大株红景天对PM2.5暴露后缺血/再灌注大鼠心肌内质网应激诱导细胞凋亡的保护作用

Sofren Attenuates Myocardial Ischemia/Reperfusion Injury Aggravated by PM2.5 Exposure in Rats via Inhibiting Endoplasmic Reticulum Stress and Apoptosis

  • 摘要: 从心肌内质网应激及其诱导的细胞凋亡水平探讨PM2.5暴露对缺血/再灌注大鼠心肌损伤的影响,以及大株红景天的保护作用及其机制。方法 应用大气细颗粒物制备PM2.5生理盐水混悬液备用,取SPF级雄性SD大鼠48只随机分为4组:①假手术组(Sham组,n=12);②缺血/再灌注组(I/R组,n=12);③PM2.5联合缺血/再灌注组(PM2.5+I/R组,n=12);④大株红景天组(PM2.5+I/R+DZ组,n=12)。Sham、I/R组术前给予PM2.5相同体积生理盐水气管内滴注,每48h 1次共3次,Sham、I/R、PM2.5+I/R组术后予用药等体积的生理盐水腹腔注射,每日1次共3d。末次给药后检测各组大鼠超声心动图,实验结束麻醉下取大鼠心脏,Western blot及qPCR法分别检测心肌内质网应激相关蛋白GRP-78、XBP1、CHOP的表达水平,TUNEL法检测心肌细胞凋亡率。结果 与I/R组相比,PM2.5+I/R组左室射血分数(LVEF)及左室短轴缩短率(LVFS)显著降低,心肌细胞凋亡率增加,GRP-78、CHOP表达在转录和蛋白表达水平明显升高,XBP1s/XBP1u明显增大(P<0.01);与PM2.5+I/R相比,PM2.5+I/R+DZ组LVEF及LVFS明显增加,心肌细胞凋亡率降低,GRP-78、CHOP表达在转录和蛋白表达水平降低(P<0.01),XBP1s/XBP1u明显减小(P<0.05)。结论 PM2.5暴露可加重心肌缺血/再灌注损伤;大株红景天可改善PM2.5暴露后大鼠心功能及心肌缺血/再灌注导致的心肌损伤,其机制可能与抑制内质网应激及细胞凋亡相关。

     

    Abstract: OBJECTIVE To investigate the effect of PM2.5 exposure on myocardial ischemia-reperfusion injury(MIRI)in rats and the protective effect and mechanism of sofren injection from myocardial endoplasmic reticulum stress and apoptosis. METHODS Particulate matter of air was collected and suspended in saline. 48 SPF Sprague-Dawley male rats were randomly divided into 4 group:①Sham-operated group(n=12); ②I/R group(n=12);③PM+I/R group(n=12);④PM2.5+I/R+DZ group. Sham-operated group, I/R group were gave the same volume of PM2.5 normal saline through intratracheal instillation before surgery, once every 48 h for 3 times, Sham-operated group, I/R group and PM2.5+I/R group were injected the same volume of normal saline for 3 days. At the end of the experiment, echocardiography was detected after anesthesia. The expression of endoplasmic reticulum stress-related protein GRP-78, XBP1and CHOP were detected by western blot and qPCR ; TUNEL was used to detect the rate of cardiomyocyte apoptosis. RESULTS Compared with I/R group, left ventricular ejection fraction (LVEF) and left ventricular fractional shortening (LVFS) in PM2.5+I/R group decreased significantly, myocardial apoptosis rate increased significantly,GRP-78, CHOP transcription and protein levels and XBP1s/XBP1u increased significantly(P<0.01). Compared with PM2.5+I/R treatment group, LVEF and LVFS of DZ group increased significantly, myocardial apoptosis rate decreased, GRP-78,CHOP expression in transcription and protein levels decreased significantly(P<0.01),XBP1s/XBP1u decreased significantly(P<0.05). CONCLUSION Exposure to PM2.5 can aggravate MIRI. Treatment of sofren injection attenuates MIRI after PM2.5 exposure. The mechanism may be related to inhibition of endoplasmic reticulum stress and apoptosis.

     

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