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橙皮苷通过 SIRT6/NLRP3 通路减轻东莨菪碱诱导的小鼠认知功能障碍。

Hesperetin attenuates cognitive dysfunction via SIRT6/NLRP3 pathway in scopolamine-induced mice.

机构信息

Science and Technology Innovation Center, Guangzhou University of Chinese Medicine, Guangdong, Guangzhou, China.

The Sixth Affiliated Hospital, Sun Yat-sen University, Guangdong, Guangzhou, China.

出版信息

Metab Brain Dis. 2023 Oct;38(7):2443-2456. doi: 10.1007/s11011-023-01250-2. Epub 2023 Jun 29.

Abstract

Neuroinflammation is a critical feature in the pathogenesis of neurodegenerative disorders such as Alzheimer's disease (AD). Hesperetin can exert anti-inflammatory, antioxidant and other neuroprotective effects. In this study, the scopolamine (SCOP)-induced cognitive dysfunction in mice model was used to evaluate the neuroprotective effects of hesperetin. Behavioral tests (Morris water maze, open field, and novel object recognition tests) were conducted to evaluate the effect of hesperetin on cognitive dysfunction behaviors. Nissl staining and Immunofluorescence were used to evaluate hippocampal neuronal damage and microglial activation in mice. The levels of proinflammatory factors, oxidant stress, and the cholinergic neurotransmitter were detected by real-time quantitative fluorescence PCR (RT-qPCR) or biochemical reagent kits. Western blotting was used to detect the relative protein expression of the sirtuin 6 (SIRT6) / NOD-like receptor thermal protein domain associated protein 3 (NLRP3) pathway. Results showed that hesperetin could ameliorate SCOP-induced cognitive impairment and neuronal damage, and regulate the levels of cholinergic neurotransmitters in the hippocampal of AD mice. Hesperetin could also enhance antioxidant defense by regulating the levels of reactive oxygen species (ROS), malondialdehyde (MDA), superoxide dismutase (SOD), and catalase (CAT). Hesperetin exerted anti-neuroinflammation effects through inhibiting of microglia activation and down-regulating the mRNA transcript levels of inflammatory cytokines, such as tumor necrosis factor α (TNF-α), interleukin-6 (IL-6), interleukin-1β (IL-1β), cyclooxygenase-2 (COX-2), and inducible nitric oxide synthase (iNOS). Meanwhile, hesperetin could attenuate the expression of NLRP3, apoptosis-associated speck-like protein containing a CARD (ASC), thioredoxin-interacting protein (TXNIP), and caspase-1 p20 and upregulate the expression of SIRT6 in SCOP-induced mice. Overall, our study suggested that hesperetin might ameliorate SCOP-induced cognitive dysfunction by improving cholinergic system dysfunction and suppressing oxidative stress and attenuating neuroinflammation via SIRT6/NLRP3 pathway in mice.

摘要

神经炎症是阿尔茨海默病(AD)等神经退行性疾病发病机制中的一个关键特征。橙皮素具有抗炎、抗氧化和其他神经保护作用。在这项研究中,使用东莨菪碱(SCOP)诱导的认知功能障碍小鼠模型来评估橙皮素的神经保护作用。进行了行为测试( Morris 水迷宫、旷场和新颖物体识别测试)来评估橙皮素对认知功能障碍行为的影响。尼氏染色和免疫荧光用于评估小鼠海马神经元损伤和小胶质细胞激活。通过实时荧光定量 PCR(RT-qPCR)或生化试剂试剂盒检测促炎因子、氧化应激和胆碱能神经递质的水平。Western blot 用于检测 SIRT6/NLRP3 通路的相对蛋白表达。结果表明,橙皮素可以改善 SCOP 诱导的认知障碍和神经元损伤,并调节 AD 小鼠海马中的胆碱能神经递质水平。橙皮素还可以通过调节活性氧(ROS)、丙二醛(MDA)、超氧化物歧化酶(SOD)和过氧化氢酶(CAT)的水平来增强抗氧化防御能力。橙皮素通过抑制小胶质细胞激活和下调炎症细胞因子(如肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)、白细胞介素-1β(IL-1β)、环氧合酶-2(COX-2)和诱导型一氧化氮合酶(iNOS)的 mRNA 转录水平发挥抗神经炎症作用。同时,橙皮素可以降低 SCOP 诱导的小鼠中 NLRP3、凋亡相关斑点样蛋白(ASC)、硫氧还蛋白相互作用蛋白(TXNIP)和半胱天冬酶-1 p20 的表达,并上调 SIRT6 的表达。总的来说,我们的研究表明,橙皮素可能通过改善胆碱能系统功能障碍、抑制氧化应激和通过 SIRT6/NLRP3 通路减轻神经炎症来改善 SCOP 诱导的认知功能障碍。

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