The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
How bile acids confer gut mucosal protection against bacteria
Abstract
Bile is a complex mixture of organic and inorganic molecules that is stored in the gallbladder and released into the proximal small intestine when a meal is eaten. Bile is both an excretory secretion, to eliminate cholesterol, bilirubin, and waste products, and a digestive secretion, to promote lipid absorption. The dominant organic constituents of bile are conjugated bile acids (also termed bile salts), glycine or taurine N-acyl amidated derivatives of bile acids that are formed from cholesterol in the liver cell. Bile acids are wedge-shaped, water soluble, amphipathic molecules with a hydrophobic side and a hydrophilic side. Adsorption of bile acid anions to lipid bilayers of dietary membrane lipids or fatty acids (derived by pancreatic lipase acting on triglyceride) increases the curvature of the bilayers, ultimately converting them to mixed micelles (1, 2). Such micellar solubilization of polar lipids greatly increases their rate of diffusion to the epithelial surface of the small intestine, and micellar solubilization is essential for the efficient absorption of lipids. Although most lipid absorption occurs in the proximal small intestine, conjugated bile acids themselves are not absorbed together with the solubilized lipids in the jejunum but pass to the distal small intestine, where they are efficiently absorbed by an active transport system present in the epithelium of the terminal ileum. Efficient intestinal reclamation of bile acids leads to the accumulation of a recycling pool of conjugated bile acids that circulates one or more times with each meal (3). Enterohepatic cycling of bile acids provides large quantities of bile acids for digestion.
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Cites
Regulation of antibacterial defense in the small intestine by the nuclear bile acid receptor
Inagaki, T., Moschetta, A., Lee, Y.-K., Peng, L., Zhao, G., Downes, M., Yu, R. T., Shelton, J. M., Richardson, J. A., Repa, J. J., et al. (2006) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0509592103 · Cited by 1,164
Fatty acid synthesis is a target for antibacterial activity of unsaturated fatty acids
Zheng, C. J., Yoo, J.-S., Lee, T.-G., Cho, H.-Y., Kim, Y.-H., & Kim, W.-G. (2005) · FEBS Letters · doi:10.1016/j.febslet.2005.08.028 · Cited by 690
Lorenzo-Zúñiga, V., Bartolí, R., Planas, R., Hofmann, A. F., Viñado, B., Hagey, L. R., Hernández, J. M., Mañé, J., Alvarez, M. A., Ausina, V., et al. (2003) · Hepatology · doi:10.1053/jhep.2003.50116 · Cited by 321
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Cited by
Jones, B. V., Begley, M., Hill, C., Gahan, C. G. M., & Marchesi, J. R. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0804437105 · Cited by 1,098
Gut-liver axis: Pathophysiological concepts and clinical implications
Tilg, H., Adolph, T. E., & Trauner, M. (2022) · Cell Metabolism · doi:10.1016/j.cmet.2022.09.017 · Cited by 843
Intestinal transport and metabolism of bile acids
Dawson, P. A., & Karpen, S. J. (2015) · Journal of Lipid Research · doi:10.1194/jlr.r054114 · Cited by 598
Bajaj, J. S., Hylemon, P. B., Ridlon, J. M., Heuman, D. M., Daita, K., White, M. B., Monteith, P., Noble, N. A., Sikaroodi, M., & Gillevet, P. M. (2012) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00152.2012 · Cited by 527
Role of bile acids and their receptors in gastrointestinal and hepatic pathophysiology
Fuchs, C. D., & Trauner, M. (2022) · Nature Reviews Gastroenterology & Hepatology · doi:10.1038/s41575-021-00566-7 · Cited by 490
Metadata
- Authors
- Hofmann, A. F., & Eckmann, L.
- Venue
- Proceedings of the National Academy of Sciences
- Published
- 2006-03-13
- Volume
- 103
- Issue
- 12
- Pages
- 4333-4334
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- OpenAlex
- W2142945080
- Cited by
- 237
- References
- 3
- FWCI
- 2.95
- Type
- journal article
- Language
- en
- Open access
- closed
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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).
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