Discover the SciOpen Platform and Achieve Your Research Goals with Ease.
Search articles, authors, keywords, DOl and etc.
Oxidative stress is one of the main ways to cause alcohol-induced liver injury, and alcoholic liver disease (ALD) has been a common health problem worldwide. Lactic acid bacteria (LAB) is also considered as a potential treatment to alleviate alcohol-induced liver injury. Lactobacillus plantarum J26 is a LAB isolated from Chinese traditional fermented dairy products with excellent probiotic effects. This study aimed to establish a mice model of alcoholic liver injury through acute-on-chronic alcohol feeding and to study the alleviating effect of pre-intake of L. plantarum J26 on alcohol-induced oxidative liver injury and focus on its potential mechanism of alleviating effect. The results showed that pre-intake of L. plantarum J26 could improve liver pathological changes, reduce lipid accumulation, increase mitochondrial ATP and mitochondrial (mtDNA) levels, and alleviate liver injury. In addition, pre-intake L. plantarum J26 can improve the level of short-chain fatty acids (SCFAs) in the intestines in mice, short chain fatty acids can be used as a signaling molecule activation of nuclear factor E2-related factor 2 (Nrf2) signaling pathway to alleviate liver oxidative stress, and maintain mitochondrial homeostasis by regulating the expression of genes related to mitochondrial dynamics and autophagy, thereby reducing cell apoptosis to alleviate alcohol-induced oxidative liver injury.
J. Rehm, C. Mathers, S. Popova, et al., Alcohol and global health and global burden of disease and injury and economic cost attributable to alcohol use and alcohol-use disorders, Lancet 373(9682) (2009) 2223-2233. https://doi.org/10.1016/s0140-6736(09)60746-7.
H. Cichoz-Lach, A. Michalak, Oxidative stress as a crucial factor in liver diseases, World J. Gastroenterol. 20(25) (2014) 8082-8091. https://doi.org/10.3748/wjg.v20.i25.8082.
J. Manthey, K.D. Shield, M. Rylett, et al., Global alcohol exposure between 1990 and 2017 and forecasts until 2030: a modelling study, Lancet 393(10190) (2019) 2493-2502. https://doi.org/10.1016/s0140-6736(18)32744-2.
J.S. Bajaj, Alcohol, liver disease and the gut microbiota, Nat. Rev. Gastroenterol. Hepatol. 16(4) (2019) 235-246. https://doi.org/10.1038/s41575-018-0099-1.
A. I. Cederbaum, Cytochrome P450 2E1-dependent oxidant stress and upregulation of anti-oxidant defense in liver cells, J. Gastroenterol. Hepatol. 21 (2006) S22-S25. https://doi.org/10.1111/j.1440-1746.2006.04595.x.
R. Hou, X. Liu, X. Wu, et al., Therapeutic effect of natural melanin from edible fungus Auricularia auricula on alcohol-induced liver damage in vitro and in vivo, Food Sci. Hum. Well. 10(4) (2021) 514-522. https://doi.org/10.1016/j.fshw.2021.04.014.
S.M. Shin, J.H. Yang, S.H. Ki, Role of the Nrf2-ARE pathway in liver diseases, Oxid. Med. Cell. Longev. 2013 (2013) 763257. https://doi.org/10.1155/2013/763257.
T. Xu, S. Hu, Y. Liu, et al., Hawk tea flavonoids as natural hepatoprotective agents alleviate acute liver damage by reshaping the intestinal microbiota and modulating the Nrf2 and NF-κB signaling pathways, Nutrients 14(17) (2022) 3662. https://doi.org/10.3390/nu14173662.
Z. Gu, F. Li, Y. Liu, et al., Exosome-like nanoparticles from Lactobacillus rhamnosus GG protect against alcohol-associated liver disease through intestinal aryl hydrocarbon receptor in mice, Hepatol Commun. 5(5) (2021) 846-864. https://doi.org/10.1002/hep4.1679.
L. Hoyles, T. Snelling, U.K. Umlai, et al., Microbiome-host systems interactions: protective effects of propionate upon the blood-brain barrier, Microbiome 6 (2018) 1-13. https://doi.org/10.1186/s40168-018-0439-y.
W. Guo, J. Liu, J. Sun, et al., Butyrate alleviates oxidative stress by regulating NRF2 nuclear accumulation and H3K9/14 acetylation via GPR109A in bovine mammary epithelial cells and mammary glands, Free Radic. Biol. Med. 152 (2020) 728-742. https://doi.org/10.1016/j.freeradbiomed.2020.01.016.
X. Peng, Y. Jiang, Protective effects of Lactobacillus plantarum NDC 75017 against lipopolysaccharide-induced liver injury in mice, Inflammation 37(5) (2014) 1599-1607. https://doi.org/10.1007/s10753-014-9886-1.
