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Neuritogenic and neuroprotective activities of fruit residues

机译:水果残留物的神经毒性和神经保护活性

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Neuritogenic and neuroprotective activities of litchi (Litchi chinensis Sonn., Sapindaceae) and salacca (Salacca edulis Reinw., Arecaceae) pericarp, and sapodilla (Achras sapota L., Sapotaceae) and tamarind Srichompu cultivar (Tamarindus indica L., Caesalpiniaceae) seed coat extracts were evaluated on cultured cholinergic P19-derived neurons. All the extracts, at a very low concentration (1 ng/mL of litchi and salacca pericarp extracts, 10 ng/mL of sapodilla and 100 ng/mL of tamarind seed coat extracts), enhanced the survival of cultured neurons (% viability more than 100%) by XTT reduction assay. The extracts were further evaluated for their neuritogenicity by observing cell morphology by phase-contrast microscopy and neuroprotective activity in serum deprivation and pre- and co-administration of hydrogen peroxide models. The phase-contrast micrographs displayed that all of the extracts possessed neurogenic activity by promoting the neurite outgrowth of the cultured neurons. Moreover, these extracts can protect neurons from oxidative stress-caused cell death in a serum deprivation model, and prevent and protect neuron cells from the toxicity of hydrogen peroxide. In this study we assured that the neuritogenic and neuroprotective activities of these extracts derived from the phenolic components and flavonoids contained in the extracts by acting as signaling molecules to enhance neuron survival and promote neurite outgrowth. These results suggest that all of the extracts are potentially sources of neuritogenic and neuroprotective components which might be used either as pharmaceutical products or dietary supplements for neurodegenerative disorder patients, for example, those suffering from Alzheimer's disease.
机译:荔枝,sal柳(Salacca edulis Reinw。,槟榔科)果皮,人心果(Achras sapota L.,Sapotaceae)和罗望子Srichompu栽培种(Tamarindus Caindia L.)的荔枝和神经保护活性。在培养的胆碱能P19衍生神经元上评估提取物。所有提取物的浓度都非常低(荔枝和Salacca果皮提取物为1 ng / mL,人心果的提取物为10 ng / mL,罗望子种皮提取物的提取率为100 ng / mL),可提高培养的神经元的存活率(生存力比100%)通过XTT还原检测。通过相差显微镜观察细胞形态和血清剥夺以及过氧化氢模型的预先和共同给药的神经保护活性,进一步评估提取物的神经原性。相差显微照片显示,所有提取物均通过促进培养的神经元的神经突向外生长而具有神经源性活性。此外,这些提取物可以在血清剥夺模型中保护神经元免受氧化应激引起的细胞死亡,并防止和保护神经元细胞免受过氧化氢的毒性。在这项研究中,我们通过提取信号分子来增强神经元的存活并促进神经突的生长,从而确保了这些提取物的神经提取活性和神经保护活性源自提取物中所含的酚类成分和类黄酮。这些结果表明,所有提取物都是潜在的神经原性和神经保护成分的来源,可用作神经退行性疾病患者(例如患有阿尔茨海默氏病的患者)的药品或膳食补充剂。

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