Liver slices in in vitro pharmacotoxicology with special reference to the use of human liver tissue

被引:83
作者
Olinga, P
Meijer, DKF
Slooff, MJH
Groothuis, GMM
机构
[1] Univ Groningen, Ctr Pharm, Dept Pharmacokinet & Drug Delivery, Groningen Inst Drug Studies, NL-9713 AV Groningen, Netherlands
[2] Univ Groningen Hosp, Dept Surg, Div Hepatobiliary Surg & Liver Transplantat, NL-9713 EZ Groningen, Netherlands
关键词
D O I
10.1016/S0887-2333(97)00097-0
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
In the early years of research in in vitro pharmacotoxicology liver slices have been used. After a decline in the application of slices in favour of the use of isolated hepatocytes and the isolated perfused liver preparation, the development of the Krumdieck slicer in the 1980s led to a 'comeback' of the technique. This review will focus on the use of human liver, with special reference to the comparison of slices with isolated hepatocytes in in vitro pharmacotoxicology. In addition, an overview on the predictive value of these in vitro systems for drug disposition and toxicity in vivo will be given. Preservation techniques for liver slices and hepatocytes will also be discussed. These techniques ensure an efficient utilization of the scarce human material. For long-term storage of liver slices and hepatocytes, cryopreservation seems most promising. However, cryopreservation is still in its infancy, and reports mainly deal with drug metabolism studies after cryopreservation. Drug toxicity, metabolism and transport data determined in slices and isolated hepatocytes, from both human and animal liver showed good correlation with the corresponding parameters measured in vivo. Therefore, the results obtained in such studies may give rise to more in-depth research on the mechanisms of pharmactoxicology in the human liver. (C) 1998 Elsevier Science Ltd.
引用
收藏
页码:77 / +
页数:23
相关论文
共 197 条
[1]   EFFECTIVE CRYOPRESERVATION AND LONG-TERM STORAGE OF PRIMARY HUMAN HEPATOCYTES WITH RECOVERY OF VIABILITY, DIFFERENTIATION, AND REPLICATIVE POTENTIAL [J].
ADAMS, RM ;
WANG, M ;
CRANE, AM ;
BROWN, B ;
DARLINGTON, GJ ;
LEDLEY, FD .
CELL TRANSPLANTATION, 1995, 4 (06) :579-586
[2]   DIFFERENTIAL EFFECTS OF CYCLOSPORIN A ON THE TRANSPORT OF BILE ACIDS BY HUMAN HEPATOCYTES [J].
AZER, SA ;
STACEY, NH .
BIOCHEMICAL PHARMACOLOGY, 1993, 46 (05) :813-819
[3]  
AZER SA, 1993, TRANSPL P, V25, P2892
[4]  
AZRI S, 1990, In Vitro Toxicology, V3, P309
[5]   FURTHER EXAMINATION OF THE SELECTIVE TOXICITY OF CCL4 IN RAT-LIVER SLICES [J].
AZRI, S ;
MATA, HP ;
REID, LL ;
GANDOLFI, AJ ;
BRENDEL, K .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1992, 112 (01) :81-86
[6]  
AZRI S, 1990, In Vitro Toxicology, V3, P127
[7]   THE INTERACTIVE TOXICITY OF CHCL3 AND BRCCL3 IN PRECISION-CUT RAT-LIVER SLICES [J].
AZRIMEEHAN, S ;
MATA, HP ;
GANDOLFI, AJ ;
BRENDEL, K .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1994, 22 (02) :172-177
[8]  
Bach PH, 1996, ATLA-ALTERN LAB ANIM, V24, P893
[9]   USE OF ORGANOTYPICAL CULTURES OF PRIMARY HEPATOCYTES TO ANALYZE DRUG BIOTRANSFORMATION IN MAN AND ANIMALS [J].
BADER, A ;
ZECH, K ;
CROME, O ;
CHRISTIANS, U ;
RINGE, B ;
PICHLMAYR, R ;
SEWING, KF .
XENOBIOTICA, 1994, 24 (07) :623-633
[10]  
BALANI SK, 1995, DRUG METAB DISPOS, V23, P185