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黄芪多糖通过内质网应激途径抑制糖尿病心肌病中心肌细胞凋亡。

Astragalus polysaccharides inhibits cardiomyocyte apoptosis during diabetic cardiomyopathy via the endoplasmic reticulum stress pathway.

机构信息

Department of Geriatrics, The Affiliated Hospital of Qingdao University, Qingdao, 266003, China.

Department of the Intensive Care Unit, The Affiliated Hospital of Qingdao University, Qingdao, 266003, China.

出版信息

J Ethnopharmacol. 2019 Jun 28;238:111857. doi: 10.1016/j.jep.2019.111857. Epub 2019 Apr 6.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Traditional Chinese medicine Astragalus membranaceus (Fisch.) Bunge (AM) has been utilized for the treatment of diabetes mellitus and its complications for centuries. Astragalus polysaccharides (APS), the main bioactive ingredient extracted from the root of AM, is prescribed widely in China and has definite cardioprotective effect during diabetic cardiomyopathy (DCM). Endoplasmic reticulum (ER) stress-induced apoptosis played a crucial role in the progression of DCM. However, the regulatory mechanisms of APS on ER stress pathway haven't been comprehensively studied so far.

AIM OF THE STUDY

The aim of this study was to identify the effect of APS on cardiomyocyte apoptosis and to investigate the mechanisms for the anti-apoptotic effect of APS during DCM.

MATERIALS AND METHODS

DCM rat model was induced by intraperitoneal streptozotocin (STZ) injection and treated with APS for 16 weeks. Cardiac function, pathological changes and apoptotic cells were assessed by echocardiography, hematoxylin-eosin (HE) staining and TUNEL assay, respectively. Expressions of key molecules in ER stress pathway were detected by Western blot analysis. Cardiomyocytes were exposed to high glucose (HG) and treated with APS for 24 h. Cell viability, apoptosis and protein expressions were assessed by MTT, flow cytometer and Western blot analysis, respectively. Moreover, lentivirus over-expressing (OE) C/EBP homologous protein (CHOP) was employed to further investigate the causative role of ER stress pathway in APS-mediated effect on cardiomyocyte apoptosis.

RESULTS

In vivo, the results demonstrated that APS could improve heart function and attenuate myocardial apoptosis in DCM rat model. Further study demonstrated that APS could down-regulate the protein expressions of activating transcription factor 6 (ATF6) and protein kinase RNA-like ER kinase (PERK) related factors of ER stress pathway. In vitro, APS significantly inhibit HG stimulated H9C2 cell apoptosis and the expressions of ATF6 and PERK related proteins of ER stress pathway. However, after CHOP-OE lentivirus transfection, the protective effects of APS were diminished as increased apoptotic rate and higher expression of CHOP.

CONCLUSIONS

APS could attenuate cardiomyocyte apoptosis via down-regulating the expression of ATF6 and PERK related factors of ER stress pathway in DCM rats and HG-stimulated H9C2 cells.

摘要

ETHNOPHARMACOLOGICAL 相关性:传统中药黄芪(膜荚黄芪)(AM)已被用于治疗糖尿病及其并发症数百年。黄芪多糖(APS)是从 AM 根中提取的主要生物活性成分,在中国被广泛应用,并且在糖尿病心肌病(DCM)期间具有明确的心脏保护作用。内质网(ER)应激诱导的细胞凋亡在 DCM 的进展中起着至关重要的作用。然而,APS 对 ER 应激途径的调节机制尚未得到全面研究。

研究目的

本研究旨在确定 APS 对心肌细胞凋亡的影响,并探讨 APS 在 DCM 期间抗凋亡作用的机制。

材料和方法

通过腹腔内链脲佐菌素(STZ)注射诱导 DCM 大鼠模型,并使用 APS 治疗 16 周。通过超声心动图、苏木精-伊红(HE)染色和 TUNEL 检测分别评估心脏功能、病理变化和凋亡细胞。通过 Western blot 分析检测 ER 应激途径中关键分子的表达。将心肌细胞暴露于高葡萄糖(HG)中,并使用 APS 处理 24 小时。通过 MTT、流式细胞仪和 Western blot 分析分别评估细胞活力、细胞凋亡和蛋白表达。此外,还使用慢病毒过表达(OE)C/EBP 同源蛋白(CHOP)进一步研究 ER 应激途径在 APS 介导的心肌细胞凋亡中的因果作用。

结果

体内研究结果表明,APS 可改善 DCM 大鼠模型的心脏功能并减轻心肌细胞凋亡。进一步的研究表明,APS 可下调 ER 应激途径中的激活转录因子 6(ATF6)和蛋白激酶 RNA 样内质网激酶(PERK)相关因子的蛋白表达。在体外,APS 显著抑制 HG 刺激的 H9C2 细胞凋亡和 ER 应激途径中 ATF6 和 PERK 相关蛋白的表达。然而,在 CHOP-OE 慢病毒转染后,APS 的保护作用减弱,因为凋亡率增加和 CHOP 表达升高。

结论

APS 可通过下调 DCM 大鼠和 HG 刺激的 H9C2 细胞中 ER 应激途径的 ATF6 和 PERK 相关因子的表达来减轻心肌细胞凋亡。

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