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1型血管紧张素II受体在大鼠脑动脉瘤形成中的作用。

Role of angiotensin II type 1 receptor in cerebral aneurysm formation in rats.

作者信息

Aoki Tomohiro, Nishimura Masaki, Kataoka Hiroharu, Ishibashi Ryota, Miyake Takashi, Takagi Yasushi, Morishita Ryuichi, Hashimoto Nobuo

机构信息

Department of Neurosurgery, Kyoto University, Graduate School of Medicine, Kyoto 606-8507, Japan.

出版信息

Int J Mol Med. 2009 Sep;24(3):353-9. doi: 10.3892/ijmm_00000239.

Abstract

Cerebral aneurysm (CA) causes catastrophic subarachnoid hemorrhage which is characterized by a high mortality and morbidity rate. CA is a common disease worldwide but to date there is no medical treatment against unruptured CAs. Thus, it is important to study the mechanisms of CA formation. Our previous report demonstrated that chronic inflammatory response in cerebral arterial bifurcation by hemodynamic stress deteriorated arterial walls and formed CA. Therefore, drugs with anti-inflammatory effects might effectively treat CA formation. As renin angiotensin system (RAS) is a major inflammatory cascade and related to various vascular diseases, including aortic aneurysms, the role of angiotensin (Ang) II type 1 receptor might contribute to the progression of CAs. However, in cerebral aneurysmal walls, Ang II type 1 receptor was not up-regulated. In addition, subcutaneously administered Ang II type 1 receptor blocker did not inhibit CA formation, nor inflammation in cerebral aneurysmal walls in rat models at a sub-suppressor dose. These results indicate that RAS might play a less important role in CA formation compared to aortic anuerysms or other vascular diseases. This suggests that there are different mechanisms between the pathogenesis of cereberal and aortic aneurysms.

摘要

脑动脉瘤(CA)可导致灾难性的蛛网膜下腔出血,其特点是死亡率和发病率很高。CA是一种全球常见疾病,但迄今为止,尚无针对未破裂CA的医学治疗方法。因此,研究CA形成的机制很重要。我们之前的报告表明,血流动力学应激导致脑动脉分叉处的慢性炎症反应会使动脉壁恶化并形成CA。因此,具有抗炎作用的药物可能有效治疗CA的形成。由于肾素血管紧张素系统(RAS)是主要的炎症级联反应,且与包括主动脉瘤在内的各种血管疾病有关,1型血管紧张素(Ang)II受体的作用可能促进CA的进展。然而,在脑动脉瘤壁中,1型Ang II受体并未上调。此外,皮下注射1型Ang II受体阻滞剂在亚抑制剂量下并不能抑制大鼠模型中CA的形成,也不能抑制脑动脉瘤壁中的炎症。这些结果表明,与主动脉瘤或其他血管疾病相比,RAS在CA形成中可能起的作用较小。这表明脑动脉瘤和主动脉瘤的发病机制之间存在不同的机制。

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