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Alcohol effects on hepatic lipid metabolism
Open accessAbstract
Alcoholic liver disease (ALD) is the most prevalent type of chronic liver disease with significant morbidity and mortality worldwide. ALD begins with simple hepatic steatosis and progresses to alcoholic steatohepatitis, fibrosis, and cirrhosis. The severity of hepatic steatosis is highly associated with the development of later stages of ALD. This review explores the disturbances of alcohol-induced hepatic lipid metabolism through altered hepatic lipid uptake, de novo lipid synthesis, fatty acid oxidation, hepatic lipid export, and lipid droplet formation and catabolism. In addition, we review emerging data on the contributions of genetics and bioactive lipid metabolism in alcohol-induced hepatic lipid accumulation.
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“It should be noted that alcohol-induced dysregulation of mitochondrial β-oxidation is considered the most significant contribution to lipid accumulation in the liver [46].”
From Pathophysiological Aspects of Alcohol Metabolism in the Liver (2021) · cites this paper as [46]
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Autophagy regulates lipid metabolism
Singh, R., Kaushik, S., Wang, Y., Xiang, Y., Novak, I., Komatsu, M., Tanaka, K., Cuervo, A. M., & Czaja, M. J. (2009) · Nature · doi:10.1038/nature07976 · Cited by 3,975
Buch, S., Stickel, F., Trépo, E., Way, M., Herrmann, A., Nischalke, H. D., Brosch, M., Rosendahl, J., Berg, T., Ridinger, M., et al. (2015) · Nature Genetics · doi:10.1038/ng.3417 · Cited by 565
Research works printed but not linked: 156
- Asrani, 2019, Burden of liver diseases in the world, J. Hepatol., 70, 151, 10.1016/j.jhep.2018.09.014 · DOI · Paper page
- Edmondson, 1967, The early stage of liver injury in the alcoholic, Medicine (Baltimore)., 46, 119, 10.1097/00005792-196703000-00006 · DOI
- Powell, 2005, Steatosis: co-factor in other liver diseases, Hepatology., 42, 5, 10.1002/hep.20750 · DOI
- Zakhari, 2006, Overview: how is alcohol metabolized by the body?, Alcohol Res. Health., 29, 245
- Carr, 2015, Insulin resistance in clinical and experimental alcoholic liver disease, Ann. N. Y. Acad. Sci., 1353, 1, 10.1111/nyas.12787 · DOI
- Zhao, 2015, FGF21 mediates alcohol-induced adipose tissue lipolysis by activation of systemic release of catecholamine in mice, J. Lipid Res., 56, 1481, 10.1194/jlr.M058610 · DOI
- Leggio, 2009, Is cortisol involved in the alcohol-related fat mass impairment? A longitudinal clinical study, Alcohol Alcohol., 44, 211, 10.1093/alcalc/agn116 · DOI
- Zhong, 2012, Chronic alcohol exposure stimulates adipose tissue lipolysis in mice: role of reverse triglyceride transport in the pathogenesis of alcoholic steatosis, Am. J. Pathol., 180, 998, 10.1016/j.ajpath.2011.11.017 · DOI
- Wei, 2013, Chronic alcohol exposure disturbs lipid homeostasis at the adipose tissue-liver axis in mice: analysis of triacylglycerols using high-resolution mass spectrometry in combination with in vivo metabolite deuterium labeling, PLoS One., 8, e55382, 10.1371/journal.pone.0055382 · DOI · Paper page
- Carr, 2013, Temporal effects of ethanol consumption on energy homeostasis, hepatic steatosis, and insulin sensitivity in mice, Alcohol. Clin. Exp. Res., 37, 1091, 10.1111/acer.12075 · DOI
- Addolorato, 1997, Energy expenditure, substrate oxidation, and body composition in subjects with chronic alcoholism: new findings from metabolic assessment, Alcohol. Clin. Exp. Res., 21, 962
- Gandhi, 1984, Alcohol-induced changes in lipids and lipoproteins, Alcohol. Clin. Exp. Res., 8, 29, 10.1111/j.1530-0277.1984.tb05027.x · DOI
- Lieber, 1984, Ethanol and lipids, Alcohol. Clin. Exp. Res., 8, 409, 10.1111/j.1530-0277.1984.tb05689.x · DOI
- Hussain, 1991, Clearance of chylomicron remnants by the low density lipoprotein receptor-related protein/alpha 2-macroglobulin receptor, J. Biol. Chem., 266, 13936, 10.1016/S0021-9258(18)92792-4 · DOI
- Willnow, 1997, Mechanisms of hepatic chylomicron remnant clearance, Diabet. Med., 14, S75, 10.1002/(SICI)1096-9136(199708)14:3+<S75::AID-DIA449>3.0.CO;2-9 · DOI
- Baraona, 1970, Effects of chronic ethanol feeding on serum lipoprotein metabolism in the rat, J. Clin. Invest., 49, 769, 10.1172/JCI106290 · DOI
- Donnelly, 2005, Sources of fatty acids stored in liver and secreted via lipoproteins in patients with nonalcoholic fatty liver disease, J. Clin. Invest., 115, 1343, 10.1172/JCI23621 · DOI · Paper page
- Stahl, 2001, Fatty acid transport proteins: a current view of a growing family, Trends Endocrinol. Metab., 12, 266, 10.1016/S1043-2760(01)00427-1 · DOI
- Zhou, 2008, Hepatic fatty acid transporter Cd36 is a common target of LXR, PXR, and PPARgamma in promoting steatosis, Gastroenterology., 134, 556, 10.1053/j.gastro.2007.11.037 · DOI
- Ronis, 2011, Effects of long-term ethanol administration in a rat total enteral nutrition model of alcoholic liver disease, Am. J. Physiol. Gastrointest. Liver Physiol., 300, G109, 10.1152/ajpgi.00145.2010 · DOI
- Clugston, 2014, CD36-deficient mice are resistant to alcohol- and high-carbohydrate-induced hepatic steatosis, J. Lipid Res., 55, 239, 10.1194/jlr.M041863 · DOI
- Berk, 2005, Increased hepatocellular uptake of long chain fatty acids occurs by different mechanisms in fatty livers due to obesity or excess ethanol use, contributing to development of steatohepatitis in both settings, Trans. Am. Clin. Climatol. Assoc., 116, 335
- Blomstrand, 1973, Studies on the ethanol-induced decrease of fatty acid oxidation in rat and human liver slices, Life Sci., 13, 1131, 10.1016/0024-3205(73)90380-9 · DOI
- Cederbaum, 1975, Effect of chronic ethanol ingestion on fatty acid oxidation by hepatic mitochondria, J. Biol. Chem., 250, 5122, 10.1016/S0021-9258(19)41286-6 · DOI
- Correnti, 2018, Ethanol and C2 ceramide activate fatty acid oxidation in human hepatoma cells, Sci. Rep., 8, 12923, 10.1038/s41598-018-31025-0 · DOI
- Reboucas, 1961, Studies on the pathogenesis of the ethanol-induced fatty liver. I. Synthesis and oxidation of fatty acids by the liver, J. Clin. Invest., 40, 1355, 10.1172/JCI104366 · DOI
- Ontko, 1973, Effects of ethanol on the metabolism of free fatty acids in isolated liver cells, J. Lipid Res., 14, 78, 10.1016/S0022-2275(20)39332-9 · DOI
- Hoek, 2002, Alcohol and mitochondria: a dysfunctional relationship, Gastroenterology., 122, 2049, 10.1053/gast.2002.33613 · DOI · Paper page
- Sonko, 1994, Effect of alcohol on postmeal fat storage, Am. J. Clin. Nutr., 59, 619, 10.1093/ajcn/59.3.619 · DOI
- Suter, 1992, The effect of ethanol on fat storage in healthy subjects, N. Engl. J. Med., 326, 983, 10.1056/NEJM199204093261503 · DOI
- You, 2004, The role of AMP-activated protein kinase in the action of ethanol in the liver, Gastroenterology., 127, 1798, 10.1053/j.gastro.2004.09.049 · DOI · Paper page
- Sachan, 1984, Ameliorating effects of carnitine and its precursors on alcohol-induced fatty liver, Am. J. Clin. Nutr., 39, 738, 10.1093/ajcn/39.5.738 · DOI
