• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

葫芦素 I 通过保护线粒体功能障碍保护 H9c2 心肌细胞免受 HO 诱导的氧化应激。

Cucurbitacin I Protects H9c2 Cardiomyoblasts against HO-Induced Oxidative Stress via Protection of Mitochondrial Dysfunction.

机构信息

Department of Veterinary Pharmacology and Toxicology, College of Veterinary Medicine, Biosafety Research Institute and Korea Zoonosis Research Institute, Chonbuk National University, Jeonju, Republic of Korea.

出版信息

Oxid Med Cell Longev. 2018 Feb 25;2018:3016382. doi: 10.1155/2018/3016382. eCollection 2018.

DOI:10.1155/2018/3016382
PMID:29682157
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5845511/
Abstract

Cucurbitacin I, a triterpenoid natural compound, exhibits various pharmacological properties, including anticancer, anti-inflammatory, and hepatoprotective properties. However, antioxidant effects of cucurbitacin I in cardiac cells are currently unknown. In the present study, we assessed the preventive effects of cucurbitacin I against the oxidative stress in H9c2 cardiomyoblasts. To evaluate antioxidant effects of cucurbitacin I in H9c2 cardiomyoblasts, HO-treated H9c2 cells were pretreated with various concentrations of the cucurbitacin I. Cell viability, reactive oxygen species (ROS) production, and apoptosis were determined to elucidate the protective effects of cucurbitacin I against HO-induced oxidative stress in H9c2 cells. In addition, we assessed the mitochondrial functions and protein expression levels of mitogen-activated protein kinases (MAPKs). Cucurbitacin I prevented the cells against cell death and ROS production and elevated the antioxidant protein levels upon oxidative stress. Furthermore, cucurbitacin I preserved the mitochondrial functions and inhibited the apoptotic responses in HO-treated cells. Cucurbitacin I also suppressed the activation of MAPK proteins (extracellular signal-regulated kinase 1/2, c-Jun N-terminal kinase, and p38). Collectively, cucurbitacin I potentially protects the H9c2 cardiomyoblasts against oxidative stress and further suggests that it can be utilized as a therapeutic agent for the prevention of oxidative stress in cardiac injury.

摘要

葫芦素 I 是一种三萜类天然化合物,具有多种药理活性,包括抗癌、抗炎和保肝作用。然而,葫芦素 I 对心肌细胞的抗氧化作用尚不清楚。本研究评估了葫芦素 I 对 H9c2 心肌细胞氧化应激的预防作用。为了评估葫芦素 I 在 H9c2 心肌细胞中的抗氧化作用,用不同浓度的葫芦素 I 预处理 HO 处理的 H9c2 细胞。测定细胞活力、活性氧(ROS)产生和细胞凋亡,以阐明葫芦素 I 对 H9c2 细胞中 HO 诱导的氧化应激的保护作用。此外,我们评估了线粒体功能和丝裂原活化蛋白激酶(MAPKs)的蛋白表达水平。葫芦素 I 可防止细胞死亡和 ROS 产生,并在氧化应激时提高抗氧化蛋白水平。此外,葫芦素 I 还可维持线粒体功能并抑制 HO 处理细胞中的凋亡反应。葫芦素 I 还抑制 MAPK 蛋白(细胞外信号调节激酶 1/2、c-Jun N 末端激酶和 p38)的激活。综上所述,葫芦素 I 可能对 H9c2 心肌细胞具有抗氧化应激作用,并进一步表明它可用作预防心脏损伤中氧化应激的治疗剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a0/5845511/32a74c975460/OMCL2018-3016382.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a0/5845511/df778c07cf62/OMCL2018-3016382.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a0/5845511/98068928fdf4/OMCL2018-3016382.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a0/5845511/ad159245b04c/OMCL2018-3016382.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a0/5845511/7c8c45d683e7/OMCL2018-3016382.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a0/5845511/32a74c975460/OMCL2018-3016382.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a0/5845511/df778c07cf62/OMCL2018-3016382.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a0/5845511/98068928fdf4/OMCL2018-3016382.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a0/5845511/ad159245b04c/OMCL2018-3016382.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a0/5845511/7c8c45d683e7/OMCL2018-3016382.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8a0/5845511/32a74c975460/OMCL2018-3016382.005.jpg

