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肉桂醛通过诱导 HO-1 减轻大鼠心肌缺血再灌注损伤。

2-methoxycinnamaldehyde from Cinnamomum cassia reduces rat myocardial ischemia and reperfusion injury in vivo due to HO-1 induction.

机构信息

Department of Urology, School of Medicine, Gyeongsang National University, Jinju, Republic of Korea.

出版信息

J Ethnopharmacol. 2012 Jan 31;139(2):605-15. doi: 10.1016/j.jep.2011.12.001. Epub 2011 Dec 9.

Abstract

ETHNOPHARMACOLOGICAL RELEVANCE

Cinnamomum cassia Blume has been used as a traditional Chinese herbal medicine for alleviation of fever, inflammation, chronic bronchitis, and to improve blood circulation.

AIM OF THE STUDY

We addressed whether 2-methoxycinnamaldehyde (2-MCA), one of active ingredients of Cinnamomum cassia, reduces vascular cell adhesion molecule-1 (VCAM-1) expression in tumor necrosis factor-alpha (TNF-α)-activated endothelial cells and protects ischemia/reperfusion (I/R)-injury due to heme oxygenase (HO)-1 induction.

MATERIALS AND METHODS

Adult male rats were subjected to 30 min of ischemia by occlusion of the left anterior descending coronary artery followed by 24h of reperfusion. Rats were randomized to receive vehicle or 2-MCA (i.v.) 10 min before reperfusion.

RESULTS

Administration of 2-MCA significantly improved I/R-induced myocardial dysfunction by increasing the values of the first derivative (±dp/dt) of left ventricular pressure and decreased infarct size. In addition, 2-MCA reduced the expression of high mobility group box 1 (HMGB1), an activator of the inflammatory cascade when released into the extracellular space, and VCAM-1 in I/R myocardium along with increase of HO-1 induction. The reduced injury was accompanied by significantly reduction of neutrophils infiltration and increased SOD activity in ischemic tissues and reduced serum level of cardiac troponin I (cTnI). Furthermore, 2-MCA significantly increased HO-1 induction by translocation of Nrf-2 from cytosol to nucleus in endothelial cells. Inhibition of VCAM-1 expression by 2-MCA was reversed both by SnPPIX, a HO-1 inhibitor and siHO-1 RNA trasfection in TNF-α-activated cells. In addition, 2-MCA significantly inhibited NF-κB luciferase activity in TNF-α-activated endothelial cells. As expected, 2-MCA significantly inhibited monocyte (U937) adhesion to endothelial cells.

CONCLUSION

We concluded that 2-MCA protects of myocardial I/R-injury due to antioxidant and anti-inflammatory action possibly by HO-1 induction which can be explained why Cinnamomum cassia has been used in inflammatory disorders.

摘要

ETHNOPHARMACOLOGICAL 相关性:肉桂 Cinnamomum cassia Blume 已被用作传统中药,用于缓解发热、炎症、慢性支气管炎,并改善血液循环。

研究目的

我们研究了 2-甲氧基肉桂醛(2-MCA),肉桂 Cinnamomum cassia 的一种活性成分,是否可以降低肿瘤坏死因子-α(TNF-α)激活的内皮细胞中血管细胞粘附分子-1(VCAM-1)的表达,并通过诱导血红素加氧酶(HO-1)来保护缺血/再灌注(I/R)损伤。

材料和方法

成年雄性大鼠通过阻塞左前降支冠状动脉缺血 30 分钟,然后再灌注 24 小时。大鼠随机接受载体或 2-MCA(静脉注射)在再灌注前 10 分钟。

结果

2-MCA 显著改善了 I/R 引起的心肌功能障碍,增加了左心室压力的一阶导数(±dp/dt)值,并减少了梗塞面积。此外,2-MCA 降低了高迁移率族蛋白 B1(HMGB1)的表达,HMGB1 是细胞外空间释放的炎症级联的激活剂,以及 I/R 心肌中的 VCAM-1,同时增加了 HO-1 的诱导。减少损伤伴随着缺血组织中中性粒细胞浸润的显著减少和 SOD 活性的增加以及血清中心脏肌钙蛋白 I(cTnI)水平的降低。此外,2-MCA 通过 Nrf-2 从细胞质向内皮细胞核易位,显著增加了 HO-1 的诱导。2-MCA 在 TNF-α 激活的细胞中通过 HO-1 抑制剂 SnPPIX 和 siHO-1 RNA 转染逆转了 VCAM-1 的表达抑制。此外,2-MCA 显著抑制了 TNF-α 激活的内皮细胞中的 NF-κB 荧光素酶活性。正如预期的那样,2-MCA 显著抑制了单核细胞(U937)与内皮细胞的粘附。

结论

我们得出结论,2-MCA 通过 HO-1 诱导来保护心肌 I/R 损伤,这可能是由于抗氧化和抗炎作用,这可以解释为什么肉桂 Cinnamomum cassia 被用于炎症性疾病。

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