• 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

丹参酮IIA通过抑制Cys-C/ Wnt信号通路对自发性高血压大鼠心脏肥大的保护作用

Protective effect of tanshinone IIA against cardiac hypertrophy in spontaneously hypertensive rats through inhibiting the Cys-C/Wnt signaling pathway.

作者信息

Feng Jun, Chen Hua-Wen, Pi Li-Juan, Wang Jin, Zhan Da-Qian

机构信息

Department of Emergency Medicine, Tongji Hospital, Huazhong University of Science and Technology, Wuhan 430030, Hubei, P.R. China.

出版信息

Oncotarget. 2017 Feb 7;8(6):10161-10170. doi: 10.18632/oncotarget.14328.

DOI:10.18632/oncotarget.14328
PMID:28053285
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5354649/
Abstract

The study aimed to investigate the protective effect of tanshinone IIA against cardiac hypertrophy in spontaneously hypertensive rats (SHRs) through the Cys-C/Wnt signaling pathway. Thirty SHRs were randomly divided into cardiac hypertrophy, low- and high-dose tanshinone IIA groups. Ten Wistar-Kyoto rats were selected as control group. The systolic blood pressure (SBP), heart weight (HW), left ventricular weight (LVW) and body weight (BW) of all rats were recorded. HE staining and qRT-PCR were applied to observe the morphology of myocardial tissue and mRNA expressions of COL1A1 and COL3A1. ELISA and Western blotting were used to measure the serum asymmetric dimethylarginine (ADMA), nitric oxide (NO) and cardiac troponin I (cTnI) levels, and the expressions of the Cys-C/Wnt signaling pathway-related proteins, eNOS and Nox4. Compared with the cardiac hypertrophy group, the SBP, HW/BW, LVW/BW, swelling degree of myocardial cells, COL1A1 and COL3A1 mRNA expressions, serum cTnI and ADMA levels, and the Cys-C/Wnt signaling pathway-related proteins and Nox4 expressions in the low- and high-dose tanshinone IIA groups were decreased, but the endothelial NO synthase (eNOS), phosphorylated eNOS (Ser1177) and NO expressions were increased. No significant difference was found between the low- and high-dose tanshinone IIA groups. Our study indicated a protective effect of tanshinone IIA against cardiac hypertrophy in SHRs through inhibiting the Cys-C/Wnt signaling pathway.

摘要

本研究旨在通过Cys-C/ Wnt信号通路探讨丹参酮IIA对自发性高血压大鼠(SHRs)心脏肥大的保护作用。将30只SHRs随机分为心脏肥大组、低剂量和高剂量丹参酮IIA组。选取10只Wistar-Kyoto大鼠作为对照组。记录所有大鼠的收缩压(SBP)、心脏重量(HW)、左心室重量(LVW)和体重(BW)。采用HE染色和qRT-PCR观察心肌组织形态及COL1A1和COL3A1的mRNA表达。采用ELISA和蛋白质印迹法检测血清不对称二甲基精氨酸(ADMA)、一氧化氮(NO)和心肌肌钙蛋白I(cTnI)水平,以及Cys-C/ Wnt信号通路相关蛋白、内皮型一氧化氮合酶(eNOS)和Nox4的表达。与心脏肥大组相比,低剂量和高剂量丹参酮IIA组的SBP、HW/BW、LVW/BW、心肌细胞肿胀程度、COL1A1和COL3A1 mRNA表达、血清cTnI和ADMA水平以及Cys-C/ Wnt信号通路相关蛋白和Nox4表达均降低,但内皮型一氧化氮合酶(eNOS)、磷酸化eNOS(Ser1177)和NO表达增加。低剂量和高剂量丹参酮IIA组之间未发现显著差异。我们的研究表明,丹参酮IIA通过抑制Cys-C/ Wnt信号通路对SHRs心脏肥大具有保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9429/5354649/65946d08bfda/oncotarget-08-10161-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9429/5354649/a750ee7cb098/oncotarget-08-10161-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9429/5354649/08a6b9a3e3fa/oncotarget-08-10161-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9429/5354649/d4682727cd12/oncotarget-08-10161-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9429/5354649/96f3ba475deb/oncotarget-08-10161-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9429/5354649/65946d08bfda/oncotarget-08-10161-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9429/5354649/a750ee7cb098/oncotarget-08-10161-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9429/5354649/08a6b9a3e3fa/oncotarget-08-10161-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9429/5354649/d4682727cd12/oncotarget-08-10161-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9429/5354649/96f3ba475deb/oncotarget-08-10161-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9429/5354649/65946d08bfda/oncotarget-08-10161-g005.jpg

