Planas E, Sánchez S, Rodriguez L, Pol O, Puig M M
Department of Pharmacology, University of Barcelona, Odontology School, Feixa LLarga s/n, Hospitalet de LLobregat, Barcelona, Spain.
Pharmacology. 2000 Apr;60(3):121-7. doi: 10.1159/000028356.
We evaluated the anti-edema/antinociceptive effects of subcutaneous free and liposomal morphine in rats with carrageenan-induced inflammation of the paw. We assessed antinociception by the paw pressure test and edema by plethysmography. Unilamellar liposomes (150-200 nm) with 0.3% morphine hydrochloride were used; encapsulation significantly reduced the rate for release of morphine in vitro. During inflammation, the antinociceptive potency of free, but not liposomal morphine increased 2.5 times; moreover, duration of the effects was prolonged by encapsulation (p < 0.001). The anti-edema effects of liposomal morphine were more pronounced (p < 0. 001) and of longer duration (p < 0.05). All the effects were reversed by naloxone. The results show that morphine encapsulation enhances the anti-edema effects and prolongs antinociception.
我们评估了皮下注射游离吗啡和脂质体吗啡对角叉菜胶诱导的大鼠爪部炎症的抗水肿/抗伤害感受作用。我们通过爪部压力试验评估抗伤害感受,通过体积描记法评估水肿。使用了含有0.3%盐酸吗啡的单层脂质体(150 - 200纳米);包封显著降低了吗啡在体外的释放速率。在炎症期间,游离吗啡而非脂质体吗啡的抗伤害感受效能增加了2.5倍;此外,包封延长了作用持续时间(p < 0.001)。脂质体吗啡的抗水肿作用更显著(p < 0.001)且持续时间更长(p < 0.05)。所有作用均被纳洛酮逆转。结果表明,吗啡包封增强了抗水肿作用并延长了抗伤害感受。