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TRK-820是一种选择性κ阿片受体激动剂,能有效改善帕金森病大鼠模型中左旋多巴诱导的运动障碍症状。

TRK-820, a selective kappa opioid receptor agonist, could effectively ameliorate L-DOPA-induced dyskinesia symptoms in a rat model of Parkinson's disease.

作者信息

Ikeda Ken, Yoshikawa Satoru, Kurokawa Takahiro, Yuzawa Natsumi, Nakao Kaoru, Mochizuki Hidenori

机构信息

Toray Industries Inc, Pharmaceutical Research Laboratories, Kamakura, Kanagawa, Japan.

出版信息

Eur J Pharmacol. 2009 Oct 12;620(1-3):42-8. doi: 10.1016/j.ejphar.2009.08.013. Epub 2009 Aug 15.

Abstract

Long-term therapy with L-3,4-dihydroxyphenylalanine (L-DOPA) in parkinsonian patients is known to lead to dyskinesia within a few years, and repeated administration of L-DOPA is also likely to alter the expression of kappa opioid receptors in the basal ganglia, especially the striatum and substantia nigra pars reticulata, suggesting that kappa opioid receptors might be deeply involved in motor functions. Therefore, effects of TRK-820 ((E)-N-[17-(cyclopropylmethyl)-4,5alpha-epoxy-3,14-dihydroxymorphinan-6beta-yl]-3-(furan-3-yl)-N-methylprop-2-enamide monohydrochloride), a selective kappa opioid receptor agonist, were investigated on rotational behavior in unilateral 6-hydroxydopamine (6-OHDA)-treated rats (hemi-parkinsonian rats) and on L-DOPA-induced dyskinesia produced by administering L-DOPA to hemi-parkinsonian rats for 3 weeks (dyskinesia rats). A single administration of subcutaneous TRK-820 significantly increased spontaneous ipsilateral rotational behavior of hemi-parkinsonian rats at 30 microg/kg though the efficacy was moderate and also significantly inhibited L-DOPA-induced dyskinesia at 10 and 30 microg/kg; this inhibition was reversed in the presence of nor-binaltorphimine, a kappa opioid receptor antagonist. In vivo microdialysis study, TRK-820 (30 microg/kg, s.c.) significantly inhibited L-DOPA-derived extracellular dopamine content in the 6-OHDA-treated striatum in dyskinesia rats, but not in hemi-parkinsonian rats. Moreover, the development of L-DOPA-induced dyskinesia was suppressed by the 3-week co-administration of TRK-820 (3 and 10 microg/kg, s.c.) with L-DOPA. These results have suggested that TRK-820 ameliorates L-DOPA-induced dyskinesia with a moderate anti-parkinsonian effect by inhibiting L-DOPA-induced excessive dopamine release through kappa opioid receptors only in dyskinesia rats; therefore, TRK-820 is expected to become a useful agent for the treatment of L-DOPA-induced dyskinesia.

摘要

已知帕金森病患者长期使用L-3,4-二羟基苯丙氨酸(L-DOPA)治疗会在几年内导致运动障碍,并且重复给予L-DOPA也可能改变基底神经节中κ阿片受体的表达,尤其是纹状体和黑质网状部,这表明κ阿片受体可能与运动功能密切相关。因此,研究了选择性κ阿片受体激动剂TRK-820((E)-N-[17-(环丙基甲基)-4,5α-环氧-3,14-二羟基吗啡喃-6β-基]-3-(呋喃-3-基)-N-甲基丙烯酰胺盐酸盐)对单侧6-羟基多巴胺(6-OHDA)处理的大鼠(半帕金森病大鼠)旋转行为以及对给半帕金森病大鼠连续3周给予L-DOPA所产生的L-DOPA诱导的运动障碍(运动障碍大鼠)的影响。皮下单次给予TRK-820在30μg/kg时显著增加了半帕金森病大鼠的自发性同侧旋转行为,尽管效果中等,并且在10和30μg/kg时也显著抑制了L-DOPA诱导的运动障碍;在κ阿片受体拮抗剂去甲纳曲酮存在的情况下,这种抑制作用被逆转。在体内微透析研究中,TRK-820(30μg/kg,皮下注射)显著抑制了运动障碍大鼠6-OHDA处理的纹状体中L-DOPA衍生的细胞外多巴胺含量,但对半帕金森病大鼠没有影响。此外,TRK-820(3和10μg/kg,皮下注射)与L-DOPA共同给药3周可抑制L-DOPA诱导的运动障碍的发展。这些结果表明,TRK-820通过仅在运动障碍大鼠中通过κ阿片受体抑制L-DOPA诱导的过量多巴胺释放,从而改善L-DOPA诱导的运动障碍并具有适度的抗帕金森病作用;因此,TRK-820有望成为治疗L-DOPA诱导的运动障碍的有用药物。

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