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本文引用的文献

1
HMGB1: a potential therapeutic target for myocardial ischemia and reperfusion injury.高迁移率族蛋白B1:心肌缺血再灌注损伤的潜在治疗靶点。
Int J Cardiol. 2012 Mar 22;155(3):489. doi: 10.1016/j.ijcard.2011.12.066. Epub 2012 Jan 10.
2
Inflammatory markers in hyperlipidemia: from experimental models to clinical practice.高脂血症中的炎症标志物:从实验模型到临床实践。
Curr Pharm Des. 2011 Dec;17(37):4132-46. doi: 10.2174/138161211798764780.
3
Hyperlipidemia stimulates the extracellular release of the nuclear high mobility group box 1 protein.高血脂症会刺激核高迁移率族蛋白 1 从细胞外释放。
Cell Tissue Res. 2011 Dec;346(3):361-8. doi: 10.1007/s00441-011-1277-4. Epub 2011 Nov 24.
4
Statins attenuate high mobility group box-1 protein induced vascular endothelial activation : a key role for TLR4/NF-κB signaling pathway.他汀类药物可减轻高迁移率族蛋白 1 诱导的血管内皮细胞激活:TLR4/NF-κB 信号通路的关键作用。
Mol Cell Biochem. 2010 Dec;345(1-2):189-95. doi: 10.1007/s11010-010-0572-9. Epub 2010 Aug 17.
5
High mobility group box-1 and cardiovascular diseases.高迁移率族蛋白盒1与心血管疾病
Saudi Med J. 2010 May;31(5):486-9.
6
Atorvastatin protects rat brains against permanent focal ischemia and downregulates HMGB1, HMGB1 receptors (RAGE and TLR4), NF-kappaB expression.阿托伐他汀可保护大鼠大脑免受永久性局灶性缺血的影响,并下调 HMGB1、HMGB1 受体(RAGE 和 TLR4)、NF-κB 的表达。
Neurosci Lett. 2010 Mar 8;471(3):152-6. doi: 10.1016/j.neulet.2010.01.030. Epub 2010 Jan 25.
7
Increased serum HMGB1 is related to the severity of coronary artery stenosis.血清高迁移率族蛋白B1升高与冠状动脉狭窄的严重程度相关。
Clin Chim Acta. 2009 Aug;406(1-2):139-42. doi: 10.1016/j.cca.2009.06.016. Epub 2009 Jun 21.
8
Increased serum HMGB1 level is associated with coronary artery disease in nondiabetic and type 2 diabetic patients.血清高迁移率族蛋白B1(HMGB1)水平升高与非糖尿病和2型糖尿病患者的冠状动脉疾病有关。
Atherosclerosis. 2009 Aug;205(2):544-8. doi: 10.1016/j.atherosclerosis.2008.12.016. Epub 2008 Dec 14.
9
Role of high-mobility group box 1 protein in post-infarction healing process and left ventricular remodelling.高迁移率族蛋白盒1在心肌梗死后愈合过程及左心室重构中的作用
Cardiovasc Res. 2009 Feb 15;81(3):565-73. doi: 10.1093/cvr/cvn291. Epub 2008 Nov 3.
10
Predictive value of coronary artery stenoses and C-reactive protein levels in patients with stable coronary artery disease.稳定型冠状动脉疾病患者冠状动脉狭窄和C反应蛋白水平的预测价值
Atherosclerosis. 2009 May;204(1):239-43. doi: 10.1016/j.atherosclerosis.2008.08.009. Epub 2008 Aug 15.

阿托伐他汀可降低高脂血症患者血清中高迁移率族蛋白B1(HMGB1)的水平。

Atorvastatin reduces serum HMGB1 levels in patients with hyperlipidemia.

作者信息

Jin Daoqun, Wu Yongbo, Zhao Lin, Guo Jie, Zhang Kai, Chen Zhiqiang

机构信息

Department of Cardiology, Central Hospital of Huangshi, Huangshi, P.R. China.

