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三七总皂苷 R1 在缺血再灌注损伤中的药理学特性及作用机制。

Pharmacological properties and mechanisms of Notoginsenoside R1 in ischemia-reperfusion injury.

机构信息

Institute of Neuroregeneration & Neurorehabilitation, Department of Pathophysiology, School of Basic Medicine, Qingdao University, Qingdao, 266071, Shandong Province, China.

Institute of Neuroregeneration & Neurorehabilitation, Department of Pathophysiology, School of Basic Medicine, Qingdao University, Qingdao, 266071, Shandong Province, China.

出版信息

Chin J Traumatol. 2023 Jan;26(1):20-26. doi: 10.1016/j.cjtee.2022.06.008. Epub 2022 Jul 3.

DOI:10.1016/j.cjtee.2022.06.008
PMID:35922249
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9912185/
Abstract

Panax notoginseng is an ancient Chinese medicinal plant that has great clinical value in regulating cardiovascular disease in China. As a single component of panax notoginosides, notoginsenoside R1 (NGR1) belongs to the panaxatriol group. Many reports have demonstrated that NGR1 exerts multiple pharmacological effects in ischemic stroke, myocardial infarction, acute renal injury, and intestinal injury. Here, we outline the available reports on the pharmacological effects of NGR1 in ischemia-reperfusion (I/R) injury. We also discuss the chemistry, composition and molecular mechanism underlying the anti-I/R injury effects of NGR1. NGR1 had significant effects on reducing cerebral infarct size and neurological deficits in cerebral I/R injury, ameliorating the impaired mitochondrial morphology in myocardial I/R injury, decreasing kidney injury molecule-1 and neutrophil gelatinase-associated lipocalin in renal I/R injury and attenuating jejunal mucosal epithelium injury in intestinal I/R injury. The various organ anti-I/R injury effects of NGR1 are mainly through the suppression of oxidative stress, apoptosis, inflammation, endoplasmic reticulum stress and promotion of angiogenesis and neurogenesis. These findings provide a reference basis for future research of NGR1 on I/R injury.

摘要

三七是一种中国传统药用植物,在中国调节心血管疾病方面具有巨大的临床价值。作为三七总皂苷的单一成分,人参皂苷 R1(NGR1)属于达玛烷二醇组。许多报道表明,NGR1 在缺血性脑卒中、心肌梗死、急性肾损伤和肠损伤中具有多种药理作用。在这里,我们概述了 NGR1 在缺血再灌注(I/R)损伤中的药理学作用的现有报道。我们还讨论了 NGR1 抗 I/R 损伤作用的化学、组成和分子机制。NGR1 对脑 I/R 损伤中减少脑梗死面积和神经功能缺损、改善心肌 I/R 损伤中受损的线粒体形态、减少肾 I/R 损伤中的肾损伤分子-1 和中性粒细胞明胶酶相关脂质运载蛋白以及减轻肠 I/R 损伤中的空肠黏膜上皮损伤有显著作用。NGR1 的各种器官抗 I/R 损伤作用主要是通过抑制氧化应激、细胞凋亡、炎症、内质网应激以及促进血管生成和神经发生。这些发现为 NGR1 对 I/R 损伤的未来研究提供了参考依据。

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Chin J Traumatol. 2023 Jan;26(1):20-26. doi: 10.1016/j.cjtee.2022.06.008. Epub 2022 Jul 3.
2
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本文引用的文献

