Department of Neurology, Nanjing First Hospital, Nanjing Medical University, Nanjing, Jiangsu Province, PR China.
Department of Neurology, Nanjing First Hospital, China Pharmaceutical University, Nanjing, Jiangsu Province, PR China.
J Alzheimers Dis. 2023;94(3):919-933. doi: 10.3233/JAD-230133.
Alzheimer's disease (AD) is the most common type of neurodegenerative disorder. There are few effective medications for halting the progression of AD. Telmisartan (TEL) is a widely used anti-hypertensive drug approved by FDA. Aside from treating hypertension, TEL has been revealed to provide protection against AD. However, the underlying mechanisms remain unclear.
To investigate the mechanisms underlying the beneficial effects of TEL against AD.
Eight-month-old APP/PS1 mice were administered with 5 mg/kg TEL once per day for 4 successive months. Nesting test, Y-maze test, and Morris water maze test were employed to assess the cognitive and executive functions. Neuronal and synaptic markers, amyloid-β (Aβ) pathology, neuroinflammation, and oxidative stress in the brains were measured. Specifically, components involved in Aβ production and degradation pathway were analyzed to explore the mechanisms underlying the therapeutic effect of TEL against Aβ pathology. The primary microglia were used to uncover the mechanisms underlying the anti-inflammatory effects of TEL in AD. Additionally, the preventive effect of TEL against AD were investigated using 4-month-old APP/PS1 mice.
TEL treatment ameliorated cognitive and executive impairments, neuronal and synaptic injury, Aβ pathology, neuroinflammation, and oxidative stress in APP/PS1 mice. The favorable effects of TEL on Aβ pathology were achieved by inhibiting enzymatic Aβ production and facilitating enzymatic and autophagic Aβ degradation. Meanwhile, the anti-inflammatory effects of TEL were accomplished via microglial PPARγ/NLRP3 pathway. The administration of TEL prior to symptom onset prevented AD-related cognitive decline and neuropathologies.
TEL represents a promising agent for AD prevention and treatment.
阿尔茨海默病(AD)是最常见的神经退行性疾病。目前很少有药物可以有效阻止 AD 的进展。替米沙坦(TEL)是一种被 FDA 批准的广泛用于治疗高血压的药物。除了治疗高血压,TEL 还被发现可以预防 AD。然而,其潜在机制尚不清楚。
研究 TEL 防治 AD 的作用机制。
将 8 月龄 APP/PS1 小鼠每天给予 5mg/kg TEL 灌胃,连续 4 个月。采用筑巢试验、Y 迷宫试验和 Morris 水迷宫试验评估认知和执行功能。测量大脑中的神经元和突触标志物、淀粉样蛋白-β(Aβ)病理学、神经炎症和氧化应激。具体来说,分析了参与 Aβ 产生和降解途径的成分,以探讨 TEL 治疗 Aβ 病理学的作用机制。使用原代小胶质细胞揭示 TEL 在 AD 中抗炎作用的机制。此外,还使用 4 月龄 APP/PS1 小鼠研究了 TEL 对 AD 的预防作用。
TEL 治疗改善了 APP/PS1 小鼠的认知和执行功能障碍、神经元和突触损伤、Aβ 病理学、神经炎症和氧化应激。TEL 对 Aβ 病理学的有益作用是通过抑制酶促 Aβ 产生和促进酶促和自噬 Aβ 降解来实现的。同时,TEL 的抗炎作用是通过小胶质细胞 PPARγ/NLRP3 通路实现的。在症状出现前给予 TEL 可预防 AD 相关的认知下降和神经病理学改变。
TEL 是一种有前途的 AD 预防和治疗药物。