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  1. Public
  2. 研究紀要
  3. Acta Medica Kindai University
  4. 35(1)2010
  1. Private
  2. 研究紀要
  3. Acta medica Kinki University
  4. 35(1)2010

Experimental study on preventive effects of statin and ARB for metabolic syndrome : using a new animal model, obese stroke-prone spontaneous hypertensive rats

https://kindai.repo.nii.ac.jp/records/10510
https://kindai.repo.nii.ac.jp/records/10510
6f81fb15-2bea-4e3c-b43c-0a5164313b1b
名前 / ファイル ライセンス アクション
AA0050842X-20100600-0033.pdf AA0050842X-20100600-0033.pdf (2.1 MB)
Item type ☆紀要論文 / Departmental Bulletin Paper(1)
公開日 2010-07-22
タイトル
タイトル Experimental study on preventive effects of statin and ARB for metabolic syndrome : using a new animal model, obese stroke-prone spontaneous hypertensive rats
言語 en
著者 Masuno, Koichi

× Masuno, Koichi

Masuno, Koichi

ja-Kana マスノ, コウイチ

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Takemori, Kumiko

× Takemori, Kumiko

Takemori, Kumiko

ja-Kana タケモリ, クミコ

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Inoue, Takao

× Inoue, Takao

Inoue, Takao

ja-Kana イノウエ, タカオ

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Yamamoto, Kazuo

× Yamamoto, Kazuo

Yamamoto, Kazuo

ja-Kana ヤマモト, カズオ

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Ito, Hiroyuki

× Ito, Hiroyuki

Ito, Hiroyuki

ja-Kana イトウ, ヒロユキ

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言語
言語 eng
キーワード
主題 SHRSP/IDmcr-fa/fa rats, HMG-CoA reductase inhibitor, angiotensin II receptor blocker, adiponectin
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 departmental bulletin paper
著者所属(翻訳)
値 Department of Pathology, Kinki University, Faculty of Medicine
著者所属(翻訳)
値 Department of Pathology, Kinki University, Faculty of Medicine
著者所属(翻訳)
値 Department of Pathology, Kinki University, Faculty of Medicine
著者所属(翻訳)
値 Department of Pathology, Kinki University, Faculty of Medicine
著者所属(翻訳)
値 Department of Pathology, Kinki University, Faculty of Medicine
版
出版タイプ NA
出版タイプResource http://purl.org/coar/version/c_be7fb7dd8ff6fe43
出版者 名前
出版者 The Kinki University Medical Association
書誌情報 en : ACTA MEDICA KINKI UNIVERSITY

巻 35, 号 1, p. 33-40, 発行日 2010-06-01
ISSN
収録物識別子タイプ ISSN
収録物識別子 03866092
抄録
内容記述タイプ Abstract
内容記述 SHRSP/IDmcr-fa/fa (SHRSP/fatty) rats are a new animal model that have the potential to develop severe hypertension, obesity, hyperlipidemia, and hyperglycemia, followed by arteriopathy and glomerulopathy in the kidneys. Thus, SHRSP/fatty rats seem to be the most severe animal model of human metabolic syndrome. Using this unique animal model, we investigated how HMG-CoA reductase inhibitor (statin), a well-known drug for hypercholesterolemia, and angiotensin II receptor blocker (ARB), a widely-used anti-hypertensive drug, affected the pathophysiology related to metabolic syndrome. The statin increased the mRNA expression of adiponectin and leptin, decreased the expression of TNF-alpha gene, and increased the secretion of high molecular weight (HMW) adiponectin, without a lipid-lowering effect. ARB increased both total adiponectin and HMW adiponectin, independent of blood pressure lowering. Histologically, the incidence of renal lesions, such as angionecrosis and glomerulosclerosis, was decreased in both treated groups. Except for well-known pharmacological effects of these drugs, the additional medicinal benefit of the statin depended on its anti-inflammatory effect, and that of ARB probably depended on its direct effect on adipocytes. It was considered that the increase of HMW adiponectin was enhanced by both pathways, and this may be a common factor of the protective effects of both drugs on pathophysiological damages in SHRSP/fatty rats.
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内容記述 application/pdf
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