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美沙酮和脑啡肽分解代谢抑制剂RB 101在自发吗啡戒断方面有类似的降低作用。

Similar decrease in spontaneous morphine abstinence by methadone and RB 101, an inhibitor of enkephalin catabolism.

作者信息

Ruiz F, Fournié-Zaluski M C, Roques B P, Maldonado R

机构信息

Unité de Pharmacochimie Moléculaire, U 266 INSERM, Université René Descartes, Faculté des Sciences Pharmaceutiques et Biologiques, Paris, France.

出版信息

Br J Pharmacol. 1996 Sep;119(1):174-82. doi: 10.1111/j.1476-5381.1996.tb15691.x.

Abstract
  1. The dual inhibitor of enkephalin degrading enzymes, RB 101, is able to block endogenous enkephalin metabolism completely, leading to potent antinociceptive responses potentiated by blockade of CCKB receptors. In this study we have investigated the effects induced by RB 101 given alone, or with the CCKB antagonist, PD-134,308, on a model of spontaneous morphine withdrawal and substitutive maintenance in rats. 2. Animals were chronically treated with morphine for 7 days followed, 36 h after the interruption of drug administration, by a maintenance treatment for 5 days with methadone (2 mg kg-1, i.p.), clonidine (0.025 mg kg-1, i.p.), RB 101 (40 mg kg-1, i.p.), PD-134,308 (3 mg kg-1, i.p.) or a combination of RB 101 plus PD-134,308. Several behavioural observations were made during this period in order to evaluate the acute effects as well as the consequence of chronic maintenance induced on spontaneous withdrawal by the different treatments. 3. Methadone was the most effective compound in decreasing the spontaneous withdrawal syndrome after acute administration. Both, methadone and RB 101 had similar effectiveness in reducing opiate abstinence during the period of substitutive treatment. PD-134,308 did not show any effect when administered alone and did not modify the effect of RB 101. 4. Naloxone (1 mg kg-1, s.c.) failed to precipitate any sign of withdrawal when injected at the end of the chronic maintenance treatment suggesting that, under the present conditions, methadone and RB 101 did not induce significant physical opiate-dependence. 5. The mildness of the side effects induced by chronic RB 101, suggests that systemically active inhibitors of enkephalin catabolism could represent a promising treatment in the maintenance of opiate addicts.
摘要
  1. 脑啡肽降解酶双重抑制剂RB 101能够完全阻断内源性脑啡肽代谢,通过阻断CCKB受体增强产生有效的抗伤害感受反应。在本研究中,我们研究了单独给予RB 101或与CCKB拮抗剂PD - 134,308联合使用对大鼠自发吗啡戒断和替代维持模型的影响。2. 动物用吗啡慢性治疗7天,在药物给药中断36小时后,用美沙酮(2毫克/千克,腹腔注射)、可乐定(0.025毫克/千克,腹腔注射)、RB 101(40毫克/千克,腹腔注射)、PD - 134,308(3毫克/千克,腹腔注射)或RB 101加PD - 134,308的组合进行5天的维持治疗。在此期间进行了多项行为观察,以评估不同治疗对急性效应以及慢性维持对自发戒断的影响。3. 美沙酮是急性给药后减轻自发戒断综合征最有效的化合物。美沙酮和RB 101在替代治疗期间减少阿片类药物戒断方面具有相似的效果。单独给予PD - 134,308没有显示任何效果,也没有改变RB 101的效果。4. 在慢性维持治疗结束时注射纳洛酮(1毫克/千克,皮下注射)未能引发任何戒断迹象,这表明在目前条件下,美沙酮和RB 101不会引起明显的身体阿片类药物依赖性。5. 慢性RB 101引起的副作用较轻,这表明脑啡肽分解代谢的全身活性抑制剂可能是维持阿片类药物成瘾者治疗的一个有前景的方法。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff59/1915744/7553466a2769/brjpharm00070-0186-a.jpg

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