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应用动物体温维持仪与仿真热气候动物舱建立大鼠经典型热射病模型的比较 被引量:4

Comparison between animal temperature controller and artificial climate chamber employed for the establishment of classical heat
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摘要 目的 比较应用动物体温维持仪与仿真热气候动物舱建立的大鼠经典型热射病(CHS)模型的异同.方法 雄性SPF级Wistar大鼠24只,随机(随机数字法)分为室温对照(C-C)组、高温对照(HS-C)组、高温麻醉(HS-A)组.HS-C和HS-A组大鼠分别使用仿真热气候动物舱和动物体温维持仪行35℃热暴露,监测各组大鼠动脉收缩压(SBP)、核心体温(Tc)变化,记录发病时间,比较两组大鼠白细胞(WBC)计数、C反应蛋白(CRP)、肿瘤坏死因子-α(TNF-α)、白介素-1β (LL-1β)等炎症指标变化及大脑、肺、肝、小肠、肾等主要器官病理改变.结果 HS-A组大鼠发病时间比HS-C组明显缩短[(40.0±4.3)minvs.(110.1±5.3) min,P<0.01],发病时SBP及Tc比HS-C组低(159.1±5.91) mmHgvs.(174.54±5.77) mmHg(1mmHg =0.133 kPa),P<0.01;(43.5±0.4)℃vs.(44.4±0.2)℃,P< 0.01).建模后两组大鼠WBC、CRP、TNF-α、IL-1β水平较C-C组均显著升高(P<0.01),且HS-A组炎性因子水平比HS-C组低(P<0.01),但WBC计数差异无统计学意义(P>0.05);两组大鼠大脑、肺、肝、小肠、肾等主要器官病理无明显改变.结论 应用动物体温维持仪建立大鼠CHS模型与仿真热气候动物舱法差异无统计学意义,并且能够明显缩短建模时间、节约成本,是一种简易、可靠而又经济的模型建立方法,可以替代仿真热气候动物舱法. Objective To investigate the differences between animal temperature controller (ATC) and artificial climate chamber (ACC) used for the establishment of classical heat stroke (CHS) rat model.Methods Twenty-four male specific pathogen-free Wistar rats were randomly (random number) and equally assigned to three groups,namely room temperature control (C-C) group,heat stroke under conscious state (HS-C) group,and heat stroke under anesthesia (HS-A) group.Rats of HS-C or HS-A group were placed into ACC or ATC,then exposed to 35 ℃ heat stress.The systolic blood pressure (SBP) and core body temperature (Tc) were monitored.The time required for onset of HS was recorded.The white blood cell count (WBC) in peripheral blood and serum levels of C-reactive protein (CRP),tumor necrosis factor-alpha (TNF-α) and interleukin-1 beta (IL-1β) were measured.The histopathological changes of major organs were also confirmed by hematoxylin-eosin (HE) staining.Results The onset time in HS-A group was significantly shorter thanthatin HS-C group [(40.0 ± 4.3) minvs.(110.1 ± 5.3) min,P〈0.01].The SBP and Tc at this moment were lower in HS-A group [(159.1 ± 5.91) mmHg vs.(174.54 ± 5.77) mmHg,P〈0.01;(43.5 ± 0.4)℃ vs.(44.4 ± 0.2)℃,P〈0.01].TheWBC,CRP,TNF-α and IL-1 β levels of these two HS groups were dramatically elevated compared with C-C group (P 〈0.01).The inflammatory cytokines levels in HS-A group were significantly lower than those in HS-C group (P 〈 0.01),but there was no difference in WBC between them (P 〉 0.05).However,there was no obvious difference in histopathological change in major organ observed between HS-A and HS-C groups.Conclusions In comparison of these two methods,ATC is similar to ACC in respect of the establishment of CHS rat model.ATC is quicker in onset of HS,and more simplified and economical than ACC and could substitute ACC.
出处 《中华急诊医学杂志》 CAS CSCD 北大核心 2015年第4期408-412,共5页 Chinese Journal of Emergency Medicine
关键词 热射病 动物模型 大鼠动物 体温维持仪 仿真热气候动物舱 Heat stroke Experiment animal model Rat Animal temperature controller Artificial climate chamber
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  • 1胡森 姚咏明.MODS的发病机制.多器官功能障碍综合征[M].北京:科学出版社,1999..
  • 2[5]Levy MM,Fink MP,Marshall JC,et al.2001 SCCM/ESICM/ACCP/ATS/SIS International Sepsis Definitions Conference [J].Crit Care Med,2003,31(4):1250-6.
  • 3[6]Bouchama A,Roberts G,Al Mohanna F,et al.Inflammatory,hemostatic,and clinical changes in a baboon experimental model for heatstroke[J].J Appl Physiol,2005,98(2):697-705.
  • 4[7]van Amersfoort ES,van Berkel TJ,Kuiper J.Receptors,mediators,and mechanisms involved in bacterial sepsis and septic shock [J].Clin Microbiol Rev,2003,16(3):379-414.
  • 5[8]Enkhbaatar P,Okajima K,Murakami K,et al.Recombinant tissue factor pathway inhibitor reduces LPS-induced pulmonary vascular injury by inhibiting leukocyte activation [J].Am J Respir Crit Care Med,2000,162(5):1752-9.
  • 6[9]Abraham E.Neutrophils and acute lung injury[J].Crit Care Med,2003,31:S195-9.
  • 7[10]Gathiram P,Wells MT,Raidoo D,et al.Portal and systemic plasma lipopolysaccharide concentrations in heat-stressed primates[J].CircShock,1988,25:223-30.
  • 8[2]Meehl GA,Tebaldi C.More intense,more frequent,and longer lasting heat waves in the 21st century[J].Science,2004,305(5686):994-7.
  • 9[3]Lin MT,Liu HH,Yang YL.Involvement of interleukin-1 receptor mechanisms in development of arterial hypotension in rat heatstroke[J].Am J Physiol,1997,273:H2072-7.
  • 10Bastland CP,Hayslett IP.The cellular action of aldosterone in target epithelia.Kindey Int,1992,42:250-253.

