Zarrindast M R, Modabber M, Sabetkasai M
Department of Pharmacology, School of Medicine, University of Tehran, Iran.
Psychopharmacology (Berl). 1993;113(2):257-61. doi: 10.1007/BF02245707.
The effects of adenosine A1 and A2 receptors on catalepsy were studied in mice. The adenosine agonists 5-N'-ethylcarboxamide-adenosine (NECA), N6-phenylisopropyladenosine (PIA) and N6-cyclohexyladenosine (CHA) induced dose dependent catalepsy. The A1 adenosine antagonist 8-phenyltheophylline (8-PT) potentiated catalepsy induced by NECA, R-PIA and CHA. However, theophylline did not potentiate but inhibited the responses induced by NECA, R-PIA and CHA. Neither 8-PT nor theophylline alone has any effect on catalepsy in mice. It is concluded that catalepsy induced by the adenosine agonists may be due to A2 receptor stimulation and that the A1 antagonism may potentiate the response.
在小鼠中研究了腺苷A1和A2受体对僵住症的影响。腺苷激动剂5-N'-乙基甲酰胺-腺苷(NECA)、N6-苯异丙基腺苷(PIA)和N6-环己基腺苷(CHA)可诱导剂量依赖性僵住症。A1腺苷拮抗剂8-苯基茶碱(8-PT)增强了由NECA、R-PIA和CHA诱导的僵住症。然而,茶碱并未增强而是抑制了由NECA、R-PIA和CHA诱导的反应。单独使用8-PT或茶碱对小鼠僵住症均无任何影响。结论是,腺苷激动剂诱导的僵住症可能是由于A2受体刺激,并且A1拮抗作用可能增强该反应。