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2
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3
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Effects of tanshinone IIA on fibrosis in a rat model of cirrhosis through heme oxygenase-1, inflammation, oxidative stress and apoptosis.丹参酮IIA通过血红素加氧酶-1、炎症、氧化应激和凋亡对肝硬化大鼠模型纤维化的影响。
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Tanshinone IIA improves miR-133 expression through MAPK ERK1/2 pathway in hypoxic cardiac myocytes.丹参酮IIA通过MAPK ERK1/2通路改善缺氧心肌细胞中miR-133的表达。
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Tanshinone IIA protects against methylglyoxal-induced injury in human brain microvascular endothelial cells.丹参酮IIA可保护人脑微血管内皮细胞免受甲基乙二醛诱导的损伤。
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Neuroprotective effect of tanshinone IIA weakens spastic cerebral palsy through inflammation, p38MAPK and VEGF in neonatal rats.丹参酮 IIA 的神经保护作用通过炎症、p38MAPK 和 VEGF 减弱新生大鼠痉挛性脑瘫。
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Protective effect of tea polyphenols on renal ischemia/reperfusion injury via suppressing the activation of TLR4/NF-κB p65 signal pathway.茶多酚通过抑制 TLR4/NF-κB p65 信号通路的激活对肾缺血/再灌注损伤的保护作用。
Gene. 2014 May 25;542(1):46-51. doi: 10.1016/j.gene.2014.03.021. Epub 2014 Mar 12.

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Pharmacokinetics and brain tissue distribution of extract in normal and cerebral ischemic rats: a comparative study.提取物在正常大鼠和脑缺血大鼠体内的药代动力学及脑组织分布:一项对比研究。
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Efficacy and Safety of Sodium Tanshinone IIA Sulfonate Injection on Hypertensive Nephropathy: A Systematic Review and Meta-Analysis.丹参酮IIA磺酸钠注射液治疗高血压肾病的疗效与安全性:一项系统评价与Meta分析
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Necrostatin-1 Attenuates Renal Ischemia and Reperfusion Injury via Meditation of HIF-1α/mir-26a/TRPC6/PARP1 Signaling.坏死抑制因子-1通过介导HIF-1α/miR-26a/TRPC6/PARP1信号通路减轻肾缺血再灌注损伤。
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本文引用的文献

1
Tanshinone IIA increases levels of NeuN, protein disulfide isomerase, and Na+/K+-ATPase and decreases evidence of microglial activation after cerebral ischemic injury.丹参酮IIA可增加NeuN、蛋白二硫键异构酶和钠钾ATP酶的水平,并减少脑缺血损伤后小胶质细胞激活的迹象。
Neuroreport. 2016 Apr 13;27(6):435-44. doi: 10.1097/WNR.0000000000000559.
2
Salvia Miltiorrhiza Root Water-Extract (Danshen) Has No Beneficial Effect on Cardiovascular Risk Factors. A Randomized Double-Blind Cross-Over Trial.丹参根水提取物(丹参)对心血管危险因素无有益作用。一项随机双盲交叉试验。
PLoS One. 2015 Jul 20;10(7):e0128695. doi: 10.1371/journal.pone.0128695. eCollection 2015.
3
Lateral intracerebroventricular injection of Apelin-13 inhibits apoptosis after cerebral ischemia/reperfusion injury.侧脑室内注射Apelin-13可抑制脑缺血/再灌注损伤后的细胞凋亡。
Neural Regen Res. 2015 May;10(5):766-71. doi: 10.4103/1673-5374.157243.
4
Tanshinone IIA protects against methylglyoxal-induced injury in human brain microvascular endothelial cells.丹参酮IIA可保护人脑微血管内皮细胞免受甲基乙二醛诱导的损伤。
Int J Clin Exp Med. 2015 Feb 15;8(2):1985-92. eCollection 2015.
5
Protective effects of tanshinone IIA on myocardial ischemia reperfusion injury by reducing oxidative stress, HMGB1 expression, and inflammatory reaction.丹参酮IIA通过减轻氧化应激、高迁移率族蛋白B1表达及炎症反应对心肌缺血再灌注损伤的保护作用。
Pharm Biol. 2015;53(12):1752-8. doi: 10.3109/13880209.2015.1005753. Epub 2015 Apr 13.
6
Tanshinone IIA attenuates the cerebral ischemic injury-induced increase in levels of GFAP and of caspases-3 and -8.丹参酮IIA可减轻脑缺血损伤诱导的胶质纤维酸性蛋白(GFAP)以及半胱天冬酶-3和-8水平的升高。
Neuroscience. 2015 Mar 12;288:105-11. doi: 10.1016/j.neuroscience.2014.12.028. Epub 2015 Jan 6.
7
Dexmedetomidine preconditioning ameliorates kidney ischemia-reperfusion injury.右美托咪定预处理减轻肾缺血再灌注损伤。
Pharmacol Res Perspect. 2014 Jun;2(3):e00045. doi: 10.1002/prp2.45. Epub 2014 Apr 22.
8
Attenuation of renal ischemia/reperfusion injury by açaí extract preconditioning in a rat model.阿萨伊提取物预处理减轻大鼠模型肾缺血/再灌注损伤
Life Sci. 2015 Feb 15;123:35-42. doi: 10.1016/j.lfs.2014.11.013. Epub 2014 Dec 2.
9
Influence of Tanshinone IIa on heat shock protein 70, Bcl-2 and Bax expression in rats with spinal ischemia/reperfusion injury.丹参酮 IIa 对脊髓缺血再灌注损伤大鼠热休克蛋白 70、Bcl-2 和 Bax 表达的影响。
Neural Regen Res. 2012 Dec 25;7(36):2882-8. doi: 10.3969/j.issn.1673-5374.2012.36.005.
10
Changes in metabolic profiles during acute kidney injury and recovery following ischemia/reperfusion.缺血/再灌注后急性肾损伤及恢复过程中的代谢谱变化。
PLoS One. 2014 Sep 5;9(9):e106647. doi: 10.1371/journal.pone.0106647. eCollection 2014.

