新型碳青霉烯类药物帕尼培南/倍他米酮对家兔的神经毒性:与中枢神经系统浓度的关系

A Kurihara, M Hisaoka, N Mikuni, K Kamoshida
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引用次数: 9

摘要

比较了新型碳青霉烯类抗生素帕尼培南/倍他米酮(PAPM/BP)与亚胺培南/西司他汀(IPM/CS)的神经毒性电位。测定癫痫发作时脑脊液中药物浓度及药物在中枢神经系统中的分布。致痫性反应与脑脊液中药物水平相关,但与循环血浆中药物水平无关。致痫性脑电图活动开始时脑脊液中PAPM的浓度几乎是IPM的两倍,表明PAPM的神经毒性活性约为IPM的一半。此外,就致痫性脑电图活动的发生率而言,在1.0-1.2 g/kg剂量范围内,PAPM/BP的毒性低于IPM/CS。静脉滴注PAPM/BP后脑脊液和脑细胞外液中PAPM的浓度与IPM/CS后IPM的浓度相当,表明两种抗生素在中枢神经系统中的分布特征相似。从这些药理作用和药物分布结果来看,PAPM/BP的神经毒性小于IPM/CS的一半。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Neurotoxicity of panipenem/betamipron, a new carbapenem, in rabbits: correlation to concentration in central nervous system.

The neurotoxic potential of panipenem/betamipron (PAPM/BP), a new carbapenem antibiotic, was compared with that of imipenem/cilastatin (IPM/CS). The drug concentration in cerebrospinal fluid (CSF) at the onset of epileptogenic electroencephalographic (EEG)-activity and the drug distribution into the central nervous system (CNS) were evaluated. Epileptogenic reactions correlated well with drug levels in CSF, but not with drug levels in circulating plasma. The concentration of PAPM in CSF at the onset of epileptogenic EEG-activity was almost twice that of IPM, suggesting that neurotoxic activity of PAPM is about half that of IPM. In addition, in terms of incidence percent for the epileptogenic EEG-activity, PAPM/BP was found to be less toxic than IPM/CS within the dose of 1.0-1.2 g/kg. Concentrations of PAPM in CSF and brain extracellular fluid after PAPM/BP i.v. infusion were comparable with those of IPM after IPM/CS infusion, indicating the similar characteristics of distribution into the CNS for the two antibiotics. From these results of pharmacologic effects and drug distributions, it is suggested that the neurotoxicity of PAPM/BP is less than half that of IPM/CS.

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