Targeting the Gut-Liver Mitochondria Axis in MASLD: Mechanisms and Therapeutic Perspectives

Yu-hang Wang , Xue-song He , Li Lin , Lu-lu Ning , Ya Zhao , Meng-xiao Zhang , Le Chen , Min Chen

Current Medical Science ›› : 1 -14.

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Current Medical Science ›› :1 -14. DOI: 10.1007/s11596-026-00190-z
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Targeting the Gut-Liver Mitochondria Axis in MASLD: Mechanisms and Therapeutic Perspectives
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Abstract

The global prevalence of metabolic dysfunction-associated steatotic liver disease (MASLD) is increasing continuously, posing a substantial threat to public health. This study examines the critical role of imbalanced interactions within the gut‒liver-mitochondrial axis in MASLD pathogenesis. Dysregulation of mitochondrial homeostasis, including metabolic disturbances, impaired quality control, and disrupted interorganelle interactions, significantly contributes to MASLD progression. Through the gut‒liver axis, the gut microbiota establishes a bidirectional regulatory network with mitochondria. Dysbiosis disrupts mitochondrial homeostasis via multiple pathways, while mitochondrial dysfunction aggravates imbalances in the gut microbiota, creating a vicious cycle. Therefore, in this study, the molecular basis of mitochondrial abnormalities was investigated, and the mechanisms of reciprocal regulation were clarified. Additionally, targeted intervention strategies, including the modulation of mitochondrial homeostasis and the regulation of the gut microbiota, are explored to provide novel therapeutic perspectives for MASLD.

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Metabolic dysfunction-associated steatotic liver disease (MASLD) / Gut-liver mitochondria axis / Mitochondrial homeostasis / Gut microbiota / Oxidative stress / Mitophagy

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Yu-hang Wang, Xue-song He, Li Lin, Lu-lu Ning, Ya Zhao, Meng-xiao Zhang, Le Chen, Min Chen. Targeting the Gut-Liver Mitochondria Axis in MASLD: Mechanisms and Therapeutic Perspectives. Current Medical Science 1-14 DOI:10.1007/s11596-026-00190-z

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References

[1]

Naghavi M, Ong KL, Aali A, et al. . Global burden of 288 causes of death and life expectancy decomposition in 204 countries and territories and 811 subnational locations, 1990–2021: a systematic analysis for the Global Burden of Disease Study 2021. Lancet., 2024, 403(10440): 2100-2132

[2]

Ong KL, Stafford LK, McLaughlin SA, et al. . Global, regional, and national burden of diabetes from 1990 to 2021,with projections of prevalence to 2050: a systematic analysis for the Global Burden of Disease Study 2021. Lancet., 2023, 402(10397): 203-234

[3]

Buzzetti E, Pinzani M, Tsochatzis EA. The multiple-hit pathogenesis of non-alcoholic fatty liver disease (NAFLD). Metabolism., 2016, 65(8): 1038-1048

[4]

Fromenty B, Roden M. Mitochondrial alterations in fatty liver diseases. J Hepatol., 2023, 78(2): 415-429

[5]

Nunnari J, Suomalainen A. Mitochondria: in sickness and in health. Cell., 2012, 148(6): 1145-1159

[6]

Yan M, Man S, Sun B, et al. . Gut liver brain axis in diseases: the implications for therapeutic interventions. Signal Transduct Target Ther., 2023, 8: 443

[7]

Pabst O, Hornef MW, Schaap FG, et al. . Gut–liver axis: barriers and functional circuits. Nat Rev Gastroenterol Hepatol., 2023, 20(7): 447-461

[8]

Tilg H, Adolph TE, Trauner M. Gut-liver axis: Pathophysiological concepts and clinical implications. Cell Metab., 2022, 34(11): 1700-1718

[9]

Hsu CL, Schnabl B. The gut-liver axis and gut microbiota in health and liver disease. Nat Rev Microbiol., 2023, 21(11): 719-733

[10]

Targher G, Tilg H, Byrne CD. Non-alcoholic fatty liver disease: a multisystem disease requiring a multidisciplinary and holistic approach. Lancet Gastroenterol Hepatol., 2021, 6(7): 578-588

[11]

Byrne CD, Targher G. NAFLD: a multisystem disease. J Hepatol., 2015, 62(1): S47-S64

[12]

Chalasani N, Younossi Z, Lavine JE, et al. . The diagnosis and management of nonalcoholic fatty liver disease: Practice guidance from the American Association for the Study of Liver Diseases. Hepatology., 2018, 67(1): 328-357

[13]

Powell EE, Wong VW, Rinella M. Non-alcoholic fatty liver disease. Lancet., 2021, 397(10290): 2212-2224

[14]