Y. Jiang, L. Li, H. Sun, et al., Induction of cytokines via NF-κB and p38 MAP kinase signalling pathways associated with the immunomodulation by Lactobacillus plantarum NDC 75017 in vitro and in vivo, J. Funct. Foods 20 (2016) 215-225. https://doi.org/10.1016/j.jff.2015.10.027.
Y. Zhang, W. Liu, Z. Wei, et al., Enhancement of functional characteristics of blueberry juice fermented by Lactobacillus plantarum, LWT-Food Sci. Technol. 139 (2021) 110590. https://doi.org/10.1016/j.lwt.2020.110590.
Y. Fan, S. Chen, F. Dang, et al., Screening and study on activity in the simulated gastrointestinal conditions of a cholesterol-lowering lactic acid bacteria, China Dairy Industry 46(9) (2018) 4-7.
A. Bertola, S. Mathews, S.H. Ki, et al., Mouse model of chronic and binge ethanol feeding (the NIAAA model), Nat. Protoc. 8(3) (2013) 627-637. https://doi.org/10.1038/nprot.2013.032.
T. Saitoh, H. Murakami, N. Hatsumi, et al., Detection of VP-16-treated HL-60 cell apoptosis by TUNEL electron microscopy, Ultrastruct. Pathol. 24(2) (2000) 99-103. https://doi.org/10.1080/01913120050118576.
A. I. Cederbaum, Y. Lu, D. Wu, Role of oxidative stress in alcohol-induced liver injury, Arch. Toxicol. 83(6) (2009) 519-548. https://doi.org/10.1007/s00204-009-0432-0.
A.M. Cassard, D. Ciocan, Microbiota, a key player in alcoholic liver disease, Clin. Mol. Hepatol. 24(2) (2018) 100-107. https://doi.org/10.3350/cmh.2017.0067.
X. Song, W. Cui, F. Meng, et al., Glucopyranose from Pleurotus geesteranus prevent alcoholic liver diseases by regulating Nrf2/HO-1-TLR4/NF-κB signalling pathways and gut microbiota, Food Funct. 13(5) (2022) 2441-2455. https://doi.org/10.1039/d1fo03486c.
Q. He, C. Yang, X. Kang, et al., Intake of Bifidobacterium lactis Probio-M8 fermented milk protects against alcoholic liver disease, J. Dairy Sci. 105(4) (2022) 2908-2921. https://doi.org/10.3168/jds.2021-21265.
L.E. Nagy, W.X. Ding, G. Cresci, et al., Linking pathogenic mechanisms of alcoholic liver disease with clinical phenotypes, Gastroenterology 150(8) (2016) 1756-1768. https://doi.org/10.1053/j.gastro.2016.02.035.
E. Ulukaya, C. Acilan, Y. Yilmaz, Apoptosis: why and how does it occur in biology?, Cell Biochem. Funct. 29(6) (2011) 468-480. https://doi.org/10.1002/cbf.1774.
L. Portt, G. Norman, C. Clapp, et al., Anti-apoptosis and cell survival: a review, Biochimica et Biophysica Acta-Molecular Cell Research 1813(1) (2011) 238-259. https://doi.org/10.1016/j.bbamcr.2010.10.010.
H.W. Liang, T.Y. Yang, C.S. Teng, et al., Mulberry leaves extract ameliorates alcohol-induced liver damages through reduction of acetaldehyde toxicity and inhibition of apoptosis caused by oxidative stress signals, Int. J. Med. Sci. 18(1) (2021) 53-64. https://doi.org/10.7150/ijms.50174.
A. Rahal, A. Kumar, V. Singh, et al., Oxidative stress, prooxidants, and antioxidants: the interplay, Biomed. Res. Int. 2014 (2014) 761264. https://doi.org/10.1155/2014/761264.
X. Tian, R. Li, Y. Jiang, et al., Bifidobacterium breve ATCC15700 pretreatment prevents alcoholic liver disease through modulating gut microbiota in mice exposed to chronic alcohol intake, J. Funct. Foods 72 (2020) 104045. https://doi.org/10.1016/j.jff.2020.104045.
X. Zeng, X. Li, C. Xu, et al., Schisandra sphenanthera extract (Wuzhi Tablet) protects against chronic-binge and acute alcohol-induced liver injury by regulating the NRF2-ARE pathway in mice, Acta. Pharm. Sin. B. 7(5) (2017) 583-592. https://doi.org/10.1016/j.apsh.2017.04.002.
R. Kandimalla, M. Manczak, X. Yin, et al., Hippocampal phosphorylated tau induced cognitive decline, dendritic spine loss and mitochondrial abnormalities in a mouse model of Alzheimer’s disease, Hum. Mol. Genet. 27(1) (2018) 30-40. https://doi.org/10.1093/hmg/ddx381.
