中文English
ISSN 1001-5256 (Print)
ISSN 2097-3497 (Online)
CN 22-1108/R
Volume 39 Issue 6
Jun.  2023
Turn off MathJax
Article Contents

Research advances in the cascade interaction between reactive oxygen species/reactive nitrogen species and the NF-κB signaling pathway in liver fibrosis

DOI: 10.3969/j.issn.1001-5256.2023.06.031
Research funding:

The Special Research Project of Traditional Chinese Medicine in Henan Province (2022ZY1167);

The Training Program for Young Scholars in Universities of Henan Province (2021GGJS084);

The Important Scientific Research Project of Universities in Henan Province (21B310003)

More Information
  • Corresponding author: LU Baoping, lbp1921@sohu.com (ORCID: 0000-0002-3707-2185)
  • Received Date: 2022-10-18
  • Accepted Date: 2022-11-16
  • Published Date: 2023-06-20
  • Liver fibrosis is a compensatory response in the process of tissue repair after chronic liver injury, and it is also a necessary pathological process in the progression of a variety of chronic liver diseases. In the pathological state, the imbalance between hepatic oxidative system and antioxidant system can lead to the excessive production or insufficient clearance of reactive oxygen species (ROS)/reactive nitrogen species (RNS), which may induce the injury of hepatocytes, expand inflammatory response, and promote the development and progression of liver fibrosis. As a master regulator of oxidative stress and inflammatory response, NF-κB plays a key role in the process of liver fibrosis. Therefore, the cascade interaction between ROS/RNS and the NF-κB signaling pathway plays a guiding role in further clarifying the pathogenesis of liver fibrosis and exploring effective prevention and treatment strategies. This article reviews and discusses the interaction between ROS/RNS and the NF-κB signaling pathway and its important role in the progression of liver fibrosis, so as to provide strategies and references for targeted therapy for liver fibrosis.

     

  • loading
  • [1]
    ZHANG J, WANG X, VIKASH V, et al. ROS and ROS-mediated cellular signaling[J]. Oxid Med Cell Longev, 2016, 2016: 4350965. DOI: 10.1155/2016/4350965.
    [2]
    RAMÍREZ A, VÁZQUEZ-SÁNCHEZ AY, CARRIÓN-ROBALINO N, et al. Ion channels and oxidative stress as a potential link for the diagnosis or treatment of liver diseases[J]. Oxid Med Cell Longev, 2016, 2016: 3928714. DOI: 10.1155/2016/3928714.
    [3]
    HE F, GUO FC, LI Z, et al. Myeloid-specific disruption of recombination signal binding protein Jκ ameliorates hepatic fibrosis by attenuating inflammation through cylindromatosis in mice[J]. Hepatology, 2015, 61(1): 303-314. DOI: 10.1002/hep.27394.
    [4]
    QIN TY, CHEN ZW. Physiological function of ROS in organism[J]. Life Sci Instrum, 2008, 6 (2): 12-16. DOI: 10.3969/j.issn.1671-7929.2008.02.003.

    秦涛余, 陈志伟. 机体内活性氧生理功能研究进展[J]. 生命科学仪器, 2008, 6(2): 12-16. DOI: 10.3969/j.issn.1671-7929.2008.02.003.
    [5]
    ZHENG RL, HUANG ZY. Free Radical Biology(The Third Edition)[M]. Beijing: Higher Education Press, 2007: 201-203.

    郑荣梁, 黄中洋. 自由基生物学(第三版)[M]. 北京: 高等教育出版社, 2007: 201-203.
    [6]
    NOGUEIRAS R, HABEGGER KM, CHAUDHARY N, et al. Sirtuin 1 and sirtuin 3: physiological modulators of metabolism[J]. Physiol Rev, 2012, 92(3): 1479-1514. DOI: 10.1152/physrev.00022.2011.
    [7]
    SÁNCHEZ-VALLE V, CHÁVEZ-TAPIA NC, URIBE M, et al. Role of oxidative stress and molecular changes in liver fibrosis: a review[J]. Curr Med Chem, 2012, 19(28): 4850-4860. DOI: 10.2174/092986712803341520.
    [8]
    WILLEMS PH, ROSSIGNOL R, DIETEREN CE, et al. Redox homeostasis and mitochondrial dynamics[J]. Cell Metab, 2015, 22(2): 207-218. DOI: 10.1016/j.cmet.2015.06.006.
    [9]
    XIA SJ, SUN T, WU JZ. Free radicals, Inflammation and Aging[J]. Pract Geriatr, 2014, 28(2): 100-103. DOI: 10.3969/j.issn.1003-9198.2014.02.004.

