Kamei C, Kitazumi K, Tsujimoto S, Yoshida T, Tasaka K
Department of Pharmacology, Faculty of Pharmaceutical Sciences, Okayama University, Japan.
J Pharmacobiodyn. 1991 Sep;14(9):509-17. doi: 10.1248/bpb1978.14.509.
The epileptogenic effects of (1R, 5S, 6S)-2-[(6,7-dihydro-5H-pyrazolo[1,2-a][1,2,4]triazolium-6- yl)]thio-6-[(R)-1-hydroxyethyl]-1-methyl-carbapenem-3-carboxylate (LJC10627), a new derivative of carbapenem were studied in comparison with those of imipenem (imipenem/cilastatin), cefazolin and penicillin G. In intraventricular injection in rats, LJC10627 caused no epileptogenic activity at a dose of 32 micrograms. In contrast, imipenem, cefazolin and penicillin G showed dose-related seizure signs, continuous rhythmic spikes or high voltage spike-wave complexes and convulsive behaviors at doses higher than 10 micrograms. After intravenous injection of LJC10627, no epileptogenic signs on the electroencephalogram (EEGs) or in behavioral symptoms were observed, even at a dose of 500 mg/kg in rats and 300 mg/kg in rabbits, respectively. By contrast, imipenem/cilastatin provoked severe seizure patterns characterized by high voltage spikes-wave complex and convulsive behavior, both in rats and rabbits, using the same doses of LJC10627. Cefazolin and penicillin G also induced obvious epileptogenic signs in both rats and rabbits after intravenous injection. From these results, it was concluded that LJC10627, unlike imipenem (imipenem/cilastatin) and cefazolin, dose not elicit epileptogenic activity, and may therefore be safely used for clinical purpose.
对碳青霉烯类新衍生物(1R, 5S, 6S)-2-[(6,7-二氢-5H-吡唑并[1,2-a][1,2,4]三唑-6-基)]硫代-6-[(R)-1-羟乙基]-1-甲基-碳青霉烯-3-羧酸酯(LJC10627)的致癫痫作用进行了研究,并与亚胺培南(亚胺培南/西司他丁)、头孢唑林和青霉素G进行比较。在大鼠脑室内注射时,LJC10627在32微克剂量下未引起致癫痫活性。相比之下,亚胺培南、头孢唑林和青霉素G在高于10微克的剂量下表现出与剂量相关的癫痫发作体征、连续节律性尖波或高电压棘慢复合波以及惊厥行为。静脉注射LJC10627后,即使在大鼠中剂量为500毫克/千克、兔子中剂量为300毫克/千克时,脑电图(EEG)或行为症状方面均未观察到致癫痫体征。相比之下,使用相同剂量的LJC10627时,亚胺培南/西司他丁在大鼠和兔子中均引发了以高电压棘慢复合波和惊厥行为为特征的严重癫痫发作模式。头孢唑林和青霉素G静脉注射后在大鼠和兔子中也诱导出明显的致癫痫体征。从这些结果得出结论,与亚胺培南(亚胺培南/西司他丁)和头孢唑林不同,LJC10627不会引发致癫痫活性,因此可能可安全用于临床。