» Articles » PMID: 33085065

Bile Acids: A Communication Channel in the Gut-Brain Axis

Overview
Specialty Biochemistry
Date 2020 Oct 21
PMID 33085065
Citations 61
Authors
Affiliations
Soon will be listed here.
Abstract

Bile acids are signalling hormones involved in the regulation of several metabolic pathways. The ability of bile acids to bind and signal through their receptors is modulated by the gut microbiome, since the microbiome contributes to the regulation and synthesis of bile acids as well to their physiochemical properties. From the gut, bacteria have been shown to send signals to the central nervous system via their metabolites, thus affecting the behaviour and brain function of the host organism. In the last years it has become increasingly evident that bile acids affect brain function, during normal physiological and pathological conditions. Although bile acids may be synthesized locally in the brain, the majority of brain bile acids are taken up from the systemic circulation. Since the composition of the brain bile acid pool may be regulated by the action of intestinal bacteria, it is possible that bile acids function as a communication bridge between the gut microbiome and the brain. However, little is known about the molecular mechanisms and the physiological roles of bile acids in the central nervous system. The possibility that bile acids may be a direct link between the intestinal microbiome and the brain is also an understudied subject. Here we review the influence of gut bacteria on the bile acid pool composition and properties, as well as striking evidence showing the role of bile acids as neuroactive molecules.

Citing Articles

The bile acid metabolome in umbilical cord blood and meconium of healthy newborns: distinct characteristics and implications.

Lu C, Gao Z, Zhang S, Du K, Xu D, Dong W PeerJ. 2024; 12:e18506.

PMID: 39686994 PMC: 11648689. DOI: 10.7717/peerj.18506.


Unlocking gut-liver-brain axis communication metabolites: energy metabolism, immunity and barriers.

Sun X, Shukla M, Wang W, Li S NPJ Biofilms Microbiomes. 2024; 10(1):136.

PMID: 39587086 PMC: 11589602. DOI: 10.1038/s41522-024-00610-9.


The bile acid chenodeoxycholic acid associates with reduced stroke in humans and mice.

Monteiro-Cardoso V, Yeo X, Bae H, Mayan D, Wehbe M, Lee S J Lipid Res. 2024; 66(1):100712.

PMID: 39577772 PMC: 11721534. DOI: 10.1016/j.jlr.2024.100712.


Every-other-day fasting inhibits pyroptosis while regulating bile acid metabolism and activating TGR5 signaling in spinal cord injury.

Song H, Pang R, Chen Z, Wang L, Hu X, Feng J Front Mol Neurosci. 2024; 17:1466125.

PMID: 39328272 PMC: 11424537. DOI: 10.3389/fnmol.2024.1466125.


Probiotic therapy modulates the brain-gut-liver microbiota axis in a mouse model of traumatic brain injury.

Amaral W, Kokroko N, Treangen T, Villapol S, Gomez-Pinilla F Biochim Biophys Acta Mol Basis Dis. 2024; 1870(8):167483.

PMID: 39209236 PMC: 11526848. DOI: 10.1016/j.bbadis.2024.167483.


References
1.
Amador M, Masingue M, Debs R, Lamari F, Perlbarg V, Roze E . Treatment with chenodeoxycholic acid in cerebrotendinous xanthomatosis: clinical, neurophysiological, and quantitative brain structural outcomes. J Inherit Metab Dis. 2018; 41(5):799-807. DOI: 10.1007/s10545-018-0162-7. View

2.
Angelin B, Bjorkhem I, Einarsson K, Ewerth S . Hepatic uptake of bile acids in man. Fasting and postprandial concentrations of individual bile acids in portal venous and systemic blood serum. J Clin Invest. 1982; 70(4):724-31. PMC: 370280. DOI: 10.1172/jci110668. View

3.
Bates G, Dorsey R, Gusella J, Hayden M, Kay C, Leavitt B . Huntington disease. Nat Rev Dis Primers. 2016; 1:15005. DOI: 10.1038/nrdp.2015.5. View

4.
Begley M, Hill C, Gahan C . Bile salt hydrolase activity in probiotics. Appl Environ Microbiol. 2006; 72(3):1729-38. PMC: 1393245. DOI: 10.1128/AEM.72.3.1729-1738.2006. View

5.
Bengmark S . Gut microbiota, immune development and function. Pharmacol Res. 2012; 69(1):87-113. DOI: 10.1016/j.phrs.2012.09.002. View