Kanda T, Shiozaki S, Shimada J, Suzuki F, Nakamura J
Pharmaceutical Research Laboratories, Kyowa Hakko Kogyo Co. Ltd., Shizuoka, Japan.
Eur J Pharmacol. 1994 May 2;256(3):263-8. doi: 10.1016/0014-2999(94)90551-7.
KF17837 is a novel selective adenosine A2A receptor antagonist. Oral administration of KF17837 (2.5, 10.0 and 30.0 mg/kg) significantly ameliorated the cataleptic responses induced by intracerebroventricular administration of an adenosine A2A receptor agonist, CGS 21680 (10 micrograms), in a dose-dependent manner. KF17837 also reduced the catalepsy induced by haloperidol (1 mg/kg i.p.) and by reserpine (5 mg/kg i.p.). These anticataleptic effects were exhibited dose dependently at doses from 0.625 and 2.5 mg/kg p.o., respectively. Moreover, KF17837 (0.625 mg/kg p.o.) potentiated the anticataleptic effects of a subthreshold dose of L-3,4-dihydroxyphenylalanine (L-DOPA; 25 mg/kg i.p.) plus benserazide (6.25 mg/kg i.p.). These results suggested that KF17837 is a centrally active adenosine A2A receptor antagonist and that the dopaminergic function of the nigrostriatal pathway is potentiated by adenosine A2A receptor antagonists. Furthermore, KF17837 may be a useful drug in the treatment of parkinsonism.
KF17837是一种新型选择性腺苷A2A受体拮抗剂。口服KF17837(2.5、10.0和30.0毫克/千克)能以剂量依赖的方式显著改善脑室内注射腺苷A2A受体激动剂CGS 21680(10微克)所诱导的僵住反应。KF17837还能减轻氟哌啶醇(1毫克/千克腹腔注射)和利血平(5毫克/千克腹腔注射)所诱导的僵住反应。这些抗僵住作用分别在口服剂量为0.625和2.5毫克/千克时呈剂量依赖性表现。此外,KF17837(口服0.625毫克/千克)能增强阈下剂量的L-3,4-二羟基苯丙氨酸(L-DOPA;25毫克/千克腹腔注射)加苄丝肼(6.25毫克/千克腹腔注射)的抗僵住作用。这些结果表明,KF17837是一种具有中枢活性的腺苷A2A受体拮抗剂,并且腺苷A2A受体拮抗剂能增强黑质纹状体通路的多巴胺能功能。此外,KF17837可能是治疗帕金森病的一种有用药物。