ratio 16:S]). Cocaine intake was limited to 8 mg/kg/day. During the first cocaine exposure (256-776 days), monkeys self-administered 3.51 (+/- 0.77) to 7.41 (+/- 0.27) mg/kg/day. During the second cocaine exposure (103-623 days), monkeys self-administered 6.18 (+/- 0.77) to 7.41 (+/- 0.27) mg/kg/day. In these prospective longitudinal studies, 48% of the menstrual cycles were of abnormal duration in the cocaine self-administration group, whereas only 6% of the menstrual cycles were abnormal in the control group. There were 19 episodes of amenorrhea (61-190 days of no menses). During cocaine self-administration, approximately one-third of the menstrual cycles were anovulatory with low mid-luteal progesterone levels of 2.04 (+/- 0.6) to 4.13 (+/- 0.5) ng/ml. Over 25% of menstrual cycles were anovulatory during cocaine withdrawal with mid-luteal progesterone levels below 5 ng/ml. These data indicate that chronic cocaine exposure can disrupt the menstrual cycle in rhesus monkeys and that menstrual cycle abnormalities often persist during cocaine withdrawal. These data are consistent with clinical studies and reports of cocaine-induced disruption of the estrous cycle in rodents.
临床研究表明,可卡因会扰乱生殖功能,但由于可卡因滥用者常常同时滥用阿片类药物和酒精,因此很难确定仅可卡因自身所产生的影响。在八只雌性恒河猴身上研究了长期自我给药可卡因对月经周期时长和孕酮基础水平的影响,并与六只未使用其他药物的对照猴偶尔单次注射可卡因剂量(0.4或0.8毫克/千克)的影响进行了比较。在接触可卡因之前,所有猴子的排卵月经周期均正常。猴子按照二级程序(固定比例2[可变比例16:S]),每天分4次自我给药可卡因(0.10毫克/千克/注射)和食物(1克香蕉颗粒)。可卡因摄入量限制在8毫克/千克/天。在首次接触可卡因期间(256 - 776天),猴子每天自我给药3.51(±0.77)至7.41(±0.27)毫克/千克。在第二次接触可卡因期间(103 - 623天),猴子每天自我给药6.18(±0.77)至7.41(±0.27)毫克/千克。在这些前瞻性纵向研究中,可卡因自我给药组中48%的月经周期时长异常,而对照组中只有6%的月经周期异常。出现了19次闭经情况(停经61 - 190天)。在自我给药可卡因期间,大约三分之一的月经周期无排卵,黄体中期孕酮水平较低,为2.04(±0.6)至4.13(±0.5)纳克/毫升。在停用可卡因期间,超过25%的月经周期无排卵,黄体中期孕酮水平低于5纳克/毫升。这些数据表明,长期接触可卡因会扰乱恒河猴的月经周期,且月经周期异常在停用可卡因期间常常持续存在。这些数据与临床研究以及关于可卡因导致啮齿动物发情周期紊乱的报告一致。