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New Approaches to Blockade of the Renin–Angiotensin–Aldosterone System: Chymase as an Important Target to Prevent Organ Damage

机译:阻断肾素-血管紧张素-醛固酮系统的新方法:胰酶作为预防器官损伤的重要靶标

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References(75) Cited-By(20) Chymase plays a crucial role in angiotensin II formation in various tissues. Angiotensin II induces gene expression of transforming growth factor (TGF)-β and matrix metalloproteinase (MMP)-9 precursors, and chymase can convert precursors of TGF-β and MMP-9 to their active forms. In cultured fibroblasts, significant increases in cell growth and TGF-β levels were observed after chymase injection; these increases were inhibited by a chymase inhibitor, but not by an angiotensin II–receptor blocker. In apolipoprotein E–deficient mice, abdominal aortic aneurysm (AAA) development depends on an increase in MMP-9 activities induced by angiotensin II infusion, but the inhibition of MMP-9 activation by a chymase inhibitor resulted in attenuation of the angiotensin II–induced AAA development. The upregulation of MMP-9 and TGF-β levels is involved in damage to various organs, but these gene expressions are not completely induced by angiotensin II alone. Therefore, chymase inhibition may be useful for attenuating MMP-9 and TGF-β levels, in addition to reducing angiotensin II formation, and this function may provide powerful organ protection. In this review, we propose the possible use of chymase inhibitors as agents to prevent organ damage.
机译:参考文献(75)Cited-By(20)胸苷酶在各种组织中血管紧张素II的形成中起着至关重要的作用。血管紧张素II诱导转化生长因子(TGF)-β和基质金属蛋白酶(MMP)-9前体的基因表达,而糜酶可以将TGF-β和MMP-9的前体转化为活性形式。在培养的成纤维细胞中,在注射糜酶后观察到细胞生长和TGF-β水平显着增加。这些增加受到糜蛋白酶抑制剂的抑制,但不受血管紧张素Ⅱ受体阻滞剂的抑制。在缺乏载脂蛋白E的小鼠中,腹主动脉瘤(AAA)的发育取决于血管紧张素II输注诱导的MMP-9活性的增加,但糜蛋白酶抑制剂对MMP-9激活的抑制导致血管紧张素II诱导的减弱AAA开发。 MMP-9和TGF-β水平的上调参与了对各种器官的损害,但是这些基因表达并不能完全由单独的血管紧张素II诱导。因此,糜蛋白酶抑制除了减少血管紧张素II的形成外,还可用于降低MMP-9和TGF-β的水平,该功能可提供强大的器官保护作用。在这篇综述中,我们建议可能使用糜酶抑制剂作为预防器官损害的药物。

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