Literature DB >> 12537968

Use of cultured cells of kidney origin to assess specific cytotoxic effects of nephrotoxins.

W Li1, D F Choy, M S Lam, T Morgan, M E Sullivan, J M Post.   

Abstract

During drug discovery, assessment of renal safety for a compound is important for further development of a candidate drug. In this study, we describe an in vitro cell-based assay capable of discerning nephrotoxicity. Three cell types, two of kidney origin and one of liver origin, were used to examine the effects of nephrotoxins. The cell types were the porcine normal kidney tubular epithelial cell line (LLC-PK1), the primary human renal proximal tubular epithelial cells (hRPTEC) and the human liver cell line (HepG2). Cytotoxicity was measured using a luciferin/luciferase assay that measures cellular ATP levels. Four known nephrotoxins, 4-aminophenol, cisplatin, cyclosporin A and paraquat, were tested in this cell-based assay to evaluate cytotoxicity on drug exposure. Kidney-derived LLC-PK1 cells and hRPTECs were found to be sensitive to selected nephrotoxins while liver-derived HepG2 cells were insensitive. Human RPTEC cells obtained from three individual donors demonstrated highly reproducible effects on drug exposure. With respect to drug discovery efforts, integration of the cell models described here are valuable for evaluation of nephrotoxic potentials during lead selection and optimization processes.

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Year:  2003        PMID: 12537968     DOI: 10.1016/s0887-2333(02)00128-5

Source DB:  PubMed          Journal:  Toxicol In Vitro        ISSN: 0887-2333            Impact factor:   3.500


  6 in total

1.  Isolation and characterization of a primary proximal tubular epithelial cell model from human kidney by CD10/CD13 double labeling.

Authors:  Cynthia Van der Hauwaert; Grégoire Savary; Viviane Gnemmi; François Glowacki; Nicolas Pottier; Audrey Bouillez; Patrice Maboudou; Laurent Zini; Xavier Leroy; Christelle Cauffiez; Michaël Perrais; Sébastien Aubert
Journal:  PLoS One       Date:  2013-06-14       Impact factor: 3.240

2.  Establishment and Validation of an In Vitro Screening Method for Traditional Chinese Medicine-Induced Nephrotoxicity.

Authors:  Zhe Ma; Xuexiao Cao; Xiao Guo; Meng Wang; Xiaoliang Ren; Ranran Dong; Rui Shao; Yan Zhu
Journal:  Evid Based Complement Alternat Med       Date:  2018-06-28       Impact factor: 2.629

Review 3.  Role of Shear Stress on Renal Proximal Tubular Cells for Nephrotoxicity Assays.

Authors:  Holly H Birdsall; Timothy G Hammond
Journal:  J Toxicol       Date:  2021-04-21

4.  Human iPSC-derived renal organoids engineered to report oxidative stress can predict drug-induced toxicity.

Authors:  M L Lawrence; M Elhendawi; M Morlock; W Liu; S Liu; A Palakkan; L F Seidl; P Hohenstein; A K Sjögren; J A Davies
Journal:  iScience       Date:  2022-02-07

5.  Fatty acid amide hydrolase-dependent generation of antinociceptive drug metabolites acting on TRPV1 in the brain.

Authors:  David A Barrière; Christophe Mallet; Anders Blomgren; Charlotte Simonsen; Laurence Daulhac; Frédéric Libert; Eric Chapuy; Monique Etienne; Edward D Högestätt; Peter M Zygmunt; Alain Eschalier
Journal:  PLoS One       Date:  2013-08-05       Impact factor: 3.240

6.  Technology Transfer of the Microphysiological Systems: A Case Study of the Human Proximal Tubule Tissue Chip.

Authors:  Courtney Sakolish; Elijah J Weber; Edward J Kelly; Jonathan Himmelfarb; Roula Mouneimne; Fabian A Grimm; John S House; Terry Wade; Arum Han; Weihsueh A Chiu; Ivan Rusyn
Journal:  Sci Rep       Date:  2018-10-05       Impact factor: 4.379

  6 in total

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