相似文献

1
Protective effect of tanshinone IIA against cardiac hypertrophy in spontaneously hypertensive rats through inhibiting the Cys-C/Wnt signaling pathway.丹参酮IIA通过抑制Cys-C/ Wnt信号通路对自发性高血压大鼠心脏肥大的保护作用
Oncotarget. 2017 Feb 7;8(6):10161-10170. doi: 10.18632/oncotarget.14328.
2
Salvianolic acid B and tanshinone IIA attenuate myocardial ischemia injury in mice by NO production through multiple pathways.丹酚酸B和丹参酮IIA通过多种途径产生一氧化氮减轻小鼠心肌缺血损伤。
Ther Adv Cardiovasc Dis. 2011 Apr;5(2):99-111. doi: 10.1177/1753944710396538. Epub 2011 Jan 31.
3
Tanshinone IIA inhibits angiotensin II-induced cell proliferation in rat cardiac fibroblasts.丹参酮 IIA 抑制血管紧张素 II 诱导的大鼠心肌成纤维细胞增殖。
Am J Chin Med. 2011;39(2):381-94. doi: 10.1142/S0192415X11008890.
4
Chronic administration of hexarelin attenuates cardiac fibrosis in the spontaneously hypertensive rat.慢性给予 hexarelin 可减轻自发性高血压大鼠的心脏纤维化。
Am J Physiol Heart Circ Physiol. 2012 Sep 15;303(6):H703-11. doi: 10.1152/ajpheart.00257.2011. Epub 2012 Jul 27.
5
Tanshinone IIA prevents cardiac remodeling through attenuating NAD (P)H oxidase-derived reactive oxygen species production in hypertensive rats.丹参酮IIA通过减弱高血压大鼠中烟酰胺腺嘌呤二核苷酸(磷酸)氧化酶衍生的活性氧生成来预防心脏重塑。
Pharmazie. 2011 Jul;66(7):517-24.
6
UBIAD1 expression is associated with cardiac hypertrophy in spontaneously hypertensive rats.UBIAD1 的表达与自发性高血压大鼠的心肌肥厚有关。
Mol Med Rep. 2019 Jan;19(1):651-659. doi: 10.3892/mmr.2018.9693. Epub 2018 Nov 26.
7
Tanshinone IIA protects against chronic intermittent hypoxia-induced myocardial injury via activating the endothelin 1 pathway.丹参酮 IIA 通过激活内皮素 1 途径保护慢性间歇性低氧诱导的心肌损伤。
Biomed Pharmacother. 2017 Nov;95:1013-1020. doi: 10.1016/j.biopha.2017.08.036. Epub 2017 Sep 13.
8
Effects of medium-chain triglyceride (MCT) application to SHR on cardiac function, hypertrophy and expression of endothelin-1 mRNA and other genes.中链甘油三酯(MCT)应用于自发性高血压大鼠(SHR)对心脏功能、心肌肥厚以及内皮素-1 mRNA和其他基因表达的影响。
J Cardiovasc Pharmacol. 2004 Nov;44 Suppl 1:S181-5. doi: 10.1097/01.fjc.0000166263.19852.fc.
9
Imatinib mesylate attenuates myocardial remodeling through inhibition of platelet-derived growth factor and transforming growth factor activation in a rat model of hypertension.甲磺酸伊马替尼通过抑制血小板衍生生长因子和转化生长因子的激活减轻高血压大鼠心肌重构。
Hypertension. 2014 Jun;63(6):1228-34. doi: 10.1161/HYPERTENSIONAHA.113.01866. Epub 2014 Mar 3.
10
Chronic administration of genistein improves endothelial dysfunction in spontaneously hypertensive rats: involvement of eNOS, caveolin and calmodulin expression and NADPH oxidase activity.长期给予染料木黄酮可改善自发性高血压大鼠的内皮功能障碍:内皮型一氧化氮合酶、小窝蛋白和钙调蛋白表达及烟酰胺腺嘌呤二核苷酸磷酸氧化酶活性的参与
Clin Sci (Lond). 2007 Feb;112(3):183-91. doi: 10.1042/CS20060185.