丹参酮IIA预处理减轻缺血/再灌注诱导的肾损伤。

Tanshinone IIA pretreatment attenuates ischemia/reperfusion-induced renal injury.

作者信息

Xu Yan-Mei, Ding Guo-Hua, Huang Jie, Xiong Yan

机构信息

Department of Nephrology, Renmin Hospital of Wuhan University, Wuhan, Hubei 430060, P.R. China.

出版信息

Exp Ther Med. 2016 Oct;12(4):2741-2746. doi: 10.3892/etm.2016.3674. Epub 2016 Sep 6.

DOI:10.3892/etm.2016.3674
PMID:27698779
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5038172/
Abstract

Tanshinone IIA is a chemical compound extracted from the root of traditional Chinese herb Bunge. Tanshinone IIA has been suggested to possess anti-inflammatory activity and antioxidizing capability. Recently, accumulating results have indicated the antitumor activity of tanshinone IIA; thus, it has attracted increasing attention. In addition, tanshinone IIA has been indicated to attenuate ischemia/reperfusion induced renal injury (I/RIRI); however, little is known regarding the underlying mechanisms involved in this process. In the present study an I/RIRI rat model was used to analyze the effects of tanshinone IIA on myeloperoxidase (MPO), TNF-α and IL-6 activities using ELISA kits. Furthermore, macrophage migration inhibitory factor (MIF), cleaved caspase-3, B-cell lymphoma 2 (Bcl-2) and p38 mitogen-activated protein kinase (MAPK) protein expression levels were evaluated using western blot analysis. The results indicated that tanshinone IIA protected renal function in I/RIRI rats. ELISA demonstrated that tanshinone IIA significantly reduced MIF, TNF-α and IL-6 activities in I/RIRI rats. Western blot analysis showed that tanshinone IIA significantly suppressed MIF, cleaved caspase-3 and p38 MAPK protein expression levels in I/RIRI rats. The present results suggest that tanshinone IIA pretreatment attenuates I/RIRI via the downregulation of MPO expression, inflammation, MIF, cleaved caspase-3 and p38 MAPK.

摘要

丹参酮IIA是从传统中药丹参的根部提取的一种化合物。丹参酮IIA被认为具有抗炎活性和抗氧化能力。最近,越来越多的研究结果表明丹参酮IIA具有抗肿瘤活性;因此,它受到了越来越多的关注。此外,丹参酮IIA已被证明可减轻缺血/再灌注诱导的肾损伤(I/RIRI);然而,关于这一过程中潜在的机制知之甚少。在本研究中,使用I/RIRI大鼠模型,通过酶联免疫吸附测定试剂盒分析丹参酮IIA对髓过氧化物酶(MPO)、肿瘤坏死因子-α(TNF-α)和白细胞介素-6(IL-6)活性的影响。此外,使用蛋白质免疫印迹分析评估巨噬细胞移动抑制因子(MIF)、裂解的半胱天冬酶-3、B细胞淋巴瘤-2(Bcl-2)和p38丝裂原活化蛋白激酶(MAPK)的蛋白表达水平。结果表明,丹参酮IIA可保护I/RIRI大鼠的肾功能。酶联免疫吸附测定显示,丹参酮IIA可显著降低I/RIRI大鼠中MIF、TNF-α和IL-6的活性。蛋白质免疫印迹分析表明,丹参酮IIA可显著抑制I/RIRI大鼠中MIF、裂解的半胱天冬酶-3和p38 MAPK的蛋白表达水平。本研究结果表明,丹参酮IIA预处理可通过下调MPO表达、炎症、MIF、裂解的半胱天冬酶-3和p38 MAPK来减轻I/RIRI。