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首页> 外文期刊>Neurochemical Research >Differential Pharmacological Actions of Methadone and Buprenorphine in Human Embryonic Kidney 293 Cells Coexpressing Human μ-Opioid and Opioid Receptor-Like 1 Receptors
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Differential Pharmacological Actions of Methadone and Buprenorphine in Human Embryonic Kidney 293 Cells Coexpressing Human μ-Opioid and Opioid Receptor-Like 1 Receptors

机译:美沙酮和丁丙诺啡在共表达人μ阿片和类阿片受体样1受体的人胚肾293细胞中的差异药理作用

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摘要

Methadone and buprenorphine are used in maintenance therapy for heroin addicts. In this study, we compared their effects on adenylate cyclase (AC) activity in human embryonic kidney (HEK) 293 cells stably overexpressing human μ-opioid receptor (MOR) and nociceptin/opioid receptor-like 1 receptor (ORL1) simultaneously. After acute exposure, methadone inhibited AC activity; however, buprenorphine induced compromised AC inhibition. When naloxone was introduced after 30 min incubation with methadone, the AC activity was enhanced. This was not observed in the case of buprenorphine. Enhancement of the AC activity was more significant when the incubation lasted for 4 h, and prolonged exposure to buprenorphine elevated the AC activity as well. The removal of methadone and buprenorphine by washing also obtained similar AC superactivation as that revealed by naloxone challenge. The study demonstrated that methadone and buprenorphine exert initially different yet eventually convergent adaptive changes of AC activity in cells coexpressing human MOR and ORL1 receptors.
机译:美沙酮和丁丙诺啡用于海洛因成瘾者的维持治疗。在这项研究中,我们比较了它们对稳定稳定表达人μ阿片受体(MOR)和伤害感受素/类阿片受体样1受体(ORL1)的人胚胎肾脏(HEK)293细胞中腺苷酸环化酶(AC)活性的影响。急性暴露后,美沙酮抑制了AC活性。但是,丁丙诺啡可导致受损的AC抑制。与美沙酮一起孵育30分钟后引入纳洛酮后,AC活性增强。在丁丙诺啡中未观察到此现象。孵育持续4小时后,AC活性的增强更为显着,长时间暴露于丁丙诺啡也会提高AC活性。通过洗涤除去美沙酮和丁丙诺啡也获得了与纳洛酮激发所揭示的相似的AC超活化。该研究表明,美沙酮和丁丙诺啡最初在共表达人类MOR和ORL1受体的细胞中发挥了不同的作用,但最终收敛了AC活性。

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