Suppr超能文献

某些抗生素对致痫特性的比较研究,包括(1Rpi,5S,6S)-2-[(6,7-二氢-5H-吡唑并[1,2-a][1,2,4]三唑鎓-6-基)]硫代-6-[(R)-1-羟乙基]-1-甲基-碳青霉烯-3-羧酸酯(LJC10627),一种具有广谱抗菌活性的碳青霉烯类抗生素。

Comparative study of certain antibiotics on epileptogenic property, including (1Rpi, 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 carbapenem antibiotic with broad antimicrobial spectrum.

作者信息

Kamei C, Kitazumi K, Tsujimoto S, Yoshida T, Tasaka K

机构信息

Department of Pharmacology, Faculty of Pharmaceutical Sciences, Okayama University, Japan.

出版信息

J Pharmacobiodyn. 1991 Sep;14(9):509-17. doi: 10.1248/bpb1978.14.509.

Abstract

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.

摘要

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。

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