Sun Hong-Lei, Zheng Ji-Wang, Wang Keng, Liu Rui-Ke, Liang Jian-Hui
National Institute on Drug Dependence, Peking University, Xue Yuan Road 38, Haidian District, Beijing 100083, PR China.
Life Sci. 2003 Jan 31;72(11):1221-30. doi: 10.1016/s0024-3205(02)02345-7.
Tramadol, an atypical opioid analgesic, stimulates both opiatergic and serotonergic systems. Here we have investigated the effect of tramadol in mice on 5-hydroxyptrytophan (5-HTP)-induced head twitch response (HTR), which is an animal model for the activation of the CNS 5-HT(2A) receptors in mice. Tramadol attenuated 5-HTP-induced HTR in a dose-dependent manner as morphine. Furthermore, the nonselective opioid receptor antagonists, naloxone and diprenorphine (M5050), reversed the effect of tramadol on 5-HTP-induced HTR dose-dependently. Interestingly, in contrast to the selective delta opioid receptor antagonist NTI, beta-FNA, a selective mu receptor antagonist, and nor-BNI, a selective kappa opioid receptor antagonist, antagonized the attenuation of 5-HTP-induced HTR by tramadol. In conclusion, administration of tramadol systemically inhibits 5-HTP-induced HTR in mice by activating opiatergic system in the CNS. Our findings show that mu and kappa opioid receptors, but not delta opioid receptor, play an important role in the regulation of serotonergic function in the CNS.
曲马多是一种非典型阿片类镇痛药,可刺激阿片能和5-羟色胺能系统。在此,我们研究了曲马多对小鼠5-羟色氨酸(5-HTP)诱导的头部抽搐反应(HTR)的影响,这是一种用于激活小鼠中枢神经系统5-HT(2A)受体的动物模型。曲马多与吗啡一样,以剂量依赖的方式减弱5-HTP诱导的HTR。此外,非选择性阿片受体拮抗剂纳洛酮和二丙诺啡(M5050)可剂量依赖性地逆转曲马多对5-HTP诱导的HTR的作用。有趣的是,与选择性δ阿片受体拮抗剂NTI不同,选择性μ受体拮抗剂β-FNA和选择性κ阿片受体拮抗剂nor-BNI可拮抗曲马多对5-HTP诱导的HTR的减弱作用。总之,全身给予曲马多可通过激活中枢神经系统的阿片能系统来抑制小鼠5-HTP诱导的HTR。我们的研究结果表明,μ和κ阿片受体而非δ阿片受体在中枢神经系统5-羟色胺能功能的调节中起重要作用。