Abstract

Bile acids are steroidal compounds, which contain 24 carbon atoms. They can be classified into two major groups: primary and secondary. The most abundant bile acids: The primary bile acids include cholic acid and chenodeoxycholic acid, while the major secondary bile acids are deoxycholic acid and litocholic acid. Bile acids are important physiological agents for intestinal absorption of nutrients and are used for biliary lipid secretion, toxic metabolites and xenobiotics. The aim of this paper is to analyze biosynthesis and biotransformation of bile acids, as preparation for practical usage in laboratory and clinical conditions. Topic: Biosynthesis and biotransformation of bile acids: The biosynthesis of bile acids is the dominant metabolic pathway for catabolism of cholesterol in humans. The classical route of biosynthesis of bile acids is embarking on the conversion of cholesterol into 7α-hydroxycholesterol using enzyme 7α-cholesterol hydroxylase (CYP7A1). This enzyme is one of the microsomal cytochrome P450 enzyme is localized exclusively in the liver. Classical road is the main road in the biosynthesis of bile acids, and its total contribution amounts to 90% for people, and 75% in mice. CYP 7A1 enzyme is considered to be sensitive to the inhibition of carbon monoxide, and the condition for the effect of NADPH, the oxygen, lecithin, and the NADPH-cytochrome P450 reductase. Bile acids are important signaling molecules and metabolic controls which activate the nuclear receptor and the G protein-coupled receptors (GPCR), a signaling lipid regulation of the liver, glucose and energy homeostasis. Also, bile acids maintain metabolic homeostasis. Biotransformation of bile acids: The conversion of cholesterol into bile acids just important for maintenance of cholesterol homeostasis, but also to prevent the accumulation of cholesterol, triglycerides and toxic metabolites as well as violations of the liver and other organs. Enterohepatic circulation of bile acids from the liver to the intestine and back to the liver occupies the most important role in the processes of absorption and distribution, as well as in metabolic regulation and homeostasis. Conclusions: This physiological process is complicated and regulates the membrane transport system in the liver and intestine by means of nuclear receptors. It is very dangerous fact that toxic bile acids may be causes of inflammation, apoptosis and cell death. On the other hand activated GPCR signaling and nuclear bile acid protects against inflammation of the liver, intestine and macrophages. Bile acid metabolism disorders cause cholestatic liver disease, dyslipidemia, fatty liver disease, cardiovascular disease and diabetes.

Highlights

  • All of the bile acids are characterized by the appearance of cyclopentanoperhydrophenanthrene ring

  • Bile acids are synthesized via the classic pathway initiated by cholesterol 7α−hydroxylase (CYP7A1), and via alternate pathways, one of which is initiated by sterol 27-hydroxylase (CYP27A1)

  • These studies used mice lacking cholesterol 7α−hydroxylase (Cyp7A1) to establish whether the loss of the classic pathway affected cholesterol homeostasis differently in males and females, and to determine if the rate of bile acid synthesis via alternate pathways was responsive to changes in the enterohepatic flux of cholesterol and bile acids

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Summary

Introduction

Bile acids are steroidal compounds, which contain 24 carbon atoms. The classical route of biosynthesis of bile acids is embarking on the conversion of cholesterol into 7α−hydroxycholesterol using enzyme 7α−cholesterol hydroxylase (CYP7A1). This enzyme is one of the microsomal cytochrome P450 enzyme is localized exclusively in the liver. Bile acids are important signaling molecules and metabolic controls which activate the nuclear receptor and the G protein-coupled receptors (GPCR), a signaling lipid regulation of the liver, glucose and energy homeostasis. Enterohepatic circulation of bile acids from the liver to the intestine and back to the liver occupies the most important role in the processes of absorption and distribution, as well as in metabolic regulation and homeostasis. Bile acid metabolism disorders cause cholestatic liver disease, dyslipidemia, fatty liver disease, cardiovascular disease and diabetes

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