» Articles » PMID: 35846774

Circadian Rhythms Coordinated With Gut Microbiota Partially Account for Individual Differences in Hepatitis B-Related Cirrhosis

Overview
Authors
Affiliations
Soon will be listed here.
Abstract

Cirrhosis is the end stage of chronic liver diseases like chronic hepatitis B. In China, hepatitis B accounts for around 60% of cases of cirrhosis. So far, clinical and laboratory indexes for the early diagnosis of cirrhosis are far from satisfactory. Nevertheless, there haven't been specific drugs for cirrhosis. Thus, it is quite necessary to uncover more specific factors which play their roles in cirrhosis and figure out the possible therapeutic targets. Among emerging factors taking part in the initiation and progression of cirrhosis, gut microbiota might be a pivot of systemic factors like metabolism and immune and different organs like gut and liver. Discovery of detailed molecular mechanism in gut microbiota and gut liver axis leads to a more promising prospect of developing new drugs intervening in these pathways. Time-based medication regimen has been proofed to be helpful in hormonotherapy, especially in the use of glucocorticoid. Thus, circadian rhythms, though haven't been strongly linked to hepatitis B and its complications, are still pivotal to various pathophysiological progresses. Gut microbiota as a potential effective factor of circadian rhythms has also received increasing attentions. Here, our work, restricting cirrhosis to the post-hepatitis B one, is aimed to summarize how circadian rhythms and hepatitis B-related cirrhosis can intersect gut microbiota, and to throw new insights on the development of new and time-based therapies for hepatitis B-related cirrhosis and other cirrhosis.

Citing Articles

Mechanisms of action of intestinal microorganisms and advances in head and neck tumors.

Xialu S, Faqiang M Discov Oncol. 2025; 16(1):303.

PMID: 40072772 PMC: 11903988. DOI: 10.1007/s12672-025-02035-y.


Protective effect of Zhizi Huangqi Shanzha formula on aflatoxin poisoning in mice and its effect on intestinal flora.

Chuanbo S, Guangpei X, Ping J, Shipping H, Cunwu C, Yanfei H J Tradit Chin Med. 2024; 44(5):926-933.

PMID: 39380223 PMC: 11462521. DOI: 10.19852/j.cnki.jtcm.2024.05.003.


Crosstalk between circadian clocks and pathogen niche.

Borrmann H, Rijo-Ferreira F PLoS Pathog. 2024; 20(5):e1012157.

PMID: 38723104 PMC: 11081299. DOI: 10.1371/journal.ppat.1012157.


The causal relationship between gut microbiota and biliary tract cancer: comprehensive bidirectional Mendelian randomization analysis.

Wang K, Wang S, Qin X, Chen Y, Chen Y, Wang J Front Cell Infect Microbiol. 2024; 14:1308742.

PMID: 38558852 PMC: 10978781. DOI: 10.3389/fcimb.2024.1308742.


Targeting the blood-brain barrier to delay aging-accompanied neurological diseases by modulating gut microbiota, circadian rhythms, and their interplays.

Wang Y, Du W, Hu X, Yu X, Guo C, Jin X Acta Pharm Sin B. 2023; 13(12):4667-4687.

PMID: 38045038 PMC: 10692395. DOI: 10.1016/j.apsb.2023.08.009.


References
1.
Mouzannar K, Fusil F, Lacombe B, Ollivier A, Menard C, Lotteau V . Farnesoid X receptor-α is a proviral host factor for hepatitis B virus that is inhibited by ligands in vitro and in vivo. FASEB J. 2018; 33(2):2472-2483. DOI: 10.1096/fj.201801181R. View

2.
Pijls K, Koek G, Elamin E, de Vries H, Masclee A, Jonkers D . Large intestine permeability is increased in patients with compensated liver cirrhosis. Am J Physiol Gastrointest Liver Physiol. 2013; 306(2):G147-53. DOI: 10.1152/ajpgi.00330.2013. View

3.
Adolph T, Grander C, Moschen A, Tilg H . Liver-Microbiome Axis in Health and Disease. Trends Immunol. 2018; 39(9):712-723. DOI: 10.1016/j.it.2018.05.002. View

4.
Lenoir M, Martin R, Torres-Maravilla E, Chadi S, Gonzalez-Davila P, Sokol H . Butyrate mediates anti-inflammatory effects of in intestinal epithelial cells through . Gut Microbes. 2020; 12(1):1-16. PMC: 7567499. DOI: 10.1080/19490976.2020.1826748. View

5.
Garrido A, Kim E, Teijeiro A, Sanchez Sanchez P, Gallo R, Nair A . Histone acetylation of bile acid transporter genes plays a critical role in cirrhosis. J Hepatol. 2021; 76(4):850-861. PMC: 8934297. DOI: 10.1016/j.jhep.2021.12.019. View