Abstract:
:As early as 1928, Cajal suggested that plaques contain a trophic substance which attracts neurites. Recently, basic fibroblast growth factor (bFGF) levels were shown to be elevated in Alzheimer's disease (AD) and localized to plaques and neurofibrillary tangles. We sought to clarify the subtype of plaques which contain bFGF and provide more detail on bFGFs neuronal and vascular localization in normal aged brain, AD brain, and Down's syndrome (DS) brain. We combined double-labeling immunocytochemistry for bFGF with heparan sulfate glycosaminoglycans, beta-amyloid, and thioflavine fluorescence. In addition, the neuritic markers tau-1 and PHF-1 were combined with bFGF staining. Eleven AD, five nondemented controls, and four DS cases were examined. Most bFGF immunopositive plaques contained numerous dystrophic fibers, indicating they were of the neuritic subtype. We also detected a variety of bFGF-positive cells, including hilar, dentate granule, pyramidal, and stellate neurons, as well as astrocytes. The basement membrane of large and small arterioles also contained bFGF. bFGF immunoreactivity within neurons, astrocytes and the vasculature was increased in AD cases relative to controls. Immunoreactivity within the DS cases was intermediate. These results suggest that bFGF is up-regulated in AD and support the hypothesis that bFGF may attract neurites into plaques. Alternatively, an injured neurite may induce bFGF production by responding glia, resulting in further neuritic attraction.
journal_name
Exp Neuroljournal_title
Experimental neurologyauthors
Cummings BJ,Su JH,Cotman CWdoi
10.1006/exnr.1993.1202subject
Has Abstractpub_date
1993-12-01 00:00:00pages
315-25issue
2eissn
0014-4886issn
1090-2430pii
S0014-4886(83)71202-1journal_volume
124pub_type
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journal_title:Experimental neurology
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abstract::The development of transgenic mouse models of amyotrophic lateral sclerosis (ALS) allows the testing of neuroprotective agents. We evaluated the effects of five agents in transgenic mice with the G93A Cu,Zn superoxide dismutase mutation. A novel inhibitor of poly(ADP-ribose) polymerase showed no effects on survival. D...
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journal_title:Experimental neurology
pub_type: 杂志文章
doi:10.1006/exnr.2002.8021
更新日期:2002-11-01 00:00:00
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pub_type: 杂志文章
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journal_title:Experimental neurology
pub_type: 杂志文章
doi:10.1016/j.expneurol.2006.08.028
更新日期:2007-02-01 00:00:00
abstract::Neonatal hypoxia ischemia (HI) is the main cause of newborn mortality and morbidity. Preclinical studies have shown that the immature rat brain is more resilient to HI injury, suggesting innate mechanisms of neuroprotection. During neonatal period brain metabolism experience changes that might greatly affect the outco...
journal_title:Experimental neurology
pub_type: 杂志文章
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journal_title:Experimental neurology
pub_type: 杂志文章
doi:10.1016/j.expneurol.2008.12.026
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journal_title:Experimental neurology
pub_type: 杂志文章
doi:10.1016/j.expneurol.2016.05.039
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journal_title:Experimental neurology
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doi:10.1016/j.expneurol.2017.10.028
更新日期:2018-02-01 00:00:00
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journal_title:Experimental neurology
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doi:10.1016/j.expneurol.2009.03.018
更新日期:2009-06-01 00:00:00
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journal_title:Experimental neurology
pub_type: 杂志文章
doi:10.1016/0014-4886(86)90126-3
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journal_title:Experimental neurology
pub_type: 杂志文章,评审
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journal_title:Experimental neurology
pub_type: 杂志文章
doi:10.1016/j.expneurol.2008.01.016
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journal_title:Experimental neurology
pub_type: 杂志文章
doi:10.1016/j.expneurol.2015.04.020
更新日期:2015-09-01 00:00:00
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journal_title:Experimental neurology
pub_type: 杂志文章
doi:10.1016/j.expneurol.2014.10.009
更新日期:2015-01-01 00:00:00
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journal_title:Experimental neurology
pub_type: 杂志文章
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pub_type: 杂志文章
doi:10.1016/j.expneurol.2008.05.019
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journal_title:Experimental neurology
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doi:10.1016/j.expneurol.2013.01.019
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journal_title:Experimental neurology
pub_type: 杂志文章
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更新日期:1987-04-01 00:00:00
abstract::Embryonic substantia nigra grafts partially reinnervate the dopamine-denervated corpus striatum when implanted adjacent to that structure. This reinnervation is generally limited to a small portion of the denervated striatum and does not completely compensate for the behavioral effects of a 6-hydroxydopamine lesion of...
journal_title:Experimental neurology
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journal_title:Experimental neurology
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doi:10.1016/j.expneurol.2017.12.010
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abstract::Cortical spreading depression (CSD) is associated with various short- and long-term physiological and neurochemical changes and has been shown to confer an increased susceptibility to accompanying ischemic injury or provide protection against a subsequent experimental ischemia. Nitric oxide is involved in the processe...
journal_title:Experimental neurology
pub_type: 杂志文章
doi:10.1006/exnr.1999.7218
更新日期:1999-12-01 00:00:00
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journal_title:Experimental neurology
pub_type: 杂志文章
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更新日期:1995-06-01 00:00:00
abstract::Gene transfer to the central nervous system provides powerful methodology for the study of gene function and gene-environment interactions in vivo, in addition to a vehicle for the delivery of therapeutic transgenes for gene therapy. The aim of the present study was to determine patterns of tropism exhibited by pseudo...
journal_title:Experimental neurology
pub_type: 杂志文章
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