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氯胺酮和吗啡在某些药理和生化效应方面存在交叉耐受性。

Cross tolerance between ketamine and morphine to some pharmacological and biochemical effects.

作者信息

De Simoni M G, Giglio R, Dal Toso G, Conforti I, Algeri S

出版信息

Neuropharmacology. 1985 Jun;24(6):541-5. doi: 10.1016/0028-3908(85)90060-7.

Abstract

Whether morphine and ketamine induced cross-tolerance to some of their common pharmacological and biochemical effects, namely analgesia and enhancement of metabolites of dopamine (DA) in the striatum and limbic area of the rat was analysed. Ketamine was given at the dose of 100 mg/kg, twice a day for 8 days. After this treatment, a challenge dose of morphine (15 mg/kg, i.p.) still induced analgesia comparable to that induced by morphine alone, showing no cross-tolerance to this effect. In contrast, the challenge dose of morphine given to ketamine-tolerant rats no longer enhanced metabolism of DA, indicating the appearance of cross-tolerance to this effect. A high degree of tolerance to morphine was obtained after the subcutaneous implantation of rats with pellets of morphine; a challenge dose of ketamine to morphine-tolerant rats induced marked analgesia, with no cross-tolerance to this pharmacological effect, while cross-tolerance was present to the biochemical effect. The existence of a high degree of reciprocal cross-tolerance in both areas and on both metabolites of DA is consistent with the hypothesis of action at a common receptor; the lack of cross-tolerance to the analgesic effect indicates that analgesia is achieved by a different mechanism for the two drugs.

摘要

分析了吗啡和氯胺酮是否会对它们的一些常见药理和生化作用产生交叉耐受性,即对大鼠纹状体和边缘区的镇痛作用以及多巴胺(DA)代谢产物的增强作用。氯胺酮以100mg/kg的剂量给药,每天两次,共8天。经过这种处理后,一剂挑战剂量的吗啡(15mg/kg,腹腔注射)仍能诱导出与单独使用吗啡时相当的镇痛效果,表明对这种作用没有交叉耐受性。相比之下,给予氯胺酮耐受大鼠的挑战剂量吗啡不再增强DA的代谢,表明对这种作用出现了交叉耐受性。在大鼠皮下植入吗啡丸剂后获得了对吗啡的高度耐受性;给予吗啡耐受大鼠一剂挑战剂量的氯胺酮可诱导出明显的镇痛作用,对这种药理作用没有交叉耐受性,而对生化作用则存在交叉耐受性。在这两个区域以及DA的两种代谢产物上都存在高度的相互交叉耐受性,这与作用于共同受体的假说一致;对镇痛作用缺乏交叉耐受性表明这两种药物通过不同的机制实现镇痛。

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