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本文引用的文献

1
Nitroglycerin enhances the propagation of cortical spreading depression: comparative studies with sumatriptan and novel kynurenic acid analogues.硝酸甘油可增强皮层扩散性抑制的传播:与舒马曲坦及新型犬尿氨酸类似物的对比研究。
Drug Des Devel Ther. 2016 Dec 20;11:27-34. doi: 10.2147/DDDT.S117166. eCollection 2017.
2
Cortical spreading depression preconditioning mediates neuroprotection against ischemic stroke by inducing AMP-activated protein kinase-dependent autophagy in a rat cerebral ischemic/reperfusion injury model.在大鼠脑缺血/再灌注损伤模型中,皮质扩散性抑制预处理通过诱导AMP激活的蛋白激酶依赖性自噬来介导对缺血性中风的神经保护作用。
J Neurochem. 2017 Mar;140(5):799-813. doi: 10.1111/jnc.13922. Epub 2017 Jan 12.
3
Incidence, hemodynamic, and electrical characteristics of spreading depolarization in a swine model are affected by local but not by intravenous application of magnesium.猪模型中扩展性去极化的发生率、血流动力学和电特性受局部应用镁的影响,但不受静脉应用镁的影响。
J Cereb Blood Flow Metab. 2016 Dec;36(12):2051-2057. doi: 10.1177/0271678X16671317. Epub 2016 Sep 28.
4
GLYX-13 Produces Rapid Antidepressant Responses with Key Synaptic and Behavioral Effects Distinct from Ketamine.GLYX-13能产生快速抗抑郁反应,其关键的突触和行为效应与氯胺酮不同。
Neuropsychopharmacology. 2017 May;42(6):1231-1242. doi: 10.1038/npp.2016.202. Epub 2016 Sep 16.
5
Contribution of prostanoid signaling to the evolution of spreading depolarization and the associated cerebral blood flow response.前列腺素信号在弥漫性去极化及其相关的脑血流反应演变中的作用。
Sci Rep. 2016 Aug 10;6:31402. doi: 10.1038/srep31402.
6
Ischemia-induced spreading depolarization in the retina.视网膜中缺血诱导的去极化扩散。
J Cereb Blood Flow Metab. 2016 Sep;36(9):1579-91. doi: 10.1177/0271678X16657836. Epub 2016 Jul 7.
7
The continuum of spreading depolarizations in acute cortical lesion development: Examining Leão's legacy.急性皮质损伤发展中去极化扩散的连续性:审视莱昂的遗产。
J Cereb Blood Flow Metab. 2017 May;37(5):1571-1594. doi: 10.1177/0271678X16654495. Epub 2016 Jan 1.
8
Recording, analysis, and interpretation of spreading depolarizations in neurointensive care: Review and recommendations of the COSBID research group.神经重症监护中扩散性去极化的记录、分析与解读:COSBID研究组的综述与建议
J Cereb Blood Flow Metab. 2017 May;37(5):1595-1625. doi: 10.1177/0271678X16654496. Epub 2016 Jan 1.
9
Changes in electrocorticographic beta frequency components precede spreading depolarization in patients with acute brain injury.急性脑损伤患者中,皮质脑电图β频率成分的变化先于扩散性去极化出现。
Clin Neurophysiol. 2016 Jul;127(7):2661-7. doi: 10.1016/j.clinph.2016.04.026. Epub 2016 May 4.
10
Modulatory Effects of Dopamine D2 Receptors on Spreading Depression in Rat Somatosensory Neocortex.多巴胺D2受体对大鼠体感新皮层扩散性抑制的调节作用
Basic Clin Neurosci. 2014 Oct;5(4):246-52.

针对扩布性去极化的已测试药理学药物的系统评价。

Systematic review of the pharmacological agents that have been tested against spreading depolarizations.

机构信息

Neurosurgery Department, University of Heidelberg, Heidelberg, Germany.

出版信息

J Cereb Blood Flow Metab. 2018 Jul;38(7):1149-1179. doi: 10.1177/0271678X18771440. Epub 2018 Apr 20.

DOI:10.1177/0271678X18771440
PMID:29673289
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6434447/
Abstract

Spreading depolarization (SD) occurs alongside brain injuries and it can lead to neuronal damage. Therefore, pharmacological modulation of SD can constitute a therapeutic approach to reduce its detrimental effects and to improve the clinical outcome of patients. The major objective of this article was to produce a systematic review of all the drugs that have been tested against SD. Of the substances that have been examined, most have been shown to modulate certain SD characteristics. Only a few have succeeded in significantly inhibiting SD. We present a variety of strategies that have been proposed to overcome the notorious harmfulness and pharmacoresistance of SD. Information on clinically used anesthetic, sedative, hypnotic agents, anti-migraine drugs, anticonvulsants and various other substances have been compiled and reviewed with respect to the efficacy against SD, in order to answer the question of whether a drug at safe doses could be of therapeutic use against SD in humans.

摘要

扩散性去极化(SD)与脑损伤同时发生,可能导致神经元损伤。因此,SD 的药理学调节可能构成一种治疗方法,以减少其有害影响并改善患者的临床结果。本文的主要目的是对所有针对 SD 进行测试的药物进行系统评价。在所检查的物质中,大多数物质已被证明可以调节某些 SD 特征。只有少数药物成功地显著抑制了 SD。我们提出了各种策略来克服 SD 的恶名昭著的危害性和药物抗性。已经编译了关于临床使用的麻醉剂、镇静剂、催眠剂、抗偏头痛药物、抗惊厥药物和各种其他物质的信息,并对其针对 SD 的疗效进行了审查,以回答一个问题,即在安全剂量下的药物是否可以对人类的 SD 具有治疗作用。