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某些β-内酰胺衍生物的致痫活性:构效关系

Epileptogenic activity of some beta-lactam derivatives: structure-activity relationship.

作者信息

De Sarro A, De Sarro G B, Ascioti C, Nisticó G

机构信息

Institute of Pharmacology, University of Messine, Italy.

出版信息

Neuropharmacology. 1989 Apr;28(4):359-65. doi: 10.1016/0028-3908(89)90030-0.

Abstract

The epileptogenic activity of several derivatives of beta-lactam was compared following their intracerebroventricular administration in rats. At a dose of 0.033 mumol/kg cefazolin was the most powerful epileptogenic compound among the drugs tested; dramatic seizure signs (nodding, clonic convulsions and sometimes escape responses) were observed repeatedly. It was approximately three times more potent than benzylpenicillin and other similar compounds, such as ceftriaxone, cefoperazone and cefamandole. No epileptogenic signs were observed with equimolar doses of cefotaxime, cefonicid and ceftizoxime. All these derivatives differ from the substitution at position 3 and at position 7 of 7-aminocephalosporanic acid. The more convulsant compounds (i.e. cefazolin and ceftezole) are both derivatives of tetrazol and show a marked similarity with pentylentetrazol. In addition, aztreonam, a compound having only the beta-lactam ring substituted with a heterocyclic ring at the 4 position, possessed convulsant properties like those of cefoperazone and cefamandole. This suggests that the beta-lactam ring is able to produce epileptogenic activity and it seems likely that substitutions at the 7-aminocephalosporanic or 6-aminopenicillanic acid may increase or reduce the epileptogenic properties of beta-lactam derivatives.

摘要

在大鼠脑室内注射几种β-内酰胺衍生物后,比较了它们的致痫活性。在剂量为0.033 μmol/kg时,头孢唑林是所测试药物中致痫性最强的化合物;反复观察到明显的癫痫发作迹象(点头、阵挛性惊厥,有时还有逃避反应)。其效力约为苄青霉素和其他类似化合物(如头孢曲松、头孢哌酮和头孢孟多)的三倍。等摩尔剂量的头孢噻肟、头孢尼西和头孢唑肟未观察到致痫迹象。所有这些衍生物在7-氨基头孢烷酸的3位和7位的取代基不同。致惊厥性更强的化合物(即头孢唑林和头孢替唑)都是四氮唑衍生物,与戊四氮有明显相似性。此外,氨曲南是一种仅在4位被杂环取代的β-内酰胺环化合物,具有与头孢哌酮和头孢孟多类似的惊厥特性。这表明β-内酰胺环能够产生致痫活性,并且7-氨基头孢烷酸或6-氨基青霉烷酸上的取代可能会增加或降低β-内酰胺衍生物的致痫特性。

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