Literature DB >> 16651812

Gene expression in cerebral ischemia: a new approach for neuroprotection.

Mónica Millán1, Juan Arenillas.   

Abstract

Cerebral ischemia is one of the strongest stimuli for gene induction in the brain. Hundreds of genes have been found to be induced by brain ischemia. Many genes are involved in neurodestructive functions such as excitotoxicity, inflammatory response and neuronal apoptosis. However, cerebral ischemia is also a powerful reformatting and reprogramming stimulus for the brain through neuroprotective gene expression. Several genes may participate in both cellular responses. Thus, isolation of candidate genes for neuroprotection strategies and interpretation of expression changes have been proven difficult. Nevertheless, many studies are being carried out to improve the knowledge of the gene activation and protein expression following ischemic stroke, as well as in the development of new therapies that modify biochemical, molecular and genetic changes underlying cerebral ischemia. Owing to the complexity of the process involving numerous critical genes expressed differentially in time, space and concentration, ongoing therapeutic efforts should be based on multiple interventions at different levels. By modification of the acute gene expression induced by ischemia or the apoptotic gene program, gene therapy is a promising treatment but is still in a very experimental phase. Some hurdles will have to be overcome before these therapies can be introduced into human clinical stroke trials. Copyright 2006 S. Karger AG, Basel.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16651812     DOI: 10.1159/000091701

Source DB:  PubMed          Journal:  Cerebrovasc Dis        ISSN: 1015-9770            Impact factor:   2.762


  3 in total

1.  Oxysophoridine protects against focal cerebral ischemic injury by inhibiting oxidative stress and apoptosis in mice.

Authors:  Teng-Fei Wang; Zhen Lei; Yu-Xiang Li; Yong-Sheng Wang; Jie Wang; Shu-Jing Wang; Yin-Ju Hao; Ru Zhou; Shao-Ju Jin; Juan Du; Juan Li; Tao Sun; Jian-Qiang Yu
Journal:  Neurochem Res       Date:  2013-11       Impact factor: 3.996

2.  P38 MAPK inhibition protects against glutamate neurotoxicity and modifies NMDA and AMPA receptor subunit expression.

Authors:  Martha Catalina Rivera-Cervantes; Rolando Castañeda-Arellano; Ruben Darío Castro-Torres; Graciela Gudiño-Cabrera; Alfredo I Feria y Velasco; Antoni Camins; Carlos Beas-Zárate
Journal:  J Mol Neurosci       Date:  2014-08-30       Impact factor: 3.444

3.  Transcriptional Response and Morphological Features of the Neurovascular Unit and Associated Extracellular Matrix After Experimental Stroke in Mice.

Authors:  Susanne Aleithe; Alexandra Blietz; Bianca Mages; Constance Hobusch; Wolfgang Härtig; Dominik Michalski
Journal:  Mol Neurobiol       Date:  2019-05-14       Impact factor: 5.590

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.