Abstract
The purpose of this study is to characterize the distribution pattern of P-gp protein levels along the entire GI tract in the Yucatan micropig, which is being developed as a model for human drug bioavailability. Small and large intestines were freshly obtained and divided into about 37 segments and 10 segments, respectively (ca., 1 foot/segment). Epithelial cells from the small intestine were obtained by an elution method; whereas, a scraping method was applied to the large intestine. Total cellular protein was isolated from the epithelial cells. Western blot analysis using P-gp antibody showed that the amount of P-gp protein increased distally from the duodenum to the ileum over approximately a 10-fold range. P-gp protein in the large intestine was present at a higher level in the central portion, but the absolute amount was much less than what was found in the small intestine.
Original language | English (US) |
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Pages (from-to) | 18-22 |
Number of pages | 5 |
Journal | Journal of Biochemical and Molecular Toxicology |
Volume | 18 |
Issue number | 1 |
DOIs | |
State | Published - 2004 |
Keywords
- Enterocytes
- Large intestine
- P-Glycoprotein
- Small intestine
- Western blot
ASJC Scopus subject areas
- Biochemistry
- Molecular Medicine
- Molecular Biology
- Toxicology
- Health, Toxicology and Mutagenesis