PMID- 7582456 OWN - NLM STAT- MEDLINE DCOM- 19951127 LR - 20201209 IS - 0007-1188 (Print) IS - 0007-1188 (Linking) VI - 115 IP - 3 DP - 1995 Jun TI - Dose-response comparisons of five lung surfactant factor (LSF) preparations in an animal model of adult respiratory distress syndrome (ARDS). PG - 451-8 AB - 1. We have examined the effects of five different lung surfactant factor (LSF) preparations in the rat lung lavage model. In this model repetitive lung lavage leads to lung injury with some similarities to adult respiratory distress syndrome with poor gas exchange and protein leakage into the alveolar spaces. These pathological sequelae can be reversed by LSF instillation soon after lavage. 2. The tested LSF preparations were: two bovine: Survanta and Alveofact: two synthetic: Exosurf and a protein-free phospholipid based LSF (PL-LSF) and one Recombinant LSF at doses of 25, 50 and 100 mg kg-1 body weight and an untreated control group. 3. Tracheotomized rats (10-12 per dose) were pressure-controlled ventilated (Siemens Servo Ventilator 900C) with 100% oxygen at a respiratory rate of 30 breaths min-1, inspiration expiration ratio of 1:2, peak inspiratory pressure (PIP) of 28 cmH2O at positive end-expiratory pressure (PEEP) of 8 cmH2O. Two hours after LSF administration, PEEP and in parallel PIP was reduced from 8 to 6 (1st reduction), from 6 to 3 (2nd reduction) and from 3 to 0 cmH2O (3rd reduction). 4. Partial arterial oxygen pressure (PaO2, mmHg) at 5 min and 120 min after LSF administration and during the 2nd PEEP reduction (PaO2(PEEP23/3)) were used for statistical comparison. All LSF preparations caused a dose-dependent increase for the PaO2(120'), whereas during the 2nd PEEP reduction only bovine and recombinant LSF exhibited dose-dependency. Exosurf did not increase PaO2 after administration of the highest dose. At the highest dose Exosurf exerted no further improvement but rather a tendency to relapse. The bovine and the Recombinant LSF are superior to both synthetic LSFpreparations.5. In this animal model and under the described specific ventilatory settings, even between bovine LSFpreparations there are detectable differences that are pronounced when compared to synthetic LSFwithout any surfactant proteins. We conclude that the difference between bovine and synthetic LSFpreparations can be overcome by addition of the surfactant protein C. FAU - Hafner, D AU - Hafner D AD - Byk Gulden, Department of Respiratory Pharmacology, Konstanz, Germany. FAU - Beume, R AU - Beume R FAU - Kilian, U AU - Kilian U FAU - Krasznai, G AU - Krasznai G FAU - Lachmann, B AU - Lachmann B LA - eng PT - Comparative Study PT - Journal Article PL - England TA - Br J Pharmacol JT - British journal of pharmacology JID - 7502536 RN - 0 (Biological Products) RN - 0 (Drug Combinations) RN - 0 (Fatty Alcohols) RN - 0 (Lipids) RN - 0 (Phospholipids) RN - 0 (Pulmonary Surfactants) RN - 0 (Recombinant Proteins) RN - 0 (SF-RI 1, bovine surfactant preparation) RN - 107-73-3 (Phosphorylcholine) RN - 3WJQ0SDW1A (Polyethylene Glycols) RN - 99732-49-7 (dipalmitoylphosphatidylcholine, hexadecanol, tyloxapol drug combination) RN - S866O45PIG (beractant) SB - IM MH - Animals MH - *Biological Products MH - Blood Gas Analysis MH - Cattle MH - Disease Models, Animal MH - Dose-Response Relationship, Drug MH - Drug Combinations MH - Fatty Alcohols/administration & dosage/pharmacology/therapeutic use MH - Feasibility Studies MH - Lipids/administration & dosage/pharmacology/therapeutic use MH - Male MH - Partial Pressure MH - *Phospholipids MH - *Phosphorylcholine MH - Polyethylene Glycols/administration & dosage/pharmacology/therapeutic use MH - Positive-Pressure Respiration MH - Pulmonary Alveoli/drug effects MH - Pulmonary Gas Exchange/*drug effects MH - Pulmonary Surfactants/administration & dosage/pharmacology/*therapeutic use MH - Pulmonary Wedge Pressure/drug effects MH - Rats MH - Rats, Sprague-Dawley MH - Recombinant Proteins/pharmacology/therapeutic use MH - Respiratory Distress Syndrome/*drug therapy MH - Trachea/drug effects PMC - PMC1908419 EDAT- 1995/06/01 00:00 MHDA- 1995/06/01 00:01 PMCR- 1996/06/01 CRDT- 1995/06/01 00:00 PHST- 1995/06/01 00:00 [pubmed] PHST- 1995/06/01 00:01 [medline] PHST- 1995/06/01 00:00 [entrez] PHST- 1996/06/01 00:00 [pmc-release] AID - 10.1111/j.1476-5381.1995.tb16354.x [doi] PST - ppublish SO - Br J Pharmacol. 1995 Jun;115(3):451-8. doi: 10.1111/j.1476-5381.1995.tb16354.x.