Del Maestro R F
Can J Physiol Pharmacol. 1982 Nov;60(11):1406-14. doi: 10.1139/y82-209.
Inflammation is associated with the accumulation and activation of phagocytic cells, such as polymorphonuclear leukocytes, and with the subsequent release and generation of a group of activated oxygen species, some of which are free radicals. These studies were carried out to assess the influence of enzymatically generated free radicals on both microvascular permeability and leukocyte adhesion. The extravasation of fluorescein-labelled dextran mean molecular weight (MW) 150 000 was used to assess microvascular permeability and methodology was developed to measure in vivo leukocyte endothelial interactions. Enzymatically generated superoxide anion radical (O-.2) was associated with an increase in macromolecular extravasation (seen primarily from postcapillary venules) and an increase in leukocyte adhesion. Macromolecular extravasation was found to be dependent on the generation of a hydroxyl radical related interaction while leukocyte adhesion was dependent on the presence of O-.2. It is suggested that the permeability alterations and increased polymorphonuclear leukocyte adhesion seen during inflammation may be partially related to the release of free radicals from inflammatory cells.
炎症与吞噬细胞(如多形核白细胞)的聚集和激活有关,也与随后一组活性氧的释放和产生有关,其中一些是自由基。进行这些研究是为了评估酶促产生的自由基对微血管通透性和白细胞黏附的影响。用平均分子量(MW)为150000的荧光素标记葡聚糖的外渗来评估微血管通透性,并开发了测量体内白细胞与内皮细胞相互作用的方法。酶促产生的超氧阴离子自由基(O₂⁻)与大分子外渗增加(主要见于毛细血管后微静脉)和白细胞黏附增加有关。发现大分子外渗依赖于与羟自由基相关的相互作用的产生,而白细胞黏附则依赖于O₂⁻的存在。有人提出,炎症期间所见的通透性改变和多形核白细胞黏附增加可能部分与炎症细胞释放自由基有关。