J-147 a Novel Hydrazide Lead Compound to Treat Neurodegeneration: CeeTox Safety and Genotoxicity Analysis.

Paul A Lapchak, Rene Bombien, Padmesh S Rajput
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引用次数: 6

Abstract

J-147 is a broad spectrum neuroprotective phenyl hydrazide compound with significant neurotrophic properties related to the induction of brain-derived neurotrophic factor (BDNF). Because this molecule is pleiotropic, it may have substantial utility in the treatment of a wide range of neurodegenerative diseases including acute ischemic stroke (AIS), traumatic brain injury(TBI), and Alzheimer's disease(AD) where both neuroprotection and neurotrophism would be beneficial. Because of the pleiotropic actions of J-147, we sought to determine the safety profile of the drug using multiple assay analysis. For CeeTox analyses, we used a rat hepatoma cell line (H4IIE) resulted in estimated CTox value (i.e.: sustained concentration expected to produce toxicity in a 14 day repeat dosing study) of 90 μM for J-147. The CeeTox panel shows that J-147 produced some adverse effects on cellular activities, in particular mitochondrial function, but only with high concentrations of the drug. J-147 was also not genetoxic with or without Aroclor-1254 treatment. For J-147, based upon extensive neuroprotection assay data previously published, and the CeeTox assay (CTox value of 90 μM) in this study, we estimated in vitro neuroprotection efficacy (EC50 range 0.06-0.115 μM)/toxicity ratio is 782.6-1500 fold and the neurotrophism (EC50 range 0.025 μM)/toxicity ratio is 3600, suggesting that there is a significant therapeutic safety window for J-147 and that it should be further developed as a novel neuroprotective-neurotrophic agent to treat neurodegenerative disease taking into account current National Institute of Neurological Disorders and Stroke (NINDS) RIGOR guidelines.

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J-147一种治疗神经退行性疾病的新型肼先导化合物:CeeTox™安全性和遗传毒性分析
J-147是一种广谱神经保护苯肼化合物,具有显著的神经营养特性,与脑源性神经营养因子(BDNF)的诱导有关。由于这种分子是多效性的,它可能在治疗包括急性缺血性中风(AIS)、创伤性脑损伤(TBI)和阿尔茨海默病(AD)在内的广泛的神经退行性疾病中具有实质性的效用,在这些疾病中,神经保护和神经营养都是有益的。由于J-147的多效性作用,我们试图通过多重分析来确定该药物的安全性。对于CeeTox分析,我们使用了大鼠肝癌细胞系(H4IIE),结果估计J-147的CTox值(即:在14天重复给药研究中预期产生毒性的持续浓度)为90 μM。CeeTox小组显示,J-147对细胞活动产生了一些不利影响,特别是线粒体功能,但只有在高浓度的药物下才会产生不利影响。无论是否使用Aroclor-1254治疗,J-147也没有遗传毒性。J-147的体外神经保护效能(EC50范围为0.06 ~ 0.115 μM)/毒性比为782.6 ~ 1500倍,神经营养作用(EC50范围为0.025 μM)/毒性比为3600倍,基于大量已发表的神经保护实验数据和本研究的CeeTox实验(CTox值为90 μM),我们估计了J-147体外神经保护效能(EC50范围为0.06 ~ 0.115 μM)/毒性比。提示J-147存在显著的治疗安全性窗口期,考虑到目前美国国家神经疾病和中风研究所(NINDS)的严格指南,应进一步开发J-147作为一种新型神经保护-神经营养剂治疗神经退行性疾病。
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