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对春黄菊和白柳提取物的多种药理学和毒理学研究:关注其作为抗偏头痛药物的潜在应用。

Multiple pharmacological and toxicological investigations on Tanacetum parthenium and Salix alba extracts: Focus on potential application as anti-migraine agents.

机构信息

Department of Pharmacy, University "G. d'Annunzio" of Chieti-Pescara, Chieti, 66100, Italy.

Department of Medical, Oral and Biotechnological Sciences, University "G. d'Annunzio" of Chieti-Pescara, Chieti, 66100, Italy.

出版信息

Food Chem Toxicol. 2019 Nov;133:110783. doi: 10.1016/j.fct.2019.110783. Epub 2019 Sep 3.

DOI:10.1016/j.fct.2019.110783
PMID:31491430
Abstract

Migraine is one of the most common neurological disorder, which has long been related to brain serotonin (5-HT) depletion and neuro-inflammation. Despite many treatment options are available, the frequent occurrence of unacceptable adverse effects further supports the research toward nutraceuticals and herbal preparations, among which Tanacetum parthenium and Salix alba showed promising anti-inflammatory and neuro-modulatory activities. The impact of extract treatment on astrocyte viability, spontaneous migration and apoptosis was evaluated. Anti-inflammatory/anti-oxidant effects were investigated on isolated rat cortexes exposed to a neurotoxic stimulus. The lactate dehydrogenase (LDH) release, nitrite levels and 5-HT turnover were evaluated, as well. A proteomic analysis was focused on specific neuronal proteins and a fingerprint analysis was carried out on selected phenolic compounds. Both extracts appeared able to exert in vitro anti-oxidant and anti-apoptotic effects. S. alba and T. parthenium extracts reduced LDH release, nitrite levels and 5-HT turnover induced by neurotoxic stimulus. The downregulation of selected proteins suggest a neurotoxicity, which could be ascribed to an elevated content of gallic acid in both S. alba and T. parthenium extracts. Concluding, both extracts exert neuroprotective effects, although the downregulation of key proteins involved in neuron physiology suggest caution in their use as food supplements.

摘要

偏头痛是最常见的神经障碍之一,长期以来一直与大脑 5-羟色胺(5-HT)耗竭和神经炎症有关。尽管有许多治疗选择,但经常出现不可接受的不良反应,这进一步支持了对营养保健品和草药制剂的研究,其中,春黄菊和柳枝稷表现出有希望的抗炎和神经调节活性。评估了提取物处理对星形胶质细胞活力、自发迁移和细胞凋亡的影响。研究了在暴露于神经毒性刺激的分离大鼠皮质上的抗炎/抗氧化作用。评估了乳酸脱氢酶(LDH)释放、亚硝酸盐水平和 5-HT 转化。还进行了针对特定神经元蛋白的蛋白质组学分析和针对选定酚类化合物的指纹分析。两种提取物都表现出体外抗氧化和抗凋亡作用。柳树皮和春黄菊提取物可降低神经毒性刺激引起的 LDH 释放、亚硝酸盐水平和 5-HT 转化。选定蛋白的下调表明存在神经毒性,这可能归因于柳树皮和春黄菊提取物中均含有较高含量的没食子酸。总之,两种提取物都具有神经保护作用,但涉及神经元生理的关键蛋白的下调表明在将它们用作食品补充剂时应谨慎。

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