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Selonsertib,一种凋亡信号调节激酶 1 抑制剂,在小鼠体内的抗神经炎症作用及脑内药代动力学特性。

Anti-neuroinflammatory Effects and Brain Pharmacokinetic Properties of Selonsertib, an Apoptosis signal-regulating Kinase 1 Inhibitor, in mice.

机构信息

Data Convergence Drug Research Center, Therapeutics & Biotechnology Division, Research Institute of Chemical Technology, 141 Gajeong-ro, Yuseong-gu, 34114, Daejeon, Korea.

College of Pharmacy, Chungnam National University, Daejeon, Korea.

出版信息

Neurochem Res. 2022 Dec;47(12):3829-3837. doi: 10.1007/s11064-022-03777-9. Epub 2022 Oct 30.

Abstract

Selonsertib is a first-in-class apoptosis signal-regulating kinase 1 (ASK1) inhibitor in clinical trials for treating NASH and diabetic kidney disease due to its anti-inflammatory and anti-fibrotic activities. In the present study, we investigated the anti-neuroinflammatory effects and brain pharmacokinetic properties of selonsertib. It inhibited inflammatory cytokines and NO production by suppressing phosphorylated ASK1 in the LPS-stimulated microglial cell line, BV2 cells. Consistent with the in vitro results, selonsertib attenuated plasma and brain TNF-α levels in the LPS-induced murine neuroinflammation model. In vitro and in vivo pharmacokinetic studies of selonsertib were conducted in support of central nervous system (CNS) drug discovery. In both Caco-2 and MDR-MDCK cells, selonsertib exhibited a high efflux ratio, showing that it is a P-gp substrate. Selonsertib was rapidly and effectively absorbed into the systemic circulation after oral treatment, with a T of 0.5 h and oral bioavailability of 74%. In comparison with high systemic exposure with C of 16.2 µg/ml and AUC of 64 µg·h/mL following oral dosing of 10 mg/kg, the brain disposition of selonsertib was limited, with C of 0.08 µg/g and Kp value of 0.004. This study demonstrates that selonsertib can be a therapeutic agent for neuroinflammatory diseases.

摘要

塞来昔替尼是一种处于临床试验阶段的凋亡信号调节激酶 1(ASK1)抑制剂,因其具有抗炎和抗纤维化作用,可用于治疗 NASH 和糖尿病肾病。在本研究中,我们研究了塞来昔替尼的抗神经炎症作用和脑内药代动力学特性。它通过抑制 LPS 刺激的小胶质细胞系 BV2 细胞中磷酸化的 ASK1,抑制炎性细胞因子和 NO 的产生。与体外结果一致,塞来昔替尼可减轻 LPS 诱导的小鼠神经炎症模型中的血浆和脑组织 TNF-α水平。为支持中枢神经系统(CNS)药物研发,我们进行了塞来昔替尼的体外和体内药代动力学研究。在 Caco-2 和 MDR-MDCK 细胞中,塞来昔替尼表现出高外排比,表明其是 P-糖蛋白(P-gp)底物。塞来昔替尼经口服给药后迅速有效地被吸收进入体循环,T 为 0.5 h,口服生物利用度为 74%。与口服 10 mg/kg 后 16.2 µg/ml 的高全身暴露浓度(C)和 64 µg·h/mL 的 AUC 相比,塞来昔替尼在脑内的分布有限,C 为 0.08 µg/g,Kp 值为 0.004。本研究表明,塞来昔替尼可能成为神经炎症性疾病的治疗药物。

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