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Calcium imaging in spinal cord slices and in vivo spinal cord using calcium-sensitive fluorescent protein

Research Project

Project/Area Number 15K15565
Research Category

Grant-in-Aid for Challenging Exploratory Research

Allocation TypeMulti-year Fund
Research Field Anesthesiology
Research InstitutionNiigata University

Principal Investigator

Kamiya Yoshinori  新潟大学, 医歯学総合病院, 特任教授 (90381491)

Co-Investigator(Kenkyū-buntansha) 馬場 洋  新潟大学, 医歯学系, 教授 (00262436)
渡部 達範  新潟大学, 医歯学総合病院, 助教 (30748330)
Co-Investigator(Renkei-kenkyūsha) SHIBUKI Katsuei  新潟大学, 脳研究所, 教授 (40146163)
TAKEBAYASHI Hirohide  新潟大学, 医歯学系, 教授 (60353439)
Research Collaborator SASAKI Mika  
Project Period (FY) 2015-04-01 – 2017-03-31
Project Status Completed (Fiscal Year 2016)
Budget Amount *help
¥3,640,000 (Direct Cost: ¥2,800,000、Indirect Cost: ¥840,000)
Fiscal Year 2016: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Fiscal Year 2015: ¥1,820,000 (Direct Cost: ¥1,400,000、Indirect Cost: ¥420,000)
Keywordsカルシウムイメージング / 遺伝子導入 / 疼痛メカニズム / 脊髄後角 / 一次知覚神経
Outline of Final Research Achievements

In this study, we aimed to introduce calcium-sensitive fluorescent protein into the spinal dorsal horn and/or dorsal root ganglia (DRG) using adeno-associated virus vector (AAV) to measure the neural activity in the spinal dorsal horn two-dimensionally. We found that the AAV vector inoculated intrathecal cavity seemed to express TurboRFP, which is a marker protein, both in the spinal cord dorsal horn and DRG 1 to 2 weeks after administration. However, due to limitations of immunohistological techniques, we could not be confirmed that the transgene-derived protein was definitely expressed in spinal dorsal horn and DRG. Therefore, it did not reach the result of the physiological experiment that was planned ahead.

Report

(3 results)
  • 2016 Annual Research Report   Final Research Report ( PDF )
  • 2015 Research-status Report

URL: 

Published: 2015-04-16   Modified: 2018-03-22  

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