- Kępka, 2019, Relation of plasma carnitine and aminotransferases to alcohol dose and time of dependence, Alcohol., 81, 62, 10.1016/j.alcohol.2019.04.004 · DOI
- Lemasters, 2006, Voltage-dependent anion channel (VDAC) as mitochondrial governator–thinking outside the box, Biochim. Biophys. Acta., 1762, 181, 10.1016/j.bbadis.2005.10.006 · DOI
- Holmuhamedov, 2009, Ethanol exposure decreases mitochondrial outer membrane permeability in cultured rat hepatocytes, Arch. Biochem. Biophys., 481, 226, 10.1016/j.abb.2008.10.036 · DOI
- Holmuhamedov, 2012, Ethanol suppresses ureagenesis in rat hepatocytes: role of acetaldehyde, J. Biol. Chem., 287, 7692, 10.1074/jbc.M111.293399 · DOI
- Mandard, 2004, Peroxisome proliferator-activated receptor α target genes, Cell. Mol. Life Sci., 61, 393, 10.1007/s00018-003-3216-3 · DOI
- Fischer, 2003, Peroxisome proliferator-activated receptor α (PPARα) agonist treatment reverses PPARα dysfunction and abnormalities in hepatic lipid metabolism in ethanol-fed mice, J. Biol. Chem., 278, 27997, 10.1074/jbc.M302140200 · DOI
- Herzig, 2018, AMPK: guardian of metabolism and mitochondrial homeostasis, Nat. Rev. Mol. Cell Biol., 19, 121, 10.1038/nrm.2017.95 · DOI
- Shearn, 2013, Increased dietary fat contributes to dysregulation of the LKB1/AMPK pathway and increased damage in a mouse model of early-stage ethanol-mediated steatosis, J. Nutr. Biochem., 24, 1436, 10.1016/j.jnutbio.2012.12.002 · DOI
- Chang, 2014, SIRT1 and other sirtuins in metabolism, Trends Endocrinol. Metab., 25, 138, 10.1016/j.tem.2013.12.001 · DOI
- Ruderman, 2010, AMPK and SIRT1: a long-standing partnership?, Am. J. Physiol. Endocrinol. Metab., 298, E751, 10.1152/ajpendo.00745.2009 · DOI · Paper page
- You, 2008, Involvement of mammalian sirtuin 1 in the action of ethanol in the liver, Am. J. Physiol. Gastrointest. Liver Physiol., 294, G892, 10.1152/ajpgi.00575.2007 · DOI
- Ajmo, 2008, Resveratrol alleviates alcoholic fatty liver in mice, Am. J. Physiol. Gastrointest. Liver Physiol., 295, G833, 10.1152/ajpgi.90358.2008 · DOI · Paper page
- Sanders, 2016, De novo lipogenesis in the liver in health and disease: more than just a shunting yard for glucose, Biol. Rev. Camb. Philos. Soc., 91, 452, 10.1111/brv.12178 · DOI
- Zhou, 2014, Disturbances in the murine hepatic circadian clock in alcohol-induced hepatic steatosis, Sci. Rep., 4, 3725, 10.1038/srep03725 · DOI
- Yen, 2008, DGAT enzymes and triacylglycerol biosynthesis, J. Lipid Res., 49, 2283, 10.1194/jlr.R800018-JLR200 · DOI · Paper page
- Foufelle, 2002, New perspectives in the regulation of hepatic glycolytic and lipogenic genes by insulin and glucose: a role for the transcription factor sterol regulatory element binding protein-1c, Biochem. J., 366, 377, 10.1042/bj20020430 · DOI
- Ji, 2006, Predominant role of sterol response element binding proteins (SREBP) lipogenic pathways in hepatic steatosis in the murine intragastric ethanol feeding model, J. Hepatol., 45, 717, 10.1016/j.jhep.2006.05.009 · DOI
- Yin, 2007, Differential gene expression and lipid metabolism in fatty liver induced by acute ethanol treatment in mice, Toxicol. Appl. Pharmacol., 223, 225, 10.1016/j.taap.2007.06.018 · DOI
- You, 2002, Ethanol induces fatty acid synthesis pathways by activation of sterol regulatory element-binding protein (SREBP), J. Biol. Chem., 277, 29342, 10.1074/jbc.M202411200 · DOI
- Esfandiari, 2010, Epigenetic regulation of hepatic endoplasmic reticulum stress pathways in the ethanol-fed cystathionine beta synthase-deficient mouse, Hepatology., 51, 932, 10.1002/hep.23382 · DOI
- Dara, 2011, The contribution of endoplasmic reticulum stress to liver diseases, Hepatology., 53, 1752, 10.1002/hep.24279 · DOI
- Peng, 2009, Adenosine signaling contributes to ethanol-induced fatty liver in mice, J. Clin. Invest., 119, 582, 10.1172/JCI37409 · DOI
- Jeong, 2008, Paracrine activation of hepatic CB1 receptors by stellate cell-derived endocannabinoids mediates alcoholic fatty liver, Cell Metab., 7, 227, 10.1016/j.cmet.2007.12.007 · DOI
- Bode, 1987, Endotoxemia in patients with alcoholic and non-alcoholic cirrhosis and in subjects with no evidence of chronic liver disease following acute alcohol excess, J. Hepatol., 4, 8, 10.1016/S0168-8278(87)80003-X · DOI
- Endo, 2007, TNF-α induces hepatic steatosis in mice by enhancing gene expression of sterol regulatory element binding protein-1c (SREBP-1c), Exp. Biol. Med. (Maywood)., 232, 614
- Horiguchi, 2008, Cell type-dependent pro- and anti-inflammatory role of signal transducer and activator of transcription 3 in alcoholic liver injury, Gastroenterology., 134, 1148, 10.1053/j.gastro.2008.01.016 · DOI
- Liangpunsakul, 2013, Activation of carbohydrate response element-binding protein by ethanol, J. Investig. Med., 61, 270, 10.2310/JIM.0b013e31827c2795 · DOI
- Marmier, 2015, Novel role for carbohydrate responsive element binding protein in the control of ethanol metabolism and susceptibility to binge drinking, Hepatology., 62, 1086, 10.1002/hep.27778 · DOI
- Gavrilova, 2003, Liver peroxisome proliferator-activated receptor γ contributes to hepatic steatosis, triglyceride clearance, and regulation of body fat mass, J. Biol. Chem., 278, 34268, 10.1074/jbc.M300043200 · DOI · Paper page
- Zhang, 2016, Hepatic peroxisome proliferator-activated receptor gamma signaling contributes to alcohol-induced hepatic steatosis and inflammation in mice, Alcohol. Clin. Exp. Res., 40, 988, 10.1111/acer.13049 · DOI
- Enomoto, 2003, Prevention of ethanol-induced liver injury in rats by an agonist of peroxisome proliferator-activated receptor-γ, pioglitazone, J. Pharmacol. Exp. Ther., 306, 846, 10.1124/jpet.102.047217 · DOI
- Tomita, 2004, Pioglitazone prevents alcohol-induced fatty liver in rats through up-regulation of c-Met, Gastroenterology., 126, 873, 10.1053/j.gastro.2003.12.008 · DOI · Paper page
- Bou Khalil, 2010, Lipin - the bridge between hepatic glycerolipid biosynthesis and lipoprotein metabolism, Biochim. Biophys. Acta., 1801, 1249, 10.1016/j.bbalip.2010.07.008 · DOI
- Hu, 2012, Regulation of hepatic lipin-1 by ethanol: role of AMP-activated protein kinase/sterol regulatory element-binding protein 1 signaling in mice, Hepatology., 55, 437, 10.1002/hep.24708 · DOI
- Hu, 2013, Hepatic-specific lipin-1 deficiency exacerbates experimental alcohol-induced steatohepatitis in mice, Hepatology., 58, 1953, 10.1002/hep.26589 · DOI
- Yin, 2012, MicroRNA-217 promotes ethanol-induced fat accumulation in hepatocytes by down-regulating SIRT1, J. Biol. Chem., 287, 9817, 10.1074/jbc.M111.333534 · DOI
- Yin, 2014, Deletion of SIRT1 from hepatocytes in mice disrupts lipin-1 signaling and aggravates alcoholic fatty liver, Gastroenterology., 146, 801, 10.1053/j.gastro.2013.11.008 · DOI
- Shen, 2010, Involvement of adiponectin-SIRT1-AMPK signaling in the protective action of rosiglitazone against alcoholic fatty liver in mice, Am. J. Physiol. Gastrointest. Liver Physiol., 298, G364, 10.1152/ajpgi.00456.2009 · DOI
- Everitt, 2013, Ethanol administration exacerbates the abnormalities in hepatic lipid oxidation in genetically obese mice, Am. J. Physiol. Gastrointest. Liver Physiol., 304, G38, 10.1152/ajpgi.00309.2012 · DOI
