Literature DB >> 19943353

Ischemic tolerance: the mechanisms of neuroprotective strategy.

Jan Lehotský1, Jozef Burda, Viera Danielisová, Miroslav Gottlieb, Peter Kaplán, Beata Saniová.   

Abstract

The phenomenon of ischemic tolerance perfectly describes this quote "What does not kill you makes you stronger." Ischemic pre- or postconditioning is actually the strongest known procedure to prevent or reverse neurodegeneration. It works specifically in sensitive vulnerable neuronal populations, which are represented by pyramidal neurons in the hippocampal CA1 region. However, tolerance is effective in other brain cell populations as well. Although, its nomenclature is "ischemic" tolerance, the tolerant phenotype can also be induced by other stimuli that lead to delayed neuronal death (intoxication). Moreover, the recent data have proven that this phenomenon is not limited to application of sublethal stimuli before the lethal stress but reversed arrangement of events, sublethal stress after lethal insult, is rather equally effective. A very important term is called "cross conditioning." Cross conditioning is the capability of one stressor to induce tolerance against another. So, since pre- or post-conditioners can be used plenty of harmful stimuli, hypo- or hyperthermia and some physiological compounds, such as norepinephrine, bradykinin. Delayed neuronal death is the slow development of postischemic neurodegeneration. This allows an opportunity for a great therapeutic window of 2-3 days to reverse the cellular death process. Moreover, it seems that the mechanisms of ischemic tolerance-delayed postconditioning could be used not only after ischemia but also in some other processes leading to apoptosis. (c) 2009 Wiley-Liss, Inc.

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Year:  2009        PMID: 19943353     DOI: 10.1002/ar.20970

Source DB:  PubMed          Journal:  Anat Rec (Hoboken)        ISSN: 1932-8486            Impact factor:   2.064


  35 in total

1.  An effective combination of two different methods of postconditioning.

Authors:  Viera Danielisova; Jozef Burda; Miroslava Nemethova; Miroslav Gottlieb; Rastislav Burda
Journal:  Neurochem Res       Date:  2012-06-19       Impact factor: 3.996

Review 2.  Ischemic conditioning-induced endogenous brain protection: Applications pre-, per- or post-stroke.

Authors:  Yuechun Wang; Cesar Reis; Richard Applegate; Gary Stier; Robert Martin; John H Zhang
Journal:  Exp Neurol       Date:  2015-04-18       Impact factor: 5.330

3.  Neuroprotection of Ischemic Preconditioning is Mediated by Anti-inflammatory, Not Pro-inflammatory, Cytokines in the Gerbil Hippocampus Induced by a Subsequent Lethal Transient Cerebral Ischemia.

Authors:  Dong Won Kim; Jae-Chul Lee; Jeong-Hwi Cho; Joon Ha Park; Ji Hyeon Ahn; Bai Hui Chen; Bich-Na Shin; Hyun-Jin Tae; Jeong Yeol Seo; Jun Hwi Cho; Il Jun Kang; Seongkweon Hong; Young-Myeong Kim; Moo-Ho Won; In Hye Kim
Journal:  Neurochem Res       Date:  2015-08-20       Impact factor: 3.996

4.  Effect of Hyperhomocysteinemia on Redox Balance and Redox Defence Enzymes in Ischemia-Reperfusion Injury and/or After Ischemic Preconditioning in Rats.

Authors:  Martin Petráš; Anna Drgová; Mária Kovalská; Zuzana Tatarková; Barbara Tóthová; Oľga Križanová; Ján Lehotský
Journal:  Cell Mol Neurobiol       Date:  2017-02-16       Impact factor: 5.046

5.  Intracellular signaling MAPK pathway after cerebral ischemia-reperfusion injury.

Authors:  Maria Kovalska; Libusa Kovalska; Martina Pavlikova; Maria Janickova; Katarina Mikuskova; Marian Adamkov; Peter Kaplan; Zuzana Tatarkova; Jan Lehotsky
Journal:  Neurochem Res       Date:  2012-03-20       Impact factor: 3.996

6.  Protection by low-dose kanamycin against noise-induced hearing loss in mice: dependence on dosing regimen and genetic background.

Authors:  Kevin K Ohlemiller; Mary E Rybak Rice; Allyson D Rosen; Scott C Montgomery; Patricia M Gagnon
Journal:  Hear Res       Date:  2011-05-27       Impact factor: 3.208

7.  Protective Effects of UCF-101 on Cerebral Ischemia-Reperfusion (CIR) is Depended on the MAPK/p38/ERK Signaling Pathway.

Authors:  Danying Su; Jing Ma; Zhuobo Zhang; Ye Tian; Baozhong Shen
Journal:  Cell Mol Neurobiol       Date:  2015-10-01       Impact factor: 5.046

8.  NMR metabolomic study of blood plasma in ischemic and ischemically preconditioned rats: an increased level of ketone bodies and decreased content of glycolytic products 24 h after global cerebral ischemia.

Authors:  Eva Baranovicova; Marian Grendar; Dagmar Kalenska; Anna Tomascova; Daniel Cierny; Jan Lehotsky
Journal:  J Physiol Biochem       Date:  2018-05-11       Impact factor: 4.158

9.  Effects of oxygen-glucose deprivation on microglial mobility and viability in developing mouse hippocampal tissues.

Authors:  Ukpong Eyo; Michael E Dailey
Journal:  Glia       Date:  2012-07-28       Impact factor: 7.452

10.  Oxygen glucose deprivation post-conditioning protects cortical neurons against oxygen-glucose deprivation injury: role of HSP70 and inhibition of apoptosis.

Authors:  Jian-Hua Zhao; Xian-Li Meng; Jian Zhang; Yong-Li Li; Yue-Juan Li; Zhe-Ming Fan
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2014-02-06
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