Saito M, Shima C, Takagi M, Ogino M, Katori M, Majima M
Department of Pharmacology, Kitasato University, School of Medicine, Sagamihara, Kanagawa, Japan.
Inflamm Res. 2002 Jul;51(7):324-31. doi: 10.1007/pl00000311.
The present experiments were performed to ascertain whether or not all plasma components are extravasated when vascular permeability is increased.
Male Sprague-Dawley strain rats (specific pathogen-free) 8 weeks old (for histamine exudation) or 9-10 weeks old (for carrageenin pleurisy) were used.
Histamine or A-carrageenin was injected into the rat right pleural cavity to induce rat pleurisy. Protein components in the inflammatory exudate and plasma were separated by high performance liquid chromatography. Coagulation time was assessed, and the fibrinogen levels in the pleural exudate were determined by thrombin time. The fibrinogen levels were also visualized by immunoblot analysis. Tumor necrosis factor-alpha (TNF-alpha, 0.4 microg/rat, intrapleurally), anti-rat CD18 monoclonal antibody (anti-CD18 antibody, 1 mg/kg, i. v.) and granulocyte-colony stimulating factor (G-CSF, 100 microg/kg, s.c. twice daily for 4 days) were used.
In the histamine-induced extravasation, the level of plasma protein components with large molecules over 900 kD in the exudate was 62% of that in the rat's own plasma. The amount of fibrinogen in the pleural exudate was 1/8 of that in the plasma and was faintly detected in immunoblot analysis, but it was clearly detected after the treatment of rats with TNF-alpha. In rat carrageenin pleurisy, fibrinogen was hardly detected in immunoblot analysis in the exudate collected 0.5 h after carrageenin, when neutrophils did not migrate into the exudate. However, it was clearly present after neutrophil migration started 2 h later The increase in the neutrophil counts in the exudate caused by G-CSF enhanced the fibrinogen level in the exudate, whereas intravenous injection of anti-CD18 antibody suppressed the fibrinogen level in immunoblot analysis.
Venular permeability increase in the rat histamine exudation induced minimal extravasation of plasma proteins with large molecules, such as fibrinogen, while fibrinogen molecule was detected in rat carrageenin-injected pleurisy, when neutrophil diapedesis occurred. Thus, only when neutrophils started to migrate into the perivascular space was fibrinogen clearly detected in the exudate.
进行本实验以确定当血管通透性增加时,血浆中的所有成分是否都会外渗。
使用8周龄(用于组胺渗出实验)或9 - 10周龄(用于角叉菜胶性胸膜炎实验)的雄性斯普拉格 - 道利品系大鼠(无特定病原体)。
将组胺或α - 角叉菜胶注入大鼠右胸腔以诱导大鼠胸膜炎。通过高效液相色谱法分离炎性渗出液和血浆中的蛋白质成分。评估凝血时间,并通过凝血酶时间测定胸腔渗出液中的纤维蛋白原水平。还通过免疫印迹分析观察纤维蛋白原水平。使用肿瘤坏死因子 - α(TNF - α,0.4微克/大鼠,胸腔内注射)、抗大鼠CD18单克隆抗体(抗CD18抗体,1毫克/千克,静脉注射)和粒细胞集落刺激因子(G - CSF,100微克/千克,皮下注射,每日两次,共4天)。
在组胺诱导的外渗中,渗出液中分子量超过900 kD的大分子血浆蛋白成分水平为大鼠自身血浆中的62%。胸腔渗出液中的纤维蛋白原量为血浆中的1/8,在免疫印迹分析中仅能微弱检测到,但在用TNF - α处理大鼠后可清晰检测到。在大鼠角叉菜胶性胸膜炎中,在注射角叉菜胶后0.5小时收集的渗出液中,当嗜中性粒细胞未迁移到渗出液中时,免疫印迹分析几乎检测不到纤维蛋白原。然而,在2小时后嗜中性粒细胞迁移开始后,纤维蛋白原明显存在。G - CSF引起的渗出液中嗜中性粒细胞计数增加增强了渗出液中的纤维蛋白原水平,而静脉注射抗CD18抗体在免疫印迹分析中抑制了纤维蛋白原水平。
大鼠组胺渗出实验中静脉通透性增加导致大分子血浆蛋白(如纤维蛋白原)的外渗极少,而在注射角叉菜胶的大鼠胸膜炎中,当嗜中性粒细胞发生渗出时可检测到纤维蛋白原分子。因此,只有当嗜中性粒细胞开始迁移到血管周围间隙时,才能在渗出液中清晰检测到纤维蛋白原。