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长期用咖啡因处理使小鼠对戊四氮诱发癫痫的易感性降低,腺苷A(2A)受体参与其中的证据。

Evidence for the involvement of the adenosine A(2A) receptor in the lowered susceptibility to pentylenetetrazol-induced seizures produced in mice by long-term treatment with caffeine.

作者信息

El Yacoubi Malika, Ledent Catherine, Parmentier Marc, Costentin Jean, Vaugeois Jean-Marie

机构信息

Unité de Neuropsychopharmacologie Expérimentale, F.R.E. 2735 C.N.R.S., I.F.R.M.P. 23, Faculté de Médecine et Pharmacie, 22 Boulevard Gambetta, 76183 Rouen Cedex, France.

出版信息

Neuropharmacology. 2008 Jul;55(1):35-40. doi: 10.1016/j.neuropharm.2008.04.007. Epub 2008 Apr 18.

Abstract

Long-term caffeine intake has been reported to decrease the susceptibility to convulsants in mice. Occurrence of seizures following long-term oral administration of caffeine (0.3g/l) was investigated using adenosine A(2A) receptor knockout (A(2A)R KO) and control (A(2A)R WT) mice. Clonic seizures induced by acute pentylenetetrazol (PTZ, 50mg/kg i.p.) were significantly attenuated in adenosine A(2A)R KO mice drinking only water and reduced by a 14-day caffeine treatment in adenosine A(2A)R WT mice. In addition we showed a protecting effect of a 21-day caffeine treatment in A(2A)R WT mice against kindled seizures induced by PTZ in an increasing dose schedule. Summing up, these protective effects against PTZ-induced seizures occurring when adenosine A(2A)R is absent or chronically blocked by a relevant dose of caffeine may be related to a decreased neuronal excitability.

摘要

据报道,长期摄入咖啡因可降低小鼠对惊厥剂的敏感性。使用腺苷A(2A)受体敲除(A(2A)R KO)小鼠和对照(A(2A)R WT)小鼠,研究了长期口服咖啡因(0.3g/l)后癫痫发作的情况。仅饮水的腺苷A(2A)R KO小鼠中,由急性戊四氮(PTZ,50mg/kg腹腔注射)诱导的阵挛性癫痫发作明显减轻,而腺苷A(2A)R WT小鼠经14天咖啡因处理后发作减少。此外,我们还表明,在腺苷A(2A)R WT小鼠中,21天咖啡因处理对按递增剂量方案由PTZ诱导的点燃性癫痫发作具有保护作用。总之,当腺苷A(2A)R不存在或被相关剂量的咖啡因长期阻断时,这些对PTZ诱导的癫痫发作的保护作用可能与神经元兴奋性降低有关。

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