2021
DOI: 10.1016/j.ejphar.2021.174497
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Resveratrol modulates Toxoplasma gondii infection induced liver injury by intervening in the HMGB1/TLR4/NF-κB signaling pathway

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Cited by 23 publications
(8 citation statements)
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“…Another probable function of resveratrol is blocking the HMGB1 by stimulating Nrf2, which could prohibit the production of ROS as well (Dong et al, 2015). Therefore, due to the contribution of HMGB1 in the dysfunction of mitochondria, resulting in the overproduction of ROS, resveratrol mitigates inflammation and stress oxidative by attenuating the expression of the HMGB1 during sepsis (Lu et al, 2021; Yang et al, 2014).…”
Section: Discussionmentioning
confidence: 99%
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“…Another probable function of resveratrol is blocking the HMGB1 by stimulating Nrf2, which could prohibit the production of ROS as well (Dong et al, 2015). Therefore, due to the contribution of HMGB1 in the dysfunction of mitochondria, resulting in the overproduction of ROS, resveratrol mitigates inflammation and stress oxidative by attenuating the expression of the HMGB1 during sepsis (Lu et al, 2021; Yang et al, 2014).…”
Section: Discussionmentioning
confidence: 99%
“…In addition, sepsis could cause edema in the liver via damaging sodium pump function, which leads to sodium hold and hepatocyte apoptosis (Lelubre & Vincent, 2018). Resveratrol could ameliorate liver damage by inhibiting the translocation of HMGB1 from the nucleus to the cytoplasm of hepatocytes in septic patients, which, at least particularly, is mediated by SIRT1 (Lu et al, 2021; Yu et al, 2019). Furthermore, resveratrol exerts a protective effect against liver injury via suppressing the production of inflammatory cytokines namely TNF‐a and IL‐1B, which are accompanied by enhanced Cytokine‐induced neutrophil chemoattractant 1(CINC‐1), aryl hydrocarbon receptor expression, and aryl hydrocarbon receptor (AhR) nuclear translocator (Arnt) in the hepatocytes (Larrosa et al, 2011; Yu et al, 2019).…”
Section: Discussionmentioning
confidence: 99%
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“…The hepatoprotective activity of resveratrol on fibrosis can be explained by its ability to produce more IL-10 to promote the polarization of M(LPS) to M(IL-4)-like macrophages (Yu et al, 2019). Resveratrol can also protect the liver by interfering with the TLR4/NF-κB signaling pathway, inhibiting the production of tumor necrosis factor-α, inducible nitric oxide synthase, and HMGB1 (Lu et al, 2021;Stewart & Bewley, 1980). However, because the content of resveratrol in wine was low, the protection of wine on the liver in our study might not come from a monomeric substance.…”
Section: Discussionmentioning
confidence: 99%
“…To begin with, ellagic acid has been found to reduce liver injury by upregulating the expression of Nrf-2 and downregulating the Bcl-2 and NF-κB signaling pathways in a rat model of CCl4-induced liver injury (Aslan et al, 2018) Toxoplasma gondii infection-induced liver injury HMGB1/TLR4/NF-κB(-) (Lu et al, 2021) CCl4-induced liver fibrosis NF-κB /AKT(-) (Zhang et al, 2016) CCl4-induced liver fibrosis PTEN/PI3K/AKT(+) (Zhu et al, 2020) Human HSC line (LX-2)cells and CCL4-induced liver fibrosis Hippo(+) (C. Li, Zhang, et al, 2021) Methionine/choline-deficient diet-induced NASH SIGIRR(+)/TLR(-)/NF-κB(-) (Che et al, 2020) HFD-induced NAFLD FAS/SREBP-1(-) (Hosseini et al, 2020) HepG2 and Hep3B PTEN/AKT(+) (Dai et al, 2020) H22-induced liver cancer CD8+CD122+Tregs(-) (Q. Zhang, Huang, et al, 2020) HepG2 and Huh7 PKA/AMPK/eEF2K(-) (Gao et al, 2021) Alcohol-aflatoxin B1-induced HCC NF-κB(-) (Rawat et al, 2020(Rawat et al, , 2021 Curcumin HSC MyD88(-) (He et al, 2017) CCL4-induce liver injury Nrf2/HO-1(+)/TGF-β1/Smad3(-) (Peng et al, 2018) Aflatoxin B(AFB1)-induced liver injury TLR4/RIPK(-) (S. Arsenic-induced hepaticinjury MAPK/NF-κB(-)/ Nrf2(+) (Xu et al, 2021) Overfeeding-induced NAFLD SIRT3(+) (Du et al, HepG2 and Huh-7 ET1/Wnt/β-catenin (J.…”
Section: Ellagic Acidmentioning
confidence: 99%