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Thrombin-Induced Responses Via Protease-Activated Receptor 1 Blocked by the Endothelium on Isolated Porcine Retinal Arterioles

https://asahikawa-med.repo.nii.ac.jp/records/5944
https://asahikawa-med.repo.nii.ac.jp/records/5944
11f255e9-3dcb-48ec-995d-1604b13adca0
名前 / ファイル ライセンス アクション
7064.pdf 7064.pdf (534.6 kB)
Item type 学位論文 / Thesis or Dissertation_02(1)
公開日 2018-10-05
タイトル
タイトル Thrombin-Induced Responses Via Protease-Activated Receptor 1 Blocked by the Endothelium on Isolated Porcine Retinal Arterioles
言語 en
言語
言語 eng
キーワード
主題Scheme Other
主題 PAR-1
キーワード
主題Scheme Other
主題 Thrombin
キーワード
主題Scheme Other
主題 endothelium blood retinal barrier
キーワード
主題Scheme Other
主題 protease-activated receptor 1
キーワード
主題Scheme Other
主題 vasoconstriction
キーワード
主題Scheme Other
主題 vasorelaxation
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_db06
資源タイプ doctoral thesis
アクセス権
アクセス権 open access
アクセス権URI http://purl.org/coar/access_right/c_abf2
著者 髙橋, 賢伍

× 髙橋, 賢伍

ja 髙橋, 賢伍

ja-Kana タカハシ, ケンゴ

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著者 ローマ字
Takahashi, Kengo
書誌情報 Current eye research

巻 43, 号 11, p. 1374-1382, 発行日 2018-11-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 0271-3683
DOI
識別子タイプ DOI
関連識別子 10.1080/02713683.2018.1496266
識別番号 その他
内容記述タイプ Other
内容記述 PMID:29966442
学位授与番号
学位授与番号 甲526
学位名
学位名 博士(医学)
学位授与機関
学位授与機関名 旭川医科大学
抄録
内容記述タイプ Abstract
内容記述 PURPOSE:
\nThrombin, a serine protease, causes organ-specific responses to vessels. However, the mechanism by which thrombin affects the retinal microcirculation remains unclear. We examined the effects of thrombin on the retinal microvasculature and signaling mechanisms.
METHODS:
\nPorcine retinal arterioles were isolated, cannulated, and pressurized (55 cmH2O) without flow in this in vitro study. Videomicroscopy techniques recorded changes in diameter in the retinal arterioles in response to thrombin at concentrations ranging from 0.001 to 20 mU/ml.
RESULTS:
\nExtraluminal administration of thrombin induced concentration-dependent vascular responses, that is, vasoconstriction at low concentrations less than 5 mU/ml and vasorelaxation with high concentrations greater than 5 mU/ml. However, intraluminal administration of thrombin (5 mU/m) did not constrict the retinal arterioles; in denuded vessels, intraluminal administration constricted the retinal arterioles. Thrombin-induced vasoconstriction was significantly (p < 0.01) suppressed by pretreatment with a protein kinase C (PKC) inhibitor and a protease-activated receptor (PAR)-1 inhibitor but not by PAR-2 and PAR-4 inhibitors or denudation. A rho kinase (ROCK) inhibitor also suppressed thrombin-induced vasoconstriction (5 mU/ml) compared with sodium nitroprusside. Endothelial denudation and pretreatment with an endothelial nitric oxide (NO) synthase inhibitor suppressed vasorelaxation caused by a high concentration of thrombin.
CONCLUSIONS:
\nA low concentration of thrombin causes vasoconstriction of smooth muscles via PAR-1, PKC, and ROCK, and a high concentration of thrombin possibly causes vasorelaxation of the retinal arterioles via nitric oxide synthase activation in the endothelium. The vascular endothelium might block signaling of thrombin-induced vasoconstriction in the retinal arterioles when administered intraluminally.
資源タイプ
内容記述タイプ Other
内容記述 application/pdf
著者版フラグ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
フォーマット
内容記述タイプ Other
内容記述 application/pdf
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