引用本文的文献

1
Harnessing the therapeutic value of Tanshinone IIA: a breakthrough therapy in cardiovascular diseases.利用丹参酮IIA的治疗价值:心血管疾病的突破性疗法。
Front Pharmacol. 2025 Jul 4;16:1620152. doi: 10.3389/fphar.2025.1620152. eCollection 2025.
2
Signaling pathways behind the biological effects of tanshinone IIA for the prevention of cancer and cardiovascular diseases.丹参酮IIA预防癌症和心血管疾病生物学效应背后的信号通路。
Naunyn Schmiedebergs Arch Pharmacol. 2025 Feb 12. doi: 10.1007/s00210-025-03857-x.
3
Proteins and DNA Sequences Interacting with Tanshinones and Tanshinone Derivatives.

本文引用的文献

1
ACE I/D Polymorphism in Hypertensive Patients of Kashmiri Population.克什米尔人群高血压患者中的ACE I/D多态性
Cardiol Res. 2010 Dec;1(1):1-7. doi: 10.4021/cr101e. Epub 2010 Nov 20.
2
Crosstalk between Beclin-1-dependent autophagy and caspase‑dependent apoptosis induced by tanshinone IIA in human osteosarcoma MG-63 cells.丹参酮IIA诱导人骨肉瘤MG-63细胞中Beclin-1依赖性自噬与半胱天冬酶依赖性凋亡之间的串扰
Oncol Rep. 2016 Oct;36(4):1807-18. doi: 10.3892/or.2016.5003. Epub 2016 Aug 4.
3
Tanshinone IIA promotes the proliferation of WB-F344 hepatic oval cells via Wnt/β-catenin signaling.
与丹参酮及丹参酮衍生物相互作用的蛋白质和DNA序列
Int J Mol Sci. 2025 Jan 20;26(2):848. doi: 10.3390/ijms26020848.
4
The role of Chinese herbal medicine in the regulation of oxidative stress in treating hypertension: from therapeutics to mechanisms.中药在治疗高血压中调节氧化应激的作用:从治疗方法到作用机制
Chin Med. 2024 Oct 29;19(1):150. doi: 10.1186/s13020-024-01022-9.
5
Targeting Oxidative Stress and Endothelial Dysfunction Using Tanshinone IIA for the Treatment of Tissue Inflammation and Fibrosis.丹参酮 IIA 通过靶向氧化应激和血管内皮功能障碍治疗组织炎症和纤维化。
Oxid Med Cell Longev. 2022 Apr 7;2022:2811789. doi: 10.1155/2022/2811789. eCollection 2022.
6
- L. Drug Pair Regulates Ferroptosis by Mediating the Neurovascular-Related Ligand-Receptor Interaction Pathway- A Potential Drug Pair for Treatment Hypertension and Prevention Ischemic Stroke.- L.药物对通过介导神经血管相关配体-受体相互作用途径调节铁死亡——一种治疗高血压和预防缺血性中风的潜在药物对。
Front Neurol. 2022 Mar 8;13:833922. doi: 10.3389/fneur.2022.833922. eCollection 2022.
7
Tanshinone IIA alleviates cardiac hypertrophy through m6A modification of galectin-3.丹参酮 IIA 通过调节半乳糖凝集素-3 的 m6A 修饰缓解心肌肥厚。
Bioengineered. 2022 Feb;13(2):4260-4270. doi: 10.1080/21655979.2022.2031388.
8
Recent Research Progress (2015-2021) and Perspectives on the Pharmacological Effects and Mechanisms of Tanshinone IIA.丹参酮IIA药理作用及机制的近期研究进展(2015 - 2021年)与展望
