WANG Hong-song,SHAN Xiao-xiao,ZHAO Guo-dong,et al.Effect and Mechanism of Banxia Baizhu Tianmatang on Atherosclerosis in ApoE-/- Mice[J].Chinese Journal of Experimental Traditional Medical Formulae,2021,27(07):9-15.
WANG Hong-song,SHAN Xiao-xiao,ZHAO Guo-dong,et al.Effect and Mechanism of Banxia Baizhu Tianmatang on Atherosclerosis in ApoE-/- Mice[J].Chinese Journal of Experimental Traditional Medical Formulae,2021,27(07):9-15. DOI: 10.13422/j.cnki.syfjx.20210301.
Effect and Mechanism of Banxia Baizhu Tianmatang on Atherosclerosis in ApoE-/- Mice
To study the effects of Banxia Baizhu Tianmatang (BBTT) on atherosclerosis in apolipoprotein-E knockout (ApoE
-/-
) mice induced by high fat diet.
Method
2
The atherosclerosis model of ApoE
-/-
mice was established with high-fat diet, and BBTT was used for intervention. The pathological changes of aorta after atherosclerosis were observed by hematoxylin-eosin (HE), oil red O and Masson staining. The changes of serum total cholesterol (TC), triglyceride (TG), high density lipoprotein cholesterol (HDL-C) and low density lipoprotein cholesterol (LDL-C) were detected by automatic biochemical analyzer. The expression levels of tumor necrosis factor-
α
(TNF-
α
), interleukin-6 (IL-6) and oxidized low density lipoprotein (ox-LDL) were detected by enzyme linked immunosorbent assay (ELISA). Total tissue proteins were extracted, quantified by protein quantification (BCA) method, and the expression of matrix metalloproteinase-9 (MMP-9) protein was detected by Western blot. Thiobarbituric acid (TBA) method was used to detect the change of malondialdehyde (MDA) content. The change of superoxide dismutase (SOD) activity was detected by 2-(2-methoxy-4-nitrophenyl)-3-(4-nitrophenyl)-5-(2,4-disulfobenzene)-2H tetrazole monosodium salt (WST-8) method.
Result
2
Compared with the control group, there was a large amount of lipid accumulation in the blood vessels of the model group, the serum levels of TG, TC, HDL-C and LDL-C significantly increased (
P
<
0.05), the expression of MMP-9 protein in the blood vessels significantly increased (
P
<
0.01), the expression levels of IL-6 and TNF-
α
in the serum increased (
P
<
0.05,
P
<
0.01), the SOD activity was significantly reduced (
P
<
0.01), and the levels of MDA and ox-LDL expression increased (
P
<
0.01). Compared with the model group, the treatment with BBTT could inhibit the accumulation of lipids in blood vessels, the TG levels were reduced in the high and medium dose groups of BBTT (
P
<
0.05), high, medium and low dose groups significantly reduced the levels of LDL-C in serum (
P
<
0.01), the expression of MMP-9 protein in blood vessels (
P
<
0.05) and IL-6 in serum (
P
<
0.01), the high-dose group down-regulated the expression of TNF-
α
in serum (
P
<
0.01) and ox-LDL (
P
<
0.01), both the high and medium-dose groups increased the level of MDA (
P
<
0.05,
P
<
0.01) and the activity of SOD (
P
<
0.05).
Conclusion
2
BBTT has a certain intervention effect on the formation of atherosclerosis aortic plaque in ApoE
-/-
mice, and its mechanism may be associated with reducing the TG and LDL-C levels, lowering blood lipid, down-regulating MMP-9 protein, protecting blood vessels from inflammatory damage, reducing ox-LDL and MDA levels, and improving SOD activity to play an antioxidant role.
SCHUETT H , OESTREICH R , WAETZIG G H , et al . Transsignaling of interleukin-6 crucially contributes to atherosclerosis in mice [J]. Arterioscler Thromb Vasc Biol , 2012 , 32 ( 2 ): 281 - 290 .
Exploration of Zhuyuwan in Treatment of Atherosclerosis from Perspective of Lipid Transport Disorder
Mechanism of Huangqi Chifengtang in Treating Atherosclerosis Based on 16S rRNA Sequencing and Metabolomics
Effect of Co-treatment Method of Stagnation of Phlegm and Blood Stasis (Danlou Tablet) on Vascular Endothelial Function in Patients with Atherosclerosis
Molecular Mechanism of Treating Different Diseases with Same Treatment of Gypenoside L Affecting Oxidative Damage HUVEC and OVCAR-3 Through EGFR/STAT3/Glycolytic Pathway
Analysis of Mechanism of Astragaloside Ⅳ in Regulating Ferroptosis Through SLC7A11/GPX4 Pathway Against Vascular Smooth Muscle Cell Proliferation
Related Author
SONG Wei
ZHANG Zhongyi
QIU Hairong
ZHAO Mei
ZHOU Zubing
SHEN Tao
ZHANG Yong
LIANG Yuqin
Related Institution
Chengdu University of Traditional Chinese Medicine(TCM)
Hospital of Chengdu University of TCM
Hubei Minzu University
Institute of TCM, Sichuan Academy of Chinese Medicine Sciences
Institute of Traditional Chinese Medicine, Heilongjiang University of Chinese Medicine