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Therapeutic hypothermia: neuroprotective mechanisms

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收录情况: ◇ SCIE

机构: [1]Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94121 USA; [2]Vet Affairs Med Ctr, San Francisco, CA 94121 USA; [3]Capital Univ Med Sci, Beijing Tiantan Hosp, Dept Neurol, Beijing 100050, Peoples R China; [4]Univ Calif San Francisco, Dept Neurol, Neurol 127,4150 Clement St, San Francisco, CA 94121 USA
出处:
DOI: 10.2741/2104
ISSN:

关键词: hypothermia temperature cerebral ischemia stroke review

摘要:
Hypothermia has long been known to be a potent putative neuroprotectant. Experimental evidence and clinical experience show that hypothermia protects the brain from cerebral injury. Recent insights into the mechanisms of cerebral ischemia and reperfusion suggest reasons why hypothermia may be an ideal modality for stroke therapy. Hypothermia protects brain tissue in multiple ways. It retards energy depletion, reduces intracellular acidosis, lessens the ischemia related accumulation of excitotoxic neurotransmitters, and attenuates the influx of intracellular calcium. Additionally, hypothermia suppresses the generation of oxygen free radicals involved in secondary damage associated with reperfusion. It also suppresses the mechanisms related to blood- brain barrier degeneration and postischemic remodeling. The clinical application of therapeutic hypothermia and its limitations will be summarized in this paper. Therapeutic hypothermia is likely to undergo phase III clinical trials in various clinical settings. Novel technologies are being developed to optimize the safety and efficacy of this promising approach.

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中科院(CAS)分区:
出版当年[2006]版:
大类 | 3 区 生物
最新[2023]版:
大类 | 4 区 生物学
小类 | 4 区 生化与分子生物学 4 区 细胞生物学
JCR分区:
出版当年[2005]版:
Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Q2 CELL BIOLOGY
最新[2023]版:
Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Q3 CELL BIOLOGY

影响因子: 最新[2023版] 最新五年平均 出版当年[2005版] 出版当年五年平均 出版前一年[2004版] 出版后一年[2006版]

第一作者:
第一作者机构: [1]Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94121 USA; [2]Vet Affairs Med Ctr, San Francisco, CA 94121 USA; [3]Capital Univ Med Sci, Beijing Tiantan Hosp, Dept Neurol, Beijing 100050, Peoples R China; [4]Univ Calif San Francisco, Dept Neurol, Neurol 127,4150 Clement St, San Francisco, CA 94121 USA
通讯作者:
通讯机构: [1]Univ Calif San Francisco, Dept Neurol, San Francisco, CA 94121 USA; [2]Vet Affairs Med Ctr, San Francisco, CA 94121 USA; [3]Capital Univ Med Sci, Beijing Tiantan Hosp, Dept Neurol, Beijing 100050, Peoples R China; [4]Univ Calif San Francisco, Dept Neurol, Neurol 127,4150 Clement St, San Francisco, CA 94121 USA
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