Front Pharmacol. 2021 Nov 8;12:778847. doi: 10.3389/fphar.2021.778847. eCollection 2021.
9
Myocardial Hypertrophy and Fibrosis Are Associated with Cardiomyocyte Beta-Catenin and TRPC6/Calcineurin/NFAT Signaling in Spontaneously Hypertensive Rats with 5/6 Nephrectomy.自发性高血压大鼠 5/6 肾切除后心肌肥厚和纤维化与心肌细胞β-连环蛋白和 TRPC6/钙调神经磷酸酶/NFAT 信号有关。
Int J Mol Sci. 2021 Apr 28;22(9):4645. doi: 10.3390/ijms22094645.
10
in Treating Cardiovascular Diseases: A Review on Its Pharmacological and Clinical Applications.治疗心血管疾病:其药理学与临床应用综述
Front Pharmacol. 2019 Jul 5;10:753. doi: 10.3389/fphar.2019.00753. eCollection 2019.
丹参酮IIA通过Wnt/β-连环蛋白信号通路促进WB-F344肝卵圆细胞的增殖。
Mol Med Rep. 2016 Feb;13(2):1501-8. doi: 10.3892/mmr.2015.4696. Epub 2015 Dec 18.
4
Hypertension: empirical evidence and implications in 2014.高血压:2014年的实证证据及影响
Open Heart. 2014 Jul 10;1(1):e000048. doi: 10.1136/openhrt-2014-000048. eCollection 2014.
5
Tanshinone IIA pretreatment renders free flaps against hypoxic injury through activating Wnt signaling and upregulating stem cell-related biomarkers.丹参酮IIA预处理通过激活Wnt信号通路和上调干细胞相关生物标志物使游离皮瓣免受缺氧损伤。
Int J Mol Sci. 2014 Oct 9;15(10):18117-30. doi: 10.3390/ijms151018117.
6
Hypertension as a risk factor for ischemic stroke in women.高血压作为女性缺血性中风的一个风险因素。
Can J Cardiol. 2014 Jul;30(7):774-82. doi: 10.1016/j.cjca.2014.01.007. Epub 2014 Jan 16.
7
Propionyl-L-carnitine induces eNOS activation and nitric oxide synthesis in endothelial cells via PI3 and Akt kinases.丙酰基左旋肉碱通过 PI3 和 Akt 激酶诱导内皮细胞中 eNOS 的激活和一氧化氮的合成。
Vascul Pharmacol. 2013 Sep-Oct;59(3-4):76-82. doi: 10.1016/j.vph.2013.07.001. Epub 2013 Jul 12.
8
Tanshinone IIA induces autophagic cell death via activation of AMPK and ERK and inhibition of mTOR and p70 S6K in KBM-5 leukemia cells.丹参酮 IIA 通过激活 AMPK 和 ERK 以及抑制 mTOR 和 p70 S6K 诱导 KBM-5 白血病细胞自噬性细胞死亡。
Phytother Res. 2014 Mar;28(3):458-64. doi: 10.1002/ptr.5015. Epub 2013 Jun 27.
9
Vaspin increases nitric oxide bioavailability through the reduction of asymmetric dimethylarginine in vascular endothelial cells.脂联素可通过降低血管内皮细胞中不对称二甲基精氨酸来增加一氧化氮的生物利用度。
PLoS One. 2012;7(12):e52346. doi: 10.1371/journal.pone.0052346. Epub 2012 Dec 28.
10
Tanshinone IIA arrests cell cycle and induces apoptosis in 786-O human renal cell carcinoma cells.丹参酮IIA使786-O人肾癌细胞的细胞周期停滞并诱导其凋亡。
Oncol Lett. 2012 May;3(5):1144-1148. doi: 10.3892/ol.2012.626. Epub 2012 Feb 29.