- Wurie, 2012, Diacylglycerol acyltransferase 2 acts upstream of diacylglycerol acyltransferase 1 and utilizes nascent diglycerides and de novo synthesized fatty acids in HepG2 cells, FEBS J., 279, 3033, 10.1111/j.1742-4658.2012.08684.x · DOI
- Qi, 2012, The use of stable isotope-labeled glycerol and oleic acid to differentiate the hepatic functions of DGAT1 and -2, J. Lipid Res., 53, 1106, 10.1194/jlr.M020156 · DOI
- Wada, 2008, Fish oil fed prior to ethanol administration prevents acute ethanol-induced fatty liver in mice, J. Hepatol., 49, 441, 10.1016/j.jhep.2008.04.026 · DOI
- Wang, 2010, Involvement and mechanism of DGAT2 upregulation in the pathogenesis of alcoholic fatty liver disease, J. Lipid Res., 51, 3158, 10.1194/jlr.M007948 · DOI
- Sugimoto, 2002, Decreased microsomal triglyceride transfer protein activity contributes to initiation of alcoholic liver steatosis in rats, J. Hepatol., 36, 157, 10.1016/S0168-8278(01)00263-X · DOI
- Nanji, 2004, Alcoholic liver injury in the rat is associated with reduced expression of peroxisome proliferator-α (PPARα)-regulated genes and is ameliorated by PPARα activation, J. Pharmacol. Exp. Ther., 310, 417, 10.1124/jpet.103.064717 · DOI
- Améen, 2005, Activation of peroxisome proliferator-activated receptor α increases the expression and activity of microsomal triglyceride transfer protein in the liver, J. Biol. Chem., 280, 1224, 10.1074/jbc.M412107200 · DOI
- Noga, 2002, An unexpected requirement for phosphatidylethanolaminen-methyltransferase in the secretion of very low density lipoproteins, J. Biol. Chem., 277, 42358, 10.1074/jbc.M204542200 · DOI
- Vance, 2005, Metabolic insights into phospholipid function using gene-targeted mice, J. Biol. Chem., 280, 10877, 10.1074/jbc.R400038200 · DOI
- Kharbanda, 2007, Betaine attenuates alcoholic steatosis by restoring phosphatidylcholine generation via the phosphatidylethanolamine methyltransferase pathway, J. Hepatol., 46, 314, 10.1016/j.jhep.2006.08.024 · DOI
- Carr, 2016, Pathophysiology of lipid droplet proteins in liver diseases, Exp. Cell Res., 340, 187, 10.1016/j.yexcr.2015.10.021 · DOI
- Li, 2013, Preservation of hepatocyte nuclear factor-4alpha contributes to the beneficial effect of dietary medium chain triglyceride on alcohol-induced hepatic lipid dyshomeostasis in rats, Alcohol. Clin. Exp. Res., 37, 587, 10.1111/acer.12013 · DOI
- Walther, 2009, The life of lipid droplets, Biochim. Biophys. Acta., 1791, 459, 10.1016/j.bbalip.2008.10.009 · DOI
- Kilwein, 2019, Lipid droplet motility and organelle contacts, Contact (Thousand Oaks)., 2
- Gluchowski, 2017, Lipid droplets and liver disease: from basic biology to clinical implications, Nat. Rev. Gastroenterol. Hepatol., 14, 343, 10.1038/nrgastro.2017.32 · DOI
- Zhou, 2012, Cidea promotes hepatic steatosis by sensing dietary fatty acids, Hepatology., 56, 95, 10.1002/hep.25611 · DOI
- Bickel, 2009, PAT proteins, an ancient family of lipid droplet proteins that regulate cellular lipid stores, Biochim. Biophys. Acta., 1791, 419, 10.1016/j.bbalip.2009.04.002 · DOI
- Dalen, 2004, Adipose tissue expression of the lipid droplet–associating proteins S3-12 and perilipin is controlled by peroxisome proliferator-activated receptor-γ, Diabetes., 53, 1243, 10.2337/diabetes.53.5.1243 · DOI
- Brasaemle, 1997, Adipose differentiation-related protein is an ubiquitously expressed lipid storage droplet-associated protein, J. Lipid Res., 38, 2249, 10.1016/S0022-2275(20)34939-7 · DOI
- Wolins, 2006, OXPAT/PAT-1 is a PPAR-induced lipid droplet protein that promotes fatty acid utilization, Diabetes., 55, 3418, 10.2337/db06-0399 · DOI
- Straub, 2008, Differential pattern of lipid droplet-associated proteins and de novo perilipin expression in hepatocyte steatogenesis, Hepatology., 47, 1936, 10.1002/hep.22268 · DOI
- Carr, 2017, Perilipin staining distinguishes between steatosis and nonalcoholic steatohepatitis in adults and children, Clin. Gastroenterol. Hepatol., 15, 145, 10.1016/j.cgh.2016.08.023 · DOI
- Motomura, 2006, Up-regulation of ADRP in fatty liver in human and liver steatosis in mice fed with high fat diet, Biochem. Biophys. Res. Commun., 340, 1111, 10.1016/j.bbrc.2005.12.121 · DOI
- Granneman, 2011, Interactions of perilipin-5 (plin5) with adipose triglyceride lipase, J. Biol. Chem., 286, 5126, 10.1074/jbc.M110.180711 · DOI
- Mak, 2008, Adipose differentiation-related protein is a reliable lipid droplet marker in alcoholic fatty liver of rats, Alcohol. Clin. Exp. Res., 32, 683, 10.1111/j.1530-0277.2008.00624.x · DOI
- Carr, 2014, Absence of perilipin 2 prevents hepatic steatosis, glucose intolerance and ceramide accumulation in alcohol-fed mice, PLoS One., 9, e97118, 10.1371/journal.pone.0097118 · DOI
- Raynard, 2002, Risk factors of fibrosis in alcohol-induced liver disease, Hepatology., 35, 635, 10.1053/jhep.2002.31782 · DOI
- Bulankina, 2009, TIP47 functions in the biogenesis of lipid droplets, J. Cell Biol., 185, 641, 10.1083/jcb.200812042 · DOI
- Carr, 2012, Reduction of TIP47 improves hepatic steatosis and glucose homeostasis in mice, Am. J. Physiol. Regul. Integr. Comp. Physiol., 302, R996, 10.1152/ajpregu.00177.2011 · DOI
- Gu, 2019, Plin3 protects against alcoholic liver injury by facilitating lipid export from the endoplasmic reticulum, J. Cell. Biochem., 120, 16075, 10.1002/jcb.28889 · DOI
- Jambunathan, 2011, FSP27 promotes lipid droplet clustering and then fusion to regulate triglyceride accumulation, PLoS One., 6, e28614, 10.1371/journal.pone.0028614 · DOI
- Xu, 2015, Fat-specific protein 27/CIDEC promotes development of alcoholic steatohepatitis in mice and humans, Gastroenterology., 149, 1030, 10.1053/j.gastro.2015.06.009 · DOI
- Tian, 2010, Variant in PNPLA3 is associated with alcoholic liver disease, Nat. Genet., 42, 21, 10.1038/ng.488 · DOI
- Stickel, 2011, Genetic variation in the PNPLA3 gene is associated with alcoholic liver injury in Caucasians, Hepatology., 53, 86, 10.1002/hep.24017 · DOI
- Stickel, 2017, The genetics of alcohol dependence and alcohol-related liver disease, J. Hepatol., 66, 195, 10.1016/j.jhep.2016.08.011 · DOI
- Basantani, 2011, Pnpla3/adiponutrin deficiency in mice does not contribute to fatty liver disease or metabolic syndrome, J. Lipid Res., 52, 318, 10.1194/jlr.M011205 · DOI
- Chen, 2010, Patatin-like phospholipase domain-containing 3/adiponutrin deficiency in mice is not associated with fatty liver disease, Hepatology., 52, 1134, 10.1002/hep.23812 · DOI
- Li, 2012, Chronic overexpression of PNPLA3I148M in mouse liver causes hepatic steatosis, J. Clin. Invest., 122, 4130, 10.1172/JCI65179 · DOI
- BasuRay, 2019, Accumulation of PNPLA3 on lipid droplets is the basis of associated hepatic steatosis, Proc. Natl. Acad. Sci. USA., 116, 9521, 10.1073/pnas.1901974116 · DOI
- Negoita, 2019, PNPLA3 variant M148 causes resistance to starvation-mediated lipid droplet autophagy in human hepatocytes, J. Cell. Biochem., 120, 343, 10.1002/jcb.27378 · DOI
- Teo, 2020, rs641738C>T near MBOAT7 promotes steatosis, NASH, fibrosis and hepatocellular carcinoma in non-alcoholic fatty liver disease: a meta-analysis, medRxiv.
