McLaughlin C L, Baile C A
Pharmacol Biochem Behav. 1983 Aug;19(2):235-40. doi: 10.1016/0091-3057(83)90045-x.
Opioids are proposed to play a role in the control of food intake since administration of opioids increase food intake while administration of opioid antagonists decrease food intake. In these experiments responses to a new opioid antagonist, nalmefene, were measured in Zucker obese and lean rats. In obese male rats 1 mg/kg nalmefene decreased the size of the first meal after a 10-hr fast and decreased 14-hr food intake, indicating nalmefene is relatively long-acting. Administration of 1 mg/kg nalmefene daily for 7 days decreased average meal size and daily food intake and increased meal frequency; feeding responses on day 7 were similar to those on day 1, suggesting a lack of development of tolerance. Food and water intake and weight gain during a 3-week treatment period were decreased more in lean rats by low doses of nalmefene (up to 0.25 mg/kg) and more in obese rats by higher doses of nalmefene (0.50 mg/kg). These responses to a new opioid antagonist further support a possible role for opioids in the control of food intake.
由于给予阿片类药物会增加食物摄入量,而给予阿片类拮抗剂会减少食物摄入量,因此有人提出阿片类药物在控制食物摄入方面发挥作用。在这些实验中,对新型阿片类拮抗剂纳美芬的反应在肥胖 Zucker 大鼠和瘦 Zucker 大鼠中进行了测量。在肥胖雄性大鼠中,1 mg/kg 的纳美芬可减少禁食 10 小时后的第一餐食量,并减少 14 小时的食物摄入量,这表明纳美芬作用时间相对较长。每天给予 1 mg/kg 的纳美芬,持续 7 天,可减少平均餐量和每日食物摄入量,并增加进餐频率;第 7 天的进食反应与第 1 天相似,表明没有产生耐受性。在为期 3 周的治疗期内,低剂量(高达 0.25 mg/kg)的纳美芬使瘦大鼠的食物和水摄入量及体重增加减少得更多,而高剂量(0.50 mg/kg)的纳美芬使肥胖大鼠的上述指标减少得更多。对新型阿片类拮抗剂的这些反应进一步支持了阿片类药物在控制食物摄入方面可能发挥的作用。