Suzuki S, Tanita T, Kubo H, Ashino Y, Chida M, Koike K, Fujimura S
Department of Surgery, Tohoku University, Sendai, Japan.
Tohoku J Exp Med. 1993 Feb;169(2):121-30. doi: 10.1620/tjem.169.121.
The purpose of this study is to determine if stimulation of pulmonary intravascular macrophages (PIMs) increase microvascular permeability in sheep. We infused latex microbeads, 1 micron in diameter, for 1 hr continuously and analysed lung hemodynamic and lymph-dynamic changes. More than 70% of latex microbeads in the lung were assigned to PIMs, and caught in their phagosomes as determined by morphological examination. This implies that infused latex microbeads predominantly stimulate PIMs. Pulmonary arterial pressure increased during the infusion period, and returned to baseline after the infusion period. Lung lymph flow increased and remained high while the lymph to plasma protein ratio ultimately increased above baseline. This implies that infusion of latex microbeads increases pulmonary microvascular permeability. The increase in lung lymph protein clearance was blocked completely by pretreatment with indomethacin, but not with a thromboxane synthetase inhibitor (OKY-046). These data indicate that the increase in microvascular permeability is mediated by an arachidonic acid cyclooxygenase metabolites but not by thromboxane. We conclude that PIMs can act as an initiator to increase pulmonary microvascular permeability by releasing arachidonic acid cyclooxygenase metabolites through their stimulation with latex beads.
本研究的目的是确定刺激肺血管内巨噬细胞(PIMs)是否会增加绵羊的微血管通透性。我们持续1小时连续输注直径为1微米的乳胶微珠,并分析肺血流动力学和淋巴动力学变化。通过形态学检查确定,肺中超过70%的乳胶微珠被PIMs摄取,并被困在它们的吞噬体中。这意味着输注的乳胶微珠主要刺激PIMs。输注期间肺动脉压升高,输注期后恢复至基线。肺淋巴流量增加并维持在较高水平,而淋巴与血浆蛋白比值最终升高至基线以上。这意味着输注乳胶微珠会增加肺微血管通透性。肺淋巴蛋白清除率的增加被吲哚美辛预处理完全阻断,但血栓素合成酶抑制剂(OKY-046)则不能阻断。这些数据表明,微血管通透性的增加是由花生四烯酸环氧化酶代谢产物介导的,而非血栓素。我们得出结论,PIMs可作为启动因子,通过乳胶微珠刺激释放花生四烯酸环氧化酶代谢产物来增加肺微血管通透性。