Cerebrovascular dysfunction is an attractive target for therapy in heat stroke

被引:37
作者
Chen, Sheng-Hsien
Niu, Ko-Chi
Lin, Mao-Tsun [1 ]
机构
[1] Chi Mei Med Ctr, Dept Med Res, Tainan 710, Taiwan
[2] Natl Cheng Kung Univ, Coll Med, Inst Clin Med, Tainan 70101, Taiwan
[3] Chi Mei Med Ctr, Dept Obstet & Gynaecol, Tainan, Taiwan
[4] Chi Mei Med Ctr, Dept Hyperbar Oxygen Therapy, Tainan, Taiwan
关键词
brain ischaemia; heatstroke; hypotension; intracranial hypertension;
D O I
10.1111/j.1440-1681.2006.04429.x
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
1. The aim of the present review is to summarize clinical observations and results of animal models that advance the knowledge of the attenuation of cerebrovascular dysfunction in the setting of heat stroke. It is a narrative review of selected published literature from Medline over the period 1959-2005. 2. All heat-stressed rodents, even under general anaesthesia, have hyperthermia, systemic inflammation, hypercoagulable state, arterial hypotension and tissue ischaemia and injury in multiple organs. These findings demonstrate that rodent heat stroke models can nearly mirror the full spectrum of human heat stroke. Experimental heat stroke fulfills the empirical triad used for the dignosis of classical human heat stroke, namely hyperthermia, central nervous system alterations and a history of heat stress. 3. These physiological dysfunctions and survival during heat stroke can be improved by whole-body or brain cooling therapy adopted immediately after the onset of heat stroke. 4. However, in the absence of body or brain cooling, these heat stroke reactions can still be reduced by the following measures: (i) fluid replacement with 3% NaCl solution, 10% human albumin or hydroxyethyl starch; (ii) intravenous delivery of anti-inflammatory drugs, free radical scavengers or interleukin-1 receptor antagonists; (iii) hyperbaric oxygen therapy; or (iv) transplantation of human umbilical cord blood cells. 5. In addition, before initiation of heat stress, prior manipulations with one of the following measures was found to be able to protect against heat stroke reactions: (i) systemic delivery of alpha-tocopherol, mannitol, inducible nitric oxide synthase inhibitors, mu-opioid receptor antagonists, endothelin ETA receptor antagonists, serotoninergic nerve depletors or receptor antagonists, or glutamate receptor antagonists; or (ii) heat shock portein 72 preconditioning. 6. There is compelling evidence that cerebrovascular dysfunction is an attractive target for therapy in heat stroke.
引用
收藏
页码:663 / 672
页数:10
相关论文
共 161 条
[1]
ELECTROCARDIOGRAPHIC ABNORMALITIES IN PATIENTS WITH HEAT-STROKE [J].
AKHTAR, MJ ;
ALNOZHA, M ;
ALHARTHI, S ;
NOUH, MS .
CHEST, 1993, 104 (02) :411-414
[2]
Nitric oxide synthases: structure, function and inhibition [J].
Alderton, WK ;
Cooper, CE ;
Knowles, RG .
BIOCHEMICAL JOURNAL, 2001, 357 (03) :593-615
[3]
Alzeer AH, 1999, INTENS CARE MED, V25, P58
[4]
Phagocytes and oxidative stress [J].
Babior, BM .
AMERICAN JOURNAL OF MEDICINE, 2000, 109 (01) :33-44
[5]
HYPERTHERMIA PROTECTS AGAINST LIGHT DAMAGE IN THE RAT RETINA [J].
BARBE, MF ;
TYTELL, M ;
GOWER, DJ ;
WELCH, WJ .
SCIENCE, 1988, 241 (4874) :1817-1820
[6]
Brain cooling during transient focal ischemia provides complete neuroprotection [J].
Barone, FC ;
Feuerstein, GZ ;
White, RF .
NEUROSCIENCE AND BIOBEHAVIORAL REVIEWS, 1997, 21 (01) :31-44
[7]
ACUTE TUBULAR NECROSIS - ANALYSIS OF 100 CASES WITH RESPECT TO MORTALITY, COMPLICATIONS, AND TREATMENT WITH AND WITHOUT DIALYSIS [J].
BLUEMLE, LW ;
WEBSTER, GD ;
ELKINTON, JR .
ARCHIVES OF INTERNAL MEDICINE, 1959, 104 (02) :180-197
[8]
ENDOTOXEMIA AND RELEASE OF TUMOR-NECROSIS-FACTOR AND INTERLEUKIN-1-ALPHA IN ACUTE HEATSTROKE [J].
BOUCHAMA, A ;
PARHAR, RS ;
ELYAZIGI, A ;
SHETH, K ;
ALSEDAIRY, S .
JOURNAL OF APPLIED PHYSIOLOGY, 1991, 70 (06) :2640-2644
[9]
Evidence for endothelial cell activation/injury in heatstroke [J].
Bouchama, A ;
Hammami, MM ;
Haq, A ;
Jackson, J ;
AlSedairy, S .
CRITICAL CARE MEDICINE, 1996, 24 (07) :1173-1178
[10]
Medical progress - Heat stroke [J].
Bouchama, A ;
Knochel, JP .
NEW ENGLAND JOURNAL OF MEDICINE, 2002, 346 (25) :1978-1988