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替米沙坦在中枢神经系统疾病中的应用。

The application of telmisartan in central nervous system disorders.

作者信息

Quan Wei, Zhang Shui-Xian, Zhang Xu-Yang, Chen Xi, Yang Chao, Li Zhi-Yu, Hu Rong

机构信息

Department of Neurosurgery, Southwest Hospital, Third Military Medical University, Chongqing, China.

Department of Neurosurgery, Zhongnan Hospital, Wuhan University, Hubei, China.

出版信息

Pharmacol Rep. 2025 Jun 19. doi: 10.1007/s43440-025-00737-2.


DOI:10.1007/s43440-025-00737-2
PMID:40536710
Abstract

Telmisartan, a well-established antihypertensive drug, has shown promising therapeutic potential for a variety of central nervous system (CNS) disorders. This review outlines the fundamental characteristics of telmisartan, focusing on its dual pharmacological effects as an angiotensin II type 1 receptor (AT1R) antagonist and a peroxisome proliferator-activated receptor (PPAR) γ activator. These mechanisms underpin its neuroprotective and anti-inflammatory effects, which are essential to its therapeutic benefits in CNS diseases. Telmisartan modulates key cellular components of the CNS, including microglia, astrocytes, oligodendrocytes, vascular endothelial cells, and neurons, thereby offering protection against neuroinflammation, oxidative stress, and neuronal damage. We summarize telmisartan's efficacy in addressing a range of neurological conditions, such as stroke, traumatic brain injury, dementia, Parkinson's disease, demyelinating diseases, psychiatric disorders, and gliomas. By targeting multiple pathways involved in these disorders, telmisartan demonstrates potential as both an adjunctive and standalone therapy. Its ability to attenuate neuroinflammation and promote cellular repair highlights its versatility in CNS disease management. This review underscores the potential of telmisartan as a valuable therapeutic option for CNS disorders, warranting continued exploration to optimize its clinical application.

摘要

替米沙坦是一种成熟的抗高血压药物,已显示出对多种中枢神经系统(CNS)疾病具有有前景的治疗潜力。本综述概述了替米沙坦的基本特性,重点关注其作为血管紧张素II 1型受体(AT1R)拮抗剂和过氧化物酶体增殖物激活受体(PPAR)γ激活剂的双重药理作用。这些机制支撑着其神经保护和抗炎作用,而这些作用对于其在中枢神经系统疾病中的治疗益处至关重要。替米沙坦调节中枢神经系统的关键细胞成分,包括小胶质细胞、星形胶质细胞、少突胶质细胞、血管内皮细胞和神经元,从而提供针对神经炎症、氧化应激和神经元损伤的保护。我们总结了替米沙坦在治疗一系列神经系统疾病方面的疗效,如中风、创伤性脑损伤、痴呆、帕金森病、脱髓鞘疾病、精神疾病和神经胶质瘤。通过靶向参与这些疾病的多种途径,替米沙坦显示出作为辅助治疗和单一治疗的潜力。其减轻神经炎症和促进细胞修复的能力突出了其在中枢神经系统疾病管理中的多功能性。本综述强调了替米沙坦作为中枢神经系统疾病有价值的治疗选择的潜力,值得继续探索以优化其临床应用。

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本文引用的文献

[1]
Effects of high salt intake on glucose metabolism, liver function, and the microbiome in rats: influence of ACE inhibitors and angiotensin II receptor blockers.

Am J Physiol Cell Physiol. 2025-4-1

[2]
Association Between Long- Versus Short-Acting Angiotensin II Receptor Antagonists and Hypotension During Anesthesia Induction: A Retrospective Study.

Asian J Anesthesiol. 2024-12-20

[3]
Acupoint catgut embedding attenuates oxidative stress and cognitive impairment in chronic cerebral ischemia by inhibiting the Ang II/AT1R/NOX axis.

Pflugers Arch. 2024-8

[4]
The angiotensin II receptors type 1 and 2 modulate astrocytes and their crosstalk with microglia and neurons in an in vitro model of ischemic stroke.

BMC Neurosci. 2024-6-26

[5]
Comparative efficacy and safety of six angiotensin II receptor blockers in hypertensive patients: a network meta-analysis.

Int J Clin Pharm. 2024-10

[6]
The role of the brain renin-angiotensin system in Parkinson´s disease.

Transl Neurodegener. 2024-4-15

[7]
Development of Telmisartan Nanocrystal-Based Dissolving Microneedle for Brain Targeting via Trigeminal Pathway: A Potentially Promising Treatment for Alzheimer's with an Improved Pharmacokinetic Profile.

ACS Appl Bio Mater. 2024-4-15

[8]
Telmisartan Protects Mitochondrial Function, Gait, and Neuronal Apoptosis by Activating the Akt/GSK3β/PGC1α Pathway in an MPTP-Induced Mouse Model of Parkinson's Disease.

J Integr Neurosci. 2024-2-4

[9]
Angiotensin type 1 receptor activation promotes neuronal and glial alpha-synuclein aggregation and transmission.

NPJ Parkinsons Dis. 2024-2-17

[10]
Modulating the polarization phenotype of microglia - A valuable strategy for central nervous system diseases.

Ageing Res Rev. 2024-1

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