    夏世金, 孙涛, 吴俊珍. 自由基、炎症与衰老[J]. 实用老年医学, 2014, 28(2): 100-103. DOI: 10.3969/j.issn.1003-9198.2014.02.004.
    [10]
    LYU YH, WU SS, WANG ZC, et al. Research progress of traditional Chinese medicine regulating reactive oxygen species(ROS) against liver fibrosis[J]. Chin Arch Tradit Chin Med, 2021, 39(6): 117-121. DOI: 10.13193/j.issn.1673-7717.

    吕艳杭, 吴姗姗, 王振常, 等. 中医药调控活性氧(ROS)抗肝纤维化的研究进展[J]. 中华中医药学刊, 2021, 39(6): 117-121. DOI: 10.13193/j.issn.1673-7717.
    [11]
    GUO R, YAN M. Cellular and molecular mechanism of liver fibrosis[J/CD]. Chin J Liver Dis(Electronic Version), 2012, 4(4): 57-62.

    郭蓉, 阎明. 肝纤维化的细胞和分子机制研究进展[J/CD]. 中国肝脏病杂志(电子版), 2012, 4(4): 57-62.
    [12]
    ZHAO J, QI YF, YU YR. Research advances in the role of oxidative stress in the development and progression of liver fibrosis[J]. J Clin Hepatol, 2019, 35(9): 2067-2071. DOI: 10.3969/j.issn.1001-5256.2019.09.040.

    赵杰, 齐永芬, 鱼艳荣. 氧化应激在肝纤维化发生发展中的作用[J]. 临床肝胆病杂志, 2019, 35(9): 2067-2071. DOI: 10.3969/j.Issn.1001-5256.2019.09.040.
    [13]
    PAIK YH, KIM J, AOYAMA T, et al. Role of NADPH oxidases in liver fibrosis[J]. Antioxid Redox Signal, 2014, 20(17): 2854-2872. DOI: 10.1089/ars.2013.5619.
    [14]
    URTASUN R, CONDE DE LA ROSA L, NIETO N. Oxidative and nitrosative stress and fibrogenic response[J]. Clin Liver Dis, 2008, 12(4): 769-790, ⅷ. DOI: 10.1016/j.cld.2008.07.005.
    [15]
    SCAMBLER T, JAROSZ-GRIFFITHS HH, LARA-REYNA S, et al. ENaC-mediated sodium influx exacerbates NLRP3-dependent inflammation in cystic fibrosis[J]. Elife, 2019, 8: e49248. DOI: 10.7554/eLife.49248.
    [16]
    ZHANG K, LIN L, ZHU Y, et al. Saikosaponin d alleviates liver fibrosis by negatively regulating the ROS/NLRP3 inflammasome through activating the ERβ pathway[J]. Front Pharmacol, 2022, 13: 894981. DOI: 10.3389/fphar.2022.894981.
    [17]
    YI J, WU S, TAN S, et al. Berberine alleviates liver fibrosis through inducing ferrous redox to activate ROS-mediated hepatic stellate cells ferroptosis[J]. Cell Death Discov, 2021, 7(1): 374. DOI: 10.1038/s41420-021-00768-7.
    [18]
    GAN D, ZHANG W, HUANG C, et al. Ursolic acid ameliorates CCl4-induced liver fibrosis through the NOXs/ROS pathway[J]. J Cell Physiol, 2018, 233(10): 6799-6813. DOI: 10.1002/jcp.26541.
    [19]
    CHUNG HK, KIM YK, PARK JH, et al. The indole derivative NecroX-7 improves nonalcoholic steatohepatitis in ob/ob mice through suppression of mitochondrial ROS/RNS and inflammation[J]. Liver Int, 2015, 35(4): 1341-1353. DOI: 10.1111/liv.12741.
    [20]
    LIU YY, LI L, LI XW, et al. Research progress of microRNAs in TLR/NF-κB signaling pathway[J]. World Latest Medicine Information, 2018, 18(A5): 115-116, 119. DOI: 10.19613/j.cnki.1671-3141.2018.105.054.

    刘毅毅, 李林, 李小薇, 等. MicroRNAs在TLR/NF-кB信号通路中的研究进展[J]. 世界最新医学信息文摘, 2018, 18(A5): 115-116, 119. DOI: 10.19613/j.cnki.1671-3141.2018.105.054.
    [21]
    SU P, FENG SS, LI QW. Research progress of the structure and function of NF-κB and IκB in different animal groups[J]. Yi Chuan, 2016, 38(6): 523-531. DOI: 10.16288/j.yczz.15-509.
    [22]
    ZHAO YW, ZHU JN. Research progress of NF-κB signaling pathway[J]. Gansu Sci Technol, 2016, 32(21): 117-123, 112. DOI: 10.3969/j.issn.1000-0952.2016.21.048.