Tilg H, Effenberger M. From NAFLD to MAFLD: when pathophysiology succeeds. Nat Rev Gastroenterol Hepatol., 2020, 17(7): 387-388

[15]

Targher G, Byrne CD, Tilg H. MASLD: a systemic metabolic disorder with cardiovascular and malignant complications. Gut., 2024, 73(4): 691-702

[16]

Wong VW, Ekstedt M, Wong GL, et al. . Changing epidemiology, global trends and implications for outcomes of NAFLD. J Hepatol., 2023, 79(3): 842-852

[17]

Yip TC, Vilar-Gomez E, Petta S, et al. . Geographical similarity and differences in the burden and genetic predisposition of NAFLD. Hepatology., 2022, 77: 1404-1427

[18]

Day CP, James OFW. Steatohepatitis: a tale of two “hits”?. Gastroenterology., 1998, 114(4): 842-845

[19]

Tilg H, Moschen AR. Evolution of inflammation in nonalcoholic fatty liver disease: the multiple parallel hits hypothesis. Hepatology., 2010, 52(5): 1836-1846

[20]

Juárez-Fernández M, Goikoetxea-Usandizaga N, Porras D, et al. . Enhanced mitochondrial activity reshapes a gut microbiota profile that delays NASH progression. Hepatology., 2023, 77(5): 1654-1669

[21]

Zhao M, Zhao L, Xiong X, et al. . TMAVA, a metabolite of intestinal microbes, is increased in plasma from patients with liver steatosis, inhibits γ-butyrobetaine hydroxylase, and exacerbates fatty liver in mice. Gastroenterology., 2020, 158(8): 2266-2281.e27

[22]

Li X, Jiang O, Chen M, et al. . Mitochondrial homeostasis: shaping health and disease. Curr Med., 2024, 3(1): 5

[23]

Kemper C, Sack MN. Linking nutrient sensing, mitochondrial function, and PRR immune cell signaling in liver disease. Trends Immunol., 2022, 43(11): 886-900

[24]

Chen W, Zhao H, Li Y. Mitochondrial dynamics in health and disease: mechanisms and potential targets. Signal Transduct Target Ther., 2023, 8: 333

[25]

Schapira AH. Mitochondrial diseases. Lancet., 2012, 379(9828): 1825-1834

[26]

Willems PHGM, Rossignol R, Dieteren CEJ, et al. . Redox homeostasis and mitochondrial dynamics. Cell Metab., 2015, 22(2): 207-218

[27]

Wang S, Long H, Hou L, et al. . The mitophagy pathway and its implications in human diseases. Signal Transduct Target Ther., 2023, 8: 304

[28]

Valente EM, Abou-Sleiman PM, Caputo V, et al. . Hereditary early-onset Parkinson’s disease caused by mutations in PINK1. Science., 2004, 304(5674): 1158-1160

[29]

Jheng HF, Tsai PJ, Guo SM, et al. . Mitochondrial fission contributes to mitochondrial dysfunction and insulin resistance in skeletal muscle. Mol Cell Biol., 2012, 32(2): 309-319

[30]

Chouchani ET, Kazak L, Jedrychowski MP, et al. . Mitochondrial ROS regulate thermogenic energy expenditure and sulfenylation of UCP1. Nature., 2016, 532(7597): 112-116

[31]

Kwong JQ, Davis J, Baines CP, et al. . Genetic deletion of the mitochondrial phosphate carrier desensitizes the mitochondrial permeability transition pore and causes cardiomyopathy. Cell Death Differ., 2014, 21(8): 1209-1217

[32]

Koliaki C, Szendroedi J, Kaul K, et al. . Adaptation of hepatic mitochondrial function in humans with non-alcoholic fatty liver is lost in steatohepatitis. Cell Metab., 2015, 21(5): 739-746

[33]

Caldwell SH, Swerdlow RH, Khan EM, et al. . Mitochondrial abnormalities in non-alcoholic steatohepatitis. J Hepatol., 1999, 31(3): 430-434

[34]

Moore MP, Cunningham RP, Meers GM, et al. . Compromised hepatic mitochondrial fatty acid oxidation and reduced markers of mitochondrial turnover in human NAFLD. Hepatology., 2022, 76(5): 1452-1465

[35]

Schuster S, Cabrera D, Arrese M, et al. . Triggering and resolution of inflammation in NASH. Nat Rev Gastroenterol Hepatol., 2018, 15(6): 349-364

[36]

Fletcher JA, Deja S, Satapati S, et al. . Impaired ketogenesis and increased acetyl-CoA oxidation promote hyperglycemia in human fatty liver. JCI Insight., 2019, 4(11): e127737

[37]

Sunny NE, Parks EJ, Browning JD, et al. . Excessive hepatic mitochondrial TCA cycle and gluconeogenesis in humans with nonalcoholic fatty liver disease. Cell Metab., 2011, 14(6): 804-810

