Literature DB >> 20725069

Preparation and incubation of precision-cut liver and intestinal slices for application in drug metabolism and toxicity studies.

Inge A M de Graaf1, Peter Olinga, Marina H de Jager, Marjolijn T Merema, Ruben de Kanter, Esther G van de Kerkhof, Geny M M Groothuis.   

Abstract

Precision-cut tissue slices (PCTS) are viable ex vivo explants of tissue with a reproducible, well defined thickness. They represent a mini-model of the organ under study and contain all cells of the tissue in their natural environment, leaving intercellular and cell-matrix interactions intact, and are therefore highly appropriate for studying multicellular processes. PCTS are mainly used to study the metabolism and toxicity of xenobiotics, but they are suitable for many other purposes. Here we describe the protocols to prepare and incubate rat and human liver and intestinal slices. Slices are prepared from fresh liver by making a cylindrical core using a drill with a hollow bit, from which slices are cut with a specially designed tissue slicer. Intestinal tissue is embedded in cylinders of agarose before slicing. Slices remain viable for 24 h (intestine) and up to 96 h (liver) when incubated in 6- or 12-well plates under 95% O(2)/5% CO(2) atmosphere.

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Year:  2010        PMID: 20725069     DOI: 10.1038/nprot.2010.111

Source DB:  PubMed          Journal:  Nat Protoc        ISSN: 1750-2799            Impact factor:   13.491


  99 in total

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Review 2.  A comparison of the performance in vitro of precision cut tissue slices and suspensions of human spleen with special reference to immunoglobulin and cytokine production.

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3.  A new technique for preparing precision-cut slices from small intestine and colon for drug biotransformation studies.

Authors:  Ruben de Kanter; Annemarie Tuin; Esther van de Kerkhof; Marcella Martignoni; Annelies L Draaisma; Marina H de Jager; Inge A M de Graaf; Dirk K F Meijer; Geny M M Groothuis
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Review 6.  Organ slices for the evaluation of human drug toxicity.

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  103 in total

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Review 5.  Antifibrotic therapies in the liver.

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6.  Parallel microfluidic chemosensitivity testing on individual slice cultures.

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9.  Ex vivo toxicological evaluation of experimental anticancer gold(i) complexes with lansoprazole-type ligands.

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10.  Anti-HIV and Anti-Hepatitis C Virus Drugs Inhibit P-Glycoprotein Efflux Activity in Caco-2 Cells and Precision-Cut Rat and Human Intestinal Slices.

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