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  1. 福島医学会
  2. Fukushima Journal of Medical Science
  3. Vol.65 (2019)

Integral role of receptor for advanced glycation end products (RAGE) in nondiabetic atherosclerosis

https://fmu.repo.nii.ac.jp/records/2001985
https://fmu.repo.nii.ac.jp/records/2001985
c663e991-0dc3-44ad-b1a5-c4d088a15614
名前 / ファイル ライセンス アクション
FksmJMedSci_65_p109.pdf FksmJMedSci_65_p109.pdf (7.1 MB)
Item type デフォルトアイテムタイプ(フル)fmu(1)
公開日 2020-01-17
タイトル
タイトル Integral role of receptor for advanced glycation end products (RAGE) in nondiabetic atherosclerosis
言語 en
作成者 Uekita, Hironori

× Uekita, Hironori

en Uekita, Hironori

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Ishibashi, Toshiyuki

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en Ishibashi, Toshiyuki

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Shiomi, Masashi

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en Shiomi, Masashi

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Koyama, Hidenori

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en Koyama, Hidenori

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Ohtsuka, Shukuko

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Yamamoto, Hiroshi

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Yamagishi, Shoichi

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Inoue, Hiroyoshi

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Itabe, Hiroyuki

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Sugimoto, Koichi

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Kamioka, Masashi

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Ohkawara, Hiroshi

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Wada, Ikuo

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Yasuchika, Takeishi

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権利情報
権利情報Resource https://creativecommons.org/licenses/by-nc-sa/4.0/
権利情報 © 2019 The Fukushima Society of Medical Science. This article is licensed under a Creative Commons [Attribution-NonCommercial-ShareAlike 4.0 International] license.
内容記述
内容記述タイプ Abstract
内容記述 An advanced glycation end products (AGE)/a receptor for AGE (RAGE) axis plays a central role in the pathogenesis of diabetic vascular remodeling. This study was conducted to clarify the role of RAGE in nondiabetic atherosclerosis. We used the aortic and coronary atherosclerotic lesions of Watanabe heritable hyperlipidemic (WHHL) rabbits prone to myocardial infarction (WHHLMI) at 1 to 14 months. Immunohistochemistry demonstrated the significant expression of RAGE as early as at 1 month with the stronger expression at 3 and 7 months, which was remarkably diminished at 14 months. RAGE expression was concordant with AGE accumulation. The major original sources of RAGE expression were macrophages and smooth muscle cells in addition to endothelial cells, and RAGE expression was distributed in the areas of phospholipid products, a component of oxidized LDL and nitrotyrosine. The concentrations of serum AGE did not alter significantly with aging. These findings suggested the expression of RAGE was induced by hyperlipidemia and oxidative stress independent of diabetes in WHHLMI rabbits. Additionally, our in vitro study showed that silencing of RAGE tended to attenuate oxidized-LDL-triggered PAI-1 expression in human cultured macrophages, as well as oxidized-LDL-induced tissue factor expression in peritoneal macrophages, suggesting a possible role of RAGE in prothrombogenic molecular regulation. In conclusion, the present study provides in vivo evidence that RAGE plays an integral role in the initiation and progression of nondiabetic atherosclerosis, suggesting that RAGE may be a novel target for treating not only diabetic but also nondiabetic vascular complications.
出版者
出版者 The Fukushima Society of Medical Science
言語
言語 eng
書誌情報 en : Fukushima Journal of Medical Science

巻 65, 号 3, p. 109-121, 発行日 2019
関連情報
関連タイプ isIdenticalTo
識別子タイプ DOI
関連識別子 https://doi.org/10.5387/fms.2019-12
関連情報
識別子タイプ PMID
関連識別子 31915324
関連情報
識別子タイプ ICHUSHI
関連識別子 2020354107
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ journal article
出版タイプ
出版タイプ VoR
出版タイプResource http://purl.org/coar/version/c_970fb48d4fbd8a85
収録物識別子
収録物識別子タイプ PISSN
収録物識別子 0016-2590
収録物識別子
収録物識別子タイプ EISSN
収録物識別子 2185-4610
収録物識別子
収録物識別子タイプ NCID
収録物識別子 AA0065246X
主題
主題Scheme Other
主題 Advanced glycation end products (AGE)
主題
主題Scheme Other
主題 RAGE
主題
主題Scheme Other
主題 Atherosclerosis
主題
主題Scheme Other
主題 WHHLMI rabbits
主題
主題Scheme Other
主題 Oxidized LDL
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