CEREBROVASCULAR DYSFUNCTION IS AN ATTRACTIVE TARGET FOR THERAPY IN HEAT STROKE

• Published in: Clinical and experimental pharmacology & physiology 2006-08, Vol.33 (8), p.663-672
• Main Authors: Chen, Sheng-Hsien, Niu, Ko-Chi, Lin, Mao-Tsun
• Format: Article
• Language: English
• Subjects: Animals; Antihypertensive Agents - pharmacology; Antihypertensive Agents - therapeutic use; Blood Coagulation - drug effects; Brain - blood supply; Brain - drug effects; Brain - enzymology; brain ischaemia; Brain Ischemia - blood; Brain Ischemia - drug therapy; Brain Ischemia - enzymology; Brain Ischemia - therapy; Cerebrovascular Circulation; Cryotherapy - methods; Disease Models, Animal; Endothelial Cells - transplantation; Endothelin Receptor Antagonists; Enzyme Inhibitors - pharmacology; Enzyme Inhibitors - therapeutic use; Fluid Therapy - methods; Free Radical Scavengers - pharmacology; Free Radical Scavengers - therapeutic use; Heat Stroke - blood; Heat Stroke - drug therapy; Heat Stroke - enzymology; Heat Stroke - therapy; heatstroke; Humans; Hyperbaric Oxygenation; hypotension; intracranial hypertension; Nitric Oxide Synthase - antagonists & inhibitors; Nitric Oxide Synthase - metabolism; Peptides, Cyclic - pharmacology; Peptides, Cyclic - therapeutic use; Receptors, Endothelin - metabolism
• ISSN: 0305-1870; 1440-1681
• DOI: 10.1111/j.1440-1681.2006.04429.x

SUMMARY 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 α‐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.