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10.1016/j.pneurobio.2015.09.008

http://scihub22266oqcxt.onion/10.1016/j.pneurobio.2015.09.008
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C4826643!4826643!26455456
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suck abstract from ncbi


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pmid26455456      Prog+Neurobiol 2016 ; 144 (ä): 103-20
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  • Astrocytes, therapeutic targets for neuroprotection and neurorestoration in ischemic stroke #MMPMID26455456
  • Liu Z; Chopp M
  • Prog Neurobiol 2016[Sep]; 144 (ä): 103-20 PMID26455456show ga
  • Astrocytes are the most abundant cell type within the central nervous system. They play essential roles in maintaining normal brain function, as they are a critical structural and functional part of the tripartite synapses and the neurovascular unit, and communicate with neurons, oligodendrocytes and endothelial cells. After an ischemic stroke, astrocytes perform multiple functions both detrimental and beneficial, for neuronal survival during the acute phase. Aspects of the astrocytic inflammatory response to stroke may aggravate the ischemic lesion, but astrocytes also provide benefit for neuroprotection, by limiting lesion extension via anti-excitotoxicity effects and releasing neurotrophins. Similarly, during the late recovery phase after stroke, the glial scar may obstruct axonal regeneration and subsequently reduce the functional outcome; however, astrocytes also contribute to angiogenesis, neurogenesis, synaptogenesis, and axonal remodeling, and thereby promote neurological recovery. Thus, the pivotal involvement of astrocytes in normal brain function and responses to an ischemic lesion designates them as excellent therapeutic targets to improve functional outcome following stroke. In this review, we will focus on functions of astrocytes and astrocyte-mediated events during stroke and recovery. We will provide an overview of approaches on how to reduce the detrimental effects and amplify the beneficial effects of astrocytes on neuroprotection and on neurorestoration post stroke, which may lead to novel and clinically relevant therapies for stroke.
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