Chandrasekar B, Melby P C, Troyer D A, Colston J T, Freeman G L
Department of Medicine, The University of Texas Health Science Center, South Texas Veterans Health Care System, San Antonio 78284-7872, USA.
Am J Pathol. 1998 Apr;152(4):925-34.
To characterize the kinetics of myocardial cytokine and inducible nitric oxide synthase (iNOS) expression in acute Chagasic cardiomyopathy, we studied a rat model of acute Trypanosoma cruzi infection. Rats were euthanized 36 hours and 5, 10, and 15 days after infection, and hearts were collected for histology, mRNA, and protein analyses. Histological analysis of myocardium showed a progressive increase in the number of amastigotes and mononuclear inflammatory cells. Organisms were first detected 5 days after intraperitoneal inoculation as isolated nests and became numerous by day 15. Northern blot analysis of total RNA revealed no signal for interleukin (IL)-1beta or tumor necrosis factor (TNF)-alpha and a weak signal for IL-6 in control hearts. High levels of expression for the three genes were detected in the infected animals at 36 hours after infection. Although IL-1beta and IL-6 levels increased steadily up to 10 days, TNF-alpha levels were the highest at 5 days, remained high at 10 days, and declined thereafter. Western blot analysis showed similar results to that of mRNA expression. No signal was detected for iNOS in the controls, but both its mRNA and protein were found in the infected animals, with levels being highest at 15 days after infection. Immunohistochemistry revealed no iNOS immunoreactivity in uninfected animals, but intense iNOS staining was detected in blood vessels of infected animals, which decreased progressively with period of infection. Positive staining for iNOS in cardiomyocytes was first detected at 36 hours after infection (at a time when there was no histological inflammatory reaction), which steadily increased, being the highest at 15 days after infection. These results indicate that, in addition to mechanical damage by T. cruzi, substantial pro-inflammatory cytokine production within the myocardium is likely to participate in the pathophysiology of acute Chagasic cardiomyopathy.
为了描述急性恰加斯病性心肌病中心肌细胞因子和诱导型一氧化氮合酶(iNOS)表达的动力学,我们研究了急性克氏锥虫感染的大鼠模型。在感染后36小时、5天、10天和15天对大鼠实施安乐死,并采集心脏进行组织学、mRNA和蛋白质分析。心肌组织学分析显示无鞭毛体和单核炎性细胞数量逐渐增加。腹腔接种后5天首次检测到病原体呈孤立巢状,到第15天数量增多。对总RNA进行Northern印迹分析发现,对照心脏中白细胞介素(IL)-1β或肿瘤坏死因子(TNF)-α无信号,IL-6有微弱信号。感染动物在感染后36小时检测到这三种基因的高水平表达。尽管IL-1β和IL-6水平在10天内稳步升高,但TNF-α水平在5天时最高,10天时仍很高,此后下降。蛋白质印迹分析结果与mRNA表达相似。对照中未检测到iNOS信号,但在感染动物中发现了其mRNA和蛋白质,感染后15天时水平最高。免疫组织化学显示未感染动物中无iNOS免疫反应性,但在感染动物的血管中检测到强烈的iNOS染色,且随感染时间逐渐减弱。感染后36小时首次在心肌细胞中检测到iNOS阳性染色(此时尚无组织学炎症反应),其水平稳步升高,在感染后15天时最高。这些结果表明,除了克氏锥虫的机械损伤外,心肌内大量促炎细胞因子的产生可能参与了急性恰加斯病性心肌病的病理生理过程。