Literature DB >> 10658615

Deficits in nerve growth factor release and tyrosine receptor kinase phosphorylation are associated with age-related impairment in long-term potentiation in the dentate gyrus.

A Kelly1, C Maguire, M A Lynch.   

Abstract

Previous findings have indicated that nerve growth factor may play a role in the expression of long-term potentiation in perforant path-granule cell synapses and that nerve growth factor treatment restores the ability of aged rats to sustain long-term potentiation. In this study, we have attempted to analyse the changes which occur in nerve growth factor release and tyrosine receptor kinase phosphorylation following tetanization in tissue prepared from dentate gyrus of young rats, as well as aged rats which did or did not sustain long-term potentiation. We report that KCl-stimulated nerve growth factor release was significantly increased in slices of the dentate gyrus or whole hippocampus, but not in synaptosomes prepared from the dentate gyrus. KCl-induced nerve growth factor release was also significantly enhanced in slices prepared from tetanized, compared with untetanized, tissue obtained from young rats and aged rats which sustained long-term potentiation; this response was absent in tissue prepared from aged rats which failed to sustain long-term potentiation, perhaps due to the enhanced basal nerve growth factor release observed in this tissue. Tetanization increased tyrosine receptor kinase phosphorylation in the dentate gyrus of young rats and aged rats which sustained long-term potentiation. In parallel with the changes in nerve growth factor release, tyrosine receptor kinase phosphorylation was markedly increased in untetanized tissue, which may contribute to the lack of effect in tetanized tissue prepared from aged rats which failed to sustain long-term potentiation. We observed that nerve growth factor concentration and tyrosine receptor kinase expression were decreased in aged, compared with young, rats. The data suggest that deficits in nerve growth factor release and subsequent signalling may contribute to age-related deficits in long-term potentiation.

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Year:  2000        PMID: 10658615     DOI: 10.1016/s0306-4522(99)00460-1

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  4 in total

1.  Age-dependent alterations in nerve growth factor (NGF)-related proteins, sortilin, and learning and memory in rats.

Authors:  Alvin V Terry; Ammar Kutiyanawalla; Anilkumar Pillai
Journal:  Physiol Behav       Date:  2010-11-06

2.  BDNF transcripts, proBDNF and proNGF, in the cortex and hippocampus throughout the life span of the rat.

Authors:  Milka Perovic; Vesna Tesic; Aleksandra Mladenovic Djordjevic; Kosara Smiljanic; Natasa Loncarevic-Vasiljkovic; Sabera Ruzdijic; Selma Kanazir
Journal:  Age (Dordr)       Date:  2012-12-21

Review 3.  Membrane lipid rafts and neurobiology: age-related changes in membrane lipids and loss of neuronal function.

Authors:  Junji Egawa; Matthew L Pearn; Brian P Lemkuil; Piyush M Patel; Brian P Head
Journal:  J Physiol       Date:  2015-10-14       Impact factor: 5.182

4.  Cholinergic Degeneration and Alterations in the TrkA and p75NTR Balance as a Result of Pro-NGF Injection into Aged Rats.

Authors:  Ashley M Fortress; Mona Buhusi; Kris L Helke; Ann-Charlotte E Granholm
Journal:  J Aging Res       Date:  2011-07-11
  4 in total

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