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Profile of the bovine acute-phase response following an intravenous bolus-dose lipopolysaccharide challengeUSDA-ARS Livestock Issues Research Unit, Lubbock, Texas, USA, jeff.carroll{at}ars.usda.gov
Department of Animal and Food Sciences, Texas Tech University, Lubbock, Texas, USA
USDA-ARS, SubTropical Agricultural Research Station, Brooksville, Florida, USA
USDA-ARS, SubTropical Agricultural Research Station, Brooksville, Florida, USA
USDA-ARS, SubTropical Agricultural Research Station, Brooksville, Florida, USA
Animal Science Division, University of Missouri-Columbia, Missouri, USA
University of Florida-IFAS, Range Cattle Research & Education Center, Ona, Florida, USA
Department of Animal and Food Sciences, Texas Tech University, Lubbock, Texas, USA
Our objective was to characterize further the acute-phase response following endotoxin (i.e. lipopolysaccharide; LPS) exposure in the bovine. Nine pure-bred Angus castrated males (i.e. steers; average body weight = 299 ± 5 kg) were used in a randomized complete block design in environmentally controlled chambers, set at thermoneutral level, to characterize the acute physiological, endocrine, immune, and acute-phase protein responses following an i.v. bolus administration of 2.5 µg of LPS/kg body weight. One day before administration of LPS, all steers were fitted with an indwelling jugular vein catheter for serial blood collection. Blood samples were collected at 30-min intervals from -2 h to 8 h relative to the LPS challenge (time 0), and serum was harvested and stored at -80 °C until analyzed for concentrations of cortisol, pro-inflammatory cytokines, and acute-phase proteins. Indicators of thermal status (i.e. rectal temperature, ruminal temperature, respiration rate, sweat rate, and skin temperatures) were measured at 30-min intervals from -1 h to 6 h relative to the challenge. Endotoxin exposure increased (P<0.05) serum concentrations of cortisol, tumor necrosis factor-
Key Words: Acute-phase response acute-phase proteins bovine cytokines lipopolysaccharide
Innate Immunity, Vol. 15, No. 2,
81-89 (2009) This article has been cited by other articles:
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