Lithocholic acid

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Lithocholic acid
2D structure for Lithocholic acid
Chemical Name (4R)-4-[(3R,5R,8R,9S,10S,13R,14S,17R)-3-hydroxy-10,13-dimethyl-2,3,4,5,6,7,
Chemical Formula C24H40O3
CAS Number 434-13-9
Chemical Information HMDB00761
Biochemical Taxonomy

  • Bile Acids

Functional Taxonomy Not Available
Nutritional Taxonomy Not Available
Metabolic Pathways Not Available
Biofluid Location

  • Bile
  • Blood

Tissue Location

  • Liver
  • Intestine

Normal Biofluid Concentrations

  • Bile: 930 (890-960) uM
  • Blood: 0.08 +/- 0.02 umol/L
  • Blood: 0.33 +/-0.04 uM

Normal Tissue Concentrations Not Available
Diseases / Conditions Related to Nutrition

  • Children with cystic fibrosis without liver disease
  • Cystic fibrosis associated with liver disease(CFLD)
  • neonatal cholestasis/extrahepatic biliary atresia (EHBA)

Other (Monogenic Disorders) Not Available
Abnormal Biofluid Concentrations

  • Blood (Children with cystic fibrosis without liver disease): 0.16 +/- 0.07 umol/L
  • Blood (Cystic fibrosis associated with liver disease(CFLD)): 0.11 +/- 0.02 uM
  • Blood (neonatal cholestasis/extrahepatic biliary atresia (EHBA)): 0.11 +/- 0.04 uM

Abnormal Tissue Concentrations Not Available
Physiological Processes Not Available
Authors:
Affiliations:

Contents

Introduction

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A bile acid formed from chenodeoxycholate by bacterial action, usually conjugated with glycine or taurine. It acts as a detergent to solubilize fats for absorption and is itself absorbed. It is used as cholagogue and choleretic. A bile acid. Bile acids are steroid acids found predominantly in bile of mammals. The distinction between different bile acids is minute, depends only on presence or absence of hydroxyl groups on positions 3, 7, and 12. Bile acids are physiological detergents that facilitate excretion, absorption, and transport of fats and sterols in the intestine and liver. Bile acids are also steroidal amphipathic molecules derived from the catabolism of cholesterol. They modulate bile flow and lipid secretion, are essential for the absorption of dietary fats and vitamins, and have been implicated in the regulation of all the key enzymes involved in cholesterol homeostasis. Bile acids recirculate through the liver, bile ducts, small intestine and portal vein to form an enterohepatic circuit. They exist as anions at physiological pH and, consequently, require a carrier for transport across the membranes of the enterohepatic tissues. The unique detergent properties of bile acids are essential for the digestion and intestinal absorption of hydrophobic nutrients. Bile acids have potent toxic properties (e.g., membrane disruption) and there are a plethora of mechanisms to limit their accumulation in blood and tissues. (PMID: 11316487, 16037564, 12576301, 11907135)


Biological Function

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Catabolism

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Diseases / Conditions Related to Nutrition

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  • Children with cystic fibrosis without liver disease
  • Cystic fibrosis associated with liver disease(CFLD)
  • neonatal cholestasis/extrahepatic biliary atresia (EHBA)

Other (Monogenic) Disorders

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Nutritional Information

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Drivers for biological variation

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Vulnerable groups

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Other resources

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Links

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