出版信息

Exp Ther Med. 2012 Dec;4(6):1124-1126. doi: 10.3892/etm.2012.732. Epub 2012 Oct 1.

DOI:10.3892/etm.2012.732
PMID:23226786
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3494102/
Abstract

High mobility group box 1 protein (HMGB1) has been identified as a novel pro-inflammatory cytokine in coronary artery disease. This study investigated the effect of atorvastatin on serum HMGB1 levels in patients with hyperlipidemia. In 72 patients with hyperlipidemia, serum total cholesterol (TC), triglycerides (TG), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDL-C) and high-sensitivity C-reactive protein (hs-CRP) were compared with the levels in 32 control patients. In hyperlipidemic patients, serum HMGB1 levels were also determined by ELISA before and after a 3-month treatment of atorvastatin (20 mg/day). TC and LDL-C levels in the hyperlipidemic group (6.37±0.94 and 4.99±0.75 mmol/l, respectively) were significantly higher compared to those in the control group (4.34±0.89 and 2.57±0.82 mmol/l, respectively) (both P<0.05). Hs-CRP and HMGB1 levels in the hyperlipidemic group (3.91±1.06 mg/l and 5.42±1.56 ng/ml, respectively) were also significantly higher compared to those in the control group (1.53±0.45 mg/l and 2.11±0.95 ng/ml, respectively) (both P<0.05). After treatment with atorvasatin for three months, TC and LDL-C levels in the hyperlipidemic group were significantly decreased compared to those prior to treatment (TC, 4.67±0.89 vs. 6.37±0.94 mmol/l and LDL-C, 2.75±0.92 vs. 4.99±0.75 mmol/l, respectively) (both P<0.05). HMGB1 and hs-CRP levels in the hyperlipidemic group (3.07±1.24 ng/ml and 1.87±0.79 mg/l, respectively) were also significantly decreased compared to levels prior to treatment (5.42±1.56 ng/ml and 3.91±1.06 mg/l, respectively) (both P<0.05). Serum HMGB1 levels are increased in patients with hyperlipidemia which could be reduced by atorvastatin.

摘要

高迁移率族蛋白B1(HMGB1)已被确认为冠状动脉疾病中的一种新型促炎细胞因子。本研究调查了阿托伐他汀对高脂血症患者血清HMGB1水平的影响。将72例高脂血症患者的血清总胆固醇(TC)、甘油三酯(TG)、高密度脂蛋白胆固醇(HDL-C)、低密度脂蛋白胆固醇(LDL-C)和高敏C反应蛋白(hs-CRP)水平与32例对照患者的水平进行比较。在高脂血症患者中,还通过酶联免疫吸附测定法(ELISA)在阿托伐他汀(20毫克/天)治疗3个月前后测定血清HMGB1水平。高脂血症组的TC和LDL-C水平(分别为6.37±0.94和4.99±0.75毫摩尔/升)显著高于对照组(分别为4.34±0.89和2.57±0.82毫摩尔/升)(均P<0.05)。高脂血症组的hs-CRP和HMGB1水平(分别为3.91±1.06毫克/升和5.42±1.56纳克/毫升)也显著高于对照组(分别为1.53±0.45毫克/升和2.11±0.95纳克/毫升)(均P<0.05)。阿托伐他汀治疗三个月后,高脂血症组的TC和LDL-C水平与治疗前相比显著降低(TC,4.67±0.89对6.37±0.94毫摩尔/升;LDL-C,2.75±0.92对4.99±0.75毫摩尔/升)(均P<0.05)。高脂血症组的HMGB1和hs-CRP水平(分别为3.07±1.24纳克/毫升和1.87±0.79毫克/升)也与治疗前水平(分别为5.42±1.56纳克/毫升和3.91±1.06毫克/升)相比显著降低(均P<0.05)。高脂血症患者的血清HMGB1水平升高,但可通过阿托伐他汀降低。