Lehr H A, Kress E, Menger M D, Friedl H P, Hübner C, Arfors K E, Messmer K
Institute for Surgical Research, University of Munich, Germany.
Free Radic Biol Med. 1993 Jun;14(6):573-81. doi: 10.1016/0891-5849(93)90138-k.
Although cigarette smoking has been identified as a major risk factor for cardiovascular diseases, the underlying pathomechanism is largely unknown. Using a dorsal skinfold chamber model in Syrian golden hamsters for intravital microscopy on striated muscle microcirculation, we investigated whether cigarette smoke (CS) affects the adhesion of circulating leukocytes to the endothelium, a constant feature of early atherogenesis and a hallmark of ischemia-reperfusion injury. Awake hamsters were exposed for 5 min to the mainstream smoke of one cigarette (2R1 research cigarette), inducing nicotine, cotinine, and carboxyhemoglobin plasma levels comparable to levels found in human smokers. In control animals (n = 7), CS exposure elicited the rolling and subsequent adhesion of fluorescently stained leukocytes to the endothelium of arterioles and postcapillary venules. Leukocyte/endothelium interaction was preceded by an early rise in xanthine oxidase activity and intravascular hemolysis. Leukocyte adhesion and xanthine oxidase (XO) activation were significantly attenuated in hamsters pretreated with superoxide dismutase (5 mg/kg, 10 min prior to CS, n = 7), suggesting a key role of superoxide in this event. These in vivo results suggest a novel pathomechanism of CS-induced cardiovascular pathology.
尽管吸烟已被确认为心血管疾病的主要危险因素,但其潜在的发病机制在很大程度上尚不清楚。我们使用叙利亚金黄地鼠的背部皮褶腔模型进行横纹肌微循环的活体显微镜检查,研究香烟烟雾(CS)是否会影响循环白细胞与内皮的黏附,这是早期动脉粥样硬化的一个持续特征,也是缺血再灌注损伤的一个标志。清醒的地鼠暴露于一支香烟(2R1研究香烟)的主流烟雾中5分钟,诱导血浆中尼古丁、可替宁和羧基血红蛋白水平与人类吸烟者体内的水平相当。在对照动物(n = 7)中,CS暴露引发了荧光染色的白细胞在小动脉和毛细血管后微静脉内皮上的滚动及随后的黏附。白细胞/内皮相互作用之前,黄嘌呤氧化酶活性和血管内溶血会提前升高。用超氧化物歧化酶预处理的地鼠(5 mg/kg,在CS暴露前10分钟,n = 7),白细胞黏附和黄嘌呤氧化酶(XO)激活显著减弱,这表明超氧化物在这一过程中起关键作用。这些体内实验结果提示了CS诱导心血管病变的一种新发病机制。