相似文献

1
Cucurbitacin I Protects H9c2 Cardiomyoblasts against HO-Induced Oxidative Stress via Protection of Mitochondrial Dysfunction.葫芦素 I 通过保护线粒体功能障碍保护 H9c2 心肌细胞免受 HO 诱导的氧化应激。
Oxid Med Cell Longev. 2018 Feb 25;2018:3016382. doi: 10.1155/2018/3016382. eCollection 2018.
2
Araloside C protects H9c2 cardiomyoblasts against oxidative stress via the modulation of mitochondrial function.山茱萸新苷 C 通过调节线粒体功能保护 H9c2 心肌细胞免受氧化应激。
Biomed Pharmacother. 2019 Sep;117:109143. doi: 10.1016/j.biopha.2019.109143. Epub 2019 Jul 8.
3
Chlorogenic acid analogues from Gynura nepalensis protect H9c2 cardiomyoblasts against HO-induced apoptosis.来自尼泊尔紫菊的绿原酸类似物可保护H9c2心肌母细胞免受HO诱导的细胞凋亡。
Acta Pharmacol Sin. 2016 Nov;37(11):1413-1422. doi: 10.1038/aps.2016.79. Epub 2016 Sep 5.
4
Naringin inhibits ROS-activated MAPK pathway in high glucose-induced injuries in H9c2 cardiac cells.柚皮苷抑制高糖诱导的H9c2心肌细胞损伤中的活性氧激活的丝裂原活化蛋白激酶(MAPK)通路。
Basic Clin Pharmacol Toxicol. 2014 Apr;114(4):293-304. doi: 10.1111/bcpt.12153. Epub 2013 Dec 11.
5
25-Hydroxyl-protopanaxatriol protects against HO-induced H9c2 cardiomyocytes injury via PI3K/Akt pathway and apoptotic protein down-regulation.25-羟基原人参三醇通过 PI3K/Akt 通路和下调凋亡蛋白对 HO 诱导的 H9c2 心肌细胞损伤起保护作用。
Biomed Pharmacother. 2018 Mar;99:33-42. doi: 10.1016/j.biopha.2018.01.039. Epub 2018 Jan 8.
6
T3 peptide, an active fragment of tumstatin, inhibits HO-induced apoptosis in H9c2 cardiomyoblasts.T3 肽,一个 tumstatin 的活性片段,抑制了 HO 诱导的 H9c2 心肌细胞凋亡。
Eur J Pharmacol. 2017 Jul 15;807:64-70. doi: 10.1016/j.ejphar.2017.04.032. Epub 2017 Apr 27.
7
Hydrogen sulfide attenuates doxorubicin-induced cardiotoxicity by inhibition of the p38 MAPK pathway in H9c2 cells.硫化氢通过抑制 H9c2 细胞中 p38 MAPK 通路减轻阿霉素诱导的心肌毒性。
Int J Mol Med. 2013 Mar;31(3):644-50. doi: 10.3892/ijmm.2013.1246. Epub 2013 Jan 15.
8
Exogenous hydrogen sulfide protects H9c2 cardiac cells against high glucose-induced injury by inhibiting the activities of the p38 MAPK and ERK1/2 pathways.外源性硫化氢通过抑制 p38MAPK 和 ERK1/2 通路的活性保护 H9c2 心肌细胞免受高糖诱导的损伤。
Int J Mol Med. 2013 Oct;32(4):917-25. doi: 10.3892/ijmm.2013.1462. Epub 2013 Aug 1.
9
The Protective Effect of INH2BP, a Novel PARP Inhibitor 5-Iodo-6-Amino-1,2-Benzopyrone, Against Hydrogen Peroxide-Induced Apoptosis Through ERK and p38 MAPK in H9c2 Cells.新型PARP抑制剂5-碘-6-氨基-1,2-苯并吡喃(INH2BP)通过ERK和p38 MAPK途径对过氧化氢诱导的H9c2细胞凋亡的保护作用
Pharmacology. 2015;96(5-6):259-70. doi: 10.1159/000439572. Epub 2015 Oct 20.
10
Overproduction of reactive oxygen species and activation of MAPKs are involved in apoptosis induced by PM2.5 in rat cardiac H9c2 cells.活性氧的过量产生和丝裂原活化蛋白激酶的激活参与了细颗粒物(PM2.5)诱导的大鼠心脏H9c2细胞凋亡。
J Appl Toxicol. 2016 Apr;36(4):609-17. doi: 10.1002/jat.3249. Epub 2015 Oct 15.

引用本文的文献

1
Supplementation with aspalathin and sulforaphane protects cultured cardiac cells against dyslipidemia-associated oxidative damage.补充羽扇豆黄素和萝卜硫素可保护培养的心脏细胞免受血脂异常相关的氧化损伤。
Metabol Open. 2025 Jan 3;25:100346. doi: 10.1016/j.metop.2025.100346. eCollection 2025 Mar.
2
Depolymerization of actin filaments by Cucurbitacin I through binding G-actin.葫芦素I通过结合G-肌动蛋白使肌动蛋白丝解聚。
Food Sci Nutr. 2023 Nov 6;12(2):881-889. doi: 10.1002/fsn3.3804. eCollection 2024 Feb.
3
Butein Ameliorates Oxidative Stress in H9c2 Cardiomyoblasts through Activation of the NRF2 Signaling Pathway.

