Evaluation of Alamar Blue reduction for the in vitro assay of hepatocyte toxicity

被引:38
作者
Slaughter, MR [1 ]
Bugelski, PJ [1 ]
O'Brien, PJ [1 ]
机构
[1] SmithKline Beecham Pharmaceut, Safety Assessment, Welwyn Garden City AL6 9AR, Herts, England
关键词
rat hepatocytes; cytotoxicity; liver;
D O I
10.1016/S0887-2333(99)00037-5
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
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 mu M CCl4, 500 mu M eugenol or 15 or 150 mu M 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. (C) 1999 Elsevier, Science Ltd. All rights reserved.
引用
收藏
页码:567 / 569
页数:3
相关论文
共 9 条
  • [1] BLAAUBOER BJ, 1994, ATLA-ALTERN LAB ANIM, V22, P231
  • [2] Microplate Alamar blue assay versus BACTEC 460 system for high-throughput screening of compounds against Mycobacterium tuberculosis and Mycobacterium avium
    Collins, LA
    Franzblau, SG
    [J]. ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1997, 41 (05) : 1004 - 1009
  • [3] EFFECTS OF SERUM-PROTEIN AND COLLOID ON THE ALAMARBLUE ASSAY IN CELL-CULTURES
    GOEGAN, P
    JOHNSON, G
    VINCENT, R
    [J]. TOXICOLOGY IN VITRO, 1995, 9 (03) : 257 - 266
  • [4] BIOCHEMICAL EVALUATION OF RAT HEPATOCYTE PRIMARY CULTURES AS A MODEL FOR CARBON-TETRACHLORIDE HEPATOTOXICITY - COMPARATIVE STUDIES INVIVO AND INVITRO
    LONG, RM
    MOORE, L
    [J]. TOXICOLOGY AND APPLIED PHARMACOLOGY, 1988, 92 (02) : 295 - 306
  • [5] A new method for continual quantitation of viable cells on endothelialized polyurethanes
    Nikolaychik, VV
    Samet, MM
    Lelkes, PI
    [J]. JOURNAL OF BIOMATERIALS SCIENCE-POLYMER EDITION, 1996, 7 (10) : 881 - 891
  • [6] PAGE B, 1993, INT J ONCOL, V3, P473
  • [7] PELOUX AF, 1992, ATLA-ALTERN LAB ANIM, V20, P8
  • [8] Seglen PO, 1976, METHOD CELL BIOL, V13, P30
  • [9] METABOLISM AND CYTOTOXICITY OF EUGENOL IN ISOLATED RAT HEPATOCYTES
    THOMPSON, DC
    CONSTANTINTEODOSIU, D
    MOLDEUS, P
    [J]. CHEMICO-BIOLOGICAL INTERACTIONS, 1991, 77 (02) : 137 - 147