Effect and mechanism of Poria cocos polysaccharides on myocardial cell apoptosis in rats with myocardial ischemia-reperfusion injury by regulating Rho-ROCK signaling pathway.
10.19540/j.cnki.cjcmm.20230816.401
- Author:
Jun XIE
1
;
Yuan-Yuan WANG
1
;
Ju-Xin LI
2
;
Feng-Min GAO
1
Author Information
1. Department of Cardiology, Hongqi Hospital Affiliated to Mudanjiang Medical College Mudanjiang 157011, China.
2. Mudanjiang Medical College Mudanjiang 157011, China.
- Publication Type:Journal Article
- Keywords:
Poria cocos polysaccharides;
Ras homologous gene-Rho-associated coiled-coil forming kinase(Rho-ROCK) signaling pathway;
apoptosis;
myocardial cells;
myocardial ischemia-reperfusion
- MeSH:
Rats;
Male;
Animals;
Myocardial Reperfusion Injury/drug therapy*;
bcl-2-Associated X Protein/metabolism*;
Rats, Sprague-Dawley;
Caspase 3/metabolism*;
Interleukin-18;
Wolfiporia;
Signal Transduction;
Myocardial Infarction/drug therapy*;
Proto-Oncogene Proteins c-bcl-2/metabolism*;
Creatine Kinase, MB Form;
Apoptosis;
Polysaccharides/pharmacology*;
Superoxide Dismutase/metabolism*;
1-(5-Isoquinolinesulfonyl)-2-Methylpiperazine/analogs & derivatives*
- From:
China Journal of Chinese Materia Medica
2023;48(23):6434-6441
- CountryChina
- Language:Chinese
-
Abstract:
This study aimed to investigate the effect and underlying mechanism of Poria cocos polysaccharides(PCP) on myocardial cell apoptosis in the rat model of myocardial ischemia-reperfusion injury(MI/RI). Male SPF-grade SD rats were randomly divided into a sham group(saline), a model group(saline), low-and high-dose PCP groups(100 and 200 mg·kg~(-1)), and a fasudil group(10 mg·kg~(-1)), with 16 rats in each group. Except for the sham group, the other four groups underwent left anterior descending coronary artery ligation for 30 min followed by reperfusion for 2 h to establish the MI/RI model. The myocardial infarct area was assessed by TTC staining. Histological changes were observed through HE staining. Myocardial cell apoptosis was evaluated using TUNEL staining. Serum lactate dehydrogenase(LDH), creatine kinase MB(CK-MB), interleukin-1β(IL-1β) and IL-18 levels, myocardial superoxide dismutase(SOD) activity and malondialdehyde(MDA) levels were detected by ELISA. Protein expression of B-cell lymphoma 2(Bcl-2), Bcl-2 associated X protein(Bax), cleaved caspase-3, Ras homolog gene A(RhoA), myosin phosphatase target subunit 1(MYPT-1), phosphorylated MYPT-1(p-MYPT-1), and Rho-associated coiled-coil forming kinase 1(ROCK 1) were measured by Western blot. Pathological staining of myocardial tissue revealed that in the model group, there was focal necrosis of myocardial tissue, myocardial cell swelling, unclear boundaries, and neutrophil infiltration. These pathological changes were alleviated in the low-and high-dose PCP groups and the fasudil group. Compared with the model group, the low-and high-dose PCP groups and the fasudil group showed significantly reduced myocardial infarct area and myocardial cell apoptosis rate. Compared with the sham group, the model group exhibited elevated serum LDH, CK-MB, IL-1β and IL-18 levels, increased MDA levels, relative protein expression of Bax, cleaved caspase-3, RhoA, ROCK1 and p-MYPT-1, and decreased myocardial SOD levels and Bcl-2 protein expression. Compared with the model group, the PCP groups and the fasudil group showed lowered serum LDH, CK-MB, IL-1β and IL-18 levels, decreased MDA levels, relative protein expression of Bax, cleaved caspase-3, RhoA, ROCK1 and p-MYPT-1, and increased myocardial SOD levels and Bcl-2 protein expression. PCP exhibited a certain preventive effect on myocardial tissue pathological damage and myocardial cell apoptosis in MI/RI rats, possibly related to the inhibition of the Rho-ROCK signaling pathway activation, thereby reducing oxidative stress and inflammatory responses.
