Morin hydrate suppresses lipoteichoic acid-induced oxidative stress-mediated inflammatory events in macrophages via augmenting Nrf2/HO-1 and antioxidant defense molecules

被引:3
|
作者
Hsieh, Cheng-Ying [1 ]
Jayakumar, Thanasekaran [2 ]
Lin, Kao-Chang [3 ,4 ]
Yen, Ting-Lin [5 ]
Hsia, Chih-Wei [3 ]
Huang, Wei-Chieh [3 ]
Sheu, Joen-Rong [3 ]
Hsia, Chih-Hsuan [3 ,6 ]
机构
[1] Taipei Med Univ, Coll Med, Sch Med, Dept Pharmacol, Taipei, Taiwan
[2] Pondicherry Univ, Dept Ecol & Environm Sci, Pondicherry, India
[3] Taipei Med Univ, Grad Inst Med Sci, Coll Med, 250 Wu Hsing St, Taipei 110, Taiwan
[4] Chi Mei Med Ctr, Dept Neurol, Tainan, Taiwan
[5] Cathay Gen Hosp, Dept Med Res, Taipei, Taiwan
[6] Shin Kong Wu Ho Su Mem Hosp, Translat Med Ctr, 95 Wen Chang Rd, Taipei 111, Taiwan
关键词
morin hydrate; oxidative stress; antioxidants; antioxidant properties; macrophages; Nrf2/HO-1; HEME; MECHANISMS; INTERPLAY; MONOXIDE; CALCIUM; NRF2;
D O I
10.1177/1721727X231199414
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
ObjectivesOxidative stress induces chronic inflammatory diseases in aerobic organisms, and antioxidants from plants represent an efficient strategy to prevent this condition. Morin hydrate (MH), a bioactive flavonoid, has a wide range of pharmacological properties, including anti-inflammatory and anti-oxidant. This study evaluated the protective effects of MH on lipoteichoic acid (LTA)-induced inflammation in RAW 264.7 macrophages by testing the main oxidative and inflammatory biomarkers and also investigating the molecular pathways involved.MethodsThe antioxidant and anti-inflammatory effects of MH were evaluated in a cell-free system and RAW264.7 cells. Quantitative real-time PCR (RT-qPCR) and assay kits were used to measure the expression of nuclear factor erythroid 2-related factor 2 (Nrf2) and heme oxygenase 1 (HO-1) mRNA, as well as the activity of antioxidant enzymes. The effects of MH on LTA-induced inducible nitric oxide synthase (iNOS), IL-1 & beta;, and TNF-& alpha; mRNA and protein expression were also evaluated by RT-qPCR and Western blotting.ResultsMH reduced DPPH and ABTS radicals in a cell-free system and LTA-induced ROS and NO production in RAW264.7 cells. MH upregulated Nrf2 and HO-1 mRNA expression and reversed LTA-mediated reduction of antioxidant enzymes, at a high concentration of 20 & mu;M pretreated cells. MH also effectively attenuated LTA-induced iNOS, IL-1 & beta;, and TNF-& alpha; mRNA and protein expression, and these effects were reversed by ML385.ConclusionsThe study found that the Nrf2/HO-1 played role in the inhibition of LTA-induced oxidative stress in macrophages by MH. This study may consider to be a promising induced macrophage-targeted strategy via regulating anti-oxidative defense to control inflammatory-related disease.
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页数:14
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