[38]

Nishikawa T, Bellance N, Damm A, et al. . A switch in the source of ATP production and a loss in capacity to perform glycolysis are hallmarks of hepatocyte failure in advance liver disease. J Hepatol., 2014, 60(6): 1203-1211

[39]

Chen Z, Tian R, She Z, et al. . Role of oxidative stress in the pathogenesis of nonalcoholic fatty liver disease. Free Radic Biol Med., 2020, 152: 116-141

[40]

Liu BH, Xu CZ, Liu Y, et al. . Mitochondrial quality control in human health and disease. Mil Med Res., 2024, 11(1): 32

[41]

Hong WL, Huang H, Zeng X, et al. . Targeting mitochondrial quality control: new therapeutic strategies for major diseases. Mil Med Res., 2024, 11(1): 59

[42]

Shin S, Kim J, Lee JY, et al. . Mitochondrial quality control: its role in metabolic dysfunction-associated steatotic liver disease (MASLD). J Obes Metab Syndr., 2023, 32(4): 289-302

[43]

Dominy JE, Puigserver P. Mitochondrial biogenesis through activation of nuclear signaling proteins. Cold Spring Harb Perspect Biol., 2013, 5(7): a015008

[44]

Qi XM, Qiao YB, Zhang YL, et al. . PGC-1α/NRF1-dependent cardiac mitochondrial biogenesis: a druggable pathway of calycosin against triptolide cardiotoxicity. Food Chem Toxicol., 2023, 171 113513

[45]

Li S, Liu C, Li N, et al. . Genome-wide coactivation analysis of PGC-1α identifies BAF60a as a regulator of hepatic lipid metabolism. Cell Metab., 2008, 8(2): 105-117

[46]

Bellanti F, Villani R, Tamborra R, et al. . Synergistic interaction of fatty acids and oxysterols impairs mitochondrial function and limits liver adaptation during nafld progression. Redox Biol., 2018, 15: 86-96

[47]

Han R, Liu Y, Li S, et al. . PINK1-PRKN mediated mitophagy: differences between in vitro and in vivo models. Autophagy., 2023, 19(5): 1396-1405

[48]

Jin S, Li Y, Xia T, et al. . Mechanisms and therapeutic implications of selective autophagy in nonalcoholic fatty liver disease. J Adv Res., 2025, 67: 317-329

[49]

El-Hattab AW, Suleiman J, Almannai M, et al. . Mitochondrial dynamics: Biological roles, molecular machinery, and related diseases. Mol Genet Metab., 2018, 125(4): 315-321

[50]

Tábara LC, Segawa M, Prudent J. Molecular mechanisms of mitochondrial dynamics. Nat Rev Mol Cell Biol., 2025, 26(2): 123-146

[51]

El-Hattab AW, Craigen WJ, Scaglia F. Mitochondrial DNA maintenance defects. Biochim Biophys Acta BBA Mol Basis Dis., 2017, 1863(6): 1539-1555

[52]

Hernández-Alvarez MI, Sebastián D, Vives S, et al. . Deficient endoplasmic reticulum-mitochondrial phosphatidylserine transfer causes liver disease. Cell., 2019, 177(4): 881-895.e17

[53]

Du J, Zhang X, Han J, et al. . Pro-inflammatory CXCR3 impairs mitochondrial function in experimental non-alcoholic steatohepatitis. Theranostics., 2017, 7(17): 4192-4203

[54]

Sidarala V, Zhu J, Levi-D’Ancona E, et al. . Mitofusin 1 and 2 regulation of mitochondrial DNA content is a critical determinant of glucose homeostasis. Nat Commun., 2022, 13: 2340

[55]

Zhang L, Xie X, Tao J, et al. . Mystery of bisphenol F-induced nonalcoholic fatty liver disease-like changes: Roles of Drp1-mediated abnormal mitochondrial fission in lipid droplet deposition. Sci Total Environ., 2023, 904 166831

[56]

Steffen J, Ngo J, Wang SP, et al. . The mitochondrial fission protein Drp1 in liver is required to mitigate NASH and prevents the activation of the mitochondrial ISR. Mol Metab., 2022, 64 101566

[57]

Song J, Herrmann JM, Becker T. Quality control of the mitochondrial proteome. Nat Rev Mol Cell Biol., 2021, 22(1): 54-70

[58]

Nie Z, Xiao C, Wang Y, et al. . Heat shock proteins (HSPs) in non-alcoholic fatty liver disease (NAFLD): from molecular mechanisms to therapeutic avenues. Biomark Res., 2024, 12(1): 120

[59]

