Experimental heatstroke in baboon: Analysis of the systemic inflammatory response

被引:57
作者
Bouchama, A
Al Mohanna, F
El-Sayed, R
Eldali, A
Saussereau, E
Collet-Martin, S
Ollivier, V
de Prost, D
Roberts, G
机构
[1] King Faisal Specialist Hosp & Res Ctr, Dept Comparat Med, Riyadh 11211, Saudi Arabia
[2] King Faisal Specialist Hosp & Res Ctr, Dept Biostat Epidemiol & Sci Comp, Riyadh 11211, Saudi Arabia
[3] King Faisal Specialist Hosp & Res Ctr, Dept Pathol & Lab Med, Riyadh 11211, Saudi Arabia
[4] Fac Xavier Bichat, INSERM, U479, F-75018 Paris, France
[5] Hop Louis Mourier, AP HP, F-92701 Colombes, France
来源
SHOCK | 2005年 / 24卷 / 04期
关键词
heat stress; hyperthermia; chemokine; cytokine; baboons;
D O I
10.1097/01.shk.0000180620.44435.9c
中图分类号
R4 [临床医学];
学科分类号
1002 ; 100602 ;
摘要
The objective of this study was to analyze the pattern of the inflammatory response to heatstroke in an experimental baboon model with a view to identifying potential target for therapeutic interventions. Blinded analysis of plasma collected from 12 juvenile baboons (Papio hamadryas) in heatstroke was used. Eight anesthetized animals were heat-stressed in an incubator at 44 degrees C to 47 degrees C until rectal temperature was 42.5 degrees C (moderate heatstroke; n = 4) or systolic arterial pressure fell to < 90 mmHg (severe heatstroke; n = 4) and were allowed to recover at room temperature. Four sham-heated animals served as a control group. We performed sequential measurement of cytokines. The rectal temperature on completion of heat stress was 42.5 degrees C +/- 0.0 degrees C and 43.3 degrees C +/- 0.1 degrees C in moderate and severe heatstroke, respectively. Heat stress elicited early, simultaneous release of anti-inflammatory cytokines and chemokines (IL-10, IL-1ra, sTNFrI and II, and IL-8). Circulating levels of IL-12p40 were significantly decreased, whereas TNF alpha, IL-1 beta, and IL-4 were below the detection limit in all animals. No baboon survived severe heatstroke; there was neurological morbidity without mortality in moderate heatstroke. Nonsurvivors displayed significantly greater activity/alterations in inflammation markers than survivors. Sham-heated animals had no evidence of inflammation activation. These results show that heatstroke activates complex systemic inflammatory and regulatory responses associated with outcome. Further definition of this ambivalent response is needed before identification of target of successful modulation may become possible.
引用
收藏
页码:332 / 335
页数:4
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