Literature DB >> 26832170

Creatine supplementation as a possible new therapeutic approach for fatty liver disease: early findings.

Rafael Deminice1, Gabriela S de Castro2, Margaret E Brosnan3, John T Brosnan3.   

Abstract

Over the last few years, consistent data have demonstrated that creatine (Cr) supplementation prevents the accumulation of fat in rat liver as well as the progression of fatty liver disease in different situations. Studies have demonstrated that Cr is effective and prevents fatty liver in high-fat and choline-deficient diets and in hepatoma cells in vitro. Because Cr synthesis is responsible for a considerable consumption of hepatic methyl groups, studies have tested the idea that Cr supplementation could modulate phospholipid formation and VLDL secretion. Studies have also demonstrated Cr is able to modulate the expression of key genes related to fatty acid oxidation in hepatocyte cell culture and in rat liver. However, to date, the mechanism by which Cr exerts protective effects against fatty liver is poorly understood. Therefore, the present review aims to summarize the studies involving the therapeutic use of Cr supplementation on fatty liver disease and to explore the mechanisms involved in one-carbon and fatty acid metabolism for the preventive effects of Cr supplementation on fat liver accumulation. Although a small number of studies have been conducted to date, we consider Cr as a new and promising therapeutic strategy to control fat accumulation in the liver as well as the progression of fatty liver disease.

Entities:  

Keywords:  Creatine supplementation; De novo fatty acid synthesis; Fatty liver disease; NAFLD; Oxidative stress; Β-oxidation

Mesh:

Substances:

Year:  2016        PMID: 26832170     DOI: 10.1007/s00726-016-2183-6

Source DB:  PubMed          Journal:  Amino Acids        ISSN: 0939-4451            Impact factor:   3.520


  5 in total

1.  Endoplasmic Reticulum Stress-induced Hepatocellular Death Pathways Mediate Liver Injury and Fibrosis via Stimulator of Interferon Genes.

Authors:  Arvin Iracheta-Vellve; Jan Petrasek; Benedek Gyongyosi; Abhishek Satishchandran; Patrick Lowe; Karen Kodys; Donna Catalano; Charles D Calenda; Evelyn A Kurt-Jones; Katherine A Fitzgerald; Gyongyi Szabo
Journal:  J Biol Chem       Date:  2016-11-03       Impact factor: 5.157

2.  Transcriptomics combined with metabolomics analysis of the mechanism of agmatine in the treatment of septic liver injury.

Authors:  Ling Huang; Lianfang Gan; Junhua Pan; Lifan Zhong; Qianru Wang; Shanjun Luo; Jia Tian; Huaping Liang
Journal:  Ann Transl Med       Date:  2022-05

3.  Chenopodium Quinoa and Salvia Hispanica Provide Immunonutritional Agonists to Ameliorate Hepatocarcinoma Severity under a High-Fat Diet.

Authors:  Jose Moisés Laparra Llopis; Daniel Brown; Blanca Saiz
Journal:  Nutrients       Date:  2020-06-30       Impact factor: 5.717

Review 4.  Common questions and misconceptions about creatine supplementation: what does the scientific evidence really show?

Authors:  Jose Antonio; Darren G Candow; Scott C Forbes; Bruno Gualano; Andrew R Jagim; Richard B Kreider; Eric S Rawson; Abbie E Smith-Ryan; Trisha A VanDusseldorp; Darryn S Willoughby; Tim N Ziegenfuss
Journal:  J Int Soc Sports Nutr       Date:  2021-02-08       Impact factor: 5.150

5.  Predicting metabolite-disease associations based on KATZ model.

Authors:  Xiujuan Lei; Cheng Zhang
Journal:  BioData Min       Date:  2019-10-26       Impact factor: 2.522

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.