Huang YH, Wang FS, Wang PW, et al. . Heat shock protein 60 restricts release of mitochondrial dsRNA to suppress hepatic inflammation and ameliorate non-alcoholic fatty liver disease in mice. Int J Mol Sci., 2022, 23(1): 577

[60]

Choi SE, Hwang Y, Lee SJ, et al. . Mitochondrial protease ClpP supplementation ameliorates diet-induced NASH in mice. J Hepatol., 2022, 77(3): 735-747

[61]

Li B, Ming H, Qin S, et al. . Redox regulation: mechanisms, biology and therapeutic targets in diseases. Signal Transduct Target Ther., 2025, 10: 72

[62]

Weng SW, Wu JC, Shen FC, et al. . Chaperonin counteracts diet-induced non-alcoholic fatty liver disease by aiding sirtuin 3 in the control of fatty acid oxidation. Diabetologia., 2023, 66(5): 913-930

[63]

Gariani K, Menzies KJ, Ryu D, et al. . Eliciting the mitochondrial unfolded protein response by nicotinamide adenine dinucleotide repletion reverses fatty liver disease in mice. Hepatology., 2016, 63(4): 1190-1204

[64]

Agyemang AF, Harrison SR, Siegel RM, et al. . Protein misfolding and dysregulated protein homeostasis in autoinflammatory diseases and beyond. Semin Immunopathol., 2015, 37(4): 335-347

[65]

Jin K, Shi Y, Zhang H, et al. . A TNFα/Miz1-positive feedback loop inhibits mitophagy in hepatocytes and propagates non-alcoholic steatohepatitis. J Hepatol., 2023, 79(2): 403-416

[66]

Skuratovskaia D, Komar A, Vulf M, et al. . IL-6 reduces mitochondrial replication, and IL-6 receptors reduce chronic inflammation in NAFLD and type 2 diabetes. Int J Mol Sci., 2021, 22(4): 1774

[67]

Tilg H, Moschen AR. Insulin resistance, inflammation, and non-alcoholic fatty liver disease. Trends Endocrinol Metab., 2008, 19(10): 371-379

[68]

Jiang T, Ruan N, Luo P, et al. . Modulation of ER-mitochondria tethering complex VAPB-PTPIP51: Novel therapeutic targets for aging-associated diseases. Ageing Res Rev., 2024, 98 102320

[69]

Elwakiel A, Mathew A, Isermann B. The role of endoplasmic reticulum–mitochondria-associated membranes in diabetic kidney disease. Cardiovasc Res., 2024, 119(18): 2875-2883

[70]

Wang J, He W, Tsai PJ, et al. . Mutual interaction between endoplasmic reticulum and mitochondria in nonalcoholic fatty liver disease. Lipds Health Dis., 2020, 19(1): 72

[71]

Smolková K, Gotvaldová K. Fatty acid trafficking between lipid droplets and mitochondria: an emerging perspective. Int J Biol Sci., 2025, 21(5): 1863-1873

[72]

Brown GT, Kleiner DE. Histopathology of nonalcoholic fatty liver disease and nonalcoholic steatohepatitis. Metabolism., 2016, 65(8): 1080-1086

[73]

Miner GE, So CM, Edwards W, et al. . PLIN5 interacts with FATP4 at membrane contact sites to promote lipid droplet-to-mitochondria fatty acid transport. Dev Cell., 2023, 58(14): 1250-1265.e6

[74]

Wu Q, Zhao M, He X, et al. . Acetylcholine reduces palmitate-induced cardiomyocyte apoptosis by promoting lipid droplet lipolysis and perilipin 5-mediated lipid droplet-mitochondria interaction. Cell Cycle., 2021, 20(18): 1890-1906

[75]

Wang H, Sreenivasan U, Hu H, et al. . Perilipin 5, a lipid droplet-associated protein, provides physical and metabolic linkage to mitochondria. J Lipid Res., 2011, 52(12): 2159-2168

[76]

Mass-Sanchez PB, Krizanac M, Štancl P, et al. . Perilipin 5 deletion protects against nonalcoholic fatty liver disease and hepatocellular carcinoma by modulating lipid metabolism and inflammatory responses. Cell Death Discov., 2024, 10: 94

[77]

Hao R, Shan S, Yang D, et al. . Peonidin-3-O-glucoside from purple corncob ameliorates nonalcoholic fatty liver disease by regulating mitochondrial and lysosome functions to reduce oxidative stress and inflammation. Nutrients., 2023, 15(2): 372

[78]

Malik N, Ferreira BI, Hollstein PE, et al. . Induction of lysosomal and mitochondrial biogenesis by AMPK phosphorylation of FNIP1. Science, 2023, 380(6642): eabj5559

[79]

Byrnes K, Blessinger S, Bailey NT, et al. . Therapeutic regulation of autophagy in hepatic metabolism. Acta Pharm Sin B., 2022, 12(1): 33-49

