Hydroxysafflor yellow A attenuates the expression of inflammatory cytokines in acute soft tissue injury

被引:30
作者
Dong, Fang [1 ]
Xue, Changjiang [1 ]
Wang, Yu [1 ]
Peng, Yuanyuan [1 ]
Zhang, Yadan [1 ]
Jin, Ming [1 ]
Zang, Baoxia [1 ]
机构
[1] Capital Med Univ, Beijing Inst Heart Lung & Blood Vessel Dis, Beijing Anzhen Hosp, Dept Pharmacol, Beijing, Peoples R China
基金
北京市自然科学基金;
关键词
TNF-ALPHA; MUSCLE; IL-6;
D O I
10.1038/srep40584
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
We examined the effect of hydroxysafflor yellow A (HSYA) on the inflammatory response to strike-induced acute soft tissue injury in rats. Soft tissue injury was induced in rat leg muscles using a strike hammer, followed by intraperitoneal administration of HSYA at 16, 32, or 64 mg/kg. After 24 h, the rats were anaesthetized, blood and muscle samples were taken. Plasma levels of interleukin (IL)-6, IL-1 beta, and tumour necrosis factor (TNF)-alpha were measured by enzyme-linked immunosorbent assay. Total RNA and protein were isolated from muscle tissue to determine the mRNA levels of IL-6, IL-1 beta, TNF-alpha, vascular cell adhesion molecule (VCAM)-1, and intercellular adhesion molecule (ICAM)-1, and the protein level of phosphorylated p38 mitogen-activated protein kinase (MAPK). Nuclear factor (NF)-kappa B expression was determined by muscle histopathology and immunohistochemistry. HSYA attenuated pathologic changes instrike-induced soft tissue inflammation. Treatment with HSYA also alleviated strike-induced increases in TNF-alpha, IL-1 beta, IL-6, VCAM-1, and ICAM-1mRNA levels and inhibited the increased activation of NF-kappa B and phosphorylation of p38 MAPK in muscle tissue. These findings suggest that HSYA effectively inhibits strike-induced inflammatory signal transduction in rats.
引用
收藏
页数:9
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