    赵运旺, 朱嘉宁. NF-κB信号通路研究进展[J]. 甘肃科技, 2016, 32(21): 117-123, 112. DOI: 10.3969/j.issn.1000-0952.2016.21.048.
    [23]
    SHEN H, SHENG L, CHEN Z, et al. Mouse hepatocyte overexpression of NF-κB-inducing kinase (NIK) triggers fatal macrophage-dependent liver injury and fibrosis[J]. Hepatology, 2014, 60(6): 2065-2076. DOI: 10.1002/hep.27348.
    [24]
    ZHU H, PING J, XU LM. Role of the nuclear factor - kappa B signaling pathway on the progress of hepatic fibrosis and the anti-fibroticmechanism of traditional Chinese medicine[J]. J Clin Hepatol, 2018, 34(4): 858-861. DOI: 10.3969/j.issn.1001-5256.2018.04.035.

    朱慧, 平键, 徐列明. NF-κB通路在肝纤维化进展和中药抗肝纤维化机制中的作用[J]. 临床肝胆病杂志, 2018, 34(4): 858-861. DOI: 10.3969/j.issn.1001-5256.2018.04.035.
    [25]
    ABBAS N, GETACHEW A, YOU K, et al. Kupffer cells mediate the recruitment of hepatic stellate cells into the localized liver damage[J]. Biochem Biophys Res Commun, 2020, 529(2): 474-479. DOI: 10.1016/j.bbrc.2020.06.041.
    [26]
    MA L, ZHAO Y, WU HY, et al. Expression of TLR4 /MyD88/NF-κB signaling pathway in cirrhosis caused by hepatitis B virus and its clinical significance[J]. Chin J Mod Med, 2021, 31(2): 72-77. DOI: 10.3969/j.issn.1005-8982.2021.21.012.

    马良, 赵阳, 伍华英, 等. TLR4、MyD88、NF-κB在乙型肝炎病毒肝硬化患者中的表达及其临床意义[J]. 中国现代医学杂志, 2021, 31(21): 72-77. DOI: 10.3969/j.issn.1005-8982.2021.21.012.
    [27]
    CUI DL. The roles of NF-κB in liver fibrosis[D]. Shijiazhuang: Hebei Medical University, 2010.

    崔东来. 抑制NF-κB诱导肝星状细胞凋亡[D]. 石家庄: 河北医科大学, 2010.
    [28]
    CHEN JY, HAO FY, LIN JQ, et al. The effect of carvedilol on the TLR4-MyD88-NF-κB signaling pathway in an animal model of liver fibrosis and its anti-liver fibrosis mechanism[J]. J Xinjiang Med Univ, 2021, 44(7): 771-776. DOI: 10.3639/j.issn.1009-5551.2021.07.002.

    陈建勇, 郝芳艳, 林近秋, 等. 卡维地洛对肝纤维化动物模型TLR4-MyD88-NF-κB信号通路的影响及其抗肝纤维化的作用机制[J]. 新疆医科大学学报, 2021, 44(7): 771-776. DOI: 10.3639/j.issn.1009-5551.2021.07.002.
    [29]
    ZHU J, FAN JR, PAN L, et al. Correlation of nuclear factor B expression with α-SMA and collagen Ⅲ expression in hepatic fibrosis in rats[J]. World Chin J Dig, 2012, 20(22): 2081-2085. https://www.cnki.com.cn/Article/CJFDTOTAL-XXHB201222019.htm

    朱净, 范建荣, 潘亮, 等. NF-κB在鼠肝纤维化组织中的表达及其与α-SMA、Ⅲ型胶原的相关性[J]. 世界华人消化杂志, 2012, 20(22): 2081-2085. https://www.cnki.com.cn/Article/CJFDTOTAL-XXHB201222019.htm
    [30]
    REEVES HL, FRIEDMAN SL. Activation of hepatic stellate cells—a key issue in liver fibrosis[J]. Front Biosci, 2002, 7: d808-d826. DOI: 10.2741/reeves.
    [31]
    FENG XY, HE PL, ZHAO W, et al. Effects of Panax notoginseng total saponins on improving nonalcoholic fatty liver disease rats and NO/iNOS/NF-κB signaling pathway[J]. Chin Tradit Patent Med, 2021, 43(1): 50-55. DOI: 10.3969/j.issn.1001-1528.2021.01.010.

