| Literature DB >> 18601951 |
Hideki Tamura1, David C Ng, Takashi Tokuda, Honda Naoki, Takuma Nakagawa, Taro Mizuno, Yumiko Hatanaka, Yasuyuki Ishikawa, Jun Ohta, Sadao Shiosaka.
Abstract
We developed an implantable one-chip biofluoroimaging device (termed biomedical photonic LSI; BpLSI) which enabled real-time molecular imaging with conventional electrophysiology in vivo in deep brain areas. The multimodal LSI enabled long-term sequential imaging of the fluorescence emitted by proteolysis-linked fluorogenic substrate. Using the BpLSI, we observed a process of stimulation-dependent modulation at synapse with multi-site (16 x 19 pixel) in widespread area and a high-speed video rate, and found that the gradual up-regulated proteolytic activity in a wide range of hippocampal CA1 area and the steep activity in local area, indicating that the proteolysis system is a basis for the fixation of long-term potentiation in post-excited synapses in the hippocampus. Mathematical data analysis confirmed the direct involvement of functional proteolysis for neural plasticity.Entities:
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Year: 2008 PMID: 18601951 DOI: 10.1016/j.jneumeth.2008.06.002
Source DB: PubMed Journal: J Neurosci Methods ISSN: 0165-0270 Impact factor: 2.390