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类胡萝卜素富集提取物通过 TrkB/Akt 通路对海马神经元细胞氧化应激的神经保护作用。

Neuroprotective Effect of Carotenoid-Rich Extract via TrkB/Akt Pathway against Oxidative Stress in Hippocampal Neuronal Cells.

机构信息

Department of Food and Nutrition, Chungnam National University, Daejeon 34134, Korea.

出版信息

Mar Drugs. 2020 Jul 19;18(7):372. doi: 10.3390/md18070372.

Abstract

In this study, we found that extract (EAEP) exhibits neuroprotective effects in oxidative stress-induced neuronal cells. EAEP improved cell viability as well as attenuated the formation of intracellular reactive oxygen species (ROS) and apoptotic bodies in glutamate-treated hippocampal neuronal cells (HT-22). Furthermore, EAEP improved the expression of brain-derived neurotrophic factor (BDNF) and antioxidant enzymes such as heme oxygenase-1 (HO-1), NAD(P)H quinine oxidoreductase-1 (NQO-1), and glutamate-cysteine ligase catalytic subunit (GCLC) via the tropomyosin-related kinase receptor B/ protein kinase B (TrkB/Akt) signaling pathway. In contrast, the pre-incubation of K252a, a TrkB inhibitor, or MK-2206, an Akt-selective inhibitor, ameliorated the neuroprotective effects of EAEP in oxidative stress-induced neuronal cells. These results suggest that EAEP protects neuronal cells against oxidative stress-induced apoptosis by upregulating the expression of BDNF and antioxidant enzymes via the activation of the TrkB/Akt pathway. In conclusion, such an effect of EAEP, which is rich in carotenoid-derived compounds, may justify its application as a food supplement in the prevention and treatment of neurodegenerative disorders.

摘要

在这项研究中,我们发现 提取物(EAEP)在氧化应激诱导的神经元细胞中表现出神经保护作用。EAEP 提高了细胞活力,并减轻了谷氨酸处理的海马神经元细胞(HT-22)中细胞内活性氧(ROS)和凋亡小体的形成。此外,EAEP 通过原肌球蛋白相关激酶受体 B/蛋白激酶 B(TrkB/Akt)信号通路改善了脑源性神经营养因子(BDNF)和抗氧化酶的表达,如血红素加氧酶-1(HO-1)、NAD(P)H 醌氧化还原酶-1(NQO-1)和谷氨酸半胱氨酸连接酶催化亚基(GCLC)。相比之下,TrkB 抑制剂 K252a 或 Akt 选择性抑制剂 MK-2206 的预孵育减轻了 EAEP 在氧化应激诱导的神经元细胞中对神经保护作用的影响。这些结果表明,EAEP 通过激活 TrkB/Akt 通路,上调 BDNF 和抗氧化酶的表达,保护神经元细胞免受氧化应激诱导的细胞凋亡。总之,富含类胡萝卜素衍生化合物的 EAEP 的这种作用可能使其作为预防和治疗神经退行性疾病的膳食补充剂得到应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3836/7404284/be38fc822289/marinedrugs-18-00372-g001.jpg

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