2012
DOI: 10.1038/bonekey.2012.202
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Estrogen-BDNF signalling in neuronal cells: toward a brain-centric approach to the cure of aging and osteoporosis

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Cited by 2 publications
(2 citation statements)
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“…Differently, the Ucp-1 gene potentiation following cold stress is associated with the enhancement of Bdnf , signaling in brain after 6 h and bone after 5 days, and down-regulation in testis. These findings are consistent with the role of BDNF signaling as a regulator of bone mass reported in previous studies (Camerino, 2012 ; Camerino et al, 2012 ).…”
Section: Discussionsupporting
confidence: 93%
“…Differently, the Ucp-1 gene potentiation following cold stress is associated with the enhancement of Bdnf , signaling in brain after 6 h and bone after 5 days, and down-regulation in testis. These findings are consistent with the role of BDNF signaling as a regulator of bone mass reported in previous studies (Camerino, 2012 ; Camerino et al, 2012 ).…”
Section: Discussionsupporting
confidence: 93%
“…These observations imply that these hormones may share common pathways in tissues, leading to cross talk between different ligand-receptor pathways. The existence of alternative pathways for the hormonal actions has been described for estrogen and androgen that act through genomic and non-genomic pathways (Falkenstein et al, 2000 ; Camerino, 2012 ; Karsenty and Oury, 2012 ; Prossnitz and Barton, 2014 ). The biological advantage of this mechanism is that the lack of effects of a specific gene following pathophysiological conditions or gene downregulation can be counterbalanced by the action of other genes (Karsenty and Oury, 2012 ).…”
Section: Discussionmentioning
confidence: 99%