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Takuya Watanabe

Researcher at Fukuoka University

Publications -  64
Citations -  1110

Takuya Watanabe is an academic researcher from Fukuoka University. The author has contributed to research in topics: Neurotransmission & Excitatory postsynaptic potential. The author has an hindex of 15, co-authored 57 publications receiving 851 citations. Previous affiliations of Takuya Watanabe include University of Massachusetts Medical School.

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Lipopolysaccharide-Activated Microglia Induce Dysfunction of the Blood–Brain Barrier in Rat Microvascular Endothelial Cells Co-Cultured with Microglia

TL;DR: The present findings suggest that LPS activates microglia to induce dysfunction of the BBB by producing reactive oxygen species through NADPH oxidase.
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Positioning of AMPA Receptor-Containing Endosomes Regulates Synapse Architecture

TL;DR: It is shown that intracellular AMPARs are transported in Rab11-positive recycling endosomes, which frequently enter dendritic spines and depend on the microtubule and actin cytoskeleton, and a mechanistic link between endosome positioning and postsynaptic structure and composition is suggested.
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Paracellular Barrier and Tight Junction Protein Expression in the Immortalized Brain Endothelial Cell Lines bEND.3, bEND.5 and Mouse Brain Endothelial Cell 4

TL;DR: Results suggest that bEND.3 cells are a convenient and useful model for evaluating BBB function, especially the paracellular barrier, as well as those of the primary mouse brain endothelial cells pMBECs.
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Decreased acetylcholine release is correlated to memory impairment in the Tg2576 transgenic mouse model of Alzheimer's disease

TL;DR: Memory impairment in Tg mice could be attributed to cholinergic synapse dysfunction that could not be caused predominantly by amyloid plaques, and measuring ACh release in this model might be a useful index for the screening of new drugs to treat the early-phase of Alzheimer's disease.
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Altered depression-related behavior and neurochemical changes in serotonergic neurons in mutant R406W human tau transgenic mice

TL;DR: It is suggested that R406W Tg mice exhibit changes in depression-related behavior involving serotonergic neurons and provide an animal model for investigating AD with depression.