Suppr超能文献

咖啡因与奥司他韦(达菲)对小鼠明暗行为和旷场行为的刺激作用。

The stimulatory effects of caffeine with oseltamivir (Tamiflu) on light-dark behavior and open-field behavior in mice.

机构信息

Department of Pharmacology, Graduate School of Pharmaceutical Sciences, Kyushu University, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.

出版信息

Neurosci Lett. 2010 Jan 22;469(2):184-8. doi: 10.1016/j.neulet.2009.11.069. Epub 2009 Dec 5.

Abstract

Abnormal behaviors and death associated with the use of oseltamivir (Tamiflu) have emerged as a major issue in influenza patients taking the drug. Here, we investigated the mechanisms underlying the effects of oseltamivir on the behavior of mice using light-dark and open-field preference tests. Oseltamivir (75 and 150 mg/kg, intraperitoneally (i.p.)) alone affected neither time spent in the open area in the light-dark preference test nor ambulation in the open-field test at 2h post-injection. However, a non-selective adenosine A(1)/A(2) receptor antagonist, caffeine (10mg/kg, i.p.) in combination with oseltamivir (150 mg/kg, i.p.) increased time spent in the open area in the light-dark preference test. This enhancement was not inhibited by a benzodiazepine receptor antagonist, flumazenil (10-20mg/kg, subcutaneously (s.c.)). Enhancement of ambulation in the open-field test was also observed when caffeine (10mg/kg, i.p.) was combined with oseltamivir (150 mg/kg, i.p.). This enhancement was inhibited by a dopamine D(2) receptor antagonist, haloperidol (0.1mg/kg, s.c.). Furthermore, an adenosine A(2) receptor antagonist, SCH58261 (3mg/kg, i.p.) in combination with oseltamivir (150 mg/kg, i.p.) increased ambulation in the open-field test, while an adenosine A(1) receptor antagonist, DPCPX (1-3mg/kg, i.p.) did not. These findings suggest that the actions of oseltamivir may involve the dopamine and adenosine systems. Our findings suggest that due to the interaction between central blockade of adenosine A(2) receptors by caffeine, and oseltamivir-induced behavioral changes, patients being treated with oseltamivir should be closely monitored.

摘要

奥司他韦(达菲)与异常行为和死亡的关联已成为流感患者使用该药物的一个主要问题。在这里,我们使用明暗偏好和旷场偏好测试研究了奥司他韦对小鼠行为的影响机制。奥司他韦(75 和 150mg/kg,腹腔内注射)单独使用,在注射后 2 小时既不影响明暗偏好测试中在开放区域的时间,也不影响旷场测试中的活动。然而,非选择性腺苷 A1/A2 受体拮抗剂咖啡因(10mg/kg,腹腔内注射)与奥司他韦(150mg/kg,腹腔内注射)联合使用,增加了明暗偏好测试中在开放区域的时间。这种增强作用不受苯二氮䓬受体拮抗剂氟马西尼(10-20mg/kg,皮下注射)的抑制。当咖啡因(10mg/kg,腹腔内注射)与奥司他韦(150mg/kg,腹腔内注射)联合使用时,旷场测试中的活动也得到增强。这种增强作用被多巴胺 D2 受体拮抗剂氟哌啶醇(0.1mg/kg,皮下注射)抑制。此外,腺苷 A2 受体拮抗剂 SCH58261(3mg/kg,腹腔内注射)与奥司他韦(150mg/kg,腹腔内注射)联合使用,增加了旷场测试中的活动,而腺苷 A1 受体拮抗剂 DPCPX(1-3mg/kg,腹腔内注射)则没有。这些发现表明,奥司他韦的作用可能涉及多巴胺和腺苷系统。我们的研究结果表明,由于咖啡因对中枢腺苷 A2 受体的阻断作用与奥司他韦引起的行为变化之间的相互作用,因此接受奥司他韦治疗的患者应密切监测。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验