Effects of different doses of dexamethasone plus flunixin meglumine on survival rate in lethal endotoxemia.docVIP
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Effects of different doses of dexamethasone plus flunixin meglumine on survival rate in lethal endotoxemia
ActaVeterinaria(Beograd),Vol.59,No.1,47-51,2009.
DOI:10.2298/AVB0901047E
UDK619.615.276
EFFECTSOFDIFFERENTDOSESOFDEXAMETHASONEPLUSFLUNIXINMEGLUMINEON
SURVIVALRATEINLETHALENDOTOXEMIA
ERA*,UNEYK*,ALTANF**,CETING*,YAZARE*andELMASM*
*UniversityofSelcuk,FacultyofVeterinaryMedicine,DepartmentofPharmacologyandToxicology,
Campus,Konya,Turkey
**UniversityofDicle,FacultyofVeterinaryMedicine,DepartmentofPharmacologyandToxicology,
Campus,Diyarbakir,Turkey
(Received4.April2008)
Effects of different doses of dexamethasone plus flunixin
meglumineonsurvivalratewereinvestigatedinlethalendotoxemia.A
totalof60Balb/Cfemalemiceweredividedinto4equalgroups.Lethal
endotoxemia(80-100%)wasinducedbylipopolysaccharideinjection
(Group 1, 1 mg, intraperinoneally). At 4 hours after the lipopoly-
saccharide injection; low-dose dexamethasone (0.6 mg/kg, SID, 5
days, intramuscularly) + flunixin meglumine (2 mg/kg, SID, 5 days,
subcutaneously),normal-dosedexamethasone(2mg/kg,SID,5days,
intramuscularly) + flunixin meglumine (2 mg/kg, SID, 5 days,
subcutaneously) and high-dose dexamethasone (10 mg/kg, SID, 5
days, intramuscularly) + flunixin meglumine (2 mg/kg, SID, 5 days,
subcutaneously)wereinjectedtoGroup2,3and4,respectively.After
the injections, survival was monitored at 7 days and 13.3%, 13.3%,
33.3%and73.3%survivalrateswereobservedinGroups1,2,3and4,
respectively. As results, high-dose dexamethasone plus flunixin
meglumine may be the treatment of choice for endotoxaemia in
animals.
Key words: lethal endotoxaemia, dexamethasone, flunixin,
survivalrate
INTRODUCTION
Septic shock is defined as sepsis-induced persistent hypotension
accompaniedbyhypoperfusionabnormalitiesororgandysfunction.Themortality
rateis50-60%insepticshock.Lipopolysaccharides(LPS)playacriticalroleinthe
pathophysiology of septic shock (Annane et al., 2004; Sanchez, 2005). When
microbes or their products (LPS) are present in the bloodstream, the same
mechanisms that are beneficial in resolving a local infection become a
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