Journal
NEUROBIOLOGY OF DISEASE
Volume 31, Issue 3, Pages 316-326Publisher
ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.nbd.2008.05.012
Keywords
beta-amyloid peptides; BDNF; neuroprotection; push-pull perfusion; indusium griseum; dentate gyrus hilus; corpus callosum; somatostatin; TrkB; trkB
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Funding
- Region Languedoc-Roussillon, Montpellier, France
- ECOS-Sud action [C04B06]
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We examined the potential protective effect of BDNF against F-amyloid-induced neurotoxicity in vitro and in vivo in rats. In neuronal cultures, BDNF had specific and dose-response protective effects on neuronal toxicity induced by A beta(1-42) and A beta(25-35). It completely reversed the toxic action induced by A beta(1-42) and partially that induced by A beta(25-35). These effects involved TrkB receptor activation since they were inhibited by K252a. Catalytic BDNF receptors (TrkB.FL) were localized in vitro in cortical neurons (mRNA and protein). In in vivo experiments, A beta(25-35) was administered into the indusium griseum or the third ventricle and several parameters were measured 7 days later to evaluate potential A beta(25-35)/BDNF interactions, i.e. local measurement of BDNF release, number of hippocampal hilar cells expressing SRIH mRNA and assessment of the corpus callosum damage (morphological examination, pyknotic nuclei counting and axon labeling with anti-MBP antibody). We conclude that BDNF possesses neuroprotective properties against toxic effects of A beta peptides. (C) 2008 Published by Elsevier Inc.
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