Suzuki T, Fukagawa Y, Yoshii T, Yanaura S
Department of Pharmacology, Hoshi University, Tokyo, Japan.
Life Sci. 1988;42(26):2729-37. doi: 10.1016/0024-3205(88)90250-0.
Morphine dependence was induced by treatment with morphine-admixed food (0.25mg/g of food) for 7 days. Withdrawal was precipitated by injecting naloxone (0.5mg/kg, s.c.). Rats treated with morphine exhibited body weight loss upon the naloxone injection. When morphine-dependent rats were injected subcutaneously with morphine, codeine, meperidine and pentazocine 30 min before the naloxone injection, these drugs significantly suppressed the naloxone-precipitated loss of body weight in a dose-dependent manner. However, body weight loss induced through coadministration of naloxone and Mr-2266 BS were not suppressed by morphine pretreatment. These results suggest that opioids protect against naloxone-precipitated loss of body weight, and that mu and kappa opiate receptors play an important role in the protection against naloxone-precipitated withdrawal.
通过用含吗啡的食物(0.25毫克/克食物)处理7天来诱导吗啡依赖。通过注射纳洛酮(0.5毫克/千克,皮下注射)引发戒断反应。注射纳洛酮后,用吗啡处理的大鼠出现体重减轻。当在注射纳洛酮前30分钟给吗啡依赖的大鼠皮下注射吗啡、可待因、哌替啶和喷他佐辛时,这些药物以剂量依赖的方式显著抑制了纳洛酮引发的体重减轻。然而,纳洛酮与Mr-2266 BS共同给药诱导的体重减轻并未被吗啡预处理所抑制。这些结果表明,阿片类药物可防止纳洛酮引发的体重减轻,并且μ和κ阿片受体在防止纳洛酮引发的戒断反应中起重要作用。