[80]

Ren Q, Sun Q, Fu J. Dysfunction of autophagy in high-fat diet-induced non-alcoholic fatty liver disease. Autophagy., 2024, 20(2): 221-241

[81]

Zeng J, Acin-Perez R, Assali EA, et al. . Restoration of lysosomal acidification rescues autophagy and metabolic dysfunction in non-alcoholic fatty liver disease. Nat Commun., 2023, 14(1): 2573

[82]

Amorim R, Simões ICM, Teixeira J, et al. . Mitochondria-targeted anti-oxidant AntiOxCIN4 improved liver steatosis in Western diet-fed mice by preventing lipid accumulation due to upregulation of fatty acid oxidation, quality control mechanism and antioxidant defense systems. Redox Biol., 2022, 55 102400

[83]

Wiese M, Bannister AJ. Two genomes, one cell: Mitochondrial-nuclear coordination via epigenetic pathways. Mol Metab., 2020, 38 100942

[84]

Xu W, Yang H, Liu Y, et al. . Oncometabolite 2-hydroxyglutarate is a competitive inhibitor of α-ketoglutarate-dependent dioxygenases. Cancer Cell., 2011, 19(1): 17-30

[85]

Hwang IY, Kwak S, Lee S, et al. . Psat1-dependent fluctuations in α-ketoglutarate affect the timing of ESC differentiation. Cell Metab., 2016, 24(3): 494-501

[86]

Wang QL, Chen Z, Lu X, et al. . Methionine metabolism dictates PCSK9 expression and antitumor potency of PD-1 blockade in MSS colorectal cancer. Adv Sci (Weinh)., 2025, 12(19): e2501623

[87]

Shyh-Chang N, Locasale JW, Lyssiotis CA, et al. . Influence of threonine metabolism on S-adenosylmethionine and histone methylation. Science., 2013, 339(6116): 222-226

[88]

Shen Y, Wei W, Zhou DX. Histone acetylation enzymes coordinate metabolism and gene expression. Trends Plant Sci., 2015, 20(10): 614-621

[89]

Pirola CJ, Gianotti TF, Burgueño AL, et al. . Epigenetic modification of liver mitochondrial DNA is associated with histological severity of nonalcoholic fatty liver disease. Gut., 2013, 62(9): 1356-1363

[90]

Pogribny IP, Tryndyak VP, Bagnyukova TV, et al. . Hepatic epigenetic phenotype predetermines individual susceptibility to hepatic steatosis in mice fed a lipogenic methyl-deficient diet. J Hepatol., 2009, 51(1): 176-186

[91]

Canfora EE, Meex RCR, Venema K, et al. . Gut microbial metabolites in obesity, NAFLD and T2DM. Nat Rev Endocrinol., 2019, 15(5): 261-273

[92]

Leung C, Rivera L, Furness JB, et al. . The role of the gut microbiota in NAFLD. Nat Rev Gastroenterol Hepatol., 2016, 13(7): 412-425

[93]

Zhang S, Zhao J, Xie F, et al. . Dietary fiber-derived short-chain fatty acids: a potential therapeutic target to alleviate obesity-related nonalcoholic fatty liver disease. Obes Rev., 2021, 22(11): e13316

[94]

Chen M, Li Y, Zhai Z, et al. . Bifidobacterium animalis subsp. lactis A6 ameliorates bone and muscle loss via modulating gut microbiota composition and enhancing butyrate production. Bone Res, 2025, 13: 28

[95]

Zhao ZH, Wang ZX, Zhou D, et al. . Sodium butyrate supplementation inhibits hepatic steatosis by stimulating liver kinase B1 and insulin-induced gene. Cell Mol Gastroenterol Hepatol., 2021, 12(3): 857-871

[96]

Steinberg GR, Hardie DG. New insights into activation and function of the AMPK. Nat Rev Mol Cell Biol., 2023, 24(4): 255-272

[97]

Liu J, Wu A, Cai J, et al. . The contribution of the gut-liver axis to the immune signaling pathway of NAFLD. Front Immunol., 2022, 13 968799

[98]

Ferro D, Baratta F, Pastori D, et al. . New insights into the pathogenesis of non-alcoholic fatty liver disease: gut-derived lipopolysaccharides and oxidative stress. Nutrients., 2020, 12(9): 2762

[99]

Ji Y, Gao Y, Chen H, et al. . Indole-3-acetic acid alleviates nonalcoholic fatty liver disease in mice via attenuation of hepatic lipogenesis, and oxidative and inflammatory stress. Nutrients., 2019, 11(9): 2062

[100]

