Reducing myocardial infarction by combination of irisin and Dendrobium nobile Lindl through inhibiting nod-like receptor protein-3-related pyroptosis and activating PINK1/Parkin-mitophagy during aging.

IF 16.4 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
Chen Ding, Chaofeng Zhang
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引用次数: 0

Abstract

Aging, a crucial risk factor for ischemic heart disease, has negative impacts on cardioprotective mechanisms. As such, there is still an unmet requirement to explore potential therapies for improving the outcomes of myocardial ischemia/reperfusion (IR) injury in elderly subjects. Here, we aimed to confirm the cardioprotective function of irisin/Dendrobium nobile Lindl (DNL) combination therapy against myocardial IR injury in aged rats, with a focus on the involvement of pyroptosis and mitophagy. Male aged Wistar rats (22-24 months old, 400-450 g; n = 54) underwent myocardial IR or sham surgery. Before IR operation, rats were pretreated with irisin (0.5 mg/kg, intraperitoneally) and/or DNL (80 mg/kg, orally) for 1 or 4 weeks, respectively, at corresponding groups. Cardiac function, lactate dehydrogenase (LDH) and cardiac-specific isoform of troponin-I (cTn-I) levels, the expression of proteins involved in pyroptosis (nod-like receptor protein-3 (NLRP3), apoptosis-associated speck-like protein, c-caspase-1, and GSDMD-N) and mitophagy (PINK1 and Parkin), and pro-inflammatory cytokines levels were evaluated after 24 h of reperfusion. Irisin/DNL combined therapy significantly restored cardiac function and decreased LDH and cTn-I levels. It also downregulated pyroptosis-related proteins, upregulated PINK1 and Parkin, and decreased pro-inflammatory cytokines secretion. Pretreatment with Mdivi-1, as mitophagy inhibitor, abolished the cardioprotective action of dual therapy. This study revealed the cardioprotective effects of irisin/DNL combination therapy against IR-induced myocardial injury in aged rats, and also showed that the mechanism might be associated with suppression of NLRP3-related pyroptosis through enhancing the activity of the PINK1/Parkin mitophagy. This combination therapy is worthy of further detailed studies due to its potential to alleviate myocardial IR injury upon aging.

鸢尾素和石斛联合用药通过抑制衰老过程中与nod样受体蛋白-3相关的焦下垂和激活PINK1/Parkin线粒体自噬来减少心肌梗死。
衰老是缺血性心脏病的重要危险因素,对心脏保护机制有负面影响。因此,探索改善老年受试者心肌缺血/再灌注(IR)损伤结果的潜在疗法仍有未满足的要求。在这里,我们旨在证实鸢尾素/石斛(DNL)联合治疗对老年大鼠心肌IR损伤的心脏保护作用,重点是焦下垂和线粒体自噬的参与。雄性Wistar大鼠(22-24个月大,400-450 g;n=54)接受心肌IR或假手术。在IR手术之前,大鼠分别用鸢尾素(0.5 mg/kg,腹膜内)和/或DNL(80 mg/kg,口服)预处理1或4周。再灌注24小时后,评估心脏功能、乳酸脱氢酶(LDH)和心脏特异性肌钙蛋白I亚型(cTn-I)水平、参与pyroptosis的蛋白质(nod样受体蛋白-3(NLRP3)、凋亡相关斑点样蛋白、c-胱天蛋白酶-1和GSDMD-N)和线粒体自噬(PINK1和Parkin)的表达,以及促炎细胞因子水平。Irisin/DNL联合治疗可显著恢复心功能,降低LDH和cTn-I水平。它还下调pyroptosis相关蛋白,上调PINK1和Parkin,并减少促炎细胞因子的分泌。Mdivi-1作为线粒体自噬抑制剂的预处理消除了双重治疗的心脏保护作用。本研究揭示了鸢尾素/DNL联合治疗对IR诱导的老年大鼠心肌损伤的心脏保护作用,并表明其机制可能与通过增强PINK1/Parkin线粒体自噬活性来抑制NLRP3相关的焦下垂有关。这种联合治疗有可能减轻衰老后的心肌IR损伤,值得进一步详细研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Accounts of Chemical Research
Accounts of Chemical Research 化学-化学综合
CiteScore
31.40
自引率
1.10%
发文量
312
审稿时长
2 months
期刊介绍: Accounts of Chemical Research presents short, concise and critical articles offering easy-to-read overviews of basic research and applications in all areas of chemistry and biochemistry. These short reviews focus on research from the author’s own laboratory and are designed to teach the reader about a research project. In addition, Accounts of Chemical Research publishes commentaries that give an informed opinion on a current research problem. Special Issues online are devoted to a single topic of unusual activity and significance. Accounts of Chemical Research replaces the traditional article abstract with an article "Conspectus." These entries synopsize the research affording the reader a closer look at the content and significance of an article. Through this provision of a more detailed description of the article contents, the Conspectus enhances the article's discoverability by search engines and the exposure for the research.
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