Enhanced neurogenesis following stroke

Each year hundreds of thousands of people must cope with the severe neurological consequences of a stroke. Current therapeutic strategies for stroke focus on acute treatment and neuroprotection. Unfortunately, these practices do little to reduce the long‐term morbidity associated with the injury. To...

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Bibliographic Details
Published inJournal of neuroscience research Vol. 73; no. 3; pp. 277 - 283
Main Authors Felling, Ryan J., Levison, Steven W.
Format Journal Article
LanguageEnglish
Published Hoboken Wiley Subscription Services, Inc., A Wiley Company 01.08.2003
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Summary:Each year hundreds of thousands of people must cope with the severe neurological consequences of a stroke. Current therapeutic strategies for stroke focus on acute treatment and neuroprotection. Unfortunately, these practices do little to reduce the long‐term morbidity associated with the injury. To develop effective therapies that promote regeneration, we must have an understanding of the cellular and molecular events involved in the recovery from an insult. Neural stem and progenitor cells are likely to be affected during this period. Here we review how the proliferation, migration, and maturation of these precursors are affected by ischemia. Furthermore, we summarize data available on the underlying mechanisms and the therapeutic implications of these studies. The studies that we review provide compelling evidence that neural precursors resident in the brain initiate a compensatory response to stroke that results in the production of new neurons. Moreover, administration of growth factors can enhance this compensatory response. Based on these encouraging results, we may eventually be able to manipulate these precursors to improve recovery of function in individuals afflicted by this devastating injury. © 2003 Wiley‐Liss, Inc.
Bibliography:ark:/67375/WNG-RN2PGCV0-F
NIH - No. MH 59950; No. HD 30705
ArticleID:JNR10670
istex:A565E6316634177A1172F59E8DF842809517AD4F
ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
ObjectType-Feature-3
ObjectType-Review-1
ISSN:0360-4012
1097-4547
DOI:10.1002/jnr.10670