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亚临界水提取法制备的板栗壳提取物的模拟胃肠道消化:通过体外试验测定生物可及性、生物活性和肠道通透性

Simulated Gastrointestinal Digestion of Chestnut ( Mill.) Shell Extract Prepared by Subcritical Water Extraction: Bioaccessibility, Bioactivity, and Intestinal Permeability by In Vitro Assays.

作者信息

Pinto Diana, Silva Ana Margarida, Dall'Acqua Stefano, Sut Stefania, Vallverdú-Queralt Anna, Delerue-Matos Cristina, Rodrigues Francisca

机构信息

REQUIMTE/LAQV, ISEP, Polytechnic of Porto, Rua Dr. António Bernardino de Almeida, 4249-015 Porto, Portugal.

Department of Pharmaceutical and Pharmacological Sciences, University of Padova, Via Marzolo 5, 35121 Padova, Italy.

出版信息

Antioxidants (Basel). 2023 Jul 12;12(7):1414. doi: 10.3390/antiox12071414.

Abstract

Chestnut shells (CSs) are an appealing source of bioactive molecules, and constitute a popular research topic. This study explores the effects of in vitro gastrointestinal digestion and intestinal permeability on the bioaccessibility and bioactivity of polyphenols from CS extract prepared by subcritical water extraction (SWE). The results unveiled higher phenolic concentrations retained after gastric and intestinal digestion. The bioaccessibility and antioxidant/antiradical properties were enhanced in the following order: oral < gastric ≤ intestinal digests, attaining 40% of the maximum bioaccessibility. Ellagic acid was the main polyphenol in the digested and undigested extract, while pyrogallol-protocatechuic acid derivative was only quantified in the digests. The CS extract revealed potential mild hypoglycemic (<25%) and neuroprotective (<75%) properties before and after in vitro digestion, along with upmodulating the antioxidant enzymes' activities and downregulating the lipid peroxidation. The intestinal permeation of ellagic acid achieved 22.89% after 240 min. This study highlighted the efficacy of the CS extract on the delivery of polyphenols, sustaining its promising use as nutraceutical ingredient.

摘要

栗壳是生物活性分子的一个有吸引力的来源,并且是一个热门的研究课题。本研究探讨了体外胃肠道消化和肠道通透性对亚临界水萃取(SWE)制备的栗壳提取物中多酚的生物可及性和生物活性的影响。结果表明,经过胃和肠道消化后,保留的酚类浓度更高。生物可及性和抗氧化/抗自由基特性按以下顺序增强:口服<胃消化≤肠道消化,达到最大生物可及性的40%。鞣花酸是消化和未消化提取物中的主要多酚,而邻苯三酚-原儿茶酸衍生物仅在消化物中被定量。栗壳提取物在体外消化前后显示出潜在的轻度降血糖(<25%)和神经保护(<75%)特性,同时上调抗氧化酶的活性并下调脂质过氧化。240分钟后,鞣花酸的肠道渗透率达到22.89%。本研究突出了栗壳提取物在多酚递送方面的功效,维持了其作为营养保健品成分的前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ee93/10376477/d2f53a31d097/antioxidants-12-01414-g001.jpg

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