Literature DB >> 28371374

Vitamin A deficiency in chronic cholestatic liver disease: Is vitamin A therapy beneficial?

Cora Freund1, Daniel N Gotthardt1.   

Abstract

Chronic cholestatic diseases are progressive diseases of the biliary tract that cause hepatic fibrosis and ultimately lead to liver failure. Liver transplantation is the sole curative option currently available, and because of high morbidity and mortality rates of these diseases, new therapeutic approaches are needed. Vitamin A is a nutrient essential for health as it regulates many processes, including epithelial growth and immunological processes. Vitamin A is primarily stored in hepatic stellate cells, and during liver injury, through an unknown mechanism, these cells lose vitamin A and convert into collagen-producing myofibroblasts, which contributes to hepatic fibrosis. Vitamin A deficiencies in chronic cholestatic diseases have been frequently reported, and therefore, retinoid metabolism has attracted a lot of attention. Retinoids have been shown to attenuate or even prevent hepatic fibrosis, and to regulate hepatic immunological response to cholestatic injury in different rodent models of chronic cholestasis. Recently, their potential as therapeutic drugs in primary sclerosing cholangitis patients was analyzed. The aim of this review is to summarize the existing knowledge and hypotheses about vitamin A role and the disease progression in cholestatic liver disease.
© 2017 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  hepatic fibrosis; hepatic stellate cells; primary biliary cholangitis; primary sclerosing cholangitis; retinoid metabolism

Mesh:

Year:  2017        PMID: 28371374     DOI: 10.1111/liv.13433

Source DB:  PubMed          Journal:  Liver Int        ISSN: 1478-3223            Impact factor:   5.828


  6 in total

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Authors:  Reham S Ibrahim; Nesrine S El-Mezayen; Alaa A El-Banna
Journal:  Sci Rep       Date:  2022-07-13       Impact factor: 4.996

2.  Vitamin A-coupled liposomes carrying TLR4-silencing shRNA induce apoptosis of pancreatic stellate cells and resolution of pancreatic fibrosis.

Authors:  Yuwei Zhang; Dan Yue; Liuliu Cheng; Anliang Huang; Nanwei Tong; Ping Cheng
Journal:  J Mol Med (Berl)       Date:  2018-03-27       Impact factor: 4.599

3.  In silico Identification and Mechanism Exploration of Hepatotoxic Ingredients in Traditional Chinese Medicine.

Authors:  Qihui Wu; Chuipu Cai; Pengfei Guo; Meiling Chen; Xiaoqin Wu; Jingwei Zhou; Yunxia Luo; Yidan Zou; Ai-Lin Liu; Qi Wang; Zaoyuan Kuang; Jiansong Fang
Journal:  Front Pharmacol       Date:  2019-05-03       Impact factor: 5.810

4.  Altered hepatic genes related to retinol metabolism and plasma retinol in patients with non-alcoholic fatty liver disease.

Authors:  Paulina Pettinelli; Bianca M Arendt; Anastasia Teterina; Ian McGilvray; Elena M Comelli; Scott K Fung; Sandra E Fischer; Johane P Allard
Journal:  PLoS One       Date:  2018-10-31       Impact factor: 3.240

5.  Altered Expression of Retinol Metabolism-Related Genes in an ANIT-Induced Cholestasis Rat Model.

Authors:  Kimitaka Takitani; Kanta Kishi; Hiroshi Miyazaki; Maki Koh; Hirofumi Tamaki; Akiko Inoue; Hiroshi Tamai
Journal:  Int J Mol Sci       Date:  2018-10-26       Impact factor: 5.923

6.  Farnesoid X receptor and bile acids regulate vitamin A storage.

Authors:  Ali Saeed; Jing Yang; Janette Heegsma; Albert K Groen; Saskia W C van Mil; Coen C Paulusma; Lu Zhou; Bangmao Wang; Klaas Nico Faber
Journal:  Sci Rep       Date:  2019-12-20       Impact factor: 4.379

  6 in total

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