    冯晓异, 何朋伦, 赵微, 等. 三七总皂苷对非酒精性脂肪肝大鼠的改善作用及对NO/iNOS/NF-κB通路的影响[J]. 中成药, 2021, 43(1): 50-55. DOI: 10.3969/j.issn.1001-1528.2021.01.010.
    [32]
    TANG H, ZENG Q, REN N, et al. Kaempferide improves oxidative stress and inflammation by inhibiting the TLR4/IκBα/NF-κB pathway in obese mice[J]. Iran J Basic Med Sci, 2021, 24(4): 493-498. DOI: 10.22038/ijbms.2021.52690.11892.
    [33]
    LIU F, FENG M, XING J, et al. Timosaponin alleviates oxidative stress in rats with high fat diet-induced obesity via activating Nrf2/HO-1 and inhibiting the NF-κB pathway[J]. Eur J Pharmacol, 2021, 909: 174377. DOI: 10.1016/j.ejphar.2021.174377.
    [34]
    LI J, WANG T, LIU P, et al. Hesperetin ameliorates hepatic oxidative stress and inflammation via the PI3K/AKT-Nrf2-ARE pathway in oleic acid-induced HepG2 cells and a rat model of high-fat diet-induced NAFLD[J]. Food Funct, 2021, 12(9): 3898-3918. DOI: 10.1039/d0fo02736g.
    [35]
    CHEN X, DING C, LIU W, et al. Abscisic acid ameliorates oxidative stress, inflammation, and apoptosis in thioacetamide-induced hepatic fibrosis by regulating the NF-кB signaling pathway in mice[J]. Eur J Pharmacol, 2021, 891: 173652. DOI: 10.1016/j.ejphar.2020.173652.
    [36]
    RODRÍGUEZ MJ, SABAJ M, TOLOSA G, et al. Maresin-1 prevents liver fibrosis by targeting Nrf2 and NF-κB, reducing oxidative stress and inflammation[J]. Cells, 2021, 10(12): 3406. DOI: 10.3390/cells10123406.
    [37]
    ZAGHLOUL RA, ZAGHLOUL AM, EL-KASHEF DH. Hepatoprotective effect of Baicalin against thioacetamide-induced cirrhosis in rats: Targeting NOX4/NF-κ B/NLRP3 inflammasome signaling pathways[J]. Life Sci, 2022, 295: 120410. DOI: 10.1016/j.lfs.2022.120410.
    [38]
    CHEN Y, ZHAO C, LIU X, et al. Plumbagin ameliorates liver fibrosis via a ROS-mediated NF-кB signaling pathway in vitro and in vivo[J]. Biomed Pharmacother, 2019, 116: 108923. DOI: 10.1016/j.biopha.2019.108923.
    [39]
    de SOUZA BASSO B, HAUTE GV, ORTEGA-RIBERA M, et al. Methoxyeugenol deactivates hepatic stellate cells and attenuates liver fibrosis and inflammation through a PPAR-γ and NF-kB mechanism[J]. J Ethnopharmacol, 2021, 280: 114433. DOI: 10.1016/j.jep.2021.114433.
    [40]
    LIU Y, KUANG Q, DAI X, et al. Deficiency in Inactive Rhomboid Protein2 (iRhom2) alleviates alcoholic liver fibrosis by suppressing inflammation and oxidative stress[J]. Int J Mol Sci, 2022, 23(14): 7701. DOI: 10.3390/ijms23147701.
    [41]
    YE L, CHEN T, CAO J, et al. Short hairpin RNA attenuates liver fibrosis by regulating the PPAR-γ and NF-κB pathways in HBV induced liver fibrosis in mice[J]. Int J Oncol, 2020, 57(5): 1116-1128. DOI: 10.3892/ijo.2020.5125.
    [42]
    SUN X, HUANG X, ZHU X, et al. HBOA ameliorates CCl4-incuded liver fibrosis through inhibiting TGF-β1/Smads, NF-κB and ERK signaling pathways[J]. Biomed Pharmacother, 2019, 115: 108901. DOI: 10.1016/j.biopha.2019.108901.
  • 加载中

Catalog

    通讯作者: 陈斌, bchen63@163.com
    • 1. 

      沈阳化工大学材料科学与工程学院 沈阳 110142

    1. 本站搜索
    2. 百度学术搜索
    3. 万方数据库搜索
    4. CNKI搜索

    Figures(1)  / Tables(1)

    Article Metrics

    Article views (640) PDF downloads(39) Cited by()
    Proportional views
    Related

    /

    DownLoad:  Full-Size Img  PowerPoint
    Return
    Return