本文引用的文献

1
The role of reactive oxygen species in myocardial redox signaling and regulation.活性氧在心肌氧化还原信号传导与调控中的作用。
Ann Transl Med. 2017 Aug;5(16):324. doi: 10.21037/atm.2017.06.17.
2
Basic Biology of Oxidative Stress and the Cardiovascular System: Part 1 of a 3-Part Series.氧化应激与心血管系统的基础生物学:三部分系列文章的第一部分
J Am Coll Cardiol. 2017 Jul 11;70(2):196-211. doi: 10.1016/j.jacc.2017.05.034.
3
Effects of Polyphenols on Oxidative Stress-Mediated Injury in Cardiomyocytes.多酚对心肌细胞氧化应激介导损伤的影响。
紫铆因通过激活NRF2信号通路改善H9c2心肌成纤维细胞中的氧化应激。
Antioxidants (Basel). 2022 Jul 23;11(8):1430. doi: 10.3390/antiox11081430.
4
Cucurbitacin I inhibits the proliferation of pancreatic cancer through the JAK2/STAT3 signalling pathway and .葫芦素I通过JAK2/STAT3信号通路抑制胰腺癌的增殖。
J Cancer. 2022 Mar 28;13(7):2050-2060. doi: 10.7150/jca.65875. eCollection 2022.
5
Use of cucurbitacins for lung cancer research and therapy.葫芦素在肺癌研究和治疗中的应用。
Cancer Chemother Pharmacol. 2021 Jul;88(1):1-14. doi: 10.1007/s00280-021-04265-7. Epub 2021 Apr 6.
6
Wenxin Keli Regulates Mitochondrial Oxidative Stress and Homeostasis and Improves Atrial Remodeling in Diabetic Rats.稳心颗粒调节糖尿病大鼠的线粒体氧化应激和动态平衡,改善心房重构。
Oxid Med Cell Longev. 2020 Feb 13;2020:2468031. doi: 10.1155/2020/2468031. eCollection 2020.
7
Protective effects of five compounds from R. Brown leaves against hypoxia/reoxygenation, HO, or adriamycin-induced injury in H9c2 cells.来自R. Brown叶的五种化合物对H9c2细胞缺氧/复氧、过氧化氢或阿霉素诱导损伤的保护作用。
Drug Des Devel Ther. 2019 May 8;13:1555-1566. doi: 10.2147/DDDT.S201816. eCollection 2019.
8
YB1 protects cardiac myocytes against H2O2‑induced injury via suppression of PIAS3 mRNA and phosphorylation of STAT3.YB1 通过抑制 PIAS3 mRNA 和磷酸化 STAT3 来保护心肌细胞免受 H2O2 诱导的损伤。
Mol Med Rep. 2019 Jun;19(6):4579-4588. doi: 10.3892/mmr.2019.10119. Epub 2019 Apr 3.
Nutrients. 2017 May 20;9(5):523. doi: 10.3390/nu9050523.
4
Global, regional, and national incidence, prevalence, and years lived with disability for 310 diseases and injuries, 1990-2015: a systematic analysis for the Global Burden of Disease Study 2015.1990 - 2015年全球、区域和国家310种疾病和损伤的发病率、患病率及伤残调整生命年:全球疾病负担研究2015的系统分析
Lancet. 2016 Oct 8;388(10053):1545-1602. doi: 10.1016/S0140-6736(16)31678-6.
5
Global, regional, and national life expectancy, all-cause mortality, and cause-specific mortality for 249 causes of death, 1980-2015: a systematic analysis for the Global Burden of Disease Study 2015.1980 - 2015年全球、区域和国家249种死因的预期寿命、全死因死亡率和死因别死亡率:全球疾病负担研究2015的系统分析
Lancet. 2016 Oct 8;388(10053):1459-1544. doi: 10.1016/S0140-6736(16)31012-1.
6
Cucurbitacin B exerts anti-cancer activities in human multiple myeloma cells in vitro and in vivo by modulating multiple cellular pathways.葫芦素B通过调节多种细胞途径在体外和体内对人多发性骨髓瘤细胞发挥抗癌活性。
Oncotarget. 2017 Jan 24;8(4):5800-5813. doi: 10.18632/oncotarget.10584.
7
Cucurbitacin I Attenuates Cardiomyocyte Hypertrophy via Inhibition of Connective Tissue Growth Factor (CCN2) and TGF- β/Smads Signalings.葫芦素I通过抑制结缔组织生长因子(CCN2)和TGF-β/Smads信号通路减轻心肌细胞肥大。
PLoS One. 2015 Aug 21;10(8):e0136236. doi: 10.1371/journal.pone.0136236. eCollection 2015.
8
Cardioprotective and cardiotoxic effects of quercetin and two of its in vivo metabolites on differentiated h9c2 cardiomyocytes.槲皮素及其两种体内代谢产物对分化的h9c2心肌细胞的心脏保护和心脏毒性作用。
Basic Clin Pharmacol Toxicol. 2015 Feb;116(2):96-109. doi: 10.1111/bcpt.12319. Epub 2014 Oct 13.
9
Mitochondrial reactive oxygen species (ROS) and ROS-induced ROS release.线粒体活性氧(ROS)与ROS诱导的ROS释放。
Physiol Rev. 2014 Jul;94(3):909-50. doi: 10.1152/physrev.00026.2013.
10
Quercetin attenuates doxorubicin cardiotoxicity by modulating Bmi-1 expression.槲皮素通过调节Bmi-1表达减轻阿霉素心脏毒性。
Br J Pharmacol. 2014 Oct;171(19):4440-54. doi: 10.1111/bph.12795. Epub 2014 Aug 14.