The objective of the proposed studies is to gain further insight into the mechanisms by which the liver removes various environmental chemicals and drugs from the blood and excretes them into the bile. The mechanism or mechanisms by which xenobiotics enter the liver will be examined by using the isolated hepatocyte technique. Further insight into the mechanisms which stimulate and regulate the development of hepatic excretory function will be examined by measuring hepatic uptake processes in rats of various ages and determining if substrates for the hepatic excretory mechanism will stimulate its development. The mechanisms responsible for the first-pass effect of xenobiotics will be examined and the importance of the first-pass effect on toxicity will be examined. Thus, by investigating the hepatic uptake and excretory mechanisms by a number of techniques, a deeper insight into the basic mechanisms of detoxification of foreign chemicals by biliary excretion will be gained, an area in which development has lagged relative to detoxification by metabolism and renal excretion.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Research Project (R01)
Project #
3R01ES003192-18S1
Application #
3250356
Study Section
Toxicology Study Section (TOX)
Project Start
1983-08-01
Project End
1989-07-31
Budget Start
1988-09-26
Budget End
1989-07-31
Support Year
18
Fiscal Year
1988
Total Cost
Indirect Cost
Name
University of Kansas
Department
Type
Schools of Medicine
DUNS #
016060860
City
Kansas City
State
KS
Country
United States
Zip Code
66160
Klaassen, Curtis D; Reisman, Scott A (2010) Nrf2 the rescue: effects of the antioxidative/electrophilic response on the liver. Toxicol Appl Pharmacol 244:57-65
Shelby, M K; Klaassen, C D (2006) Induction of rat UDP-glucuronosyltransferases in liver and duodenum by microsomal enzyme inducers that activate various transcriptional pathways. Drug Metab Dispos 34:1772-8
Cherrington, Nathan J; Slitt, Angela L; Li, Ning et al. (2004) Lipopolysaccharide-mediated regulation of hepatic transporter mRNA levels in rats. Drug Metab Dispos 32:734-41
Shelby, M K; Cherrington, N J; Vansell, N R et al. (2003) Tissue mRNA expression of the rat UDP-glucuronosyltransferase gene family. Drug Metab Dispos 31:326-33
Cherrington, Nathan J; Slitt, Angela L; Maher, Jonathan M et al. (2003) Induction of multidrug resistance protein 3 (mrp3) in vivo is independent of constitutive androstane receptor. Drug Metab Dispos 31:1315-9
Guo, Grace L; Johnson, David R; Klaassen, Curtis D (2002) Postnatal expression and induction by pregnenolone-16alpha-carbonitrile of the organic anion-transporting polypeptide 2 in rat liver. Drug Metab Dispos 30:283-8
Guo, Grace L; Choudhuri, Supratim; Klaassen, Curtis D (2002) Induction profile of rat organic anion transporting polypeptide 2 (oatp2) by prototypical drug-metabolizing enzyme inducers that activate gene expression through ligand-activated transcription factor pathways. J Pharmacol Exp Ther 300:206-12
Johnson, David R; Habeebu, Sultan S M; Klaassen, Curtis D (2002) Increase in bile flow and biliary excretion of glutathione-derived sulfhydryls in rats by drug-metabolizing enzyme inducers is mediated by multidrug resistance protein 2. Toxicol Sci 66:16-26
Johnson, David R; Guo, Grace L; Klaassen, Curtis D (2002) Expression of rat Multidrug Resistance Protein 2 (Mrp2) in male and female rats during normal and pregnenolone-16alpha-carbonitrile (PCN)-induced postnatal ontogeny. Toxicology 178:209-19
Brady, James M; Cherrington, Nathan J; Hartley, Dylan P et al. (2002) Tissue distribution and chemical induction of multiple drug resistance genes in rats. Drug Metab Dispos 30:838-44

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