Immunofluorescent analysis of plasma fibronectin incorporation into the lung during acute inflammatory vascular injury.
Immunofluorescent analysis of plasma fibronectin incorporation into the lung during acute inflammatory vascular injury.
复制标题
急性炎症性血管损伤期间血浆纤连蛋白掺入肺部的免疫荧光分析。
DOI:
10.1164/ajrccm/148.2.467
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发表时间:
1993
期刊:
影响因子:
--
通讯作者:
Guinta,C
中科院分区:
文献类型:
--
作者:
Charash,WE;Vincent,PA;Saba,TM;Minnear,FL;McKeown-Longo,PJ;Migliozzi,JA;Lewis,MA;Lewis,E;Guinta,C
Adult male sheep (25 to 35 kg) were fasted of solid food for 48 h before surgery. General anesthesia was induced with 2.5% thiopental sodium (15 mg/kg: Abbott Laboratories, Chicago, IL). The animals were endotracheally intubated and mechanically ventilated (Harvard Apparatus, Mills, MA) at a rate of 18 breaths/min and a tidal volume of 12 ml/kg. The sheep were maintained on inhalation of 77.5 to 78% N20, 21% 02'and 1 to 1.5% halothane. Surgical preparation of the lung lymph fistula as well as the prefemoral lymph fistula was performed under sterile conditions during the same operative interval (1 to 1.5 h), as described previously (14). The surgical approach was through a right thoracotomy via the seventh intercostal space. For the lung fistula, the posterior portion of the caudal mediastinal lymph node was ligated to minimize contamination of lung lymph by diaphragmatic lymphatics. The right common carotid artery was aseptically cannulated with a polyethylene (PE-240) catheter impregnated with 2% tridodecylmethyl ammonium chloride-(TDMAC)-heparin complex. The external jugular vein was aseptically cannulated with a No. 8.5 French Cordis introducer (Cordis Laboratories, Miami, FL). The cannulas were externalized along the right lateral side of the neck. The incision was closed with No. 0 silk. Sheep recovered in a special postoperative metabolic recovery unit with free access to food and water.