- Caddeo, 2019, MBOAT7 is anchored to endomembranes by six transmembrane domains, J. Struct. Biol., 206, 349, 10.1016/j.jsb.2019.04.006 · DOI
- Yamashita, 2003, Reverse reaction of lysophosphatidylinositol acyltransferase functional reconstitution of coenzyme A-dependent transacylation system, J. Biol. Chem., 278, 30382, 10.1074/jbc.M303391200 · DOI
- Magné, 2013, The minor allele of the missense polymorphism Ser251Pro in perilipin 2 (PLIN2) disrupts an α-helix, affects lipolysis, and is associated with reduced plasma triglyceride concentration in humans, FASEB J., 27, 3090, 10.1096/fj.13-228759 · DOI
- Lin, 2013, Pharmacological promotion of autophagy alleviates steatosis and injury in alcoholic and non-alcoholic fatty liver conditions in mice, J. Hepatol., 58, 993, 10.1016/j.jhep.2013.01.011 · DOI
- Ding, 2010, Autophagy reduces acute ethanol-induced hepatotoxicity and steatosis in mice, Gastroenterology., 139, 1740, 10.1053/j.gastro.2010.07.041 · DOI · Paper page
- Ni, 2013, Critical role of FoxO3a in alcohol-induced autophagy and hepatotoxicity, Am. J. Pathol., 183, 1815, 10.1016/j.ajpath.2013.08.011 · DOI
- Thomes, 2015, Acute and chronic ethanol administration differentially modulate hepatic autophagy and transcription factor EB, Alcohol. Clin. Exp. Res., 39, 2354, 10.1111/acer.12904 · DOI
- Rasineni, 2017, Ethanol-induced steatosis involves impairment of lipophagy, associated with reduced Dynamin2 activity, Hepatol. Commun., 1, 501, 10.1002/hep4.1063 · DOI
- Schulze, 2017, Ethanol exposure inhibits hepatocyte lipophagy by inactivating the small guanosine triphosphatase Rab7, Hepatol. Commun., 1, 140, 10.1002/hep4.1021 · DOI
- Clugston, 2017, The hepatic lipidome: a gateway to understanding the pathogenes is of alcohol-induced fatty liver, Curr. Mol. Pharmacol., 10, 195, 10.2174/1874467208666150817111419 · DOI
- Clugston, 2011, Altered hepatic lipid metabolism in C57BL/6 mice fed alcohol: a targeted lipidomic and gene expression study, J. Lipid Res., 52, 2021, 10.1194/jlr.M017368 · DOI
- Fernando, 2010, 1H and 31P NMR lipidome of ethanol-induced fatty liver, Alcohol. Clin. Exp. Res., 34, 1937, 10.1111/j.1530-0277.2010.01283.x · DOI
- Fernando, 2011, Lipidomic changes in rat liver after long-term exposure to ethanol, Toxicol. Appl. Pharmacol., 255, 127, 10.1016/j.taap.2011.05.022 · DOI
- Bosner, 1988, Receptor-like function of heparin in the binding and uptake of neutral lipids, Proc. Natl. Acad. Sci. USA., 85, 7438, 10.1073/pnas.85.20.7438 · DOI
- Athenstaedt, 2006, The life cycle of neutral lipids: synthesis, storage and degradation, Cell. Mol. Life Sci., 63, 1355, 10.1007/s00018-006-6016-8 · DOI
- Shimizu, 2009, Lipid mediators in health and disease: enzymes and receptors as therapeutic targets for the regulation of immunity and inflammation, Annu. Rev. Pharmacol. Toxicol., 49, 123, 10.1146/annurev.pharmtox.011008.145616 · DOI
- Bradford, 2008, Metabolomic profiling of a modified alcohol liquid diet model for liver injury in the mouse uncovers new markers of disease, Toxicol. Appl. Pharmacol., 232, 236, 10.1016/j.taap.2008.06.022 · DOI
- Loftus, 2011, Metabonomic investigation of liver profiles of nonpolar metabolites obtained from alcohol-dosed rats and mice using high mass accuracy MSn analysis, J. Proteome Res., 10, 705, 10.1021/pr100885w · DOI
- Zhao, 2011, Ethanol-induced alterations in fatty acid-related lipids in serum and tissues in mice, Alcohol. Clin. Exp. Res., 35, 229, 10.1111/j.1530-0277.2010.01338.x · DOI
- Jang, 2012, Metabolic profiling of an alcoholic fatty liver in zebrafish (Danio rerio), Mol. Biosyst., 8, 2001, 10.1039/c2mb25073j · DOI
- Fernando, 2012, Hepatic lipid profiling of deer mice fed ethanol using (1)H and (3)(1)P NMR spectroscopy: a dose-dependent subchronic study, Toxicol. Appl. Pharmacol., 264, 361, 10.1016/j.taap.2012.07.026 · DOI
- Nanji, 1995, Dietary saturated fatty acids: a novel treatment for alcoholic liver disease, Gastroenterology., 109, 547, 10.1016/0016-5085(95)90344-5 · DOI
- You, 2005, Role of adiponectin in the protective action of dietary saturated fat against alcoholic fatty liver in mice, Hepatology., 42, 568, 10.1002/hep.20821 · DOI
- Chen, 2015, Supplementation of saturated long-chain fatty acids maintains intestinal eubiosis and reduces ethanol-induced liver injury in mice, Gastroenterology., 148, 203, 10.1053/j.gastro.2014.09.014 · DOI · Paper page
- Ramirez, 2013, Insulin resistance, ceramide accumulation and endoplasmic reticulum stress in experimental chronic alcohol-induced steatohepatitis, Alcohol Alcohol., 48, 39, 10.1093/alcalc/ags106 · DOI
- Longato, 2012, Insulin resistance, ceramide accumulation, and endoplasmic reticulum stress in human chronic alcohol-related liver disease, Oxid. Med. Cell. Longev., 2012, 479348, 10.1155/2012/479348 · DOI
- Chavez, 2012, A ceramide-centric view of insulin resistance, Cell Metab., 15, 585, 10.1016/j.cmet.2012.04.002 · DOI
- Liangpunsakul, 2010, Inhibitory effect of ethanol on AMPK phosphorylation is mediated in part through elevated ceramide levels, Am. J. Physiol. Gastrointest. Liver Physiol., 298, G1004, 10.1152/ajpgi.00482.2009 · DOI
- Hannun, 2011, Many ceramides, J. Biol. Chem., 286, 27855, 10.1074/jbc.R111.254359 · DOI
- Williams, 2018, A novel role for ceramide synthase 6 in mouse and human alcoholic steatosis, FASEB J., 32, 130, 10.1096/fj.201601142R · DOI
- Tong, 2014, Therapeutic reversal of chronic alcohol-related steatohepatitis with the ceramide inhibitor myriocin, Int. J. Exp. Pathol., 95, 49, 10.1111/iep.12052 · DOI
- Deaciuc, 2000, Apoptosis and dysregulated ceramide metabolism in a murine model of alcohol-enhanced lipopolysaccharide hepatotoxicity, Alcohol. Clin. Exp. Res., 24, 1557, 10.1111/j.1530-0277.2000.tb04575.x · DOI
- Liangpunsakul, 2012, Imipramine blocks ethanol-induced ASMase activation, ceramide generation, and PP2A activation, and ameliorates hepatic steatosis in ethanol-fed mice, Am. J. Physiol. Gastrointest. Liver Physiol., 302, G515, 10.1152/ajpgi.00455.2011 · DOI
- Fernandez, 2013, ASMase is required for chronic alcohol induced hepatic endoplasmic reticulum stress and mitochondrial cholesterol loading, J. Hepatol., 59, 805, 10.1016/j.jhep.2013.05.023 · DOI
- Schlemmer, 2005, Hepatic phospholipids in alcoholic liver disease assessed by proton-decoupled 31P magnetic resonance spectroscopy, J. Hepatol., 42, 752, 10.1016/j.jhep.2004.12.032 · DOI
- Vance, 1988, The methylation of phosphatidylethanolamine, Prog. Lipid Res., 27, 61, 10.1016/0163-7827(88)90005-7 · DOI
- Cui, 1996, Expression of phosphatidylethanolamine n-methyltransferase-2 is markedly enhanced in long term choline-deficient rats, J. Biol. Chem., 271, 2839, 10.1074/jbc.271.5.2839 · DOI
- Barak, 1973, Relationship of ethanol to choline metabolism in the liver: a review, Am. J. Clin. Nutr., 26, 1234, 10.1093/ajcn/26.11.1234 · DOI
- Duce, 1988, S-adenosyl-L-methionine synthetase and phospholipid methyltransferase are inhibited in human cirrhosis, Hepatology., 8, 65, 10.1002/hep.1840080113 · DOI
- Lieber, 1994, Hepatic phosphatidylethanolamine methyltransferase activity is decreased by ethanol and increased by phosphatidylcholine, Alcohol. Clin. Exp. Res., 18, 592, 10.1111/j.1530-0277.1994.tb00915.x · DOI
- Lu, 2000, Changes in methionine adenosyltransferase and S-adenosylmethionine homeostasis in alcoholic rat liver, Am. J. Physiol. Gastrointest. Liver Physiol., 279, G178, 10.1152/ajpgi.2000.279.1.G178 · DOI
- Lieber, 1994, Phosphatidylcholine protects against fibrosis and cirrhosis in the baboon, Gastroenterology., 106, 152, 10.1016/S0016-5085(94)95023-7 · DOI
- Lieber, 2003, II. Veterans Affairs Cooperative Study of polyenylphosphatidylcholine in alcoholic liver disease, Alcohol. Clin. Exp. Res., 27, 1765, 10.1097/01.ALC.0000093743.03049.80 · DOI
- Li, 2006, The ratio of phosphatidylcholine to phosphatidylethanolamine influences membrane integrity and steatohepatitis, Cell Metab., 3, 321, 10.1016/j.cmet.2006.03.007 · DOI
Cited by
Sorted by citations
Items 101–200 of 253
Zhuge, H., Pan, Y., Lai, S., Chang, K., Ding, Q., Cao, W., Song, Q., Li, S., Dou, X., & Ding, B. (2024) · Heliyon · doi:10.1016/j.heliyon.2024.e31195 · Cited by 9
“While at the same time, DGAT2, an essential protein in lipid synthesis [14], was similarly down-regulated by PGF (Fig.”
