Leon Lisa R, Helwig Bryan G
Thermal Mountain Medicine Division, US Army Research Institute of Environmental Medicine, Kansas Street, Building 42, Natick, Massachusetts 01760-5007, USA.
Front Biosci (Schol Ed). 2010 Jun 1;2(3):916-38. doi: 10.2741/s111.
Environmental heat exposure represents one of the most deadly natural hazards in the United States. Heat stroke is a life-threatening illness that affects all segments of society with few effective treatment strategies to mitigate the long-term debilitating consequences of this syndrome. Although the etiologies of heat stroke are not fully understood, the long-term sequelae are thought to be due to a systemic inflammatory response syndrome (SIRS) that ensues following heat-induced tissue injury. Endotoxin and cytokines have been implicated as key mediators of the heat-induced SIRS, based almost exclusively on correlative data that show high circulating concentrations of these substances in heat stroke patients and animal models. However, endotoxin and cytokine neutralization studies have not consistently supported this hypothesis indicating that the mechanisms of heat stroke morbidity / mortality remain poorly understood. This review discusses the current understanding of the role of endotoxin and cytokines in heat-induced SIRS. Insight is provided into genetic conditions that may predispose to heat stroke and potential therapeutic strategies that may be efficacious against the adverse consequences of this debilitating illness.
在美国,暴露于环境高温是最致命的自然灾害之一。中暑是一种危及生命的疾病,影响着社会各阶层,几乎没有有效的治疗策略来减轻该综合征的长期衰弱后果。虽然中暑的病因尚未完全明了,但人们认为其长期后遗症是由热诱导组织损伤后随之而来的全身炎症反应综合征(SIRS)所致。内毒素和细胞因子被认为是热诱导SIRS的关键介质,这几乎完全基于相关数据,这些数据显示中暑患者和动物模型中这些物质的循环浓度很高。然而,内毒素和细胞因子中和研究并未始终支持这一假说,这表明中暑发病/死亡机制仍未得到充分理解。本综述讨论了目前对内毒素和细胞因子在热诱导SIRS中作用的认识。还深入探讨了可能易患中暑的遗传条件以及可能有效对抗这种衰弱疾病不良后果的潜在治疗策略。