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  • 1徐昌盛,刘文革.热射病研究进展[J].中华急诊医学杂志,2005,14(7):609-611. 被引量:35
  • 2Wei Ma,Zuo-Ren Wang,Lei Shi,Yue Yuan.Expression of macrophage inflammatory protein-1αin Kupffer cells following liver ischemia or reperfusion injury in rats[J].World Journal of Gastroenterology,2006,12(24):3854-3858. 被引量:5
  • 3余樱,张兆辉,杨波,曾庆杏.溶血磷脂酸对血脑屏障通透性的影响及其机制[J].中华急诊医学杂志,2006,15(12):1109-1112. 被引量:8
  • 4al- Mashhadani S A,Gader A G ,al f larlhi S S,et al. The coag ulopathy of heat stroke=aheraticms in coagulation and fibri nolysis in heat stroke patietlls during the pilgrimage(llaj) toMakkah[J]. Blood Coagul Fibrinolysis, 1994,5 (5) : 731-736.
  • 5Sucholeiki R. Heatstroke[J]. Semin Neurol, 2005,25 (3) : 307- 314.
  • 6Leon L R,Helwig B G. Heat stroke=Role of the systemic in flammatory response[J]. J Appl Physiol, 2010,109 ( 6 ) :1980- 1988.
  • 7LeonL R. Heat stroke and cytokines[J]. Prog Brain Res, 2007,162(6) :481-524.
  • 8Bouchama A, Knochel J P. Heat stroke[J]. N Engl J Med, 2002,346 (25)[J].1978-1988.
  • 9Bouchama A,Bridey F, Hammami M M, et al. Activation of coagulation and fibrinolysis in heatstroke[J]. Thrornb Haem- ost,1996,76(6):909 915.
  • 10Levine M, LoVecchio F,Ruha A M, et al. Influence of drug use on morbidity and mortality in heatstroke[J]. J Med Toxi- col,2012,8(3) :252 257.

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