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

机译:通过肠肝胆汁运输控制胆固醇稳态-反馈机制的作用

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摘要

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.
机译:胆固醇的稳态通过在合成,饮食吸收,胆汁盐的利用和排泄之间的严格调节来实现。这些过程通过三种已知的反馈机制进行调节,即肝细胞胆汁盐合成的自负调节和肠道胆汁盐对胆固醇吸收和排泄的积极调节。肠肝胆固醇代谢的模型与胆固醇的饮食投入一起用于了解反馈作用。分析表明负反馈在维持胆固醇的生理水平中的重要性。此外,肠道胆汁盐对胆固醇吸收/排泄过程的正反馈在血浆胆固醇稳态中起着重要作用。在家族性高胆固醇血症(FH)下,肝肠可逆胆汁转运的扰动表明,胆盐从肠到肝脏的转运增加会降低肝胆固醇的吸收率。在这种情况下,肠内胆汁盐转运减少两倍,导致血浆胆固醇水平降低约20%,从而使其恢复正常。这表明胆汁运输控制策略提出了另一种治疗方法,可以有效地减少胆固醇的吸收以达到胆固醇的稳态。

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