School of Public Health and Preventive Medicine, Monash University, 553 St Kilda Road, Melbourne, VIC, 3004, Australia.
Menzies Institute for Medical Research, University of Tasmania, Hobart, TAS, Australia.
Curr Hypertens Rep. 2024 Jan;26(1):1-19. doi: 10.1007/s11906-023-01266-0. Epub 2023 Sep 21.
To provide an overview of the association between angiotensin II receptor blocker (ARB) use and cognitive outcomes.
ARBs have previously shown greater neuroprotection compared to other anti-hypertensive classes. The benefits are primarily attributed to the ARB's effect on modulating the renin-angiotensin system via inhibiting the Ang II/AT1R pathway and activating the Ang II/AT2R, Ang IV/AT4R, and Ang-(1-7)/MasR pathways. These interactions are associated with pleiotropic neurocognitive benefits, including reduced β-amyloid accumulation and abnormal hyperphosphorylation of tau, ameliorated brain hypo-fusion, reduced neuroinflammation and synaptic dysfunction, better neurotoxin clearing, and blood-brain barrier function restoration. While ACEis also inhibit AT1R, they simultaneously lower Ang II and block the Ang II/AT2R and Ang IV/AT4R pathways that counterbalance the potential benefits. ARBs may be considered an adjunctive approach for neuroprotection. This preliminary evidence, coupled with their underlying mechanistic pathways, emphasizes the need for future long-term randomized trials to yield more definitive results.
探讨血管紧张素Ⅱ受体阻滞剂(ARB)的使用与认知结局之间的关系。
与其他抗高血压药物相比,ARB 先前显示出更大的神经保护作用。其益处主要归因于 ARB 通过抑制血管紧张素Ⅱ/AT1R 途径和激活血管紧张素Ⅱ/AT2R、血管紧张素 IV/AT4R 和血管紧张素-(1-7)/MasR 途径来调节肾素-血管紧张素系统。这些相互作用与多种神经认知益处相关,包括减少β-淀粉样蛋白积累和 tau 的异常过度磷酸化、改善脑低融合、减少神经炎症和突触功能障碍、更好地清除神经毒素以及恢复血脑屏障功能。虽然 ACEi 也抑制 AT1R,但它们同时降低血管紧张素Ⅱ并阻断血管紧张素Ⅱ/AT2R 和血管紧张素 IV/AT4R 途径,从而抵消了潜在的益处。ARB 可被视为神经保护的辅助治疗方法。这些初步证据,加上其潜在的机制途径,强调需要进行未来的长期随机试验以获得更明确的结果。