Synergistic effect of a recombinant N-terminal fragment of bactericidal/permeability-increasing protein and cefamandole in treatment of rabbit gram-negative sepsis

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Veröffentlicht in:	Antimicrobial Agents and Chemotherapy 1996-01, Vol.40 (1), p.65-69
Hauptverfasser:	LIN, Y, LEACH, W. J, AMMONS, W. S
Format:	Artikel
Sprache:	eng
Schlagworte:	Amino Acid Sequence Animals Anti-Infective Agents Anti-Infective Agents - therapeutic use Anti-Infective Agents - toxicity Antibacterial agents Antibiotics. Antiinfectious agents. Antiparasitic agents Antimicrobial Cationic Peptides Biological and medical sciences Blood Gas Analysis Blood Glucose - metabolism Blood Proteins Blood Proteins - chemistry Blood Proteins - therapeutic use Blood Proteins - toxicity Cefamandole Cefamandole - therapeutic use Cefamandole - toxicity Cephalosporins Cephalosporins - therapeutic use Cephalosporins - toxicity Colony Count, Microbial Drug Synergism Endotoxins - blood Escherichia coli Infections Escherichia coli Infections - blood Escherichia coli Infections - drug therapy Escherichia coli Infections - mortality Escherichia coli Infections - physiopathology Hemodynamics - drug effects Lactates - blood Male Medical sciences Membrane Proteins Pharmacology. Drug treatments Rabbits Recombinant Proteins Recombinant Proteins - therapeutic use Recombinant Proteins - toxicity Shock, Septic Shock, Septic - blood Shock, Septic - drug therapy Shock, Septic - mortality Shock, Septic - physiopathology
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Zusammenfassung:	Services AAC Citing Articles Google Scholar PubMed Related Content Social Bookmarking CiteULike Delicious Digg Facebook Google+ Mendeley Reddit StumbleUpon Twitter current issue AAC About AAC Subscribers Authors Reviewers Advertisers Inquiries from the Press Permissions & Commercial Reprints ASM Journals Public Access Policy AAC RSS Feeds 1752 N Street N.W. • Washington DC 20036 202.737.3600 • 202.942.9355 fax • journals@asmusa.org Print ISSN: 0066-4804 Online ISSN: 1098-6596 Copyright © 2014 by the American Society for Microbiology. For an alternate route to AAC .asm.org, visit: AAC
ISSN:	0066-4804 1098-6596
DOI:	10.1128/aac.40.1.65