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2019 Fiscal Year Final Research Report

Establishment of treatment for acute ischemic stroke focusing on TRPV4

Research Project

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Project/Area Number 19K21303
Project/Area Number (Other) 18H06198 (2018)
Research Category

Grant-in-Aid for Research Activity Start-up

Allocation TypeMulti-year Fund (2019)
Single-year Grants (2018)
Review Section 0902:General internal medicine and related fields
Research InstitutionKyushu University

Principal Investigator

Tanaka Koji  九州大学, 大学病院, 医員 (50722344)

Project Period (FY) 2018-08-24 – 2020-03-31
KeywordsTRPV4 / ノックアウトマウス / 脳梗塞 / アストロサイト / 脳浮腫
Outline of Final Research Achievements

In the acute phase of ischemia-reperfusion, hypoperfusion associated with ischemia and reperfusion in microvascular regions and disruption of the blood brain barrier (BBB) contribute to post-ischemic brain injury. We aimed to clarify whether brain injury following transient middle cerebral artery occlusion (tMCAO) is ameliorated in Transient Receptor Potential Vanilloid 4 (TRPV4) knockout (Trpv4-/-) mice.
Compared with WT mice, Trpv4-/- mice showed reduced ischemia-induced lesion volume and reduced water content and Evans blue leakage in the ipsilateral hemisphere alongside milder neurological symptoms after the tMCAO. The loss of zonula occludens-1 and occludin proteins in the ipsilateral hemisphere after the tMCAO was attenuated in Trpv4-/- mice. Transmission electron microscopy revealed that parenchymal microvessels in the ischemic lesion were compressed and narrowed by the swollen endfeet of astrocytes in WT mice, but these effects were markedly ameliorated in Trpv4-/- mice.

Free Research Field

脳血管障害

Academic Significance and Societal Importance of the Research Achievements

本研究結果から、急性期にTransient Receptor Potential Vanilloid 4 (TRPV4)を抑制することは再灌流直後のアストロサイト足突起の浮腫を軽減しblood brain barrierを保持することで脳保護的に働くと推察された。
主幹動脈閉塞を伴う急性期脳梗塞に対する急性期再開通療法の進歩が著しい近年において、虚血再灌流後の脳損傷に対する脳保護効果を示した本研究結果の意義は大きいと考えられる。

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Published: 2021-02-19  

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