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Therapeutic targets of neuroprotection and neurorestoration in ischemic stroke: Applications for natural compounds from medicinal herbs.缺血性脑卒中的神经保护和神经修复治疗靶点:药用植物天然化合物的应用。
Biomed Pharmacother. 2022 Apr;148:112719. doi: 10.1016/j.biopha.2022.112719. Epub 2022 Feb 12.
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Xuesaitong injection treating acute myocardial infarction: A systematic review and meta-analysis.血塞通注射液治疗急性心肌梗死的系统评价和 Meta 分析。
Medicine (Baltimore). 2021 Sep 17;100(37):e27027. doi: 10.1097/MD.0000000000027027.
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Notoginsenoside R1 intervenes degradation and redistribution of tight junctions to ameliorate blood-brain barrier permeability by Caveolin-1/MMP2/9 pathway after acute ischemic stroke.
肢体缺血再灌注损伤中关键基因及免疫浸润机制的鉴定:一项生物信息学与实验研究
Front Immunol. 2025 May 9;16:1491928. doi: 10.3389/fimmu.2025.1491928. eCollection 2025.
4
NGR1 reduces neuronal apoptosis through regulation of ITGA11 following subarachnoid hemorrhage.NGR1通过调控蛛网膜下腔出血后的ITGA11来减少神经元凋亡。
Mol Med Rep. 2025 Mar;31(3). doi: 10.3892/mmr.2025.13432. Epub 2025 Jan 10.
5
Notoginsenoside R1 Attenuates Cisplatin-Induced Ototoxicity by Inducing Heme Oxygenase-1 Expression and Suppressing Oxidative Stress.三七总皂苷 R1 通过诱导血红素加氧酶-1 的表达和抑制氧化应激减轻顺铂诱导的耳毒性。
Int J Mol Sci. 2024 Oct 24;25(21):11444. doi: 10.3390/ijms252111444.
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Methane saline suppresses ferroptosis via the Nrf2/HO-1 signaling pathway to ameliorate intestinal ischemia-reperfusion injury.甲烷盐水通过 Nrf2/HO-1 信号通路抑制铁死亡,从而改善肠缺血再灌注损伤。
Redox Rep. 2024 Dec;29(1):2373657. doi: 10.1080/13510002.2024.2373657. Epub 2024 Jul 18.
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BMC Endocr Disord. 2023 Jul 6;23(1):140. doi: 10.1186/s12902-023-01402-6.
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三七总皂苷 R1 通过 Cav-1/MMP2/9 通路干预紧密连接的降解和重分布改善急性缺血性脑卒中后血脑屏障通透性。
Phytomedicine. 2021 Sep;90:153660. doi: 10.1016/j.phymed.2021.153660. Epub 2021 Jul 25.
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The Composite of 3, 4-Dihydroxyl-Phenyl Lactic Acid and Notoginsenoside R1 Attenuates Myocardial Ischemia and Reperfusion Injury Through Regulating Mitochondrial Respiratory Chain.3,4-二羟基苯乳酸与三七皂苷R1的复合物通过调节线粒体呼吸链减轻心肌缺血再灌注损伤。
Front Physiol. 2021 Jul 12;12:538962. doi: 10.3389/fphys.2021.538962. eCollection 2021.
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Notoginsenoside R1 protects hypoxia-reoxygenation deprivation-induced injury by upregulation of miR-132 in H9c2 cells.三七总皂苷 R1 通过上调 H9c2 细胞中 miR-132 对缺氧/复氧剥夺诱导的损伤起保护作用。
Hum Exp Toxicol. 2021 Dec;40(12_suppl):S29-S38. doi: 10.1177/09603271211025589. Epub 2021 Jul 2.
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Notoginsenoside R1 activates the NAMPT-NAD-SIRT1 cascade to promote postischemic angiogenesis by modulating Notch signaling.三七总皂苷 R1 通过调节 Notch 信号通路激活烟酰胺磷酸核糖转移酶-NAD-SIRT1 级联反应促进缺血后血管生成。
Biomed Pharmacother. 2021 Aug;140:111693. doi: 10.1016/j.biopha.2021.111693. Epub 2021 May 21.
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Notoginsenoside R1 Improves Cerebral Ischemia/Reperfusion Injury by Promoting Neurogenesis via the BDNF/Akt/CREB Pathway.三七皂苷R1通过BDNF/Akt/CREB通路促进神经发生改善脑缺血/再灌注损伤
Front Pharmacol. 2021 May 7;12:615998. doi: 10.3389/fphar.2021.615998. eCollection 2021.
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Oxid Med Cell Longev. 2021 Mar 13;2021:8868941. doi: 10.1155/2021/8868941. eCollection 2021.
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