Nd. Nader et al., Systemic perfluorocarbons suppress the acute lung inflammation after gastric acid aspiration in rats, ANESTH ANAL, 90(2), 2000, pp. 356-361
Citations number
30
Categorie Soggetti
Aneshtesia & Intensive Care","Medical Research Diagnosis & Treatment
Perflurocarbons (PFCs) are used during Liquid ventilation and as hemoglobin
substitutes. PFCs reduce free radical generation and damage to the lung du
ring Liquid ventilation. Thus, we examined the effects of parenteral admini
stration of PFCs on lung injury after acid aspiration. Rats were treated wi
th intraperitoneal injection of either FC-77 or IV injection of Fluosol. Co
ntrols received intraperitoneal or IV normal saline (NS) before or at the t
ime of injury and then were injured by instillation of NS + HCl (pH = 1.25)
into their lungs via a tracheotomy. The animals were exposed to air or 98%
oxygen, breathing spontaneously. The rats were injected with 0.05 mu Ci of
I-125-albumin (bovine serum albumin) before injury. The extent of lung inj
ury was assessed 5 h postinjury by compliance and lung albumin permeability
index measurement. Myeloperoxidase (MPO) activity and histologic examinati
on were used to assess neutrophilic infiltration. Both FC-77 and Fluosol de
creased the permeability index compared with controls (1.05 +/- 0.08: 1.08
+/- 0.12 respectively, versus 1.34 +/- 0.21) and improved lung compliance a
fter intratracheal instillation of 1.2 mL/kg of HCl/NS, pH = 1.25 + hyperox
ia injury (P < 0.05). Lung MPO activity decreased in the FC-77 group and wa
s associated with a concomitant decrease in neutrophil infiltration. MPO ac
tivity of the spleen increased after FC-77 treatment. The administration of
FC-77 decreased the severity of lung permeability changes associated with
acid in the presence or absence of hyperoxia exposure. These data suggest t
hat attenuation of neutrophilic infiltration by PFCs decreases lung injury.
Implications: Intraperitoneally administered perfluorocarbons in rats atte
nuate the neutrophilic infiltration in the lung after acid aspiration, ther
eby decreasing the alveolar protein leakage and improving pulmonary complia
nce.