Baumann M H, Schuster C R, Rothman R B
Clinical Psychopharmacology Section, NIDA, NIH, Baltimore, MD 21224, USA.
Drug Alcohol Depend. 1996 May;41(1):71-4. doi: 10.1016/0376-8716(96)01234-3.
The combined administration of phentermine and fenfluramine (PHEN/FEN) has been used as a treatment for obesity. Recent evidence suggests that this drug mixture may also be an effective medication for substance abuse disorders, including cocaine dependence. It is well-established that repeated high-dose fenfluramine causes serotonin (5-HT) terminal degeneration in laboratory animals, and no studies have addressed possible interactions between phentermine and fenfluramine. The purpose of the present work was to examine the effect of phentermine coadministration on fenfluramine-induced depletion of 5-HT in mouse forebrain. In addition, because of the potential for cocaine abuse in drug addicts taking PHEN/FEN as a medication, we examined the effects of PHEN/FEN on forebrain 5-HT levels in the presence or absence of cocaine. Fenfluramine (0, 3, 10, 30 mg/kg, s.c. twice daily for 4 days) caused a dose-dependent reduction in forebrain 5-HT without affecting dopamine or norepinephrine. Phentermine coadministration (7 mg/kg, s.c. twice daily for 4 days) did not significantly alter the 5-HT-depleting effect of fenfluramine. Likewise, cocaine (10 mg/kg, i.p.), administered 60 min prior to or 60 min after PHEN/FEN, had no effect on the PHEN/FEN-induced decrease in central 5-HT. The present results indicate that doses of phentermine far above those typically administered to humans do not potentiate the 5-HT-depleting effect of repeated high-dose fenfluramine. Moreover, exposure to cocaine does not significantly alter the long-term neurochemical actions of the PHEN/FEN mixture.
苯丁胺和芬氟拉明联合用药(PHEN/FEN)曾被用作治疗肥胖症的药物。最近有证据表明,这种药物组合可能也是治疗药物滥用障碍(包括可卡因成瘾)的有效药物。众所周知,反复高剂量使用芬氟拉明会导致实验动物的血清素(5-HT)终末变性,且尚无研究探讨苯丁胺和芬氟拉明之间可能存在的相互作用。本研究的目的是检验联合使用苯丁胺对芬氟拉明诱导的小鼠前脑5-HT耗竭的影响。此外,鉴于服用PHEN/FEN作为药物的吸毒者存在滥用可卡因的可能性,我们研究了在有或没有可卡因的情况下PHEN/FEN对前脑5-HT水平的影响。芬氟拉明(0、3、10、30毫克/千克,皮下注射,每日两次,共4天)导致前脑5-HT呈剂量依赖性降低,而不影响多巴胺或去甲肾上腺素。联合使用苯丁胺(7毫克/千克,皮下注射,每日两次,共4天)并未显著改变芬氟拉明的5-HT耗竭作用。同样,在PHEN/FEN给药前60分钟或给药后60分钟注射可卡因(10毫克/千克,腹腔注射),对PHEN/FEN诱导的中枢5-HT降低没有影响。目前的结果表明,远远高于通常给人类使用的苯丁胺剂量不会增强反复高剂量芬氟拉明的5-HT耗竭作用。此外,接触可卡因并不会显著改变PHEN/FEN混合物的长期神经化学作用。