The action of zymosan on octanoate transport and metabolism in the isolated perfused rat liver
| Autor: | Alice M. Derbocio, Carlos Lopez, Adelar Bracht, Lívia Bracht, Emy Luiza Ishii-Iwamoto |
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| Rok vydání: | 2009 |
| Předmět: |
Male
Health Toxicology and Mutagenesis Toxicology Biochemistry Microcirculation chemistry.chemical_compound Animals Rats Wistar Molecular Biology Cell Size chemistry.chemical_classification Diminution Chromatography Ion Transport Zymosan Cell Membrane Albumin Fatty acid General Medicine Metabolism Dilution Rats Perfusion Membrane chemistry Liver Molecular Medicine Caprylates |
| Zdroj: | Journal of biochemical and molecular toxicology. 23(3) |
| ISSN: | 1099-0461 |
| Popis: | The effects of zymosan on transport, distribution, and metabolism of octanoate in the perfused rat liver were investigated using the multiple-indicator dilution technique. Livers were perfused with 300 µM octanoate in the absence or in the presence of 100 µg/mL zymosan. Tracer amounts of [1-14C]octanoate, [3H] water, and [131I]albumin were injected into the portal vein, and the effluent perfusate was fractionated. The normalized dilution curves were analyzed by means of a space-distributed variable transit time model. Zymosan decreased the space into which octanoate undergoes flow-limited distribution, possibly the first cellular exchanging pool represented by plasma membranes and their adjacencies. However, the rate of transfer of octanoate from the plasma membrane into the rest of the cell was not modified as indicated by the similar values of the influx rates and also the net uptake of octanoate per unit of accessible cellular volume. However, when referred to the wet weight of the liver, the net uptake of octanoate was 37.5% reduced, a value corresponding to the diminution of the cellular accessible space. It can be concluded that an exclusion of a fraction of the liver parenchyma from the microcirculation is the main mechanism by which zymosan reduces the metabolism of exogenous octanoate. © 2009 Wiley Periodicals, Inc. J Biochem Mol Toxicol 23:155–165, 2009; Published online in Wiley InterScience (www.interscience.wiley.com). DOI 10.1002/jbt.20269 |
| Databáze: | OpenAIRE |
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