Morales Melissa, Anderson Rachel I, Spear Linda P, Varlinskaya Elena I
Center for Development and Behavioral Neuroscience, Department of Psychology, Binghamton University, P.O. Box 6000, Binghamton, New York, 13902-6000.
Dev Psychobiol. 2014 May;56(4):700-12. doi: 10.1002/dev.21137. Epub 2013 Jun 10.
The kappa opioid receptor (KOR) antagonist, nor-binaltorphimine (nor-BNI), was used to investigate the role of the KOR system in mediating ethanol intake. On P25 (adolescent) or P67 (adult) male and female rats were individually housed and given ad libitum access to food and water. The experimental procedure was initiated on P28 or P70: animals were given 30 min/day access to a 10% ethanol/supersaccharin solution every other day (3 baseline exposures). On the day after the final baseline test, rats were injected with nor-BNI (0, 2.5, 5, 10 mg/kg), with testing initiated 24 hr later (30-min access every other day, 3 test exposures). Nor-BNI (10 mg/kg) increased ethanol intake in adult males, whereas the same dose decreased intake in adult females, suggesting pronounced sex differences in KOR-associated mediation of ethanol intake in adulthood. There was no impact of nor-BNI in adolescent animals of either sex, suggesting that the KOR may play less of a role in modulating ethanol intake during adolescence.
κ阿片受体(KOR)拮抗剂诺-纳曲酮(nor-BNI)被用于研究KOR系统在介导乙醇摄入中的作用。在出生后第25天(青春期)或第67天(成年期),将雄性和雌性大鼠单独饲养,并给予自由采食和饮水的机会。实验程序于出生后第28天或第70天开始:每隔一天给予动物30分钟接触10%乙醇/超级糖精溶液的机会(3次基线暴露)。在最后一次基线测试后的第二天,给大鼠注射诺-纳曲酮(0、2.5、5、10毫克/千克),24小时后开始测试(每隔一天30分钟接触,3次测试暴露)。诺-纳曲酮(10毫克/千克)增加了成年雄性大鼠的乙醇摄入量,而相同剂量则降低了成年雌性大鼠的摄入量,这表明成年期KOR相关的乙醇摄入介导存在明显的性别差异。诺-纳曲酮对任何性别的青春期动物均无影响,这表明KOR在调节青春期乙醇摄入中可能发挥的作用较小。