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Trichosanthis Pericarpium Aqueous Extract Protects H9c2 Cardiomyocytes from Hypoxia/Reoxygenation Injury by Regulating PI3K/Akt/NO Pathway
被引:29
|作者:
Chu, Donghai
[1
,2
]
Zhang, Zhenqiu
[1
]
机构:
[1] Liaoning Univ Tradit Chinese Med, 77 Shengming 1st Rd, Dalian 11600, Liaoning, Peoples R China
[2] Liaoning Inst Sci & Technol, 76 Xianghuai Rd, Benxi 117004, Liaoning, Peoples R China
来源:
关键词:
trichosanthis pericarpium;
hypoxia/reoxygenation;
apoptosis;
PI3K/AKT/NO;
NITRIC-OXIDE;
MYOCARDIAL-ISCHEMIA;
IN-VIVO;
ISCHEMIA/REPERFUSION INJURY;
DIABETIC CARDIOMYOPATHY;
INFLAMMATORY RESPONSE;
REPERFUSION INJURY;
INDUCED APOPTOSIS;
PEROXYNITRITE;
CELLS;
D O I:
10.3390/molecules23102409
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
Trichosanthis Pericarpium (TP) is a traditional Chinese medicine for treating cardiovascular diseases. In this study, we investigated the effects of TP aqueous extract (TPAE) on hypoxia/reoxygenation (H/R) induced injury in H9c2 cardiomyocytes and explored the underlying mechanisms. H9c2 cells were cultured under the hypoxia condition induced by sodium hydrosulfite for 30 min and reoxygenated for 4 h. Cell viability was measured by MTT assay. The amounts of LDH, NO, eNOS, and iNOS were tested by ELISA kits. Apoptotic rate was detected by Annexin V-FITC/PI staining. QRT-PCR was performed to analyze the relative mRNA expression of Akt, Bcl-2, Bax, eNOS, and iNOS. Western blotting was used to detect the expression of key members in the PI3K/Akt pathway. Results showed that the pretreatment of TPAE remarkably enhanced cell viability and decreased apoptosis induced by H/R. Moreover, TPAE decreased the release of LDH and expression of iNOS. In addition, TPAE increased NO production and Bcl-2/Bax ratio. Furthermore, the mRNA and protein expression of p-Akt and eNOS were activated by TPAE pretreatment. On the contrary, a specific inhibitor of PI3K, LY294002 not only inhibited TPAE-induced p-Akt/eNOS upregulation but alleviated its anti-apoptotic effects. In conclusion, results indicated that TPAE protected against H/R injury in cardiomyocytes, which consequently activated the PI3K/Akt/NO signaling pathway.
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页数:16
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