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  1. Public
  2. 研究紀要
  3. ACTA MEDICA KINDAI UNIVERSITY
  4. 21(2)1996

Pharmacological investigation of peptide-induced vasorelaxation in the isolated intrarenal arteries of stroke-prone spontaneously hypertensive rats

https://kindai.repo.nii.ac.jp/records/2003052
https://kindai.repo.nii.ac.jp/records/2003052
5fd5ecaf-4ef9-493b-bf7a-660f5ab2769c
名前 / ファイル ライセンス アクション
AA0050842X-19960600-0123.pdf AA0050842X-19960600-0123.pdf (1.1 MB)
アイテムタイプ 紀要論文 / departmental bulletin paper(1)
公開日 2025-07-07
タイトル
タイトル Pharmacological investigation of peptide-induced vasorelaxation in the isolated intrarenal arteries of stroke-prone spontaneously hypertensive rats
言語 en
作成者 Gao, Yujing

× Gao, Yujing

en Gao, Yujing
Kinki University

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言語
言語 eng
キーワード
主題 Atrial natriuretic peptide (ANP), brain natriuretic peptide (BNP), calcitonin gene-related peptide (CGRP), intrarenal artery, SHRSP, vasoactive intestinal peptide (VIP), vasorelaxation
内容記述
内容記述タイプ Abstract
内容記述 This study was designed to investigate the effects of various vasodilator peptides in the isolated intrarenal arteries (IRA) of stroke-prone spontaneously hypertensive rats (SHRSP). In noradrenaline-precontracted IRA of 6-7 month old rats, calcitonin gene-related peptide (CGRP) provoked significantly greater endothelium-independent relaxation in SHRSP than in Wistar-Kyoto rats (WKY) with pD₂ estimates of 8.85 and 8.13 respectively (p<0.01). This relaxation was reversibly inhibited by human CGRP₈₋₃₇ (10⁻⁶ M), a CGRP₁ receptor antagonist. Amylin amide and adrenomedullin also produced greater relaxation in SHRSP than in WKY with pD₂ values of 7.59 and 7.4 for SHRSP and of 7.04 and 7.02 for WKY, respectively (p<0.01). No significant differences between SHRSP and WKY were observed in the endothelium-independent relaxation responses to atrial natriuretic peptide (ANP), brain natriuretic peptide (BNP), c-type natriuretic peptide, vasoactive intestinal peptide (VIP), and peptide histidine isoleucine. Bradykinin produced minor endothelium-dependent vasodilation similarly in the two strains. Substance P and neurokinin A did not relax the IRA at all. Furthermore, response to CGRP was also evaluated in younger SHRSP. It was found that reactivity to CGRP was still significantly greater in SHRSP aged 3 and 1.5 months than in age-matched WKY. In addition, a notable decline in the magnitude of CGRP-induced response was found in WKY as the age increased from 1.5 to 6-7 months, whereas in SHRSP no such age-related decrease was observed. Neither significant differences between the two strains nor significant age-dependent variations in either strain were found in relaxation responses to dibutyryl cyclic AMP, forskolin, and 3-isobutyl-1-methylxanthine. Incubation with glibenclamide (10⁻⁶ M) did not affect CGRP-induced relaxation in both SHRSP and WKY at all the ages used. In summary, the present results show that several peptides, such as CGRP, ANP, BNP, and VIP, are able to relax rat IRA remarkably, suggesting their possible role in modulating intrarenal vascular tone. In SHRSP, a significantly increased relaxation response to CGRP₁ receptor stimulation and lack of age-related reduction of this enhanced response are demonstrated. These changes found in SHRSP may not be a post-receptor event relating to second messengers like cyclic AMP, or to ATP-dependent potassium channels.
言語 en
出版者
出版者 The Kinki University Medical Association
言語 en
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
出版タイプ
出版タイプ AM
出版タイプResource http://purl.org/coar/version/c_ab4af688f83e57aa
収録物識別子
収録物識別子タイプ PISSN
収録物識別子 03866092
開始ページ
開始ページ 123
終了ページ
終了ページ 137
書誌情報 en : ACTA MEDICA KINKI UNIVERSITY

巻 21, 号 2, p. 123-137, 発行日 1996-06
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