Souza Danielle G, Pinho Vanessa, Soares Adriana C, Shimizu Takao, Ishii Satoshi, Teixeira Mauro M
Departamento de Bioquímica e Imunologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil.
Br J Pharmacol. 2003 Jun;139(4):733-40. doi: 10.1038/sj.bjp.0705296.
1 The reperfusion of ischemic tissues may be associated with local and systemic inflammation that prevents the full benefit of blood flow restoration. The present study aimed to confirm a role for platelet-activating factor receptor(s) (PAFR) during ischemia and reperfusion injury by using genetically modified mice deficient in the PAFR (PAFR(-/-) mice) and to evaluate comparatively the effectiveness of pharmacological treatment using the PAFR antagonist UK-74,505 (modipafant). 2 The reperfusion of the ischemic superior mesenteric artery (SMA) induced marked local (intestine) and remote (lungs) tissue injury, as assessed by the increase in vascular permeability, neutrophil influx and intestinal hemorrhage and in the production of TNF-alpha. There was also a systemic inflammatory response, as shown by the increase in serum TNF-alpha concentrations and marked reperfusion-associated lethality. 3 After reperfusion of the ischemic SMA, PAFR(-/-) mice had little tissue or systemic inflammation and lethality was delayed, but not prevented, in these mice. Interestingly, the reperfusion-associated increases in tissue concentrations of IL-10 were significantly greater in PAFR(-/-) than wild-type mice. 4 Pretreatment with PAFR antagonist UK-74,505 (1 mg kg(-1)) markedly prevented tissue injury, as assessed by the increase in vascular permeability, neutrophil accumulation, hemorrhage and TNF-alpha concentrations in the intestine and lungs. In contrast, UK-74,505 failed to affect reperfusion-associated lethality and increases in serum TNF-alpha when used at 1 mg kg(-1). 5 Reperfusion-associated lethality and increase in serum TNF-alpha were only affected when a supra-maximal dose of the antagonist was used (10 mg kg(-1)). At this dose, UK-74,505 also induced a marked enhancement of reperfusion-associated increases in tissue concentrations of IL-10. However, at the same dose, UK-74,505 failed to prevent reperfusion-associated lethality in PAFR(-/-) mice any further. 6 The present studies using genetically modified animals and a receptor antagonist firmly establish a role of PAFR activation for the local, remote and systemic inflammatory injury and lethality which follows reperfusion of the ischemic SMA in mice. Moreover, it is suggested that high doses of PAFR antagonists need to be used if the real efficacy of these compounds is to be tested clinically.
1 缺血组织的再灌注可能与局部和全身炎症相关,这会妨碍血流恢复带来的全部益处。本研究旨在通过使用缺乏血小板活化因子受体(PAFR)的基因修饰小鼠(PAFR(-/-)小鼠)来证实PAFR在缺血再灌注损伤中的作用,并比较评估使用PAFR拮抗剂UK-74,505(莫地帕泛)进行药物治疗的效果。2 缺血肠系膜上动脉(SMA)的再灌注诱导了明显的局部(肠道)和远处(肺)组织损伤,通过血管通透性增加、中性粒细胞浸润、肠道出血以及TNF-α产生增加来评估。还存在全身炎症反应,表现为血清TNF-α浓度升高和明显的再灌注相关致死率。3 缺血SMA再灌注后,PAFR(-/-)小鼠几乎没有组织或全身炎症,并且这些小鼠的致死率延迟但未被阻止。有趣的是,PAFR(-/-)小鼠中与再灌注相关的IL-10组织浓度升高明显大于野生型小鼠。4 用PAFR拮抗剂UK-74,505(1 mg kg(-1))预处理可显著预防组织损伤,通过肠道和肺中血管通透性增加、中性粒细胞积聚、出血以及TNF-α浓度升高来评估。相比之下,UK-74,505以1 mg kg(-1)使用时未能影响再灌注相关致死率和血清TNF-α升高。5 仅当使用超最大剂量的拮抗剂(10 mg kg(-1))时,再灌注相关致死率和血清TNF-α升高才受到影响。在此剂量下,UK-74,505还诱导了再灌注相关的组织IL-10浓度升高的显著增强。然而,在相同剂量下,UK-74,505未能进一步预防PAFR(-/-)小鼠的再灌注相关致死率。6 本研究使用基因修饰动物和受体拮抗剂,明确证实了PAFR激活在小鼠缺血SMA再灌注后引起的局部、远处和全身炎症损伤及致死率中的作用。此外,提示如果要在临床上测试这些化合物的实际疗效,需要使用高剂量的PAFR拮抗剂。