L. Bonet-Ponce, S. Saez-Atienzar, C. da Casa, et al., On the mechanism underlying ethanol-induced mitochondrial dynamic disruption and autophagy response, Biochim. Biophys. Acta Mol. Basis Dis. 1852(7) (2015) 1400-1409. https://doi.org/10.1016/j.bbadis.2015.03.006.
N. Matsuda, S. Sato, K. Shiba, et al., PINK1 stabilized by mitochondrial depolarization recruits Parkin to damaged mitochondria and activates latent Parkin for mitophagy, J. Cell Biol. 189(2) (2010) 211-221. https://doi.org/10.1083/jcb.200910140.
J.A. Williams, H.M. Ni, Y. Ding, et al., Parkin regulates mitophagy and mitochondrial function to protect against alcohol-induced liver injury and steatosis in mice, Am. J. Physiol. Gastrointest. Liver Physio. 309(5) (2015) G324-G340. https://doi.org/10.1152/ajpgi.00108.2015.
Y. Aman, T. Schmauck-Medina, M. Hansen, et al., Autophagy in healthy aging and disease, Nature Aging 1(8) (2021) 634-650. https://doi.org/10.1038/s43587-021-00098-4.
C. Zhang, J. Lin, J. Ge, et al., Selenium triggers Nrf2-mediated protection against cadmium-induced chicken hepatocyte autophagy and apoptosis, Toxicol. in Vitro 44 (2017) 349-356. https://doi.org/10.1016/j.tiv.2017.07.027.
H. Zhao, S. Liu, H. Zhao, et al., Protective effects of fucoidan against ethanol-induced liver injury through maintaining mitochondrial function and mitophagy balance in rats, Food Funct. 12(9) (2021) 3842-3854. https://doi.org/10.1039/d0fo03220d.
J.A. Williams, W.X. Ding, Targeting Pink1-Parkin-mediated mitophagy for treating liver injury, Pharmacol. Res. 102 (2015) 264-269. https://doi.org/10.1016/j.phrs.2015.09.020.
C.W. Lin, H. Zhang, M. Li, et al., Pharmacological promotion of autophagy alleviates steatosis and injury in alcoholic and non-alcoholic fatty liver conditions in mice, J. Hepatol. 58(5) (2013) 993-999. https://doi.org/10.1016/j.jhep.2013.01.011.
X. Chao, H.M. Ni, W.X. Ding, Insufficient autophagy: a novel autophagic flux scenario uncovered by impaired liver TFEB-mediated lysosomal biogenesis from chronic alcohol-drinking mice, Autophagy 14(9) (2018) 1646-1648. https://doi.org/10.1080/15548627.2018.1489170.
R.C. Chen, L.M. Xu, S.J. Du, et al., Lactobacillus rhamnosus GG supernatant promotes intestinal barrier function, balances T-reg and T(H)17 cells and ameliorates hepatic injury in a mouse model of chronic-binge alcohol feeding, Toxicol. Lett. 241 (2016) 103-110. https://doi.org/10.1016/j.toxlet.2015.11.019.
J. Hanus, A. Kolkin, J. Chimienti, et al., 4-Acetoxyphenol prevents RPE oxidative stress-induced necrosis by functioning as an NRF2 stabilizer, Invest. Ophthalmol. Visual. Sci. 56(9) (2015) 5048-5059. https://doi.org/10.1167/iovs.15-16401.
K. Chan, X.D. Han, Y. W. Kan, An important function of Nrf2 in combating oxidative stress: detoxification of acetaminophen, PNAS 98(8) (2001) 4611-4616. https://doi.org/10.1073/pnas.081082098.
T.E. Adolph, C. Grander, A.R. Moschen, et al., Liver-microbiome axis in health and disease, Trends Immunol. 39(9) (2018) 712-723. https://doi.org/10.1016/j.it.2018.05.002.
Z. Zhou, W. Zhong, Targeting the gut barrier for the treatment of alcoholic liver disease, Liver Research 1(4) (2017) 197-207. https://doi.org/10.1016/j.livres.2017.12.004.
Q. Zhang, N. Hu, Effects of metformin on the gut microbiota in obesity and type 2 diabetes mellitus, Diabet. Metab. Synd. Ob. 13 (2020) 5003-5014. https://doi.org/10.2147/dmso.S286430.
H. Endo, M. Niioka, N. Kobayashi, et al., Butyrate-producing probiotics reduce nonalcoholic fatty liver disease progression in rats: new insight into the probiotics for the gut-liver axis, PLoS ONE 8(5) (2013) e63388. https://doi.org/10.1371/journal.pone.0063388.
C. Gonzalez-Bosch, E. Boorman, P.A. Zunszain, et al., Short-chain fatty acids as modulators of redox signaling in health and disease, Redox. Biology. 47 (2021) 102165. https://doi.org/10.1016/j.redox.2021.102165.
892
Views
285
Downloads
0
Crossref
0
Web of Science
0
Scopus
0
CSCD
Altmetrics
This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).