Zhao ZH, Xin FZ, Zhou D, et al. . Trimethylamine N-oxide attenuates high-fat high-cholesterol diet-induced steatohepatitis by reducing hepatic cholesterol overload in rats. World J Gastroenterol., 2019, 25(20): 2450-2462

[101]

Guo J, Shi CX, Zhang QQ, et al. . Interventions for non-alcoholic liver disease: a gut microbial metabolites perspective. Therap Adv Gastroenterol., 2022, 15: 17562848221138676

[102]

Di Vincenzo F, Del Gaudio A, Petito V, et al. . Gut microbiota, intestinal permeability, and systemic inflammation: a narrative review. Intern Emerg Med., 2024, 19(2): 275-293

[103]

Rosadini CV, Kagan JC. Early innate immune responses to bacterial LPS. Curr Opin Immunol., 2017, 44: 14-19

[104]

Mohammad S, Thiemermann C. Role of metabolic endotoxemia in systemic inflammation and potential interventions. Front Immunol., 2021, 11 594150

[105]

Brenner C, Galluzzi L, Kepp O, et al. . Decoding cell death signals in liver inflammation. J Hepatol., 2013, 59(3): 583-594

[106]

Albillos A, de Gottardi A, Rescigno M. The gut-liver axis in liver disease: Pathophysiological basis for therapy. J Hepatol., 2020, 72(3): 558-577

[107]

Lin S, Wang S, Wang P, et al. . Bile acids and their receptors in regulation of gut health and diseases. Prog Lipid Res., 2023, 89 101210

[108]

Samson N, Bosoi CR, Roy C, et al. . HSDL2 links nutritional cues to bile acid and cholesterol homeostasis. Sci Adv., 2024, 10(22): eadk9681

[109]

Cheng Y, Xiang X, Liu C, et al. . Transcriptomic analysis reveals lactobacillus reuteri alleviating alcohol-induced liver injury in mice by enhancing the farnesoid X receptor signaling pathway. J Agric Food Chem., 2022, 70(39): 12550-12564

[110]

Duan X, Meng Q, Wang C, et al. . Calycosin attenuates triglyceride accumulation and hepatic fibrosis in murine model of non-alcoholic steatohepatitis via activating farnesoid X receptor. Phytomedicine., 2017, 25: 83-92

[111]

Watanabe M, Houten SM, Wang L, et al. . Bile acids lower triglyceride levels via a pathway involving FXR, SHP, and SREBP-1c. J Clin Invest., 2004, 113(10): 1408-1418

[112]

Peng A, Liu S, Fang L, et al. . Inonotus obliquus and its bioactive compounds alleviate non-alcoholic fatty liver disease via regulating FXR/SHP/SREBP-1c axis. Eur J Pharmacol., 2022, 921 174841

[113]

Li T, Chiang JYL. Bile acid signaling in metabolic disease and drug therapy. Pharmacol Rev., 2014, 66(4): 948-983

[114]

Gonzalez FJ, Jiang C, Patterson AD. An intestinal microbiota–farnesoid X receptor axis modulates metabolic disease. Gastroenterology., 2016, 151(5): 845-859

[115]

Hegyi P, Maléth J, Walters JR, et al. . Guts and gall: bile acids in regulation of intestinal epithelial function in health and disease. Physiol Rev., 2018, 98(4): 1983-2023

[116]

Shum M, Ngo J, Shirihai OS, et al. . Mitochondrial oxidative function in NAFLD: Friend or foe?. Mol Metab., 2021, 50 101134

[117]

Negi CK, Babica P, Bajard L, et al. . Insights into the molecular targets and emerging pharmacotherapeutic interventions for nonalcoholic fatty liver disease. Metabolism., 2022, 126 154925

[118]

Gutierrez-Mariscal FM, Arenas-de Larriva AP, Limia-Perez L, et al. . Coenzyme Q10 supplementation for the reduction of oxidative stress: clinical implications in the treatment of chronic diseases. Int J Mol Sci., 2020, 21(21): 7870

[119]

Vrentzos E, Ikonomidis I, Pavlidis G, et al. . Six-month supplementation with high dose coenzyme Q10 improves liver steatosis, endothelial, vascular and myocardial function in patients with metabolic-dysfunction associated steatotic liver disease: a randomized double-blind, placebo-controlled trial. Cardiovasc Diabetol., 2024, 23(1): 245

[120]

Lee SW, Lee YJ, Baek SM, et al. . Mega-dose vitamin C ameliorates nonalcoholic fatty liver disease in a mouse fast-food diet model. Nutrients., 2022, 14(11): 2195

[121]

Caldwell S. NASH Therapy: omega 3 supplementation, vitamin E, insulin sensitizers and statin drugs. Clin Mol Hepatol., 2017, 23(2): 103-108

[122]

