INHIBITION OF PULMONARY SURFACTANT BIOPHYSICAL ACTIVITY BY CATIONIC POLYAMINO ACIDS

被引:10
作者
BUMMER, PM [1 ]
AZIZ, S [1 ]
GILLESPIE, MN [1 ]
机构
[1] UNIV KENTUCKY,COLL PHARM,DIV PHARMACOL & EXPTL THERAPEUT,LEXINGTON,KY 40536
关键词
PULMONARY SURFACTANT; MONOLAYER; SURFACE PRESSURE; POLYAMINO ACID;
D O I
10.1023/A:1016297118227
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Purpose. The purpose of this study is to investigate the interaction of cationic polyamino acids, polylysine and polyarginine, with rat pulmonary surfactant at the air/water interface. Methods. Surface pressure measurements of rat pulmonary surfactant in the presence and absence of polyamino acids were carried out in both dynamic and static modes. Results. In dynamic cycle studies, compression and expansion of adsorbed surfactant films in the presence of the cationic polyamino acids resulted in a delayed attainment of the plateau surface pressure. In area studies of spread surfactant films at constant surface pressure, cationic polyamino acids in the subphase resulted in an increase in film area. Increased film area was also observed when a polyamino acid was injected beneath films of dipalmitoyl-phosphatidylcholine/phosphatidylglycerol. In the presence of the cationic polyamino acids, the equilibrium surface pressure (at constant film area) of pulmonary surfactant was elevated in a concentration- and molecular weight-dependent manner. Conclusions, These data indicate that the model cationic peptides interact with surfactant lipid, possibly electrostatically with phosphatidylglycerol. It is concluded that the surface activity of pulmonary surfactant is significantly inhibited by the presence of the polycations, possibly by the formation of a mixed lipid/polyamino acid film.
引用
收藏
页码:1658 / 1663
页数:6
相关论文
共 29 条
[1]   REVERSIBLE AND IRREVERSIBLE INACTIVATION OF PREFORMED PULMONARY SURFACTANT SURFACE-FILMS BY CHANGES IN SUBPHASE CONSTITUENTS [J].
AMIRKHANIAN, JD ;
TAEUSCH, HW .
BIOCHIMICA ET BIOPHYSICA ACTA, 1993, 1165 (03) :321-326
[2]   PHYSICAL-PROPERTIES OF AN EFFECTIVE LUNG SURFACTANT [J].
BANGHAM, AD ;
MORLEY, CJ ;
PHILLIPS, MC .
BIOCHIMICA ET BIOPHYSICA ACTA, 1979, 573 (03) :552-556
[3]  
Birdi KS, 1989, LIPID BIOPOLYMER MON
[4]   SQUEEZE-OUT FROM MIXED MONOLAYERS OF DIPALMITOYLPHOSPHATIDYLCHOLINE AND EGG PHOSPHATIDYLGLYCEROL [J].
BOONMAN, A ;
MACHIELS, FHJ ;
SNIK, AFM ;
EGBERTS, J .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1987, 120 (02) :456-468
[5]   PENETRATION OF PHOSPHOLIPID MONOLAYERS BY CARDIOTOXINS [J].
BOUGIS, P ;
ROCHAT, H ;
PIERONI, G ;
VERGER, R .
BIOCHEMISTRY, 1981, 20 (17) :4915-4920
[6]   SURFACTANT DISPOSITION IN RATS WITH MONOCROTALINE-INDUCED PNEUMOTOXICITY [J].
BUMMER, PM ;
BAUGHN, JA ;
SANDERS, LP ;
ABSHER, KR ;
OCONNOR, WN ;
OLSON, JW ;
GILLESPIE, MN .
TOXICOLOGY, 1994, 90 (1-2) :53-62
[7]  
Chien YW, 1992, NOVEL DRUG DELIVERY
[8]   SURFACE-ANALYSIS OF LIPID LAYERS AT AIR WATER INTERFACES [J].
CHUNG, JB ;
HANNEMANN, RE ;
FRANSES, EI .
LANGMUIR, 1990, 6 (11) :1647-1655
[9]  
Creighton T. E., 1984, PROTEINS STRUCTURES, V2nd
[10]   SPECIFIC INTERACTION OF MYELIN BASIC PROTEIN WITH LIPIDS AT AIR-WATER INTERFACE [J].
DEMEL, RA ;
LONDON, Y ;
GEURTSVA.WS ;
VOSSENBERG, FG ;
VANDEENE.LL .
BIOCHIMICA ET BIOPHYSICA ACTA, 1973, 311 (04) :507-519