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西洋参和延胡索有效成分通过减轻氧化应激和内质网应激保护心肌。

Effective Components of Panax quinquefolius and Corydalis tuber Protect Myocardium through Attenuating Oxidative Stress and Endoplasmic Reticulum Stress.

机构信息

Cardiovascular Center, Xiyuan Hospital, China Academy of Chinese Medical Sciences, Beijing 100091, China.

出版信息

Evid Based Complement Alternat Med. 2013;2013:482318. doi: 10.1155/2013/482318. Epub 2013 Jun 24.

Abstract

Both oxidative stress and endoplasmic reticulum stress (ERS) have been implicated in carcinogenesis and neurological diseases, while there are few reports about the mechanisms of them in the progression of acute myocardial infarction (AMI). This study examined oxidative stress and ERS in a rat model of AMI and evaluated their role in therapy by metoprolol and effective components of Panax quinquefolius and Corydalis tuber (EPC). In the present study a rat model of AMI was established by ligation of the left anterior descending coronary artery. After oral administration of metoprolol or low-to-high doses of EPC for 2 weeks, serum malondialdehyde (MDA), superoxide dismutase (SOD), and 8-iso-prostaglandin F2 α (8-iso-PGF2 α ) were detected using enzyme-linked immunosorbent assay (ELISA). Quantitative real-time PCR and Western blotting were used to examine mRNA and protein expressions of the hallmarks of ERS-glucose-regulated protein-78 (GRP78) and CCAAT/enhancer-binding protein homologous protein (CHOP). We confirmed that both metoprolol and moderate-to-high dose of EPC decreased 8-iso-PGF2 α serum level and downregulated the mRNA and protein expressions of GRP78 and CHOP in myocardium, while EPC also increased SOD serum level. These results indicated that metoprolol and EPC protect the myocardium by attenuating oxidative stress and ERS induced by myocardial infarction, highlighting the ERS pathways as potential therapeutic targets for AMI.

摘要

氧化应激和内质网应激(ERS)都与癌症发生和神经疾病有关,而关于它们在急性心肌梗死(AMI)进展中的机制的报道很少。本研究在 AMI 大鼠模型中研究了氧化应激和 ERS,并通过美托洛尔以及西洋参和延胡索的有效成分(EPC)评估了它们在治疗中的作用。在本研究中,通过结扎左前降支冠状动脉建立 AMI 大鼠模型。口服美托洛尔或低至高剂量 EPC 2 周后,采用酶联免疫吸附试验(ELISA)检测血清丙二醛(MDA)、超氧化物歧化酶(SOD)和 8-异前列腺素 F2α(8-iso-PGF2α)。实时定量 PCR 和 Western blot 用于检测 ERS 标志物葡萄糖调节蛋白 78(GRP78)和 CCAAT/增强子结合蛋白同源蛋白(CHOP)的 mRNA 和蛋白表达。我们证实,美托洛尔和中至高剂量的 EPC 均可降低 8-iso-PGF2α血清水平,并下调心肌中 GRP78 和 CHOP 的 mRNA 和蛋白表达,而 EPC 还可增加 SOD 血清水平。这些结果表明,美托洛尔和 EPC 通过减轻心肌梗死后的氧化应激和 ERS 来保护心肌,强调 ERS 途径可能是 AMI 的潜在治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6e5a/3707262/9b85eaf9f0d6/ECAM2013-482318.001.jpg

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