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Dexmedetomidine combined with propofol attenuates myocardial ischemia/reperfusion injury by activating the AMPK signaling pathway
被引:4
作者:

Yang, Ke
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机构:
Fuwai Yunnan Cardiovasc Hosp, Dept Anesthesiol, 528 Shahu North Rd, Kunming 650000, Yunnan, Peoples R China Fuwai Yunnan Cardiovasc Hosp, Dept Anesthesiol, 528 Shahu North Rd, Kunming 650000, Yunnan, Peoples R China

Ma, Yinhong
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h-index: 0
机构:
Fuwai Yunnan Cardiovasc Hosp, Dept Anesthesiol, 528 Shahu North Rd, Kunming 650000, Yunnan, Peoples R China Fuwai Yunnan Cardiovasc Hosp, Dept Anesthesiol, 528 Shahu North Rd, Kunming 650000, Yunnan, Peoples R China

Xie, Chunmei
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h-index: 0
机构:
Fuwai Yunnan Cardiovasc Hosp, Dept Anesthesiol, 528 Shahu North Rd, Kunming 650000, Yunnan, Peoples R China Fuwai Yunnan Cardiovasc Hosp, Dept Anesthesiol, 528 Shahu North Rd, Kunming 650000, Yunnan, Peoples R China

Zhao, Haoxing
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机构:
Fuwai Yunnan Cardiovasc Hosp, Dept Anesthesiol, 528 Shahu North Rd, Kunming 650000, Yunnan, Peoples R China Fuwai Yunnan Cardiovasc Hosp, Dept Anesthesiol, 528 Shahu North Rd, Kunming 650000, Yunnan, Peoples R China

Dai, Zheng
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Fuwai Yunnan Cardiovasc Hosp, Dept Anesthesiol, 528 Shahu North Rd, Kunming 650000, Yunnan, Peoples R China Fuwai Yunnan Cardiovasc Hosp, Dept Anesthesiol, 528 Shahu North Rd, Kunming 650000, Yunnan, Peoples R China

Wang, Xiaoqi
论文数: 0 引用数: 0
h-index: 0
机构:
Fuwai Yunnan Cardiovasc Hosp, Dept Anesthesiol, 528 Shahu North Rd, Kunming 650000, Yunnan, Peoples R China Fuwai Yunnan Cardiovasc Hosp, Dept Anesthesiol, 528 Shahu North Rd, Kunming 650000, Yunnan, Peoples R China
机构:
[1] Fuwai Yunnan Cardiovasc Hosp, Dept Anesthesiol, 528 Shahu North Rd, Kunming 650000, Yunnan, Peoples R China
来源:
关键词:
Myocardial ischemia/reperfusion injury;
Dexmedetomidine;
Propofol;
AMPK signaling pathway;
Apoptosis;
Autophagy;
ISCHEMIA-REPERFUSION INJURY;
PROTECTS;
D O I:
10.1016/j.heliyon.2023.e22054
中图分类号:
O [数理科学和化学];
P [天文学、地球科学];
Q [生物科学];
N [自然科学总论];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Objective: Myocardial ischemia/reperfusion (MI/R) injury is a major cause of cardiac tissue damage, with high disability and death rates. Although both dexmedetomidine (Dex) and propofol (PPF) have been indicated to alleviate MI/R injury in rat models, the effects of the combined use of these two drugs remain unclear. This study aimed to investigate the combined effects of Dex and PPF against MI/R injury and related mechanisms. Methods: A rat model of MI/R injury was established and used to explore the combined effects of Dex and PPF on MI/R injury. Hematoxylin-eosin (HE) and Masson staining were used for histopathological evaluation. 2,3,5-triphenyltetrazolium chloride (TTC), echocardiography, terminal deoxynucleotidyl transferase dUTP nick-end labeling (TUNEL) staining were used to determine myocardial infarction size, cardiac function, and apoptosis, respectively. Enzyme-linked immunosorbent assay (ELISA) was performed to assess myocardial function and oxidative stress (OS). Autophagy was observed through transmission electron microscopy. Moreover, western blotting was conducted to detect autophagy markers and the AMPK pathway. Results: The combination of Dex and PPF alleviated histopathological injury, reduced myocardial infarction, and rescued cardiac dysfunction in MI/R rats. Furthermore, Dex combined with PPF decreased the levels of MDA and ROS and increased the SOD level in MI/R rats. Besides, Dex combined with PPF inhibited myocardial apoptosis in MI/R rats. After combined treatment with Dex and PPF, the number of autophagosomes, expression levels of Beclin-1 and LC3II/LC3I were elevated, while the expression levels of p62 were reduced in MI/R rats. The combined use of Dex and PPF activated the AMPK pathway in MI/R rats. Compound C (an AMPK inhibitor) could abolish the combined effects of Dex and PPF on alleviating myocardial injury and enhancing autophagy in MI/R rats. Conclusion: The combination of Dex and PPF attenuated MI/R injury in rats, which may be associated with the activation of the AMPK signaling pathway.
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