Abstract

During the last 80 years there have been extraordinary advances in our knowledge of the chemistry and biology of bile acids. We present here a brief history of the major achievements as we perceive them. Bernal, a physicist, determined the X-ray structure of cholesterol crystals, and his data together with the vast chemical studies of Wieland and Windaus enabled the correct structure of the steroid nucleus to be deduced. Today, C24 and C27 bile acids together with C27 bile alcohols constitute most of the bile acid "family". Patterns of bile acid hydroxylation and conjugation are summarized. Bile acid measurement encompasses the techniques of GC, HPLC, and MS, as well as enzymatic, bioluminescent, and competitive binding methods. The enterohepatic circulation of bile acids results from vectorial transport of bile acids by the ileal enterocyte and hepatocyte; the key transporters have been cloned. Bile acids are amphipathic, self-associate in solution, and form mixed micelles with polar lipids, phosphatidylcholine in bile, and fatty acids in intestinal content during triglyceride digestion. The rise and decline of dissolution of cholesterol gallstones by the ingestion of 3,7-dihydroxy bile acids is chronicled. Scientists from throughout the world have contributed to these achievements.

Highlights

  • During the last 80 years there have been extraordinary advances in our knowledge of the chemistry and biology of bile acids

  • We found that cholyl conjugates were 70% bound, and dihydroxy conjugates were >95% bound in human serum [251], so the glomerular filtrate should contain mostly conjugates of cholic acid in humans

  • The breakthrough came with the identification of FGF15 and FGF19 as a protein released by the ileal enterocyte in response to farnesoid X receptor (FXR) induction by bile acids

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Summary

THE EBB AND FLOW OF MEDICAL INTEREST IN BILE ACIDS

After the elucidation of the true chemical structure of bile acids in 1932 (see below), there was little interest in bile acids in the Western world. In 1952, Bridgwater and Haslewood [98] synthesized a defined side chain starting from the steroid nucleus They showed that their product was identical to 3␣,7␣,12␣-trihydroxy-5␤-cholestan-27oic acid, the major bile acid isolated from the bile of crocodiles and alligators, and they confirmed its structure by X-ray diffraction. A detailed review of some of the experimental work elucidating the nature of the A/B ring junction in various bile acids is available in Fieser and Fieser’s comprehensive text on steroids [7] It was Windaus who introduced the prefix allo to denote 5␣ (A/B trans) bile acids. In each of these classes, there are 5␣ and 5␤ epimers Within these three great classes, and for a given A/B ring junction, the pattern of hydroxylation, on the steroid nucleus and side chain or both, defines each individual bile alcohol or bile acid. Such bile acids occur in mice when the canalicular bile salt export pump (BSEP) has been deleted genetically [116]

Tinamou Ancient birds
Enzymatic and competitive binding assays
Diagnostic utility of plasma bile acid levels
Determinants of bile acid profiles in body fluids
Perturbations of the enterohepatic circulation in disease
PHYSICOCHEMICAL ASPECTS OF BILE ACIDS
Physical chemistry of bile and cholesterol gallstone disease
Gallstone dissolution by oral bile acids
Acceleration of dissolution by extracorporeal shockwave lithotripsy
Topical dissolution with organic solvents
Findings
Concurrent advances in gallstone management
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