BackgroundCheng, J., Lei, Z., Fang, C., Jia, W. P., & Xu, Y. (2024) · Food Bioscience · doi:10.1016/j.fbio.2024.104072 · Cited by 8
Low sphingolipid levels predict poor survival in patients with alcohol-related liver disease
Kronborg, T., Gao, Q., Trošt, K., Ytting, H., O'Connell, M., Werge, M., Thing, M., Gluud, L., Hamberg, O., Møller, S., et al. (2023) · JHEP Reports · doi:10.1016/j.jhepr.2023.100953 · Cited by 9
Zonal expression of StARD1 and oxidative stress in alcoholic-related liver disease
Fucho, R., Solsona‐Vilarrasa, E., Torres, S., Núñez, S., Insausti-Urkia, N., Edo, A., Calvo, M., Bosch, A., Martin, G., Enrich, C., et al. (2023) · Journal of Lipid Research · doi:10.1016/j.jlr.2023.100413 · Cited by 11
“Alcohol metabolism alters the imbalance between the biosynthesis and catabolism of lipids leading to hepatic steatosis (9).”
BackgroundSingle ethanol binge causes severe liver injury in mice fed Western diet
Yeh, Y.-T., Wu, X.-D., Ma, Y.-Y., Ying, Z., He, L., Xue, B.-Z., Shi, H., Choi, Y., & Yu, L.-Q. (2023) · Hepatology Communications · doi:10.1097/hc9.0000000000000174 · Cited by 9
“Alcohol intake is known to suppress the hepatic transcription of genes related to fatty acid oxidation.[41] F IGURE 6 Western diet plus single ethanol binge synergistically induces hepatic ER stress.”
BackgroundThomes, P. G., Strupp, M. S., Donohue, T. M., Kubik, J. L., Sweeney, S. A., Mahmud, R., Schott, M. B., Schulze, R. J., McNiven, M. A., & Casey, C. A. (2023) · Journal of Biological Chemistry · doi:10.1016/j.jbc.2023.103071 · Cited by 10
Mitochondria–endoplasmic reticulum contact sites in hepatocytic senescence
Kumar, P., Hassan, M., Tacke, F., & Engelmann, C. (2026) · Cellular & Molecular Biology Letters · doi:10.1186/s11658-025-00809-4 · Cited by 9
“Alcohol-induced mitochondrial dysfunction inhibits fatty acid oxidation, leading to intrahepatic lipid accumulation [165, 166].”
Zhao, M., Li, B., Meng, X., Zhang, Y., Xuan, F., Li, L., Li, S., Xu, Y., & Wang, Y. (2025) · Phytochemistry Reviews · doi:10.1007/s11101-025-10094-w · Cited by 4
“In addition, a large amount of alcohol dehydrogenation and oxidation increases the ratio of NAD/NADH and weakens the circulation of tricarboxylic acid, resulting in the weakening of oxidative decomposition of fatty acids and the accumulation of neutral fats in the liver (Jeon and Carr 2020).”
Cheng, J., Luo, M., Zhou, D.-D., Huang, S., Xiong, R.-G., Wu, S., Saimaiti, A., Li, B., Shang, A., Tang, G., et al. (2024) · Foods · doi:10.3390/foods13162521 · Cited by 6
Metabolic Rewiring During Metastasis: The Interplay Between the Environment and the Host
Vandekeere, A., Kharraz, S. E., Altea‐Manzano, P., & Fendt, S. (2024) · Annual Review of Cancer Biology · doi:10.1146/annurev-cancerbio-062822-122840 · Cited by 9
Wu, Y. S., Lin, Y.-L., Kao, Y.-F., Chen, J.-W., Chen, Y.-C., & Chen, Y.-C. (2023) · Environmental Toxicology · doi:10.1002/tox.24072 · Cited by 8
“39 Therefore, the decreases of serum and liver lipids by supplementing GBHP01 ™ may normalize lipid dyshomeostasis in livers during the chronic alcohol consumption.”
BackgroundPokhrel, S., Dilts, M., Stahl, Z., Boehme, S., Frame, G., Chiang, J. Y. L., & Ferrell, J. M. (2023) · Hepatology Communications · doi:10.1097/hc9.0000000000000138 · Cited by 10
“Alcohol consumption causes metabolic alterations that can occur as soon as 2 weeks in rodents.[17] LeiberDeCarli ethanol + binge diet-induced complications involve increased ALT and AST levels, reduced fatty acid oxidation, and enhanced lipogenesis.”
BackgroundIturrospe, E., Robeyns, R., Silva, K. M., Lavoir, M. C. A., Boeckmans, J., Vanhaecke, T., Nuijs, A. L. N., & Covaci, A. (2023) · Archives of Toxicology · doi:10.1007/s00204-023-03470-y · Cited by 8
Jung, H., You, S., Choi, S., Kang, C.-H., & Kim, G. (2022) · Microorganisms · doi:10.3390/microorganisms10122488 · Cited by 10
“Alcohol consumption increases the fat synthesis and reduces fatty acid oxidation, leading to metabolic disorders and excessive lipid accumulation [36].”
BackgroundInfluentialYan, C., Tian, Z.-X., Yuan, R., Liu, Y., Wang, W., & Liu, Z.-G. (2025) · Phytomedicine · doi:10.1016/j.phymed.2025.157324 · Cited by 7
Wang, W.-M., Zhou, K., Fu, Z.-Y., Huang, Y., Deng, J.-J., Fan, D.-D., & Yang, H.-X. (2025) · Journal of Ginseng Research · doi:10.1016/j.jgr.2025.08.003 · Cited by 7
“Alcohol disrupts hepatic lipid metabolism by inducing insulin resistance in adipose tissue, inhibiting mitochondrial β -oxidation, impairing the VLDL assembly and secretion [6,7].”
The effects of cynaroside on lipid metabolism and lipid-related diseases: a mechanistic overview
Cen, C., Li, J., Zhou, P., Fisher, D. P., Hiền, N. T. T., Musabaev, E. I., Pronyuk, K., & Zhao, L. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1648614 · Cited by 6
Bexarotene regulates zebrafish embryonic development by activating Wnt signaling pathway
Zha, W., Wang, Z., Hu, W., Ge, C., Yuan, W., Shen, Q., Li, W., Chen, W., Tang, J., Xiao, Z., et al. (2025) · Life Sciences · doi:10.1016/j.lfs.2025.123664 · Cited by 6
Cheng, E. Y., & Mirzaei, A. (2024) · Medical Hypotheses · doi:10.1016/j.mehy.2024.111497 · Cited by 6
Shinde, S. S., Chakole, S. V., & Humane, S. (2024) · Cureus · doi:10.7759/cureus.54052 · Cited by 5
“If alcohol consumption continues, this condition can progress to more severe forms of ALD [7].”
BackgroundTherapeutic targets in alcohol-associated liver disease: progress and challenges
Adekunle, A. D., Adejumo, A., & Singal, A. K. (2023) · Therapeutic Advances in Gastroenterology · doi:10.1177/17562848231170946 · Cited by 14
Role of triglycerides as a predictor of autoimmune hepatitis with cirrhosis
Wang, P., Wang, Y.-Q., Liu, H., Han, X., Yi, Y.-Y., Wang, X., & Li, X. (2022) · Lipids in Health and Disease · doi:10.1186/s12944-022-01716-9 · Cited by 7
Algburi, A. F., Dursun, İ., & Garip, Ş. (2022) · Life Sciences · doi:10.1016/j.lfs.2022.121102 · Cited by 9
Koga, T., & Peters, J. M. (2021) · Biological and Pharmaceutical Bulletin · doi:10.1248/bpb.b21-00486 · Cited by 9
Saiman, Y., Hooks, R., & Carr, R. M. (2020) · Current Hepatology Reports · doi:10.1007/s11901-020-00539-5 · Cited by 8
Self-citationCoffee for the liver: a mechanistic approach
Vargas-Pozada, E. E., Ramos‐Tovar, E., Márquez-Quiroga, L. V., Ortega-Carballo, K. J., & Muriel, P. (2025) · Biochemical Pharmacology · doi:10.1016/j.bcp.2025.117338 · Cited by 9
Zheng, J., Gaspar, R. C., Sakuma, I., Hubbard, B. T., Zhang, D., Nasiri, A. R., Kahn, M., Perelis, M., Samuel, V. T., Petersen, K. F., et al. (2025) · Diabetologia · doi:10.1007/s00125-025-06539-8 · Cited by 6
“In addition, we also observed changes in enzymes and metabolites that would promote increased hepatic FAO in the Cideb KD mice [15], as reflected by a ~90% decrease in ACC2 levels (Fig.”
