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Angiotensin-(1-7) and angiotensin-(1-9): assessment as therapeutic targets in acute vascular injury and remodelling

Angiotensin-(1-7) and angiotensin-(1-9): assessment as therapeutic targets in acute vascular injury and remodelling
血管紧张素-(1-7) 和血管紧张素-(1-9):作为急性血管损伤和重塑治疗靶点的评估
批准号:
MR/L019108/1
负责人:
Stuart Nicklin
金额:
$45.61万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2014
资助国家:
英国
项目状态:
已结题
起止时间:
2014 至 --

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中文摘要
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英文摘要
Heart disease is commonly caused by the buildup of fat or plaques in blood vessels that deliver blood to the heart, causing them to become blocked. To unblock blood vessels doctors use two approaches, in one a balloon is inserted into the blockage and inflated to clear it and in another a piece of vein is removed from the patients leg and implanted into the heart to bypass the blockage. Both approaches are effective to treat the patients, however damage to the blood vessel by the inflated balloon or to the vein used to bypass the blockage by the high blood pressure in the heart cause these treatments to fail, by triggering overgrowth of the blood vessels causing them to become blocked again. Currently, there is a need for new treatments to prevent this failure. We have identified a new potential therapeutic target that may be able to prevent this overgrowth. The body produces specific hormones which travel via the bloodstream and engage with receptors which contribute to the normal function of blood vessels, the heart and kidney. The main hormone from this system, angiotensin II, can become overactive and contribute to the development of cardiovascular diseases, including the adverse vascular overgrowth which blocks blood vessels. We have identified an alternative hormone in this pathway which can block the growth of the cells in blood vessels and potentially prevent the vessels from becoming blocked. Here, we will investigate this hormone more fully to understand how it functions and to test whether it has therapeutic benefit in animal models of vessel blockage. This will help us understand the function better and highlight whether it is a suitable molecular to develop into a therapeutic drug in the future.
期刊论文(10)
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会议论文
Angiotensin-(1-7) and angiotensin-(1-9) inhibit vascular smooth muscle cell growth and migration in vitro and vascular remodelling in vivo
血管紧张素-(1-7) 和血管紧张素-(1-9) 抑制血管平滑肌细胞体外生长和迁移以及体内血管重塑
DOI: 10.1016/j.atherosclerosis.2015.04.158
发表时间: 2015
期刊: Atherosclerosis
影响因子: 5.3
作者: [McKinney C]
通讯作者: McKinney C
DOI: 10.1080/14789450.2018.1493927
发表时间: 2018-07
期刊: Expert review of proteomics
影响因子: 3.4
作者: [Delles C, Carrick E, Graham D, Nicklin SA]
通讯作者: Nicklin SA
178 Angiotensin-(1-9) inhibits vascular smooth muscle cell proliferation and migration in vitro and neointimal formation in vivo
178 血管紧张素-(1-9) 抑制体外血管平滑肌细胞增殖和迁移以及体内新内膜形成
DOI: 10.1136/heartjnl-2015-308066.178
发表时间: 2015
期刊: Heart
影响因子: 5.7
作者: [McKinney C]
通讯作者: McKinney C
Angiotensin-(1-9) inhibits vascular smooth muscle cell proliferation and migration in vitro and neointimal formation in vivo
血管紧张素-(1-9) 抑制血管平滑肌细胞体外增殖和迁移以及体内新内膜形成
DOI: --
发表时间:
期刊: Submitted
影响因子: --
作者: [McKinney CA]
通讯作者: McKinney CA
9
    Dissecting the mechanism of action of the renin angiotensin hormone angiotensin1-9
    • 批准号:
      G0901161/1
    • 项目类别:
      Research Grant
    • 资助金额:
      $48.87万
    • 财政年份:
      2010
    • 负责人:
      Stuart Nicklin
    • 依托单位:
    Development of efficient disease-regulated expression cassettes for gene therapy using microRNA targeting sequences
    • 批准号:
      BB/F006667/1
    • 项目类别:
      Research Grant
    • 资助金额:
      $42.99万
    • 财政年份:
      2008
    • 负责人:
      Stuart Nicklin
    • 依托单位:
    国内基金
    海外基金
    新型 Cyclic Apelin-12 环肽拮抗 Ang II 和 Apelin-13 诱导的心 肌肥厚及其机制
    • 批准号:
      2024JJ9370
    • 项目类别:
      省市级项目
    • 资助金额:
      --
    • 批准年份:
      2024
    • 负责人:
      欧阳雪 倩
    • 依托单位:
    内源性Angiotensin Ⅱ通过脊髓背角星形胶质细胞谷氨酸转运体-1 (GLT-1)调控糖尿病神经病理性痛的机制研究
    • 批准号:
      81871088
    • 项目类别:
      面上项目
    • 资助金额:
      56.0万元
    • 批准年份:
      2018
    • 负责人:
      严喜胜
    • 依托单位:
    Renin-Angiotensin System在介导机械通气所致肺微血管内皮细胞功能障碍中的作用及其机制研究
    • 批准号:
      81372100
    • 项目类别:
      面上项目
    • 资助金额:
      70.0万元
    • 批准年份:
      2013
    • 负责人:
      毛燕飞
    • 依托单位:
    具有调控VSMC增殖信号通路的新型二氢黄酮类小分子的构建及其调控机制研究
    • 批准号:
      81172938
    • 项目类别:
      面上项目
    • 资助金额:
      45.0万元
    • 批准年份:
      2011
    • 负责人:
      李青山
    • 依托单位: