Department of Neurology, Hanyang University Guri Hospital, 153, Gyeongchun-ro, Guri, 11923, South Korea.
GemVax & Kael Co., Ltd, Seongnam-si, Republic of Korea.
Mol Neurobiol. 2021 Apr;58(4):1806-1818. doi: 10.1007/s12035-020-02253-1. Epub 2021 Jan 6.
Angiotensin II receptor blockers (ARBs) have been shown to exert neuroprotective effects by suppressing inflammatory and apoptotic responses. In the present study, the effects of the ARB telmisartan on the NLRP3 inflammasome induced by oxygen-glucose deprivation (OGD) in neural stem cells (NSCs) were investigated, as well as their possible association with the activation of the PI3K pathway. Cultured NSCs were treated with different concentrations of telmisartan and subjected to various durations of OGD. Cell counting, lactate dehydrogenase, bromodeoxyuridine, and colony-forming unit assays were performed to measure cell viability and proliferation. In addition, the activity of intracellular signaling pathways associated with the PI3K pathway and NLRP3 inflammasome was evaluated. Telmisartan alone did not affect NSCs up to a concentration of 10 μM under normal conditions but showed toxicity at a concentration of 100 μM. Moreover, OGD reduced the viability of NSCs in a time-dependent manner. Nevertheless, treatment with telmisartan increased the viability and proliferation of OGD-injured NSCs. Furthermore, telmisartan promoted the expression of survival-related proteins and mRNA while inhibiting the expression of death-related proteins induced by OGD. In particular, telmisartan attenuated OGD-dependent expression of the NLRP3 inflammasome and its related signaling proteins. These beneficial effects of telmisartan were blocked by a PI3K inhibitor. Together, these results indicate that telmisartan attenuated the activation of the NLRP3 inflammasome by triggering the PI3K pathway, thereby contributing to neuroprotection.
血管紧张素 II 受体阻滞剂(ARBs)通过抑制炎症和细胞凋亡反应发挥神经保护作用。本研究旨在探讨 ARB 替米沙坦对氧葡萄糖剥夺(OGD)诱导的神经干细胞(NSCs)中 NLRP3 炎性体的影响,以及其与 PI3K 通路激活的可能关联。培养的 NSCs 用不同浓度的替米沙坦处理,并进行不同时间的 OGD。通过细胞计数、乳酸脱氢酶、溴脱氧尿苷和集落形成单位测定来测量细胞活力和增殖。此外,评估了与 PI3K 通路和 NLRP3 炎性体相关的细胞内信号通路的活性。替米沙坦在正常条件下,浓度高达 10μM 时对 NSCs 没有影响,但在浓度为 100μM 时表现出毒性。此外,OGD 以时间依赖性方式降低 NSCs 的活力。然而,替米沙坦处理增加了 OGD 损伤的 NSCs 的活力和增殖。此外,替米沙坦促进了与生存相关的蛋白和 mRNA 的表达,同时抑制了 OGD 诱导的死亡相关蛋白的表达。特别是,替米沙坦减轻了 OGD 依赖性 NLRP3 炎性体及其相关信号蛋白的表达。这种替米沙坦的有益作用被 PI3K 抑制剂阻断。总之,这些结果表明,替米沙坦通过触发 PI3K 通路来减轻 NLRP3 炎性体的激活,从而有助于神经保护。