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Receptor for Advanced Glycation End-Product Antagonist Reduces Blood–Brain Barrier Damage After Intracerebral Hemorrhage
Author(s) -
Fan Yang,
Zhe Wang,
John H. Zhang,
Jiping Tang,
Xin Liu,
Liang Tan,
Qingyuan Huang,
Hua Feng
Publication year - 2015
Publication title -
stroke
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.397
H-Index - 319
eISSN - 1524-4628
pISSN - 0039-2499
DOI - 10.1161/strokeaha.114.008336
Subject(s) - medicine , rage (emotion) , hmgb1 , occludin , proinflammatory cytokine , pharmacology , blood–brain barrier , evans blue , neuroprotection , intracerebral hemorrhage , endocrinology , nitric oxide synthase , receptor , inflammation , nitric oxide , chemistry , tight junction , central nervous system , biology , biochemistry , neuroscience , subarachnoid hemorrhage
To determine whether the receptor for advanced glycation end-products (RAGE) plays a role in early brain injury from intracerebral hemorrhage (ICH), RAGE expression and activation after injury were examined in a rat model of ICH with or without administration of a RAGE-specific antagonist (FPS-ZM1).

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