Tamayo L, Contreras E
Pharmacology. 1983;26(6):297-302. doi: 10.1159/000137815.
Effects of valproic acid administration on morphine analgesia and on morphine tolerance and dependence were investigated in mice. Valproate increased the reaction time to thermal stimulation in naive animals. This effect was additive with morphine when valproate was administered shortly before the analgesic. However, an antagonism was observed if a 4-hour period elapsed between valproate and morphine administration. When administered to mice receiving a sustained release preparation of morphine, valproate antagonized the development of tolerance to morphine. Valproate elicited a dual action on the abstinence signs observed after naloxone administration in morphine-treated mice. The effect consisted in a reduction of abstinence behavior if the anticonvulsant was administered a few minutes before naloxone; the same treatment increased the severity of the abstinence behavior when valproate was injected 1 h before the precipitating dose of naloxone. In this latter schedule, concomitant administration of gamma-vinyl-GABA failed to reduce the severity of the convulsions observed during the abstinence syndrome. These results suggest that valproate is metabolized to a compound responsible for decreased analgesia and intensified withdrawal signs.
在小鼠中研究了丙戊酸给药对吗啡镇痛、吗啡耐受性和依赖性的影响。丙戊酸盐增加了未用药动物对热刺激的反应时间。当在镇痛剂给药前不久给予丙戊酸盐时,这种作用与吗啡具有相加性。然而,如果丙戊酸盐和吗啡给药之间间隔4小时,则观察到拮抗作用。当给予接受吗啡缓释制剂的小鼠时,丙戊酸盐拮抗对吗啡耐受性的发展。丙戊酸盐对吗啡治疗的小鼠给予纳洛酮后观察到的戒断症状产生双重作用。如果在纳洛酮给药前几分钟给予抗惊厥药,其作用在于减少戒断行为;当在引发剂量的纳洛酮前1小时注射丙戊酸盐时,相同的处理增加了戒断行为的严重程度。在后一种给药方案中,同时给予γ-乙烯基-GABA未能减轻戒断综合征期间观察到的惊厥严重程度。这些结果表明,丙戊酸盐代谢为一种导致镇痛作用减弱和戒断症状加重的化合物。