4.6 Review

MOLECULAR PHYSIOLOGY OF BILE ACID SIGNALING IN HEALTH, DISEASE, AND AGING

Journal

PHYSIOLOGICAL REVIEWS
Volume 101, Issue 2, Pages 683-731

Publisher

AMER PHYSIOLOGICAL SOC
DOI: 10.1152/physrev.00049.2019

Keywords

FXR; metabolic syndrome; microbiome; NAFLD; TGR5

Categories

Funding

  1. EPFL
  2. Swiss National Science Foundation (SNSF) [310030_189178, CRSII5_180317/1]
  3. AXA Research Fund
  4. Marie Sklodowska-Curie fellowship (EU H2020)
  5. Swiss National Science Foundation (SNF) [310030_189178, CRSII5_180317] Funding Source: Swiss National Science Foundation (SNF)

Ask authors/readers for more resources

Bile acids have become important signaling molecules in the body, enabling inter-tissue communication and exerting pleiotropic physiological effects. The chemical variety of bile acids, largely determined by the gut microbiome, allows for complex adaptive responses in the body. This review discusses the mechanisms by which bile acid receptors coordinate various aspects of physiology and presents new therapeutic strategies for diseases related to pathological bile acid signaling.
Over the past two decades, bile acids (BAs) have become established as important signaling molecules that enable fine-tuned inter-tissue communication from the liver, their site of production, over the intestine, where they are modified by the gut microbiota, to virtually any organ, where they exert their pleiotropic physiological effects. The chemical variety of BAs, to a large extent determined by the gut microbiome, also allows for a complex fine-tuning of adaptive responses in our body. This review provides an overview of the mechanisms by which BA receptors coordinate several aspects of physiology and highlights new therapeutic strategies for diseases underlying pathological BA signaling.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available