Issue 103, 2014

Control of cholesterol homeostasis by entero-hepatic bile transport – the role of feedback mechanisms

Abstract

Cholesterol homeostasis is achieved through a tight regulation between synthesis, dietary absorption, utilization of bile salts, and excretion. These processes are regulated through three known feedback mechanisms, namely auto-negative regulation of hepatic bile salt synthesis, and positive regulation of intestinal bile salts on cholesterol absorption and excretion. A model for entero-hepatic cholesterol metabolism in conjunction with dietary inputs for cholesterol was used to obtain insights into the role of the feedback. The analysis demonstrated the significance of the negative feedback in maintaining physiological levels of cholesterol. Furthermore, the positive feedback by the intestinal bile salts on the cholesterol absorption/excretion processes plays an important role in plasma cholesterol homeostasis. Under familial hypercholesterolemia (FH), perturbations in the hepato-intestinal reversible bile transport revealed that an increase in the transport of bile salts from the intestine to the liver decreased the hepatic cholesterol absorption rate. Under such a condition, a twofold decrease in intestinal bile salt transport resulted in an approximately 20% reduction in the plasma cholesterol level, thereby restoring it to normalcy. This suggests that the bile transport control strategy presents an alternative therapeutic method that can effectively reduce cholesterol absorption to attain cholesterol homeostasis.

Graphical abstract: Control of cholesterol homeostasis by entero-hepatic bile transport – the role of feedback mechanisms

Supplementary files

Article information

Article type
Paper
Submitted
28 Aug 2014
Accepted
22 Oct 2014
First published
24 Oct 2014

RSC Adv., 2014,4, 58964-58975

Author version available

Control of cholesterol homeostasis by entero-hepatic bile transport – the role of feedback mechanisms

S. Mishra, P. R. Somvanshi and K. V. Venkatesh, RSC Adv., 2014, 4, 58964 DOI: 10.1039/C4RA09397F

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