Multi-omics signature of healthy versus unhealthy lifestyles reveals associations with diseases
Fu, G., Rushing, B. R., Graves, L. M., Nieman, D. C., Pellegrini, M. A., Soldano, M., Thompson, M. J., Sakaguchi, C. A., Pathmasiri, W., & Sumner, S. (2025) · Human Genomics · doi:10.1186/s40246-025-00817-7 · Cited by 7
Tao, Y., Wang, H.-N., Peng, Y.-N., Chen, Y., Liu, X., Qi, G., Wang, H., Bai, L., & Qian, Y.-B. (2025) · Hepatology Communications · doi:10.1097/hc9.0000000000000731 · Cited by 6
“[17,47] 28] Conversely, CERK-mediated conversion of ceramide to C1P is hepatoprotective, promoting cell survival by modulating oxidative stress and inflammation.”
Chen, L., Liu, Q., Li, X., Zhang, L., Dong, W., Li, Q., Su, H., Luo, G., Huang, Y., & Yang, X. (2025) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2025.177320 · Cited by 6
He, Z., Deng, S., Wu, Z., Cui, Z., Mei, H., Wang, J., Wang, K., & Zhang, Y. (2024) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2024.119117 · Cited by 5
Insulin Resistance Surrogates May Predict HTN-HUA in Young, Non-Obese Individuals
Zuo, Y.-Q., Gao, Z., Yin, Y.-L., Yang, X., Guan, X., & Feng, P. (2024) · Diabetes Metabolic Syndrome and Obesity · doi:10.2147/dmso.s482184 · Cited by 7
“…HTN, HUA and HTN+HUA; TG/HDL-C ratio had a better predictive value for HUA than TyG-BMI in young, non-obese individuals; TyG-BMI had a better predictive value for HTN in young, non-obese individuals; TG/HDL-C ratio and TyG-BMI had high predictive value for HTN-HUA in young, non-obese individuals.”
BackgroundA novel phosphodiesterase inhibitor for the treatment of chronic liver injury and metabolic diseases
Staller, D. W., Panigrahi, S. S., Jayasinghe, Y. P., Dong, Y., Mahto, S., Kumar, V., Ronning, D. R., & Mahato, R. I. (2024) · Hepatology · doi:10.1097/hep.0000000000000999 · Cited by 10
“…degradation of triglycerides (TGs) stored in WAT and increased circulating free fatty acids, which can contribute to the progression of SLD. [11] The translatability of PDE4 inhibitors has been stymied by their poor efficacy and adverse effects such as severe gastrointestinal upset and…”
Targeting cAMP signaling and phosphodiesterase 4 for liver disease treatment
Ma, J., Staller, D. W., & Mahato, R. I. (2024) · Medicinal Chemistry Research · doi:10.1007/s00044-024-03267-3 · Cited by 6
Intestinal Microbiotas and Alcoholic Hepatitis: Pathogenesis and Therapeutic Value
Zheng, J., Li, Z., & Xu, H. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241914809 · Cited by 9
“Ultimately, they can lead to severe cirrhosis, hepatic failure, or even hepatocellular carcinoma, making alcohol one of the leading causes of death among patients with liver disease [3,4].”
Zhou, X., Yu, J., Wan, Q., Wang, W., Yu, X., You, J., Ouyang, H. X., Chen, X., Yuan, C., Huang, S., et al. (2022) · Journal of Functional Foods · doi:10.1016/j.jff.2022.105284 · Cited by 7
Zhang, X., Huang, Y., Chen, B., Li, Q., Wu, P., Chen, W.-H., Wu, R., & Li, C. (2024) · Frontiers in Pharmacology · doi:10.3389/fphar.2024.1392338 · Cited by 5
“Disturbance of the Frontiers in Pharmacology frontiersin.org 13 lipid metabolism will result in progression of hepatic steatosis, which is the early stage of alcoholic liver injury (Jeon and Carr, 2020).”
BackgroundMiRNA-Seq reveals key MicroRNAs involved in fat metabolism of sheep liver
Fei, X.-J., Jin, M.-L., Yuan, Z.-H., Li, T.-T., Lu, Z.-K., Wang, H., Lu, J., Quan, K., Yang, J., He, M., et al. (2023) · Frontiers in Genetics · doi:10.3389/fgene.2023.985764 · Cited by 5
Neuman, M. G., Seitz, H. K., Tuma, P. L., Osna, N. A., Casey, C. A., Kharbanda, K. K., Cohen, L. B., Malnick, S. D. H., Adhikari, R., Mitra, R., et al. (2022) · Experimental and Molecular Pathology · doi:10.1016/j.yexmp.2022.104750 · Cited by 6
Maccioni, R., Tambaro, S., Doro, L., Bassareo, V., Peana, A. T., & Acquas, E. (2026) · Antioxidants · doi:10.3390/antiox15020216 · Cited by 6
“The alcoholic liver, in response to excessive alcohol consumption, undergoes a metabolic derangement rooted in compromised lipid metabolism; this impairment is characterized by abnormal esterification of cholesterol, excessive synthesis of triglycerides, and elevated LDL levels [97].”
Treatment approaches for alcohol use disorder with metabolic dysfunction
Wagner, A. C., Jung, J., Pacher, P., & Lohoff, F. W. (2025) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2025.108957 · Cited by 4
Yuan, S., Gao, P., Lei, J., Sun, J., Fang, X., Tu, P., Lu, Y., & Jiang, Y. (2025) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2025.120626 · Cited by 4
Lei, Y., Zhu, Y., Ni, W., Shi, J., Seto, W., & Li, J. (2025) · Alimentary Pharmacology & Therapeutics · doi:10.1111/apt.70335 · Cited by 5
“Moreover, alcohol inhibits lipid output and LDL catabolism, leading to substantial accumulation of LDL in hepatocytes [82].”
Lipid Droplet Dynamics in Alcoholic Steatohepatitis
Omar, D. Y., Willoughby, M. M., Mostafa, N., Otakhor, K. O., Bhatt, S., Zaidi, M. A. A., & Schott, M. B. (2025) · American Journal Of Pathology · doi:10.1016/j.ajpath.2025.07.010 · Cited by 5
“15 Additionally, alcohol suppresses LD catabolism by inhibiting both lipolysis and lipophagy.”
Andaloro, S., Gaetano, V. D., Cardone, F., Ianiro, G., Cerrito, L., Pallozzi, M., Stella, L., Gasbarrini, A., & Ponziani, F. R. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms26157345 · Cited by 5
Systems metabolic insights into kaempferol-mediated alleviation of alcoholic fatty liver disease
Song, C.-M., Li, L., Li, J., & Yao, J. (2025) · Frontiers in Endocrinology · doi:10.3389/fendo.2025.1610613 · Cited by 4
“Alterations in sphingolipid metabolism and primary bile acid biosynthesis further highlight KPF ’ s role in modulating lipid-associated pathways (33, 34).”
Analyzing the effects of human error on automated driving takeovers
Yu, Z., Zhao, X., Jiang, K., Deng, Q., Yu, S.-Y., Huang, Z., Chen, J., Chen, Y., & Zhai, L. (2025) · Cognition Technology & Work · doi:10.1007/s10111-025-00794-w · Cited by 5
“This effect has been widely documented in existing literature (Bishehsari et al. 2017; Jeon and Carr 2020).”
Fu, Z.-W., Zhou, J.-F., Pan, H., Yang, S., Pan, Z., Shen, Y., Yao, J., & Hu, J. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1575280 · Cited by 4
“Existing researches have demonstrated that ethanol contributes to the accumulation of lipids in the liver by in fl uencing hepatic lipid uptake, stimulating lipogenesis, hindering fatty acid oxidation, and affecting lipid export from the liver (Jeon and Carr, 2020).”
Güleken, Z., Sarıbal, D., Mırsal, H., Cebulski, J., Ceylan, Z., & Depciuch, J. (2025) · Journal of Biophotonics · doi:10.1002/jbio.202400550 · Cited by 3
“As ethanol is metabolized in the liver, fatty acids accumulate and may undergo lipid peroxidation, potentially leading to fibrosis [14].”
Huang, J.-W., Zhou, K., Li, J.-Y., Xu, Z., Wu, X.-Q., Chen, T.-T., Wang, D.-N., Pan, H.-F., Huang, S., Liu, T., et al. (2025) · Phytomedicine · doi:10.1016/j.phymed.2025.156598 · Cited by 4
Wu, J., Huang, E., McMullen, M. R., Singh, V., Mrdjen, M., Bellar, A., Wang, L., Welch, N., Dasarathy, J., Dasarathy, S., et al. (2024) · Hepatology Communications · doi:10.1097/hc9.0000000000000547 · Cited by 4
The pharmacological management of alcohol-related cirrhosis: what’s new?
