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首页> 外文期刊>Metabolic brain disease >Neuroprotective effects of some seaweeds against Zn - induced neuronal damage in HT-22 cells via modulation of redox imbalance, inhibition of apoptosis and acetylcholinesterase activity
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Neuroprotective effects of some seaweeds against Zn - induced neuronal damage in HT-22 cells via modulation of redox imbalance, inhibition of apoptosis and acetylcholinesterase activity

机译:通过调制氧化还原性失衡,抑制细胞凋亡和乙酰胆碱酯酶活性的HT-22细胞中一些海藻对HT-22细胞神经元损伤的神经保护作用

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摘要

Zinc plays an important role in neuronal signaling and neurotransmission. However, dyshomeostasis of this metal or its accumulation in the brain has been linked with neurological disorders such as Alzheimer's disease and Parkinson's disease. In this study, the neuroprotective effects of Ecklonia maxima (KPM), Gracilaria gracilis (GCL), Ulva lactuca (ULT) and Gelidium pristoides (MNP) in Zn -induced neurotoxicity in HT-22 cells was examined. Cells were treated with Zinc sulphate and/or aqueous - ethanol extracts and cell viability, apoptosis, acetylcholinesterase activity, including some antioxidant enzymes (catalase and superoxide dismutase activity) and glutathione (GSH) levels were determined. Malondialdehyde and nitric oxide levels produced in the Zn and/or seaweed extract treated cells were also determined. Prior treatment with the seaweed extracts improved cell viability and inhibited Zn - induced cell death. Acetylcholinesterase activity was significantly high in Zn treated cells compared to the control. Pre-treatment with the seaweed extracts triggered a decrease in acetylcholinesterase activity in Zn - treated cells. Furthermore, treatment with Zn caused a significant reduction in GSH levels as well as a decrease in superoxide dismutase and catalase activities. In contrast, the seaweed extract increased antioxidant enzyme activities and GSH levels. An increase in malondialdehyde and nitric oxide levels was also reversed after treatment with the seaweed extracts. These results suggest that the seaweed extracts improved cholinergic transmission disrupted by Zn - induced neurotoxicity and protected the cells against oxidative damage and neuroinflammation. The neuroprotective effects of the seaweed extracts could be linked to their bioactive constituents. Hence these seaweeds are potential sources of active ingredients with neuroprotective potentials and could be used for the development of functional foods and/or nutraceuticals.
机译:锌在神经元信令和神经递质中起着重要作用。然而,这种金属的脱节性或其在大脑中的积累已经与神经系统疾病相似,例如阿尔茨海默病和帕金森病。在本研究中,研究了Ecklonia Maxima(KPM),Gracilaria Glacilis(GCL),ULVA Lactuca(ULT)和Gelidium(MNP)在HT-22细胞中的神经毒性中的神经保护作用。用硫酸锌和/或乙醇萃取物和细胞活力,细胞凋亡,乙酰胆碱酯酶活性,包括一些抗氧化酶(过氧化氢酶和超氧化物歧化酶活性)和谷胱甘肽(GSH)水平的细胞。还测定了在Zn和/或海藻提取物处理的细胞中产生的丙二醛和一氧化物水平。用海藻提取物提取细胞活力并抑制Zn诱导的细胞死亡。与对照相比,乙酰胆碱酯酶活性在Zn处理细胞中显着高。用海藻提取物预处理引发Zn处理细胞中乙酰胆碱酯酶活性的降低。此外,用Zn处理导致GSH水平的显着降低以及超氧化物歧化酶和过氧化氢酶活性的降低。相比之下,海藻提取抗氧化酶活性和GSH水平。在用海藻提取物处理后,丙二醛和一氧化氮水平的增加也逆转。这些结果表明,海藻提取物改善受Zn诱导的神经毒性破坏的胆碱能传播,并保护细胞免受氧化损伤和神经炎症。海藻提取物的神经保护作用可以与其生物活性成分联系起来。因此,这些海藻是具有神经保护潜力的活性成分的潜在来源,可用于开发功能性食品和/或营养保健品。

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