Xie Hong, Wang Chen, Wu Xuemei, Liu Xia, Qiao Shigang, Liu Chunfeng, Liu Hong
Department of Anesthesiology, the Second Affiliated Hospital of Soochow University, Suzhou 215004, China;
J Biomed Res. 2012 Jan;26(1):37-43. doi: 10.1016/S1674-8301(12)60005-0.
Parthenolide (PTN), a selective nuclear factor kappa B (NF-κB) inhibitor, has been used extensively to inhibit NF-κB activation. The duration of the inhibitory effect of PTN on NF-κB in vivo remains unclear. This study was to determine whether a lipopolysaccharide (LPS) challenge 6, 12 and 24 h after the administration of PTN could activate NF-κB. Rats were devided into five groups. The rats in the PTN, PTN+LPS and DMSO groups were injected intraperitoneally with PTN or DMSO. After 6, 12 or 24 h, LPS was administered in LPS and PTN+LPS groups. The expressions of NF-κB p50, IκBα and p-IκBα were inhibited in both PTN and PTN+LPS group at end of 6 and 12 h and no effects at 24 h. In summary, myocardial NF-κB expression occurs 1 h after the administration of LPS. PTN blocks this effect given at 6 h and no inhibitory effect 24 h after administration in vivo.
小白菊内酯(PTN)是一种选择性核因子κB(NF-κB)抑制剂,已被广泛用于抑制NF-κB的激活。PTN在体内对NF-κB的抑制作用持续时间尚不清楚。本研究旨在确定在给予PTN后6、12和24小时进行脂多糖(LPS)刺激是否会激活NF-κB。将大鼠分为五组。PTN组、PTN+LPS组和DMSO组的大鼠腹腔注射PTN或DMSO。6、12或24小时后,LPS组和PTN+LPS组给予LPS。在6小时和12小时结束时,PTN组和PTN+LPS组中NF-κB p50、IκBα和p-IκBα的表达均受到抑制,而在24小时时无影响。总之,LPS给药1小时后心肌NF-κB表达出现。PTN在给药后6小时给予可阻断此效应,而在体内给药24小时后无抑制作用。