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Tolerance to ischemia - an increasingly complex biology.耐受缺血——一门日益复杂的生物学。
Transl Stroke Res. 2013 Feb;4(1):40-50. doi: 10.1007/s12975-012-0246-x. Epub 2013 Jan 11.
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Transl Stroke Res. 2013 Feb;4(1):51-5. doi: 10.1007/s12975-012-0218-1. Epub 2012 Nov 22.
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Genetics and genomics of ischemic tolerance: focus on cardiac and cerebral ischemic preconditioning.缺血耐受的遗传学和基因组学:关注心脏和脑缺血预处理。
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Epigenetics and the environment: in search of the "toleroasome" vital to execution of ischemic preconditioning.表观遗传学与环境:探寻执行缺血预处理的关键“耐受体”。
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Putative endogenous mediators of preconditioning-induced ischemic tolerance in rat brain identified by genomic and proteomic analysis.通过基因组和蛋白质组学分析鉴定的大鼠脑中预处理诱导的缺血耐受的假定内源性介质。
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Further application of hyperbaric oxygen in prostate cancer.高压氧在前列腺癌中的进一步应用。
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Regulation of gene expression in ischemic preconditioning in the brain.脑缺血预处理中基因表达的调控
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Magnesium induces preconditioning of the neonatal brain via profound mitochondrial protection.镁通过深度的线粒体保护诱导新生儿脑的预处理。
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Dynamic changes in DNA methylation in ischemic tolerance.缺血耐受中DNA甲基化的动态变化。
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Ischemic conditioning-induced endogenous brain protection: Applications pre-, per- or post-stroke.缺血预处理诱导的内源性脑保护:在卒中前、卒中时或卒中后的应用。
Exp Neurol. 2015 Oct;272:26-40. doi: 10.1016/j.expneurol.2015.04.009. Epub 2015 Apr 18.

本文引用的文献

1
The end of "small science"?“小科学”的终结?
Science. 2012 Sep 28;337(6102):1583. doi: 10.1126/science.1230529.
2
Gene expression analysis to identify molecular correlates of pre- and post-conditioning derived neuroprotection.基因表达分析鉴定预处理和后处理诱导的神经保护的分子相关性。
J Mol Neurosci. 2012 Jun;47(2):322-39. doi: 10.1007/s12031-012-9751-3. Epub 2012 Apr 1.
3
Differential DNA methylation patterns define status epilepticus and epileptic tolerance.差异性 DNA 甲基化模式定义了癫痫持续状态和癫痫耐受状态。
J Neurosci. 2012 Feb 1;32(5):1577-88. doi: 10.1523/JNEUROSCI.5180-11.2012.
4
Remote ischemic limb preconditioning after subarachnoid hemorrhage: a phase Ib study of safety and feasibility.蛛网膜下腔出血后肢体远程缺血预处理:安全性和可行性的 Ib 期研究。
Stroke. 2011 May;42(5):1387-91. doi: 10.1161/STROKEAHA.110.605840. Epub 2011 Mar 17.
5
Functional identification of neuroprotective molecules.神经保护分子的功能鉴定。
PLoS One. 2010 Nov 24;5(11):e15008. doi: 10.1371/journal.pone.0015008.
6
Neuroprotection induced in vitro by ischemic preconditioning and postconditioning: modulation of apoptosis and PI3K-Akt pathways.缺血预处理和后处理诱导的体外神经保护:细胞凋亡和 PI3K-Akt 通路的调节。
J Mol Neurosci. 2011 Mar;43(3):428-42. doi: 10.1007/s12031-010-9461-7. Epub 2010 Oct 15.
7
Epileptic tolerance is associated with enduring neuroprotection and uncoupling of the relationship between CA3 damage, neuropeptide Y rearrangement and spontaneous seizures following intra-amygdala kainic acid-induced status epilepticus in mice.癫痫耐受与神经保护有关,并使内侧杏仁核红藻氨酸诱导的癫痫持续状态后 CA3 损伤、神经肽 Y 重排和自发性癫痫之间的关系解耦。
Neuroscience. 2010 Dec 1;171(2):556-65. doi: 10.1016/j.neuroscience.2010.09.003. Epub 2010 Sep 17.
8
MicroRNAs induced during ischemic preconditioning.缺血预处理诱导的 microRNAs。
Stroke. 2010 Aug;41(8):1646-51. doi: 10.1161/STROKEAHA.110.579649. Epub 2010 Jun 24.
9
Possible involvement of DNA methylation in NKCC1 gene expression during postnatal development and in response to ischemia.可能涉及 DNA 甲基化在 NKCC1 基因表达在出生后发育过程中和对缺血的反应。
J Neurochem. 2010 Jul;114(2):520-9. doi: 10.1111/j.1471-4159.2010.06772.x. Epub 2010 Apr 28.
10
Polycomb group proteins as epigenetic mediators of neuroprotection in ischemic tolerance.多梳蛋白作为缺血耐受中神经保护的表观遗传介质。
Sci Signal. 2010 Mar 2;3(111):ra15. doi: 10.1126/scisignal.2000502.

耐受缺血——一门日益复杂的生物学。

Tolerance to ischemia - an increasingly complex biology.

机构信息

Neuroscience Institute, Morehouse School of Medicine, 720 Westview Drive SW, Atlanta, GA, 30310-1495 ; Department of Neurobiology, Morehouse School of Medicine, 720 Westview Drive SW, Atlanta, GA, 30310-1495 ; Department of Pharmacology, Morehouse School of Medicine, 720 Westview Drive SW, Atlanta, GA, 30310-1495.

出版信息

Transl Stroke Res. 2013 Feb;4(1):40-50. doi: 10.1007/s12975-012-0246-x. Epub 2013 Jan 11.

DOI:10.1007/s12975-012-0246-x
PMID:23504451
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3596882/
Abstract

In this review we identify and discuss some of the genomics studies of preconditioning and the ischemic tolerance phenomenon. Such studies have been attempted in multiple species, using different array technologies and with different preconditioning and tolerance models. In addition, studies are starting to reveal epigenetic mechanisms and modifiers of tolerance and preconditioning. Together these studies are starting to reveal some of the immense complexity of the ischemic tolerance phenomenon, yet further studies await to be performed.

摘要

在这篇综述中,我们确定并讨论了一些关于预处理和缺血耐受现象的基因组学研究。这些研究已经在多个物种中进行,使用了不同的阵列技术和不同的预处理和耐受模型。此外,研究开始揭示耐受和预处理的表观遗传机制和修饰因子。这些研究一起开始揭示缺血耐受现象的巨大复杂性,但还需要进行更多的研究。