Transepithelial resistance and inulin permeability as endpoints in in vitro nephrotoxicity testing

被引:28
作者
Duff, T
Carter, S
Feldman, G
McEwan, G
Pfaller, W
Rhodes, P
Ryan, M
Hawksworth, G
机构
[1] Univ Aberdeen, Dept Med & Therapeut, Aberdeen AB25 2ZD, Scotland
[2] Univ Aberdeen, Dept Biomed Sci, Aberdeen AB25 2ZD, Scotland
[3] GlaxoSmithKline, Ware SG12 0DP, Herts, England
[4] Natl Univ Ireland Univ Coll Dublin, Dept Pharmacol, Dublin 4, Ireland
[5] Univ Innsbruck, Inst Physiol, A-6010 Innsbruck, Austria
来源
ATLA-ALTERNATIVES TO LABORATORY ANIMALS | 2002年 / 30卷
关键词
in vitro testing; medium-throughput screening; nephrotoxicity; nephrotoxins; transepithelial resistance; transmembrane flux;
D O I
10.1177/026119290203002S08
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 [基础医学];
摘要
Transepithelial electrical resistance (R-T) and the flux of fluorescein isothiocyanate (FITC) across Madin Darby canine kidney (MDCK) strain 1 cells and porcine epithelial kidney (LLC-PK1) monolayers were compared between three laboratories for a range of nephrotoxins. The precision of the REMS AutoSampler was similar to that of the Ussing chamber and the ENDOHM(R) technique, but superior to using chopstick electrodes, for measurements of resistance. The nephrotoxins used were selective for the proximal tubule, and in all cases, LLC-PK1 cells were more sensitive than MDCK cells. In most cases, change in R-T was a more sensitive indicator of damage than alterations in FITC flux. The REMS system provides high intra-plate precision for R-T measurements and is a higher throughput system, which is applicable to screening for nephrotoxicity in vitro.
引用
收藏
页码:53 / 59
页数:7
相关论文
共 7 条
[1]
PRIMARY CULTURES OF RABBIT RENAL PROXIMAL TUBULE CELLS .3. COMPARATIVE CYTOTOXICITY OF INORGANIC AND ORGANIC MERCURY [J].
ALEO, MD ;
TAUB, ML ;
KOSTYNIAK, PJ .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1992, 112 (02) :310-317
[2]
Role of cytochrome P-450 as a source of catalytic iron in cisplatin-induced nephrotoxicity [J].
Baliga, R ;
Zhang, ZW ;
Baliga, M ;
Ueda, N ;
Shah, SV .
KIDNEY INTERNATIONAL, 1998, 54 (05) :1562-1569
[3]
Targeting of membrane transporters in renal epithelia: when cell biology meets physiology [J].
Brown, D .
AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2000, 278 (02) :F192-F201
[4]
Molecular physiology and pathophysiology of tight junctions - I. Biogenesis of tight junctions and epithelial polarity [J].
Cereijido, M ;
Shoshani, L ;
Contreras, RG .
AMERICAN JOURNAL OF PHYSIOLOGY-GASTROINTESTINAL AND LIVER PHYSIOLOGY, 2000, 279 (03) :G477-G482
[5]
A ROLE FOR OXYGEN FREE-RADICALS IN AMINONUCLEOSIDE NEPHROSIS [J].
DIAMOND, JR ;
BONVENTRE, JV ;
KARNOVSKY, MJ .
KIDNEY INTERNATIONAL, 1986, 29 (02) :478-483
[6]
Pfaller W, 2000, DEV AN VET, V31, P291
[7]
Validation and nephrotoxicity of a simplified once-daily aminoglycoside dosing schedule and guidelines for monitoring therapy [J].
Prins, JM ;
Weverling, GJ ;
deBlok, K ;
vanKetel, RJ ;
Speelman, P .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 1996, 40 (11) :2494-2499