Verma, N., Vinod, A. P., & Singal, A. K. (2024) · Expert Opinion on Pharmacotherapy · doi:10.1080/14656566.2024.2409941 · Cited by 4
“[ 117] As a result, the liver accumulates free fatty acids, which triggers hepatic inflammation by triggering chemokine synthesis, activating the inflammasome, and initiating TLR-4-mediated inflammatory pathways.”
Park, W., Kim, Y., & Cho, S. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25158526 · Cited by 3
“Alcohol-induced lipid accumulation in the liver results from the chronic or binge consumption of alcohol [42].”
BackgroundHasken, J. M., de Vries, M. D., Marais, A., May, P., Parry, C., Seedat, S., Mooney, S., & Smith, S. M. (2022) · Nutrients · doi:10.3390/nu14245367 · Cited by 4
“alcohol exposure [43] and could suggest an inefficient oxidation of acyl-CoA species.”
Yang, C., Zhao, Y., Luo, Z., Hu, Y., Wang, S., Hu, S., Yao, Y., Pan, L., Shen, C., & Xu, T. (2022) · Planta Medica · doi:10.1055/a-1878-3991 · Cited by 4
“Many studies have shown that the specific pathogenesis of ALD is complex, among which inflammation and lipid metabolism disorders caused by alcohol metabolism play key roles in the occurrence and development of ALD [3,4].”
BackgroundByun, J., Shin, J., Choi, Y. J., & Choung, S. (2021) · International Journal of Food Science & Technology · doi:10.1111/ijfs.14983 · Cited by 5
Efficacy of Probiotic Treatment in Alcoholic Liver Disease: A Systematic Review of Animal Studies
Sosnowski, K., Kucharski, R., & Przybyłkowski, A. (2026) · Nutrients · doi:10.3390/nu18040608 · Cited by 3
Mittal, A., & Sharma, S. (2025) · Nutrition Research · doi:10.1016/j.nutres.2025.11.004 · Cited by 3
Patterns of lipid profile and genetic variations in South Asians
Rahmanian, M. (2025) · Cardiovascular Diabetology · doi:10.1186/s40842-025-00246-4 · Cited by 3
“Alcohol abuse decreases the oxidation of fatty acids by the liver and is associated with an increase in VLDL and triglyceride levels [23].”
Physiological Mechanisms Vulnerable to Alcohol‐Induced Alterations: Role in Chronic Comorbidities
Simon, L., Couvillion, K. E., Donovan, M. E., Gallegos, E. M., Souza‐Smith, F. M., & Molina, P. E. (2025) · Comprehensive physiology · doi:10.1002/cph4.70057 · Cited by 4
“At the same time, dysregulated hepatic AMPK signaling and direct regulatory effects of alcohol on transcription of genes lead to maladaptive increases in de novo lipogenesis (Mackowiak et al. 2024; You and Arteel 2019; Jeon and Carr 2020).”
Zhou, Y., Yang, Z., Liu, S., Xie, S.-A., Zhang, Q., Zhang, S., Zhu, S., & Wu, S. (2025) · BMC Gastroenterology · doi:10.1186/s12876-025-04165-7 · Cited by 3
“With impaired liver function hindering alcohol metabolism, alcohol may further damage the liver and alter metabolic pathways [22].”
Saito, T., George, J., Ozaki, K., Tsuchishima, M., & Tsutsumi, M. (2025) · Molecular Medicine · doi:10.1186/s10020-025-01210-9 · Cited by 2
“Alcohol-associated liver disease is the most prevalent type of chronic liver disease that begins with simple steatosis and progresses to steatohepatitis, fibrosis, and cirrhosis (Jeon and Carr 2020).”
InfluentialLi, J., Liu, Z., Du, Y., Zhong, Z., Tu, Z., Zhou, W.-J., Chen, Z., Wang, L., Zhang, X.-X., & Li, T. (2025) · Food Bioscience · doi:10.1016/j.fbio.2025.106434 · Cited by 3
Advances in the study of the mechanism of action of miR‑22 in liver lesions (Review)
Wang, M., Wang, X., Wang, Y., Gai, Y., Ye, J., Xu, X., & You, X. (2024) · Oncology Letters · doi:10.3892/ol.2024.14674 · Cited by 3
“…and has the potential to develop into HCC. ALD is closely linked to hepatic steatosis, with alcohol affecting hepatic lipid metabo‑ lism by altering how the liver takes up lipids, synthesizes lipids, oxidizes fatty acids, exports lipids, forms lipid droplets and undergoes catabolism (100).”
BackgroundTherapeutic perspectives on PDE4B inhibition in adipose tissue dysfunction and chronic liver injury
Staller, D. W., Bennett, R. G., & Mahato, R. I. (2024) · Expert Opinion on Therapeutic Targets · doi:10.1080/14728222.2024.2369590 · Cited by 6
“To compound things further, chronic ethanol intake has been correlated to increased CD36 expression on hepatocyte membranes, increasing the uptake of circulating FAs into the liver parenchyma [61,62].”
Ethanol enhances selenoprotein P expression via ERK-FoxO3a axis in HepG2 cells
Chen, J., Mita, Y., & Noguchi, N. (2024) · Journal of clinical biochemistry and nutrition · doi:10.3164/jcbn.23-104 · Cited by 3
Hepatoprotective Effect of Annulohypoxylon stygium Melanin on Acute Alcoholic Liver Injury in Mice
Liu, R., Mo, C., Wei, X.-T., & Ma, A.-M. (2024) · Applied Biochemistry and Biotechnology · doi:10.1007/s12010-024-04863-0 · Cited by 3
“Disturbance of lipid metabolism is one of the manifestations of alcoholic liver injury, and large intake of alcohol promotes TG and TC synthesis [24].”
Liu, D., Luo, Y., Zheng, Y., Ji, R., & Zhou, Y. (2023) · European Journal of Gastroenterology & Hepatology · doi:10.1097/meg.0000000000002566 · Cited by 2
Apple Consumption Protects against Acute Ethanol-Induced Liver Injury in Rats
Wang, C., Ma, C.-N., Liu, X.-L., Sun, Q., Zhang, Q., Lin, Y., Yan, C.-X., & Hu, D.-G. (2023) · Applied Sciences · doi:10.3390/app13085112 · Cited by 3
Mărginean, I., Cazacu, S., Marginean, C., Popescu, M., Iacob, G., Popescu, M.-S., & Vere, C. (2026) · Biomedicines · doi:10.3390/biomedicines14030531 · Cited by 2
“Excessive lipid accumulation in hepatocytes occurs when the liver increases the uptake of circulating fatty acids (FAs) or activates de novo lipogenesis, leading to the synthesis of lipids within the liver itself [20,21].”
Willis, C. R. G., Ganjayi, M. S., Brown, A. M., Moser, S. E., Szewczyk, N. J., Clark, B. C., & Baumann, C. W. (2026) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.70240 · Cited by 2
“…of liver Got1 and Gpt (Data S1 ), as well as a lower hepatic PC:PE ratio, which is a hallmark of impaired hepatocyte membrane integrity that leads to progression of steatosis into steatohepatitis (Li et al., 2006 ) and is indicative of ALD in both patients and animal models (Jeon & Carr, 2020 ).”
Cao, H.-J., Han, D., Lu, J., Qi, D., & Li, F. (2026) · Journal of Drug Delivery Science and Technology · doi:10.1016/j.jddst.2025.107688 · Cited by 2
Yang, F., Li, X., Sun, J., Pang, X., Hu, Y., Chen, C., Lu, Y., & Lv, F. (2026) · Food Bioscience · doi:10.1016/j.fbio.2026.108352 · Cited by 2
Limami, Y., Wahnou, H., Ndayambaje, M., Hba, S., Chgari, O., Ammara, M., Kebbaj, R. E., Naya, A., Oudghiri, M., & Duval, R. E. (2025) · WIREs Mechanisms of Disease · doi:10.1002/wsbm.70005 · Cited by 3
Sui, Y., Zhang, R., Liu, G., Liu, Y., Du, Y., Zhang, Y., Fu, S., Nie, Z., Qin, H., & Ma, L. (2025) · International Journal of Cardiology · doi:10.1016/j.ijcard.2025.133644 · Cited by 1
Choi, Y., & Son, C. (2025) · 대한한의학회지 · doi:10.13048/jkm.25016 · Cited by 3
Sim, S.-Y., Cho, H.-D., & Lee, S.-B. (2025) · Foods · doi:10.3390/foods14050861 · Cited by 2
“Alcoholic fatty liver disease refers to the enlargement of the liver in response to the accumulation of more than 5% triglycerides [52].”
