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原花青素对 PC12 细胞中 Aβ诱导损伤的神经抗炎作用。

Anti-Neuroinflammatory Property of Phlorotannins from on Aβ-Induced Damage in PC12 Cells.

机构信息

Department of Food Science and Nutrition, College of Health Sciences, Dong-A University, 37, Nakdong-daero 550 beon-gil, Saha-gu, Busan 49315, Korea.

Center for Silver-Targeted Biomaterials, Brain Busan 21 Plus Program, Graduate School, Dong-A University, Nakdong-daero 550 beon-gil, Saha-gu, Busan 49315, Korea.

出版信息

Mar Drugs. 2018 Dec 22;17(1):7. doi: 10.3390/md17010007.

Abstract

Alzheimer disease (AD) is a neurodegenerative disorder characterized by excessive accumulation of amyloid-beta peptide (Aβ) and progressive loss of neurons. Therefore, the inhibition of Aβ-induced neurotoxicity is a potential therapeutic approach for the treatment of AD. is an edible brown seaweed, which has been recognized as a rich source of bioactive derivatives, mainly phlorotannins. In this study, phlorotannins including eckol, dieckol, 8,8'-bieckol were used as potential neuroprotective candidates for their anti-apoptotic and anti-inflammatory effects against Aβ-induced damage in PC12 cells. Among the tested compounds, dieckol showed the highest effect in both suppressing intracellular oxidative stress and mitochondrial dysfunction and activation of caspase family. Three phlorotannins were found to inhibit TNF-α, IL-1β and PGE₂ production at the protein levels. These result showed that the anti-inflammatory properties of our compounds are related to the down-regulation of proinflammatory enzymes, iNOS and COX-2, through the negative regulation of the NF-κB pathway in Aβ-stimulated PC12 cells. Especially, dieckol showed the strong anti-inflammatory effects via suppression of p38, ERK and JNK. However, 8,8'-bieckol markedly decreased the phosphorylation of p38 and JNK and eckol suppressed the activation of p38. Therefore, the results of this study indicated that dieckol from might be applied as a drug candidate for the development of new generation therapeutic agents against AD.

摘要

阿尔茨海默病(AD)是一种神经退行性疾病,其特征是淀粉样β肽(Aβ)的过度积累和神经元的逐渐丧失。因此,抑制 Aβ诱导的神经毒性是治疗 AD 的一种潜在治疗方法。裙带菜是一种可食用的棕色海藻,已被认为是生物活性衍生物的丰富来源,主要是岩藻多酚。在这项研究中,岩藻多酚包括岩藻依醇、双岩藻酚、8,8'-双岩藻酚被用作潜在的神经保护候选物,因为它们具有抗细胞凋亡和抗炎作用,可以对抗 Aβ诱导的 PC12 细胞损伤。在测试的化合物中,双岩藻酚在抑制细胞内氧化应激和线粒体功能障碍以及半胱天冬酶家族的激活方面表现出最高的效果。三种岩藻多酚被发现可抑制 TNF-α、IL-1β 和 PGE₂ 的蛋白质水平。这些结果表明,我们的化合物具有抗炎特性,这与通过负向调节 Aβ 刺激的 PC12 细胞中的 NF-κB 途径,下调促炎酶 iNOS 和 COX-2 有关。特别是,双岩藻酚通过抑制 p38、ERK 和 JNK 表现出强烈的抗炎作用。然而,8,8'-双岩藻酚显著降低了 p38 和 JNK 的磷酸化,而岩藻依醇抑制了 p38 的激活。因此,这项研究的结果表明,裙带菜中的双岩藻酚可能被应用于开发新一代治疗 AD 的药物候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/878d/6356621/46f5bb1fae61/marinedrugs-17-00007-g001.jpg

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