Takahashi M, Tokuyama S
Department of Pharmacoinformatics, Faculty of Pharmaceutical Sciences, Nagasaki University, Japan.
Methods Find Exp Clin Pharmacol. 1998 Jan-Feb;20(1):77-84. doi: 10.1358/mf.1998.20.1.485635.
Pharmacological and physiological effects of ginseng on actions induced by opioids and psychostimulants are summarized. Analgesic effects of opioids, such as morphine and U-50, 488H, were blocked by ginseng in a nonopioid dependent manner. Furthermore, ginseng inhibited the tolerance to and dependence on morphine, and eliminated the suppressive effect of the development of morphine tolerance by coexposure to footshock stress, but not psychological stress. On the other hand, behavior sensitization (reverse tolerance to their ambulation-accelerating effect) to morphine, methamphetamine and cocaine was also inhibited by ginseng. Interestingly, ginseng also inhibited the appearance of the recurrent phenomenon (reappearance of the sensitized state was observed at the time of readministration of methamphetamine and cocaine even after a 30-day discontinuation of drug administration) of the effect of methamphetamine and cocaine. The conditioned place preference of methamphetamine and cocaine was completely blocked by ginseng. These findings provide evidence that ginseng may be useful clinically for the prevention of abuse and dependence of opioids and psychostimulants.
人参对阿片类药物和精神兴奋剂所致行为的药理及生理作用进行了综述。人参以非阿片类药物依赖的方式阻断了吗啡和U - 50、488H等阿片类药物的镇痛作用。此外,人参抑制了对吗啡的耐受性和依赖性,并消除了通过同时暴露于足部电击应激而非心理应激所产生的对吗啡耐受性发展的抑制作用。另一方面,人参也抑制了对吗啡、甲基苯丙胺和可卡因的行为敏化(对其行走加速作用的反向耐受性)。有趣的是,人参还抑制了甲基苯丙胺和可卡因作用的复发现象(即使在停药30天后再次给予甲基苯丙胺和可卡因时,仍观察到致敏状态的再次出现)。人参完全阻断了甲基苯丙胺和可卡因的条件性位置偏爱。这些发现提供了证据,表明人参在临床上可能有助于预防阿片类药物和精神兴奋剂的滥用及依赖。