Ritzenthaler, J. D., Ekuban, A., Horsman, B., Roman, J., & Watson, W. H. (2025) · Alcoholism Clinical and Experimental Research · doi:10.1111/acer.15533 · Cited by 2
Diagnosis, Evaluation, and Management of Severe Hypertriglyceridemia
Krishnamurthy, A., Homan, E. A., & Kim, S. M. (2025) · Current Cardiovascular Risk Reports · doi:10.1007/s12170-025-00758-9 · Cited by 4
Acetylation of proximal cysteine-lysine pairs by alcohol metabolism
McGinnis, C. D., Harris, P. S., Graham, B. I. M., Marentette, J., Michel, C. R., Saba, L. M., Reisdorph, R. M., Roede, J. R., & Fritz, K. S. (2024) · Redox Biology · doi:10.1016/j.redox.2024.103462 · Cited by 3
Wang, S.-M., Jing, D.-Z., Li, M.-F., Duan, H.-A., Ding, X., Peng, J., Li, X., & Zhu, Y. (2024) · Frontiers in Nutrition · doi:10.3389/fnut.2024.1467025 · Cited by 2
“Moreover, alcohol can hinder the oxidative decomposition of fat, causing fat to accumulate in the liver and abdomen and leading to obesity (33, 34).”
Zhao, M., Zhang, Q., Lin, Y., Zhang, D., & Cao, H. (2024) · PLoS ONE · doi:10.1371/journal.pone.0310184 · Cited by 3
Lee, M., Park, J., Kim, D., Park, S.-H., Jung, J., Jun, W., Kim, O., Baek, K.-S., Kim, O., & Lee, J. (2024) · Journal of Medicinal Food · doi:10.1089/jmf.2024.k.0111 · Cited by 2
“29,30 Therefore, the inhibition of SREBP-1c expression or increased expressions of AMPK and PPAR-a might attenuate fatty liver development.”
Social Media and Health Literacy: Negative Influence or an Emerging Reality?
Aguilar, S. R., Gonçalves, A. C. F., Guimarães, T. A., Almeida, M. T. C., Andrade, M. C., & de Paula-Júnior, W. (2024) · Revista de Gestão Social e Ambiental · doi:10.24857/rgsa.v18n5-158 · Cited by 2
Small-molecule chemical probes for the potential therapeutic targets in alcoholic liver diseases
Dogra, A., & Li, F. (2023) · Liver Research · doi:10.1016/j.livres.2023.09.001 · Cited by 3
Hepatic macrophage mediated immune response in liver steatosis driven carcinogenesis
Tu, T., Alba, M. M., Datta, A. A., Hong, H., Hua, B., Jia, Y., Khan, J., Nguyen, P., Niu, X., Pammidimukkala, P., et al. (2022) · Frontiers in Oncology · doi:10.3389/fonc.2022.958696 · Cited by 3
“Non-alcoholic fatty liver disease (NAFLD) and non-alcoholic steatohepatitis (NASH) develop in patients with metabolic syndromes including obesity, IR and diabetes (9, 10) whereas alcoholic liver disease (ALD) and ASH (alcoholic steatohepatitis) are caused by excessive alcohol drinking which also contributes to lipid m…”
BackgroundKupffer cells are protective in alcoholic steatosis
Köhler, N., Höring, M., Czepukojc, B., Rose, T. D., Buechler, C., Kröhler, T., Haybaeck, J., Liebisch, G., Pauling, J. K., Kessler, S. M., et al. (2022) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2022.166398 · Cited by 4
Longo, M., Meroni, M., Paolini, E., & Dongiovanni, P. (2026) · Metabolites · doi:10.3390/metabo16090608 · Cited by 1
“Concurrently, alcohol intake impairs the hepatic secretion of very-low-density lipoproteins (VLDL) and upregulates lipogenic transcription factors such as SREBP-1c and Cluster of differentiation 36 (CD36) [45].”
Liu, J., Li, K., Deng, Y., Li, X., Yang, R., Huang, P., Li, C., Zhao, Y., Du, F., Chen, Y., et al. (2026) · Pharmacological Research · doi:10.1016/j.phrs.2026.108410 · Cited by 1
Small Extracellular Vesicles in Alcohol Use Disorders: A Scoping Review
Severtsev, V. V., Kamalieva, E. R., Sklyar, E., Pevunova, A. R., Finko, E. V., Galeeva, M. S., & Ivanets, N. N. (2026) · Consortium Psychiatricum · doi:10.17816/cp15803 · Cited by 1
“Furthermore, alcohol disrupts overall lipid metabolism, potentially leading to global alterations in signaling processes mediated by various lipid sEVs [41].”
Dai, C., Qin, W.-X., Ge, Z.-F., Cai, H., Zhu, H.-M., Ding, H.-Z., & Bi, H. (2026) · Food Bioscience · doi:10.1016/j.fbio.2026.108898 · Cited by 1
Yang, N., Li, X., Wang, X.-J., Huang, K.-X., Tang, W.-X., & Zhang, X.-S. (2026) · Fenxi huàxué · doi:10.1016/j.cjac.2026.100726 · Cited by 1
Wang, H., Liu, H., Wang, M.-X., Chi, T.-J., Liu, F.-T., Qu, X.-Y., Mu, Y., Xu, Q., & Wang, Q.-B. (2026) · Nutrients · doi:10.3390/nu18050872 · Cited by 1
“Prior studies have reported that specific saturated fatty acid diets, such as 12% palmitic acid plus 85% stearic acid, exerted protective effects in ALD models [37].”
Zhu, H., Zikela, L., Wang, D., Yu, Z., Zhu, Y., Zhou, H., Li, X., Wu, Y., & Han, Q. (2026) · Phytomedicine · doi:10.1016/j.phymed.2026.157977 · Cited by 1
Yu, S., Xia, Y., Zhang, C., Han, X., Feng, X., Li, L., Ma, H., & Xu, J. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262412173 · Cited by 1
“Alcohol exposure modulates numerous lipid-regulating transcription factors and lipogenic enzymes, thereby enhancing hepatic TG accumulation [9].”
Matsumori, R., Tanaka, M., Sato, T., Akiyama, Y., Hosaka, I., Nakata, K., Kawaharata, W., Aida, H., Nishizawa, K., Kouzu, H., et al. (2025) · Journal of Atherosclerosis and Thrombosis · doi:10.5551/jat.65939 · Cited by 4
“An alcohol-induced increase in hepatic TG production may lead to hypertriglyceridemia and contribute to hepatic steatosis 61) .”
Duan, M.-Y., Wu, Y., Zhang, J., Azeem, S., Dong, Y., Gai, Z.-H., Zhu, J.-G., Fang, S.-G., & Gu, S.-B. (2025) · Antioxidants · doi:10.3390/antiox14091038 · Cited by 1
“…by alcohol dehydrogenase (ADH) to acetaldehyde and subsequently by aldehyde dehydrogenase (ALDH) to acetate; with chronic intake, the microsomal ethanol-oxidizing system (largely CYP2E1) is induced and contributes substantially to acetaldehyde and reactive oxygen species (ROS) generation [3,4].”
Sheykhmagomedova, P., Popov, I., Sergeeva, E., Popova, O., Abisalova, I., & Sajaya, L. (2025) · Problems of Biological Medical and Pharmaceutical Chemistry · doi:10.29296/25877313-2025-07-10 · Cited by 1
Cai, J., Wang, S., Feng, Y., Zheng, L., Liang, Q.-H., Liang, Y., & Ye, X. (2025) · Hepatology Forum · doi:10.14744/hf.2024.2024.0030 · Cited by 1
“[19,20,25] Consequently, ETOH treatment can significantly increase cellular fat content by upregulating these three genes.”
Sales, I. M., Damacena, F. C., Zandonade, E., & Sampaio, K. N. (2025) · BMJ Open · doi:10.1136/bmjopen-2024-088084 · Cited by 2
“The combination of these measures would have great power in preventing the progression of hypertension and CVD among these workers, directly impacting the excellence of the service provided to the population.”
Metadata
- Authors
- Jeon, S., & Carr, R.
- Affiliations
- University of Pennsylvania (US)
- Corresponding author
- Carr, Rotonya
- Venue
- Journal of Lipid Research
- Publisher
- Elsevier BV
- Published
- 2020-04
- Volume
- 61
- Issue
- 4
- Pages
- 470-479
- ISSN
- 0022-2275 (ISSN-L)
- PMC
- PMC7112138
- OpenAlex
- W3005408539
- Cited by
- 326
- References
- 161
- Citations by year
- 2026: 58 · 2025: 78 · 2024: 76 · 2023: 49 · 2022: 45 · 2021: 13 · 2020: 7
- FWCI
- 4.37
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Lipid Research (publishedVersion, cc-by)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- National Institutes of Health (R01 AA026302-02, P30 DK0503060)
- Topics
- Health Sciences › Medicine › Pathology and Forensic Medicine › Alcohol Consumption and Health Effects
- Health Sciences › Medicine › Hepatology › Liver Disease Diagnosis and Treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Lipid metabolism and biosynthesis
- Keywords
- alcoholic liver disease, hepatic lipid metabolism, hepatic steatosis, alcoholic steatohepatitis, fatty acid oxidation, de novo lipogenesis, lipid export, lipid droplet formation, genetic susceptibility, bioactive lipids, liver fibrosis
- MeSH terms
- Ethanol, Animals, Humans, Liver, Lipogenesis, Lipid Metabolism
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