Yamamoto M, Kensler TW, Motohashi H. The KEAP1-NRF2 system: a thiol-based sensor-effector apparatus for maintaining redox homeostasis. Physiol Rev., 2018, 98(3): 1169-1203

[123]

Loboda A, Damulewicz M, Pyza E, et al. . Role of Nrf2/HO-1 system in development, oxidative stress response and diseases: an evolutionarily conserved mechanism. Cell Mol Life Sci., 2016, 73(17): 3221-3247

[124]

Xu L, Nagata N, Ota T. Impact of glucoraphanin-mediated activation of Nrf2 on non-alcoholic fatty liver disease with a focus on mitochondrial dysfunction. Int J Mol Sci., 2019, 20(23): 5920

[125]

Li Y, Deng X, Tan X, et al. . Protective role of curcumin in disease progression from non-alcoholic fatty liver disease to hepatocellular carcinoma: a meta-analysis. Front Pharmacol., 2024, 15: 1343193

[126]

Undamatla R, Fagunloye OG, Chen J, et al. . Reduced mitophagy is an early feature of NAFLD and liver-specific PARKIN knockout hastens the onset of steatosis, inflammation and fibrosis. Sci Rep., 2023, 13: 7575

[127]

Narendra DP, Youle RJ. The role of PINK1-Parkin in mitochondrial quality control. Nat Cell Biol., 2024, 26(10): 1639-1651

[128]

Li X, Shi Z, Zhu Y, et al. . Cyanidin-3-O-glucoside improves non-alcoholic fatty liver disease by promoting PINK1-mediated mitophagy in mice. Br J Pharmacol., 2020, 177(15): 3591-3607

[129]

Tian M, Hou J, Liu Z, et al. . BNIP3 in hypoxia-induced mitophagy: Novel insights and promising target for non-alcoholic fatty liver disease. Int J Biochem Cell Biol., 2024, 168 106517

[130]

Kuang Y, Ma K, Zhou C, et al. . Structural basis for the phosphorylation of FUNDC1 LIR as a molecular switch of mitophagy. Autophagy., 2016, 12(12): 2363-2373

[131]

Egan DF, Shackelford DB, Mihaylova MM, et al. . Phosphorylation of ULK1 (hATG1) by AMP-activated protein kinase connects energy sensing to mitophagy. Science., 2011, 331(6016): 456-461

[132]

Chen M, Zhu JY, Mu WJ, et al. . Cdo1-Camkk2-AMPK axis confers the protective effects of exercise against NAFLD in mice. Nat Commun., 2023, 14(1): 8391

[133]

Afonso MB, Islam T, Magusto J, et al. . RIPK3 dampens mitochondrial bioenergetics and lipid droplet dynamics in metabolic liver disease. Hepatology., 2023, 77(4): 1319-1334

[134]

Desjardins EM, Smith BK, Day EA, et al. . The phosphorylation of AMPKβ1 is critical for increasing autophagy and maintaining mitochondrial homeostasis in response to fatty acids. Proc Natl Acad Sci U S A., 2022, 119(48): e2119824119

[135]

Longo M, Meroni M, Paolini E, et al. . Mitochondrial dynamics and nonalcoholic fatty liver disease (NAFLD): new perspectives for a fairy-tale ending?. Metabolism., 2021, 117 154708

[136]

Elbadawy M, Tanabe K, Yamamoto H, et al. . Evaluation of the efficacy of mitochondrial fission inhibitor (Mdivi-1) using non-alcoholic steatohepatitis (NASH) liver organoids. Front Pharmacol., 2023, 14: 1243258

[137]

Afonso MB, David JC, Alves MI, et al. . Intricate interplay between cell metabolism and necroptosis regulation in metabolic dysfunction-associated steatotic liver disease: a narrative review. Metabolism., 2024, 158 155975

[138]

Pawlak M, Lefebvre P, Staels B. Molecular mechanism of PPARα action and its impact on lipid metabolism, inflammation and fibrosis in non-alcoholic fatty liver disease. J Hepatol., 2015, 62(3): 720-733

[139]

Wang X, Wang J, Ying C, et al. . Fenofibrate alleviates NAFLD by enhancing the PPARα/PGC-1α signaling pathway coupling mitochondrial function. BMC Pharmacol Toxicol., 2024, 25(1): 7

[140]

Li R, Xin T, Li D, et al. . Therapeutic effect of Sirtuin 3 on ameliorating nonalcoholic fatty liver disease: The role of the ERK-CREB pathway and Bnip3-mediated mitophagy. Redox Biol., 2018, 18: 229-243

[141]

Zhu Y, Tan JK, Liu J, et al. . Roles of traditional and next-generation probiotics on non-alcoholic fatty liver disease (NAFLD) and non-alcoholic steatohepatitis (NASH): a systematic review and network meta-analysis. Antioxidants (Basel)., 2024, 13(3): 329

