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Oroxylin A Induces BDNF Expression on Cortical Neurons through Adenosine A2(A) Receptor Stimulation: A Possible Role in Neuroprotection

Authors
Jeon, Se JinBak, HaerangSeo, JungeunHan, So MinLee, Sung HoonHan, Seol-HeuiKwon, Kyoung JaRyu, Jong HoonCheong, Jae HoonKo, Kwang HoYang, Sung-IlChoi, Ji WoongPark, Seung HwaShin, Chan Young
Issue Date
31-Jan-2012
Publisher
KOREAN SOC APPLIED PHARMACOLOGY
Keywords
Oroxylin A; BDNF; CREB; Adenosine A2(A) receptor; CGS21680; ZM241385
Citation
BIOMOLECULES & THERAPEUTICS, v.20, no.1, pp.27 - 35
Journal Title
BIOMOLECULES & THERAPEUTICS
Volume
20
Number
1
Start Page
27
End Page
35
URI
https://scholarworks.bwise.kr/gachon/handle/2020.sw.gachon/16618
DOI
10.4062/biomolther.2012.20.1.027
ISSN
1976-9148
Abstract
Oroxylin A is a flavone isolated from a medicinal herb reported to be effective in reducing the inflammatory and oxidative stresses. It also modulates the production of brain derived neurotrophic factor (BDNF) in cortical neurons by the transactivation of cAMP response element-binding protein (CREB). As a neurotrophin, BDNF plays roles in neuronal development, differentiation, synaptogenesis, and neural protection from the harmful stimuli. Adenosine A2(A) receptor colocalized with BDNF in brain and the functional interaction between A2(A) receptor stimulation and BDNF action has been suggested. In this study, we investigated the possibility that oroxylin A modulates BDNF production in cortical neuron through the regulation of A2(A) receptor system. As expected, CGS21680 (A2(A) receptor agonist) induced BDNF expression and release, however, an antagonist, ZM241385, prevented oroxylin A-induced increase in BDNF production. Oroxylin A activated the PI3K-Akt-GSK-3 beta signaling pathway, which is inhibited by ZM241385 and the blockade of the signaling pathway abolished the increase in BDNF production. The physiological roles of oroxylin A-induced BDNF production were demonstrated by the increased neurite extension as well as synapse formation from neurons. Overall, oroxylin A might regulate BDNF production in cortical neuron through A2(A) receptor stimulation, which promotes cellular survival, synapse formation and neurite extension.
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