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齐墩果酸通过调节 STC-1 和解偶联蛋白 2 信号减轻阿尔茨海默病中的氧化应激。

Oleanolic acid alleviates oxidative stress in Alzheimer's disease by regulating stanniocalcin-1 and uncoupling protein-2 signalling.

机构信息

Department of Neurology, Xidian Group Hospital, Xi'an, China.

出版信息

Clin Exp Pharmacol Physiol. 2020 Jul;47(7):1263-1271. doi: 10.1111/1440-1681.13292. Epub 2020 Mar 11.

Abstract

Oxidative stress is thought to play an important role in the occurrence and development of Alzheimer's disease (AD) and antioxidants may delay or even treat AD. Oleanolic acid (OA) exhibits antioxidant properties against many diseases. However, its effects on oxidative stress in AD remain unclear. Here, we explored the role and mechanism of action of OA in N2a/APP695swe cells exposed to oxidative stress. The cells were incubated with different concentrations of OA (0, 5, 8, 10, 15, and 25 μmol/L) for 24 hours. Higher concentrations of OA (10, 15, and 25 μmol/L) significantly suppressed the apoptosis, caspase-3 activity, reactive oxygen species level, and β amyloid (Aβ) content and increased the viability of these cells. OA (10 μmol/L) also increased the expression of stanniocalcin-1 (STC-1) and uncoupling protein-2 (UCP2) in N2a/APP695swe cells. STC-1 interference markedly reversed the effect of OA on UCP2, indicating that OA may regulate UCP2 expression in N2a/APP695swe cells via STC-1. Moreover, UCP2 inhibition significantly reversed the OA-mediated effects on cell viability, caspase-3 activity, reactive oxygen species, and Aβ level. Thus, OA regulates UCP2 expression via STC-1 to alleviate oxidative stress and Aβ level in N2a/APP695swe cells.

摘要

氧化应激被认为在阿尔茨海默病(AD)的发生和发展中起重要作用,抗氧化剂可能延缓甚至治疗 AD。齐墩果酸(OA)对许多疾病表现出抗氧化特性。然而,其在 AD 中对氧化应激的影响尚不清楚。在这里,我们研究了 OA 在 N2a/APP695swe 细胞暴露于氧化应激时的作用和作用机制。将细胞用不同浓度的 OA(0、5、8、10、15 和 25μmol/L)孵育 24 小时。较高浓度的 OA(10、15 和 25μmol/L)显著抑制细胞凋亡、半胱天冬酶-3 活性、活性氧水平和β淀粉样蛋白(Aβ)含量,并增加这些细胞的活力。OA(10μmol/L)还增加了 N2a/APP695swe 细胞中 stanniocalcin-1(STC-1)和解偶联蛋白-2(UCP2)的表达。STC-1 干扰明显逆转了 OA 对 UCP2 的作用,表明 OA 可能通过 STC-1 调节 N2a/APP695swe 细胞中 UCP2 的表达。此外,UCP2 抑制显著逆转了 OA 介导的对细胞活力、半胱天冬酶-3 活性、活性氧和 Aβ水平的影响。因此,OA 通过 STC-1 调节 UCP2 的表达,以减轻 N2a/APP695swe 细胞中的氧化应激和 Aβ水平。

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