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用于肝细胞毒性体外测定的alamar蓝还原法评估

Evaluation of alamar blue reduction for the in vitro assay of hepatocyte toxicity.

作者信息

Slaughter M R, Bugelski P J, O'Brien P J

机构信息

Safety Assessment, SmithKline Beecham Pharmaceuticals, The Frythe, Welwyn, Herts AL6 9AR, UK.

出版信息

Toxicol In Vitro. 1999 Aug-Oct;13(4-5):567-9. doi: 10.1016/s0887-2333(99)00037-5.

Abstract

Alamar Blue (AB) reduction is a promising new in vitro assay which is simple to conduct and amenable to repeated measurements and high-throughput screening; however, evaluation with hepatocytes has not been reported. Accordingly, we compared AB reduction with established markers of hepatocyte viability and cell density. Primary rat hepatocytes were allowed to adhere to collagen-coated 96-well plates, then exposed for 16 hours to culture medium, 0.7% dimethyl sulfoxide (DMSO) in medium, 500 mum CCl(4), 500 mum eugenol or 15 or 150 mum of a novel substituted indoline (the latter three in medium with 0.7% DMSO; medium also contained hydrocortisone during exposure period). Using a spectrophotometric plate reader, AB reduction was compared with lactate dehydrogenase release (LDH) release, neutral red (NR) uptake, total protein (TP) and cell seed density. AB reduction showed a linear relationship and good correlation with NR uptake, LDH release, TP and cell density. AB assay precision varied with cell density, but was similar to other assays in cytotoxicity screening. Good correlation with cell density indicates AB to have the potential for assessment of hepatocyte proliferation. From the results reported here, we recommend further evaluation and optimization of a protocol for application of AB reduction as a test for cytotoxicity and proliferation in primary hepatocyte cultures.

摘要

alamar蓝(AB)还原法是一种很有前景的新型体外检测方法,操作简单,适合重复测量和高通量筛选;然而,尚未见其用于肝细胞的评估报道。因此,我们将AB还原法与已确立的肝细胞活力及细胞密度标志物进行了比较。将原代大鼠肝细胞接种于胶原包被的96孔板,然后分别置于培养基、含0.7%二甲基亚砜(DMSO)的培养基、500μmol/L四氯化碳(CCl₄)、500μmol/L丁香酚或15或150μmol/L一种新型取代吲哚啉(后三种置于含0.7%DMSO的培养基中;暴露期间培养基中还含有氢化可的松)中培养16小时。使用分光光度计酶标仪,将AB还原法与乳酸脱氢酶释放(LDH)、中性红(NR)摄取、总蛋白(TP)及细胞接种密度进行比较。AB还原法与NR摄取、LDH释放、TP及细胞密度呈线性关系且相关性良好。AB检测的精密度随细胞密度而异,但在细胞毒性筛选中与其他检测方法相似。与细胞密度的良好相关性表明AB法有评估肝细胞增殖的潜力。根据本文报道的结果,我们建议进一步评估和优化AB还原法的方案,以用于原代肝细胞培养中细胞毒性和增殖的检测。

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