Mechanism of extract of Ginseng Radix et Rhizoma, Notoginseng Radix et Rhizoma and Chuanxiong Rhizoma on SIRT1 autophagy pathway of endothelial cell senescence induced by hydrogen peroxide.
10.19540/j.cnki.cjcmm.20210922.703
- Author:
Cheng-Kui XIU
1
;
Ying-Kun FU
2
;
Qiang WANG
3
;
Xue WANG
1
;
Yan-Hong HU
1
;
Ye WU
1
;
Jing YANG
1
;
Yan LEI
1
Author Information
1. Beijing Key Laboratory of Research of Chinese Medicine on Preventional and Treatment for Major Diseases,Experimental Research Center, China Academy of Chinese Medical Sciences Beijing 100700, China.
2. Guang'anmen Hospital, China Academy of Chinese Medical Sciences Beijing 100056, China.
3. Wangjing Hospital, China Academy of Chinese Medical Sciences Beijing 100102, China.
- Publication Type:Journal Article
- Keywords:
extract of Ginseng Radix et Rhizoma,Notoginseng Radix et Rhizoma,and Chuanxiong Rhizoma;
senescence;
senescence of endothelial cells;
vascular senescence
- MeSH:
Autophagy;
Cells, Cultured;
Cellular Senescence;
Drugs, Chinese Herbal/pharmacology*;
Endothelial Cells/drug effects*;
Hydrogen Peroxide;
Panax/chemistry*;
Sirtuin 1/genetics*
- From:
China Journal of Chinese Materia Medica
2021;46(23):6216-6223
- CountryChina
- Language:Chinese
-
Abstract:
This study aims to explore the effect of extract of Ginseng Radix et Rhizoma, Notoginseng Radix et Rhizoma, and Chuanxiong Rhizoma(hereinafter referred to as GNS) on the SIRT1-autophagy pathway of endothelial cell senescence induced by hydrogen peroxide(H_2O_2). To be specific, vascular endothelial cells were classified into the blank control group(control), model group(model), model + DMSO group(DMSO), resveratrol group(RESV), and GNS low-dose(GNS-L), medium-dose(GNS-M), and high-dose(GNS-H) groups. They were treated with H_2O_2 for senescence induction except the control. After intervention of cells in each group with corresponding drugs for 24 h, cell growth status was observed under an inverted microscope, and the formation of autophagosome under the transmission electron microscope. In addition, the changes of microtubule-associated protein 1 light chain 3β(LC3 B) were detected by immunofluorescence staining. The autophagy flux was tracked with the autophagy double-labeled adenovirus(mRFP-GFP-LC3) fusion protein. Dansylcadaverine(MDC) staining was employed to determine the autophagic vesicles, and Western blot the expression of sirtuin 1(SIRT1), ubiquitin-binding protein p62, and LC3Ⅱ. After H_2O_2 induction, cells demonstrated slow growth, decreased adhesion ability, raised number of SA-β-gal-stained blue ones, a certain number of autophagosomes with bilayer membrane and secondary lysosomes in the cytoplasm, and slight rise of autophagy flux level. Compared with the model group, GNS groups showed improved morphology, moderate adhesion ability, complete and smooth membrane, decreased SA-β-gal-stained blue cells, many autophagosomes, autophagic vesicles, and secondary lysosomes in the cytoplasm, increased autophagolysosomes, autophagy flux level, and fluorescence intensity of LC3 B and MDC, up-regulated expression of SIRT1 and LC3Ⅱ, and down-regulated expression of p62, suggesting the improvement of autophagy level. GNS can delay the senescence of vascular endothelial cells. After the intervention, the autophagy flux and related proteins SIRT1, LC3Ⅱand p62 changed significantly, and the autophagy level increased significantly. However, EX527 weakened the effect of Chinese medicine in delaying vascular senescence. GNS may delay the senescence of vascular endothelial cells through the SIRT1 autophagy pathway.
