Therapeutic Potential of Nutraceuticals against Drug-Induced Liver Injury

被引:0
作者
Sethi, Namya [1 ]
Khokhar, Manoj [1 ]
Mathur, Mitali [1 ]
Batra, Yashi [1 ]
Mohandas, Amal [1 ]
Tomo, Sojit [1 ]
Rao, Mahadev [2 ]
Banerjee, Mithu [1 ]
机构
[1] All India Inst Med Sci, Dept Biochem, Basni Phase 2, Jodhpur 342005, Rajasthan, India
[2] Manipal Acad Higher Educ, Manipal Coll Pharmaceut Sci, Dept Pharm Practice, Manipal, Karnataka, India
关键词
drug-induced liver injury; polyphenols; terpenes; Nrf-2; oxidative stress; TRANSCATHETER ARTERIAL CHEMOEMBOLIZATION; UNFOLDED PROTEIN RESPONSE; INDUCED OXIDATIVE STRESS; DOUBLE-BLIND; ELLAGIC ACID; GALLIC ACID; CELL-DEATH; INDUCED HEPATOTOXICITY; LIPID-PEROXIDATION; REPERFUSION INJURY;
D O I
10.1055/s-0044-1791559
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Drug-induced liver injury (DILI) continues to be a major concern in clinical practice, thus necessitating a need for novel therapeutic approaches to alleviate its impact on hepatic function. This review investigates the therapeutic potential of nutraceuticals against DILI, focusing on examining the underlying molecular mechanisms and cellular pathways. In preclinical and clinical studies, nutraceuticals, such as silymarin, curcumin, and N-acetylcysteine, have demonstrated remarkable efficacy in attenuating liver injury induced by diverse pharmaceutical agents. The molecular mechanisms underlying these hepatoprotective effects involve modulation of oxidative stress, inflammation, and apoptotic pathways. Furthermore, this review examines cellular routes affected by these nutritional components focusing on their influence on hepatocytes, Kupffer cells, and stellate cells. Key evidence highlights that autophagy modulation as well as unfolded protein response are essential cellular processes through which nutraceuticals exert their cytoprotective functions. In conclusion, nutraceuticals are emerging as promising therapeutic agents for mitigating DILI, by targeting different molecular pathways along with cell processes involved in it concurrently.
引用
收藏
页码:430 / 456
页数:27
相关论文
共 293 条
  • [81] A study of the effect of Nigella sativa (Black seeds) in isoniazid (INH)-induced hepatotoxicity in rabbits
    Hassan, Anwar S.
    Ahmed, Jawad H.
    Al-Haroon, Sawsan S.
    [J]. INDIAN JOURNAL OF PHARMACOLOGY, 2012, 44 (06) : 678 - 682
  • [82] The Nrf2 regulatory network provides an interface between redox and intermediary metabolism
    Hayes, John D.
    Dinkova-Kostova, Albena T.
    [J]. TRENDS IN BIOCHEMICAL SCIENCES, 2014, 39 (04) : 199 - 218
  • [83] Antioxidants Maintain Cellular Redox Homeostasis by Elimination of Reactive Oxygen Species
    He, Long
    He, Ting
    Farrar, Shabnam
    Ji, Linbao
    Liu, Tianyi
    Ma, Xi
    [J]. CELLULAR PHYSIOLOGY AND BIOCHEMISTRY, 2017, 44 (02) : 532 - 553
  • [84] Heidari R., 2015, ADV PHARM BULL
  • [85] Beneficial effects of naringenin in liver diseases: Molecular mechanisms
    Hernandez-Aquino, Erika
    Muriel, Pablo
    [J]. WORLD JOURNAL OF GASTROENTEROLOGY, 2018, 24 (16) : 1679 - 1707
  • [86] The Unfolded Protein Response and Cell Fate Control
    Hetz, Claudio
    Papa, Feroz R.
    [J]. MOLECULAR CELL, 2018, 69 (02) : 169 - 181
  • [87] Saskatoon and wild blueberries have higher anthocyanin contents than other Manitoba berries
    Hosseinian, Farah S.
    Beta, Trust
    [J]. JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2007, 55 (26) : 10832 - 10838
  • [88] Flavones: Food Sources, Bioavailability, Metabolism, and Bioactivity
    Hostetler, Gregory L.
    Ralston, Robin A.
    Schwartz, Steven J.
    [J]. ADVANCES IN NUTRITION, 2017, 8 (03) : 423 - 435
  • [89] Rifampicin-Induced Hepatic Lipid Accumulation: Association with Up-Regulation of Peroxisome Proliferator-Activated Receptor γ in Mouse Liver
    Huang, Jia-Hui
    Zhang, Cheng
    Zhang, Da-Gang
    Li, Lu
    Chen, Xi
    Xu, De-Xiang
    [J]. PLOS ONE, 2016, 11 (11):
  • [90] Protective Effect of Flavonoids from Ziziphus jujuba cv. Jinsixiaozao against Acetaminophen-Induced Liver Injury by Inhibiting Oxidative Stress and Inflammation in Mice
    Huang, Weizhen
    Wang, Yongjie
    Jiang, Xiaoyan
    Sun, Yueyue
    Zhao, Zhongxi
    Li, Siying
    [J]. MOLECULES, 2017, 22 (10)