CGS-21680
茶碱
腺苷
腺苷受体
黄嘌呤
化学
焦虑症
兴奋剂
咖啡因
腺苷A1受体
腺苷受体拮抗剂
药理学
可可碱
内科学
内分泌学
受体
生物
生物化学
医学
抗焦虑药
酶
作者
Masahiro Imaizumi,S Miyazaki,K Onodera
出处
期刊:PubMed
日期:1994-11-01
卷期号:16 (9): 639-44
被引量:34
摘要
We investigated the effects of adenosine receptor antagonists, caffeine, theophylline, 8-phenyltheophylline, and 8-cyclopentyl-1,3-dipropylxanthine (DPCPX), in a light/dark test in mice. All antagonists decreased the time spent in the light zone in this test, which suggested that these compounds have anxiogenic effects. The anxiogenic effects of theophylline were reduced by pretreatment with CGS 21680, an A2-selective agonist, but not by N6-cyclopentyladenosine (CPA), an A1-selective agonist. However, the antagonism of the theophylline-induced anxiogenic effects by CGS21680 was only observed in the time spent in the light zone, and DPCPX-induced anxiogenic effects were neither reversed by CGS 21680 nor by CPA. Finally, it is notable that xanthine-derived adenosine antagonists tested here commonly showed anxiogenic effects in the light/dark test in mice. It is suggested that there is a minor contribution of adenosine receptors to these effects, although theophylline-induced anxiogenic effects were antagonized by an A2 receptor agonist.
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