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头孢菌素在大鼠中的致痫活性及其构效关系。

Epileptogenic activity of cephalosporins in rats and their structure-activity relationship.

作者信息

Kamei C, Sunami A, Tasaka K

出版信息

Epilepsia. 1983 Aug;24(4):431-9. doi: 10.1111/j.1528-1157.1983.tb04913.x.

Abstract

The epileptogenic properties of 10 cephalosporins and penicillin G were compared by intraventricular application to rats. At doses greater than 32 micrograms per head, cefazolin provoked tremendous seizure signs, a spike-and-wave complex appeared in close succession for more than 30 min, and severe convulsions were observed repeatedly. Reactions to cefotiam, ceftezole, and cephaloridine were almost equal to reactions to penicillin. No epileptogenic signs were observed on EEGs, and no behavioral symptoms were observed after administration of 1,000 micrograms of cephalexin and cephradine per head. Reactions to cephapirin, cefmetazole, cephalothin, and ceftizoxime exhibited less marked epileptogenic features; activity was diminished in that order on EEGs and in behavioral signs. Compounds substituted with two different heterocyclic rings at position 7 (R1) and position 3 (R2) of 7-aminocephalosporanic acid were potent in producing epileptogenic signs both on EEGs and in behaviors. Compounds substituted with a heterocyclic ring at either position of 7-aminocephalosporanic acid were less potent. Compounds such as ceftizoxime, cephalexin, and cephradine, substituted at R2 with small groups, were almost incapable of producing epileptogenic activity. This may indicate that the substitution of a heterocyclic ring at position 3 will provoke the convulsive actions.

摘要

通过向大鼠脑室内给药,比较了10种头孢菌素和青霉素G的致癫痫特性。当剂量大于每只32微克时,头孢唑林引发剧烈的癫痫症状,出现尖波和慢波复合波并持续超过30分钟,且反复观察到严重惊厥。头孢替安、头孢替唑和头孢噻啶的反应与青霉素的反应几乎相同。每只给予1000微克头孢氨苄和头孢拉定后,脑电图上未观察到致癫痫迹象,也未观察到行为症状。头孢匹林、头孢美唑、头孢噻吩和头孢唑肟的反应表现出不太明显的致癫痫特征;脑电图和行为体征的活性按该顺序降低。在7-氨基头孢烷酸的7位(R1)和3位(R2)被两个不同杂环取代的化合物在脑电图和行为上均具有很强的致癫痫迹象。在7-氨基头孢烷酸的任一位置被一个杂环取代的化合物活性较低。在R2位被小基团取代的化合物,如头孢唑肟、头孢氨苄和头孢拉定,几乎不能产生致癫痫活性。这可能表明在3位取代杂环会引发惊厥作用。

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