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

被引:23
作者
Deminice, Rafael [1 ]
de Castro, Gabriela S. [2 ]
Brosnan, Margaret E. [3 ]
Brosnan, John T. [3 ]
机构
[1] Univ Estadual Londrina, Fac Phys Educ & Sport, Dept Phys Educ, Rodovia Celso Garcia Cid,Pr 445 Km 380, Londrina, Parana, Brazil
[2] Univ Southampton, Human Dev & Hlth Acad Unit, Fac Med, Southampton SO16 6YD, Hants, England
[3] Mem Univ Newfoundland, Dept Biochem, St John, NF, Canada
关键词
NAFLD; Fatty liver disease; Creatine supplementation; B-oxidation; De novo fatty acid synthesis; Oxidative stress; ACTIVATED PROTEIN-KINASE; PHOSPHATIDYLETHANOLAMINE N-METHYLTRANSFERASE; INSULIN-RESISTANCE; HEPATIC STEATOSIS; DEFICIENT MICE; PPAR-GAMMA; IN-VIVO; NONALCOHOLIC STEATOHEPATITIS; BETAINE SUPPLEMENTATION; OXIDATIVE STRESS;
D O I
10.1007/s00726-016-2183-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:1983 / 1991
页数:9
相关论文
共 67 条
[51]   Clinical approaches to non-alcoholic fatty liver disease [J].
Schwenger, Katherine J. P. ;
Allard, Johane P. .
WORLD JOURNAL OF GASTROENTEROLOGY, 2014, 20 (07) :1712-1723
[52]   Effects of Purified Eicosapentaenoic and Docosahexaenoic Acids in Nonalcoholic Fatty Liver Disease: Results From the WELCOME* Study [J].
Scorletti, Eleonora ;
Bhatia, Lokpal ;
McCormick, Keith G. ;
Clough, Geraldine F. ;
Nash, Kathryn ;
Hodson, Leanne ;
Moyses, Helen E. ;
Calder, Philip C. ;
Byrne, Christopher D. .
HEPATOLOGY, 2014, 60 (04) :1211-1221
[53]  
Selhub J, 2002, J Nutr Health Aging, V6, P39
[54]   Polymorphism of the PEMT gene and susceptibility to nonalcoholic fatty liver disease (NAFLD) [J].
Song, JN ;
da Costa, KA ;
Fischer, LM ;
Kohlmeier, M ;
Kwock, L ;
Wang, SL ;
Zeisel, SH .
FASEB JOURNAL, 2005, 19 (10) :1266-1271
[55]  
Stead LM, 2006, AM J CLIN NUTR, V83, P5
[56]   Methylation demand and homocysteine metabolism: effects of dietary provision of creatine and guanidinoacetate [J].
Stead, LM ;
Au, KP ;
Jacobs, RL ;
Brosnan, ME ;
Brosnan, JT .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2001, 281 (05) :E1095-E1100
[57]   Differential regulation of AMPK activation in leptin- and creatine-deficient mice [J].
Stockebrand, Malte ;
Sauter, Kathrin ;
Neu, Axel ;
Isbrandt, Dirk ;
Choe, Chi-un .
FASEB JOURNAL, 2013, 27 (10) :4147-4156
[58]   Roles of PPARs in NAFLD: Potential therapeutic targets [J].
Tailleux, Anne ;
Wouters, Kristiaan ;
Staels, Bart .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR AND CELL BIOLOGY OF LIPIDS, 2012, 1821 (05) :809-818
[59]   Impact of increased PPARγ activity in adipocytes in vivo on adiposity, insulin sensitivity and the effects of rosiglitazone treatment [J].
Takasawa, Katsuko ;
Kubota, Naoto ;
Terauchi, Yasuo ;
Kadowaki, Takashi .
ENDOCRINE JOURNAL, 2008, 55 (04) :767-776
[60]   Evolution of Inflammation in Nonalcoholic Fatty Liver Disease: The Multiple Parallel Hits Hypothesis [J].
Tilg, Herbert ;
Moschen, Alexander R. .
HEPATOLOGY, 2010, 52 (05) :1836-1846