Effect of methyl eugenol on hypoxia/reoxygenation injury of human renal tubular epithelial cells and its mechanism.
10.19540/j.cnki.cjcmm.20210918.402
- Author:
Bai-Cheng KUANG
1
;
Shuai-Heng HOU
1
;
G Ji ZHAN
1
;
Meng-Qin WANG
1
;
Jia-Si ZHANG
1
;
Kai-Lun SUN
1
;
Zhi-Heng WANG
1
;
Qing-Wen LI
1
;
Nian-Qiao GONG
1
Author Information
1. Key Laboratory of Organ Transplantation, Chinese Academy of Medical Sciences, Key Laboratory of Organ Transplantation, National Health Commission of the People's Republic of China,Key Laboratory of Organ Transplantation, Ministry of Education, Institute of Organ Transplantation, Tongji Hospital, Tongji Medical College, Huazhong University of Science and Technology Wuhan 430030,China.
- Publication Type:Journal Article
- Keywords:
HK-2 cell;
Nox4;
Nrf2;
hypoxia/reoxygenation;
methyl eugenol
- MeSH:
Apoptosis;
Epithelial Cells/metabolism*;
Eugenol/pharmacology*;
Heme Oxygenase-1/metabolism*;
Humans;
Hypoxia;
NF-E2-Related Factor 2/metabolism*;
Oxidative Stress;
Reactive Oxygen Species;
Reperfusion Injury/drug therapy*
- From:
China Journal of Chinese Materia Medica
2021;46(24):6502-6510
- CountryChina
- Language:Chinese
-
Abstract:
This study aimed to investigate the effect of methyl eugenol(ME) on hypoxia/reoxygenation(H/R)-induced injury of human renal tubular epithelial HK-2 cells and its mechanism. The viability of HK-2 cells cultured with different concentrations of ME and exposed to H/R was detected by cell counting kit-8(CCK-8) assay. The effect of ME on the morphology of HK-2 cells was observed under an inverted microscope. The content of intracellular reactive oxygen species in different groups was detected after 2',7'-dichlorodihydrofluorescein diacetate(DCFH-DA) fluorescence staining. Cell apoptosis was determined by flow cytometry. Changes in mitochondrial membrane potential were monitored by JC-1 dye. The concentrations of nuclear factor erythroid 2 related factor 2(Nrf2), heme oxygenase-1(HO-1), and nicotinamide adenine dinucleotide phosphatase oxidase 4(Nox4) were measured by Western blot, followed by the assay of Nrf2 concentration changes in cytoplasm and nucleus by confocal fluorescence staining. The results showed that when the concentration of ME was 0-40 μmol·L~(-1), the activity of HK-2 cells was not affected. Compared with the model group, ME enhanced the activity of HK-2 cells and the cell morphology was normal. As revealed by further experiments, ME inhibited the release of reactive oxygen species and the decline in mitochondrial membrane potential of HK-2 cells after H/R injury, promoted Nrf2/HO-1 expression and Nrf2 translocation to the nucleus, and down-regulated the expression of Nox4, thereby significantly reducing apoptosis. This protective effect of ME could be reversed by the specific Nrf2 inhibitor ML385. These findings have preliminarily proved that ME effectively protected HK-2 cells against H/R injury, which might be related to its promotion of Nrf2/HO-1 signaling pathway and inhibition of Nox4. Such exploration on the possible mechanism of ME in the treatment of renal ischemia-reperfusion injury(IRI) and protection of organ function from the perspective of antioxidant stress has provided reference for related research on the treatment of acute kidney injury with traditional Chinese medicine.
