Characterization of calves exhibiting a novel inheritable TNF-α hyperresponsiveness to endotoxin:: associations with increased pathophysiological complications

被引:25
作者
Elsasser, TH
Blum, JW
Kahl, S
机构
[1] USDA ARS, Growth Biol Lab, Beltsville, MD 20705 USA
[2] Univ Bern, Inst Anim Genet Nutr & Housing, Div Nutr & Physiol, Bern, Switzerland
关键词
cytokine; inflammatory stress; disease susceptibility;
D O I
10.1152/japplphysiol.01050.2004
中图分类号
Q4 [生理学];
学科分类号
071003 ;
摘要
A subpopulation of calves, herein termed "hyperresponders" (HPR), was identified and defined by the patterns of plasma TNF-alpha concentrations that developed following two challenges with endotoxin (LPS, 0.8 mu g Escherichia coli 055: B5 LPS/kg(0.75) live body wt) separated by 5 days. The principle characteristic of HPR calves was a failure to develop tolerance to repeated LPS challenge that was evident in the magnitude of the TNF-alpha concentrations and prolonged severity of pathological sequellae. Whereas calves failing to develop LPS tolerance were identified on the basis of their excessive in vivo plasma TNF-alpha concentration responses, in vitro TNF-alpha responses of peripheral blood mononuclear cells isolated from each calf and challenged with LPS or PMA did not correlate or predict the magnitude of in vivo plasma TNF response of the calf. Intentional breeding to obtain calves from bulls and/or cows documented as HPR resulted in offspring displaying the HPR character when similar progeny calves were tested with LPS in vivo, with extensive controls in place to account for sources of variability in the general TNF-alpha response to LPS that might compromise interpretation of the data. Feed intake, clinical serology and hematology profiles, and acute-phase protein responses of HPR calves following LPS were significantly different from those of calves displaying tolerance. These results suggest that the pattern of plasma TNF-alpha changes that evolve from a low-level double LPS challenge effectively reveal the presence of a genetic potential for animals to display excessive or prolonged pathological response to LPS-related stress and compromised prognosis for recovery.
引用
收藏
页码:2045 / 2055
页数:11
相关论文
共 73 条
[11]   Low molecular weight heparin prevents the pulmonary hemodynamic and pathomorphologic effects of endotoxin in a porcine acute lung injury model [J].
Darien, BJ ;
Fareed, J ;
Centgraf, KS ;
Hart, AP ;
MacWilliams, PS ;
Clayton, MK ;
Wolf, H ;
Kruse-Elliott, KT .
SHOCK, 1998, 9 (04) :274-281
[12]   Mechanisms underlying growth hormone effects in augmenting nitric oxide production and protein tyrosine nitration during endotoxin challenge [J].
Elsasser, TH ;
Kahl, S ;
Macleod, C ;
Nicholson, B ;
Sartin, JL ;
Li, CJ .
ENDOCRINOLOGY, 2004, 145 (07) :3413-3423
[13]   RECOMBINANT BOVINE SOMATOTROPIN BLUNTS PLASMA TUMOR-NECROSIS-FACTOR-ALPHA, CORTISOL, AND THROMBOXANE-B-2 RESPONSES TO ENDOTOXIN IN-VIVO [J].
ELSASSER, TH ;
FAYER, R ;
RUMSEY, TS ;
HARTNELL, GF .
ENDOCRINOLOGY, 1994, 134 (03) :1082-1088
[14]   Adrenomedullin has multiple roles in disease stress: Development and remission of the inflammatory response [J].
Elsasser, TH ;
Kahl, S .
MICROSCOPY RESEARCH AND TECHNIQUE, 2002, 57 (02) :120-129
[15]  
Elsasser TH, 2000, BIOLOGY OF ANIMAL STRESS, P77, DOI 10.1079/9780851993591.0077
[16]  
ELSASSER TH, 1989, J ANIM SCI, V67, P128
[17]   Physiological responses to repeated endotoxin challenge are selectively affected by recombinant bovine somatotropin administration to calves [J].
Elsasser, TH ;
Richards, M ;
Collier, R ;
Hartnell, GF .
DOMESTIC ANIMAL ENDOCRINOLOGY, 1996, 13 (01) :91-103
[18]   Underlying disease stress augments plasma and tissue adrenomedullin (AM) responses to endotoxin:: Colocalized increases in AM and inducible nitric oxide synthase within pancreatic islets [J].
Elsasser, TH ;
Sartin, JL ;
Martínez, A ;
Kahl, S ;
Montuenga, L ;
Pío, R ;
Fayer, R ;
Miller, MJ ;
Cuttitta, F .
ENDOCRINOLOGY, 1999, 140 (11) :5402-5411
[19]   ENDOTOXEMIA IN PREGNANT COWS - COMPARISONS OF MATERNAL AND FETAL EFFECTS UTILIZING THE CHRONICALLY CATHETERIZED FETUS [J].
FOLEY, GL ;
SCHLAFER, DH ;
ELSASSER, TH ;
MITCHELL, M .
THERIOGENOLOGY, 1993, 39 (03) :739-762
[20]   TUMOR-NECROSIS-FACTOR IN THE PATHOPHYSIOLOGY OF INFECTION AND SEPSIS [J].
FONG, Y ;
LOWRY, SF .
CLINICAL IMMUNOLOGY AND IMMUNOPATHOLOGY, 1990, 55 (02) :157-170