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Updated: May 5, 2026

Using Multi-fluorinated Bile Acids and In Vivo Magnetic Resonance Imaging to Measure Bile Acid Transport
Published on: November 27, 2016
Na+-dependent bile acid transport in the ileum: the balance between diarrhea and constipation
A J van Tilburg1, F W de Rooij, M van Blankenstein
1Department of Internal Medicine II, University Hospital Dijkzigt, Rotterdam, The Netherlands.
Insights
Ileal bile acid transport is linked to bile acid levels. Low transport is seen in constipation and ileal disease, while high transport occurs with bile acid-losing diarrhea.
Area of Science:
- Gastroenterology
- Hepatology
- Molecular Biology
Background:
- Bile acid malabsorption is a common cause of diarrhea.
- Ileal Na+-dependent bile acid transport is crucial for bile acid reabsorption.
Purpose of the Study:
- To quantify ileal bile acid transport in various gastrointestinal conditions.
- To investigate the relationship between bile acid transport and bile acid loss.
Main Methods:
- Uptake of 3H-taurocholate into ileal brush-border membrane vesicles was measured.
- Vesicles were prepared from 158 patients across 10 diagnostic categories.
Main Results:
- Ileal bile acid transport was significantly decreased in ileal disease, partial ileal resection, and constipation.
- Increased bile acid transport was observed in patients with bile acid-losing diarrhea.
- Normal transport was found in irritable bowel syndrome, colon polyps, colitis, post-surgery, and diarrhea without bile acid loss.
Conclusions:
- Ileal Na+-dependent bile acid transport is reduced in conditions with low bile acid loss (e.g., constipation) and increased in conditions with high bile acid loss.
- Bile acid availability to ileal enterocytes may regulate ileal bile acid transport.
Abstract:
Ileal Na+-dependent bile acid transport was quantified in vitro as the uptake of 3H-taurocholate into brush-border membrane vesicles. Vesicles were prepared from ileal biopsies of 158 patients placed in 10 diagnostic categories. Active bile acid transport (expressed as picomoles taurocholate uptake per milligram brush-border membrane protein per 15 s, median and interquartile ranges indicated) did not differ significantly in 6 categories: irritable bowel syndrome (71, 35-97; n = 21), colon polyps (42, 30-89; n = 29), colitis (62, 33-91; n = 31), postvagotomy or postcholecystectomy (69, 37-97; n = 11), diarrhea without increased bile acid loss (58, 48-85; n = 12), and lack of gastrointestinal pathology (74, 45-103; n = 22). A decreased active bile acid transport was found in 3 categories: ileal disease (4, 1-36; n = 11), partial ileal resection (5, 1-35; n = 5), and constipation (41, 22-50; n = 8). Bile acid transport was increased in patients with bile acid-losing diarrhea with endoscopically and histologically normal ilea (111, 94-135; n = 8). These findings indicate that a low fecal bile acid loss, presumed to be present in constipated patients, is associated with a low Na+-dependent ileal bile acid transport and a high bile acid loss is associated with a high active bile acid transport. Ileal bile acid transport might be regulated by the availability of bile acids to the ileal enterocytes.
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