Special Medical Service Center, The First Affiliated Hospital of Sun Yat‑Sen University, Guangzhou, Guangdong 510080, P.R. China.
Department of Rehabilitation, Sun Yat‑Sen Memorial Hospital, Sun Yat‑Sen University, Guangzhou, Guangdong 510080, P.R. China.
Mol Med Rep. 2020 Nov;22(5):4320-4328. doi: 10.3892/mmr.2020.11508. Epub 2020 Sep 14.
Hypertension is one of the critical risk factors of cerebrovascular disease. Caveolin‑1 (Cav‑1) has been suggested to be involved in the development of hypertension; however, the underlying mechanism remains largely unknown. Therefore, the present study aimed to investigate the mechanism underlying Cav‑1 in hypertension. In the present study, the hypertension model was induced by infusion of angiotensin II (Ang‑II) in rats. Cell Counting Kit‑8 assay was used to detect the viability of human umbilical vein endothelial cells (HUVECs). Flow cytometry was used to determine the apoptosis of HUVECs. Transmission electron microscopy was utilized to address the thickness of the vessel walls. Reverse transcription‑quantitative PCR, western blotting and immunofluorescence staining were used to assess the mechanism of cav‑1/Notch1 involved in hypertensive vascular remodeling. In the present study, an Ang‑II‑induced hypertension model was successfully established in rats. With this model, it was found that the expression levels of cav‑1 and Notch1 were significantly increased in brain tissues in the hypertension group compared with the sham‑operated group. In cultured HUVECs, knockdown of cav‑1 regulated Ang‑II‑induced HUVEC viability and apoptosis, and modulated hypertensive vascular remodeling, which was mediated by the Notch pathway. The data of the present study demonstrated that the cav‑1/Notch signaling plays an important role in the regulation of Ang‑II‑induced hypertension and vascular remodeling.
高血压是脑血管疾病的关键危险因素之一。小窝蛋白-1(Cav-1)已被认为参与高血压的发生,但其中的潜在机制仍知之甚少。因此,本研究旨在探讨 Cav-1 在高血压中的作用机制。在本研究中,通过向大鼠输注血管紧张素 II(Ang-II)来诱导高血压模型。使用细胞计数试剂盒-8 检测人脐静脉内皮细胞(HUVEC)的活力。通过流式细胞术检测 HUVEC 的凋亡情况。采用透射电子显微镜观察血管壁的厚度。逆转录-定量 PCR、western blot 和免疫荧光染色用于评估 cav-1/Notch1 参与高血压血管重塑的机制。在本研究中,成功建立了 Ang-II 诱导的高血压大鼠模型。使用该模型发现,与假手术组相比,高血压组脑组织中 cav-1 和 Notch1 的表达水平显著升高。在培养的 HUVEC 中,cav-1 的敲低调节 Ang-II 诱导的 HUVEC 活力和凋亡,并通过 Notch 通路调节高血压血管重塑。本研究的数据表明,cav-1/Notch 信号通路在调节 Ang-II 诱导的高血压和血管重塑中发挥重要作用。