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姜黄素通过其抗氧化和神经保护作用改善了壬基酚诱导的记忆缺陷和神经毒性。

Thymoquinone Improved Nonylphenol-Induced Memory Deficit and Neurotoxicity Through Its Antioxidant and Neuroprotective Effects.

机构信息

Student Research Committee, Babol University of Medical Sciences, Babol, Iran.

Cellular and Molecular Biology Research Center, Health Research Institute, Babol University of Medical Sciences, Ganjafrooz Blvd, Babol, Iran.

出版信息

Mol Neurobiol. 2022 Jun;59(6):3600-3616. doi: 10.1007/s12035-022-02807-5. Epub 2022 Mar 30.

Abstract

Nonylphenol (NP), a well-known endocrine-disrupter chemical, has several harmful effects on the central nervous system including neuroendocrine disruption, cognitive impairment, and neurotoxicity. Thymoquinone (TQ) is a main bioactive compound in the black seeds of Nigella sativa that has antioxidant, anti-inflammatory, and neuroprotective properties. Here, we investigated the neuroprotective effect of TQ against NP-induced memory deficit and neurotoxicity in rats. To induce memory impairment, NP (25 mg/kg) was used as gavage in male Wistar rats for 21 days. TQ (2.5, 5, and 10 mg/kg) was intraperitoneally administered in NP-treated animals. The morris water maze test was performed to assess spatial learning and memory. The hippocampal tissues were isolated from the brain for histopathological evaluation. Biochemical, molecular, and cellular tests were performed to quantify oxidant (malondialdehyde; MDA)/antioxidant (superoxide dismutase (SOD), total antioxidant capacity (TAC), and reduced glutathione (GSH) parameters) as well as markers for astrocytic activation (glial fibrillary acidic protein; GFAP) and neuronal death (alpha-synuclein; α-syn). Results showed TQ (5 mg/kg) significantly improved NP-induced memory impairment. Histological data revealed a significant increase in the number of necrotic cells in hippocampus, and TQ treatment markedly decreased this effect. The GSH and TAC levels were significantly increased in TQ-treated groups compared to NP group. The molecular analysis indicated that NP increased GFAP and decreased α-syn expression and TQ treatment did the reverse. In vitro study in astrocytes isolated from mice brain showed that TQ significantly increased cell viability in NP-induced cytotoxicity. This study strongly indicates that TQ has neuroprotective effects on NP-induced neurotoxicity through reducing oxidative damages and neuroinflammation. This study investigates the behavioral neurotoxicity induced by Nonylphenol (NP) and the protective effects of Thymoquinone (TQ) as a potent antioxidant compound using molecular, cell culture, histopathological and biochemical techniques.

摘要

壬基酚(NP)是一种众所周知的内分泌干扰化学物质,对中枢神经系统有多种有害影响,包括神经内分泌紊乱、认知障碍和神经毒性。百里醌(TQ)是黑种草子中的一种主要生物活性化合物,具有抗氧化、抗炎和神经保护特性。在这里,我们研究了 TQ 对 NP 诱导的大鼠记忆损伤和神经毒性的神经保护作用。为了诱导记忆损伤,将 NP(25mg/kg)作为灌胃剂用于雄性 Wistar 大鼠 21 天。将 TQ(2.5、5 和 10mg/kg)腹腔内给予 NP 处理的动物。通过 Morris 水迷宫测试评估空间学习和记忆。从大脑中分离出海马齿组织进行组织病理学评估。进行生化、分子和细胞测试,以定量氧化剂(丙二醛;MDA)/抗氧化剂(超氧化物歧化酶(SOD)、总抗氧化能力(TAC)和还原型谷胱甘肽(GSH)参数)以及星形胶质细胞激活标志物(胶质纤维酸性蛋白;GFAP)和神经元死亡标志物(α-突触核蛋白;α-syn)。结果表明,TQ(5mg/kg)显著改善了 NP 诱导的记忆损伤。组织学数据显示海马体中坏死细胞数量显着增加,而 TQ 处理显着降低了这种作用。与 NP 组相比,TQ 处理组的 GSH 和 TAC 水平显着增加。分子分析表明,NP 增加了 GFAP 并降低了 α-syn 的表达,而 TQ 处理则相反。从老鼠大脑中分离的星形胶质细胞的体外研究表明,TQ 显着增加了 NP 诱导的细胞毒性中的细胞活力。这项研究强烈表明,TQ 通过减少氧化损伤和神经炎症对 NP 诱导的神经毒性具有神经保护作用。本研究使用分子、细胞培养、组织病理学和生化技术研究了壬基酚(NP)引起的行为神经毒性和百里醌(TQ)作为一种有效的抗氧化化合物的保护作用。

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