1998
DOI: 10.1073/pnas.95.19.11429
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Transient expression and transport of brain-derived neurotrophic factor in the male zebra finch’s song system during vocal development

Abstract: The distribution of brain-derived neurotrophic factor (BDNF) in the song system of male zebra finches changes with posthatching age. At day 20, the hyperstriatum ventrale, pars caudale is the only song nucleus in which neurons showed BDNF immunoreactivity. At day 45, the staining in hyperstriatum ventrale, pars caudale was denser than at day 20 and the robust nucleus of the archistriatum, another song nucleus, showed BDNF labeling. By day 65, two additional song nuclei, area X and the lateral magnocellular nuc… Show more

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Cited by 60 publications
(39 citation statements)
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“…In situ hybridization has revealed mRNA in HVC specifically at 30 -35 days of age in males but not females (Dittrich et al, 1999), and cells ventral to HVC at 20 days of age. Immunohistochemistry detected specific labeling in the male HVC from days 20 through 65, with a sharp reduction by adulthood (Akutagawa and Konishi, 1998). However, in another study the protein was expressed at comparable levels in late juvenile (55-60-day-old) males and adult males and females.…”
Section: Summary and Future Directionsmentioning
confidence: 84%
“…In situ hybridization has revealed mRNA in HVC specifically at 30 -35 days of age in males but not females (Dittrich et al, 1999), and cells ventral to HVC at 20 days of age. Immunohistochemistry detected specific labeling in the male HVC from days 20 through 65, with a sharp reduction by adulthood (Akutagawa and Konishi, 1998). However, in another study the protein was expressed at comparable levels in late juvenile (55-60-day-old) males and adult males and females.…”
Section: Summary and Future Directionsmentioning
confidence: 84%
“…Other evidence that L M AN supplies trophic support for RA development is that (1) early L M AN lesions cause massive RA cell death, which can be rescued by inf usion of neurotrophins, including BDN F (Johnson et al, 1997), (2) BDN F can be anterogradely transported from L M AN to R A (Johnson et al, 1997), and (3) BDN F expression is developmentally regulated, with highest expression in R A coinciding with the height of sensorimotor learning (Akutagawa and Konishi, 1998). Activitydependent expression of neurotrophins can homeostatically regulate synaptic strength (Rutherford et al, 1997.…”
Section: Discussionmentioning
confidence: 99%
“…More recently, BDNF/ TrkB signaling has been implicated in learning and memory by directly examining its role in a variety of learning paradigms in behaving animals. Despite the fact that BDNF has been shown to play a critical role in a variety of learning paradigms in mice Qiao et al 1998;Aloe et al 1999;Croll et al 1999;Horger et al 1999), monkeys (Tokuyama et al 2000), zebra finches (Akutagawa and Konishi 1998;Wade 2000), and chicks (Johnston et al 1999;Johnston and Rose 2001), the behavioral tests used in those studies were not as hippocampal-dependent as spatial learning or contextual fear conditioning. We focus here on behavioral evidence obtained using specific hippocampal-mediated spatial learning and contextual fear conditioning paradigms.…”
Section: Bdnf Signaling Is Necessary For Hippocampal-dependent Learningmentioning
confidence: 99%