[142]

Han Y, Ling Q, Wu L, et al. . Akkermansia muciniphila inhibits nonalcoholic steatohepatitis by orchestrating TLR2-activated γδT17 cell and macrophage polarization. Gut Microbes., 2023, 15(1): 2221485

[143]

Wang L, Jiao T, Yu Q, et al. . Bifidobacterium bifidum shows more diversified ways of relieving non-alcoholic fatty liver compared with Bifidobacterium adolescentis. Biomedicines., 2021, 10(1): 84

[144]

Yang Z, Su H, Lv Y, et al. . Inulin intervention attenuates hepatic steatosis in rats via modulating gut microbiota and maintaining intestinal barrier function. Food Res Int., 2023, 163 112309

[145]

Wei W, Wong CC, Jia Z, et al. . Parabacteroides distasonis uses dietary inulin to suppress NASH via its metabolite pentadecanoic acid. Nat Microbiol., 2023, 8(8): 1534-1548

[146]

Fotschki B, Juśkiewicz J, Jurgoński A, et al. . Fructo-oligosaccharides and pectins enhance beneficial effects of raspberry polyphenols in rats with nonalcoholic fatty liver. Nutrients., 2021, 13(3): 833

[147]

Shou D, Luo Q, Tang W, et al. . Hepatobiliary and pancreatic: Multi-donor fecal microbiota transplantation attenuated high-fat diet-induced hepatic steatosis in mice by remodeling the gut microbiota. J Gastroenterol Hepatol., 2023, 38(12): 2195-2205

[148]

Craven L, Rahman A, Nair Parvathy S, et al. . Allogenic fecal microbiota transplantation in patients with nonalcoholic fatty liver disease improves abnormal small intestinal permeability: a randomized control trial. Am J Gastroenterol., 2020, 115(7): 1055-1065

[149]

Xue L, Deng Z, Luo W, et al. . Effect of fecal microbiota transplantation on non-alcoholic fatty liver disease: a randomized clinical trial. Front Cell Infect Microbiol., 2022, 12 759306

[150]

Bibbò S, Settanni CR, Porcari S, et al. . Fecal microbiota transplantation: screening and selection to choose the optimal donor. J Clin Med., 2020, 9(6): 1757

[151]

Woodworth MH, Carpentieri C, Sitchenko KL, et al. . Challenges in fecal donor selection and screening for fecal microbiota transplantation: a review. Gut Microbes., 2017, 8(3): 225-237

[152]

Zheng Y, Wang S, Wu J, et al. . Mitochondrial metabolic dysfunction and non-alcoholic fatty liver disease: new insights from pathogenic mechanisms to clinically targeted therapy. J Transl Med., 2023, 21(1): 510

[153]

Mansouri A, Gattolliat CH, Asselah T. Mitochondrial dysfunction and signaling in chronic liver diseases. Gastroenterology., 2018, 155(3): 629-647

[154]

Wiest R, Albillos A, Trauner M, et al. . Targeting the gut-liver axis in liver disease. J Hepatol., 2017, 67(5): 1084-1103

[155]

Atabaki-Pasdar N, Ohlsson M, Viñuela A, et al. . Predicting and elucidating the etiology of fatty liver disease: a machine learning modeling and validation study in the IMI DIRECT cohorts. PLoS Med., 2020, 17(6): e1003149

[156]

Ding J, Liu H, Zhang X, et al. . Integrative multiomic analysis identifies distinct molecular subtypes of NAFLD in a Chinese population. Sci Transl Med., 2024, 16(772): eadh9940

[157]

Betrapally NS, Gillevet PM, Bajaj JS. Changes in the intestinal microbiome and alcoholic and nonalcoholic liver diseases: causes or effects?. Gastroenterology., 2016, 150(8): 1745-1755.e3

[158]

Aron-Wisnewsky J, Vigliotti C, Witjes J, et al. . Gut microbiota and human NAFLD: disentangling microbial signatures from metabolic disorders. Nat Rev Gastroenterol Hepatol., 2020, 17(5): 279-297

[159]

Le Roy T, Llopis M, Lepage P, et al. . Intestinal microbiota determines development of non-alcoholic fatty liver disease in mice. Gut., 2013, 62(12): 1787-1794

[160]

Moschen AR, Kaser S, Tilg H. Non-alcoholic steatohepatitis: a microbiota-driven disease. Trends Endocrinol Metab., 2013, 24(11): 537-545

Funding

Natural Science Foundation of Hubei Province(2023AFB170 to MC)

National Natural Science Foundation of China(No. 81902665 to LC)

RIGHTS & PERMISSIONS

The Author(s), under exclusive licence to the Huazhong University of Science and Technology

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