Screening inducers of neuronal BDNF gene transcription using primary cortical cell cultures from BDNF-luciferase transgenic mice.
Mamoru FukuchiYui OkunoHironori NakayamaAoi NakanoHisashi MoriSatoru MitazakiYuka NakanoKazufumi ToumeMichiko JoIchiro TakasakiKazuki WatanabeNaotoshi ShibaharaKatsuko KomatsuAkiko TabuchiMasaaki TsudaPublished in: Scientific reports (2019)
Brain-derived neurotrophic factor (BDNF) is a key player in synaptic plasticity, and consequently, learning and memory. Because of its fundamental role in numerous neurological functions in the central nervous system, BDNF has utility as a biomarker and drug target for neurodegenerative and neuropsychiatric disorders. Here, we generated a screening assay to mine inducers of Bdnf transcription in neuronal cells, using primary cultures of cortical cells prepared from a transgenic mouse strain, specifically, Bdnf-Luciferase transgenic (Bdnf-Luc) mice. We identified several active extracts from a library consisting of 120 herbal extracts. In particular, we focused on an active extract prepared from Ginseng Radix (GIN), and found that GIN activated endogenous Bdnf expression via cAMP-response element-binding protein-dependent transcription. Taken together, our current screening assay can be used for validating herbal extracts, food-derived agents, and chemical compounds for their ability to induce Bdnf expression in neurons. This method will be beneficial for screening of candidate drugs for ameliorating symptoms of neurological diseases associated with reduced Bdnf expression in the brain, as well as candidate inhibitors of aging-related cognitive decline.
Keyphrases
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- spinal cord
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- stem cells
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- metabolic syndrome
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- gene expression
- mesenchymal stem cells
- adipose tissue
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- adverse drug