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首页> 外文期刊>Journal of Medicinal Plants Research >Antioxidant and anti-acetylcholinesterase activity of commercially available medicinal infusions after in vitro gastrointestinal digestion
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Antioxidant and anti-acetylcholinesterase activity of commercially available medicinal infusions after in vitro gastrointestinal digestion

机译:体外消化后市售药物输注液的抗氧化和抗乙酰胆碱酯酶活性

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Cynara cardunculus,?Fraxinus?angustifolia??and?Pterospartum tridentatum?are plants commercialized in Portugal for digestion-related ailments, among others. The aim of this study was to identify the chemical composition of the infusions and determine the inhibition of acetylcholinesterase, the antioxidant activity, and to evaluate if the chemical composition and activities remained after?in vitro?gastrointestinal digestion. These activities can be related with the traditional uses of these plants. The toxicity of the infusions was also tested with Caco-2 cells, a model of intestinal cells. The composition of the plant extracts revealed mainly flavonoids and phenolic acids. The antioxidant activity measured as half maximal effective concentration (EC50) values ranged from 19 to 120 μg/ml and the acetylcholinesterase inhibition activity of the three extracts determined as half inhibitory concentration (IC50) was between 1 and 2.5 mg/ml. The composition and the biochemical activities remained after the?in vitro?gastrointestinal digestion. The infusions showed no toxicity against Caco-2 cell lines. The antioxidant activity and inhibition of acetylcholinesterase were maintained during the digestive process, and therefore can be important mechanisms for the therapeutic effects attributed to the infusions under evaluation, namely to treat digestive problems. Even though the infusions presented biochemical activities, they were not toxic for the intestine cell line.
机译:Cynara cardunculus,“ Fraxinus”,“ Angustifolia”和“ Pterospartum tridentatum”是在葡萄牙商业化用于消化相关疾病的植物。这项研究的目的是确定输液的化学成分并确定对乙酰胆碱酯酶的抑制作用,抗氧化活性,并评估体外消化道消化后化学成分和活性是否仍然存在。这些活动可能与这些植物的传统用途有关。还使用肠细胞模型Caco-2细胞测试了输液的毒性。植物提取物的成分主要显示类黄酮和酚酸。以最大最大有效浓度(EC50)的一半值衡量的抗氧化活性范围为19至120μg/ ml,确定为半抑制浓度(IC50)的三种提取物的乙酰胆碱酯酶抑制活性为1至2.5 mg / ml。体外消化道消化后,其成分和生化活性得以保留。输注液显示对Caco-2细胞系无毒性。在消化过程中保持了抗氧化活性和对乙酰胆碱酯酶的抑制作用,因此可能是评估输液的治疗效果的重要机制,即治疗消化问题。即使输注显示出生化活性,它们对肠细胞系也没有毒性。

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