Effects of bile acids and taurine on the lipid fluidity of hepatic microsomes in normal and bile duct-ligated rats--a spin label study.

Abstract

In cholestasis and obstructive jaundice, hepatic bile acids and taurine content increase significantly and bile acids change in compositions. For example, increases in cholic acid, beta-muricholic acid and taurine-conjugated bile acids occur in rats. In this study, to clarify the significance of changes in bile acid composition in obstructive jaundice, the effects of various bile acids and taurine on the fluidity of the hepatic microsomal membrane were studied by the electron spin resonance spin-label method in normal and bile duct-ligated (for 10 days) rats. The flow properties (order parameter) of the shallow and deep layers of the membrane were determined with 5- and 12-doxyl stearic acid, respectively. Bile acids mainly affected the fluidity of the shallow membrane layer. The fluidity of the hepatic microsomal membrane was decreased in bile duct-ligated rats. Conjugated cholic acid (taurine-conjugated cholic acid, glycine-conjugated cholic acid and non-conjugated beta-muricholic acid exerted effects that increased fluidity in comparison with non-conjugated cholic acid and chenodeoxycholic acid, a precursor of beta-muricholic acid. Taurine had no clear effect on fluidity. In conclusion, cholic acid conjugation and beta-muricholic acid formation may be mechanisms which protect against the decrease in lipid fluidity of hepatic biomembranes in cholestasis or obstructive jaundice. Taurine may also affect fluidity through the formation of taurine-conjugated bile acids.

• Authors: T Nakashima, T Shima, Y Sakamoto, T Nakajima, Y Seto, A Sano, M Iwai, T Okanoue, K Kashima
• Journal: Journal of hepatology (J Hepatol) Vol. 18 Issue 1 Pg. 74-9 (Apr 1993) ISSN: 0168-8278 [Print] Netherlands
• PMID: 8393465 (Publication Type: Journal Article)

Chemical References

• Bile Acids and Salts
• Membrane Lipids
• Spin Labels
• Taurine

Topics

• Animals
• Bile Acids and Salts (pharmacology)
• Cholestasis, Intrahepatic (physiopathology)
• Disease Models, Animal
• Electron Spin Resonance Spectroscopy
• Intracellular Membranes (physiology)
• Ligation
• Male
• Membrane Fluidity (physiology)
• Membrane Lipids (physiology)
• Microsomes, Liver (drug effects)
• Rats
• Rats, Wistar
• Reference Values
• Spin Labels
• Taurine (pharmacology)