Suppr超能文献

大鼠大脑皮层切片中嘌呤释放对钠和钙的依赖性。

Sodium and calcium dependence of purine release from rat cerebral cortical slices.

作者信息

Di Iorio P, Ballerini P, Ciccarelli R, Tacconelli L, Caciagli F

机构信息

Institute of Neuroscience, University of Chieti, Medical School, Italy.

出版信息

Pharmacol Res Commun. 1988 Jun;20(6):511-25. doi: 10.1016/s0031-6989(88)80078-x.

Abstract

Electrically evoked purine release from rat cerebral cortical slices was evaluated, using a HPLC analysis combined with radioactivity measurement of the identified fractions. Two different pools of released purines have been identified: one probably related to cell metabolism and the other strictly linked to the nervous transmission. Since a linear increase, due to the stimulation frequencies, was found for the purines released from this second pool, a possible dependence on sodium and calcium transmembrane fluxes was evaluated. Pretreatment of the slices with TTX (5 x 10(-7) M) caused only a partial inhibitory effect on purine release (50%). This effect was probably related to the drug activity on the neuronal component of slices, since TTX induces an almost complete inhibition of purine release from isolated neurons "in cultures" and does not affect it from glial cells. Verapamil (1 x 10(-4) M), a calcium-channel blocker at glial and neuronal level, and TEA (3 x 10(-2) M), a specific inhibitor of calcium-mediated potassium efflux from glial cells, administered to the slices alone or in combination, showed a partial calcium-dependence of purine release. These results suggest a glial role in modulation of electrically-evoked purine release. These cells could exert a "buffering action" that regulates the calcium-mediated potassium availability, by which neuronal activity might be influenced.

摘要

采用高效液相色谱分析结合对鉴定组分的放射性测量,评估了大鼠大脑皮质切片电诱发的嘌呤释放。已鉴定出两种不同的释放嘌呤池:一种可能与细胞代谢有关,另一种与神经传递紧密相关。由于从第二个池中释放的嘌呤随刺激频率呈线性增加,因此评估了其对钠和钙跨膜通量的可能依赖性。用TTX(5×10⁻⁷ M)预处理切片仅对嘌呤释放产生部分抑制作用(50%)。这种作用可能与药物对切片神经元成分的活性有关,因为TTX几乎完全抑制“培养的”分离神经元的嘌呤释放,而对胶质细胞的嘌呤释放没有影响。维拉帕米(1×10⁻⁴ M)是一种在胶质细胞和神经元水平上的钙通道阻滞剂,四乙铵(3×10⁻² M)是一种特异性抑制胶质细胞钙介导的钾外流的抑制剂,单独或联合应用于切片时,显示嘌呤释放存在部分钙依赖性。这些结果表明胶质细胞在调节电诱发的嘌呤释放中起作用。这些细胞可能发挥“缓冲作用”,调节钙介导的钾的可用性,借此可能影响神经元活动。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验