1984
DOI: 10.1016/0006-2952(84)90105-9
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Sulfation in isolated enterocytes of guinea pig: Dependence on inorganic sulfate

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Cited by 21 publications
(5 citation statements)
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“…mrp2, an important member of the ABC family of transporters (20), is a candidate for pumping conjugated compounds out of the intestinal cells. mrp2 is principally expressed in the proximal small intestine and follows a pattern of distribution similar to that of conjugating enzymes (10,25,33,38,41). Regulation of mrp2 expression during perinatal events may determine the fate and, consequently, the toxicity of xenobiotics introduced into the maternal intestine.…”
Section: Discussionmentioning
confidence: 99%
See 1 more Smart Citation
“…mrp2, an important member of the ABC family of transporters (20), is a candidate for pumping conjugated compounds out of the intestinal cells. mrp2 is principally expressed in the proximal small intestine and follows a pattern of distribution similar to that of conjugating enzymes (10,25,33,38,41). Regulation of mrp2 expression during perinatal events may determine the fate and, consequently, the toxicity of xenobiotics introduced into the maternal intestine.…”
Section: Discussionmentioning
confidence: 99%
“…Thus mrp2, or canalicular multispecific organic anion transporter, mediates the ATP-dependent transport of glucuronide, sulfate, and glutathione conjugates across the apical domain not only of hepatocytes and renal tubular cells (22) but also of enterocytes. mrp2 protein is preferentially localized in the proximal intestine and gradually decreases from the jejunum to the distal ileum (33), following a pattern of distribution similar to that of the conjugating enzymes in the rat (10,25,38,41). In addition, mrp2 expression is highest at the tip region of the intestinal villus.…”
mentioning
confidence: 99%
“…While the incidence of cancer in the human small intestine is only 0.1-0.3% of all malignant neoplasms, that in the colon is 15%, and is the second most prevalent cancer in the United States (American Cancer Society 1989). In contrast, the small intestine has 3 times greater glucuronosyl transferase (Hanninen et al 1968), 30 times greater glutathione-S-transferase activity (Siegers et al 1988), and significantly higher sulphotransferase activity (Schwartz and Schwenk 1984;Hanninen et al 1987;Cappiello et al 1990). Moreover, the isoenzyme composition of each of three enzyme systems, glucuronosyltransferase, glutathione-S-transferase and cytochrome P-450 was greater in the small intestine than in the colon (Peters et al 199 1).…”
Section: Figsmentioning
confidence: 98%
“…at ASPET Journals on May 7, 2018 dmd.aspetjournals.org intestinal wall, from duodenum to ileum (Clifton and Kaplowitz, 1977;Pinkus et al, 1977;Schwarz and Schwenk, 1984;Dubey and Singh, 1988a). The human intestinal CYP3A4 shows a slightly lower level at the duodenum before levels rise again at the jejunum, then finally decreasing toward the ileum .…”
Section: Intestinal Drug Transport and Metabolismmentioning
confidence: 99%