Smits S E
Res Commun Chem Pathol Pharmacol. 1976 Dec;15(4):689-96.
Single-dose physical dependence on morphine, as indicated by the mouse withdrawal jumping test, was reduced in a dose-related fashion by co-administration of naloxone. In the same dose range, naloxone also antagonized the antinociceptive effect of morphine in the mouse writhing test. Dose-response data revealed essentially the same ED50's for naloxone in both tests. These results indicate that naloxone does indeed block the development of morphine-induced single-dose physical dependence in mice and that it does so as effectively as it blocks morphine-induced inhibition of writhing.
如小鼠戒断跳跃试验所示,通过联合使用纳洛酮,吗啡单剂量身体依赖性以剂量相关方式降低。在相同剂量范围内,纳洛酮在小鼠扭体试验中也拮抗了吗啡的镇痛作用。剂量反应数据显示,在两项试验中纳洛酮的半数有效剂量(ED50)基本相同。这些结果表明,纳洛酮确实能阻断小鼠体内吗啡诱导的单剂量身体依赖性的发展,而且其阻断效果与阻断吗啡诱导的扭体抑制效果一样有效。