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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/594411f255e9-3dcb-48ec-995d-1604b13adca0
名前 / ファイル | ライセンス | アクション |
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7064.pdf (534.6 kB)
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Item type | 学位論文 / Thesis or Dissertation_02(1) | |||||
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公開日 | 2018-10-05 | |||||
タイトル | ||||||
言語 | en | |||||
タイトル | Thrombin-Induced Responses Via Protease-Activated Receptor 1 Blocked by the Endothelium on Isolated Porcine Retinal Arterioles | |||||
言語 | ||||||
言語 | eng | |||||
キーワード | ||||||
主題 | PAR-1 | |||||
キーワード | ||||||
主題 | Thrombin | |||||
キーワード | ||||||
主題 | endothelium blood retinal barrier | |||||
キーワード | ||||||
主題 | protease-activated receptor 1 | |||||
キーワード | ||||||
主題 | vasoconstriction | |||||
キーワード | ||||||
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 |
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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 |
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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. |
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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 |