Peanut skin polyphenols inhibit proliferation of leukemia cells in vitro, and its A-type procyanidins selectively pass through a Caco-2 intestinal barrier

IF 3.4 2区 农林科学 Q2 FOOD SCIENCE & TECHNOLOGY Journal of Food Science Pub Date : 2025-02-14 DOI:10.1111/1750-3841.70018
Pornpat (Aom) Jantip, Chandra K. Singh, Yaa Asantewaa Kafui Klu, Nihal Ahmad, Bradley W. Bolling
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Abstract

Increased consumption of nuts is associated with reduced risk of some forms of cancer, including leukemia. Peanut skins are not typically retained during food processing but are a potential source of anticarcinogenic polyphenols. There are limited data about the antileukemic activity and bioavailability of peanut skin polyphenols. This study determined the polyphenol profile of raw peanut skin extract (PSE), its antiproliferative activity toward Jurkat cells, and intestinal bioavailability and metabolism using a Caco-2 intestinal monolayer model. High-resolution mass spectrometry (UHPLC–Q-Orbitrap) was used to analyze PSE and extracts of PSE-treated Jurkat cells to determine PSE polyphenols associated with antiproliferative activity. PSE reduced Jurkat cell viability, indicating its antiproliferative activity. PSE contained at least 63 polyphenols, including phenolic acids, proanthocyanidins, and prenylated flavonoids, among others. Multiple PSE polyphenols, particularly proanthocyanidins with A-type bonds, interacted with Jurkat cells. In Caco-2 cells, PSE intestinal bioavailability was limited to (+)-catechin, quercetin, procyanidin A2, and tentatively procyanidin A1. Caco-2 cells metabolized PSE polyphenols, including the methylation of A-type procyanidin dimer. Thus, these cell-based studies demonstrate that raw peanut skins contain intestinal bioavailable polyphenols with potential antileukemic properties. PSE polyphenols, including A-type proanthocyanidins, were metabolized by intestinal cells. Thus, the antileukemic activity of PSE polyphenols is modulated by the bioavailability and metabolism of A-type proanthocyanidins.

Practical Application

Raw peanut skins are rich in polyphenols, including A-type proanthocyanidins. Extracts of peanut skins inhibit the growth of cultured leukemia cells, and peanut A-type proanthocyanidins are associated with this effect. Peanut skins are not typically retained in food processing, so further research and development are needed to recover or retain these compounds and document their health-promoting activities in human research studies.

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花生皮多酚抑制白血病细胞增殖,其a型原花青素选择性通过Caco-2肠屏障
多吃坚果可以降低患某些癌症的风险,包括白血病。在食品加工过程中,花生皮通常不会被保留,但它是抗癌多酚的潜在来源。关于花生皮多酚的抗白血病活性和生物利用度的数据有限。本研究采用Caco-2肠道单层模型测定了生花生皮提取物(PSE)的多酚谱、对Jurkat细胞的抗增殖活性以及肠道生物利用度和代谢。采用高分辨率质谱法(UHPLC-Q-Orbitrap)分析PSE和PSE处理Jurkat细胞的提取物,以确定PSE多酚与抗增殖活性相关。PSE降低Jurkat细胞活力,表明其抗增殖活性。PSE含有至少63种多酚,包括酚酸、原花青素和烯酰化类黄酮等。多种PSE多酚,特别是具有a型键的原花青素,与Jurkat细胞相互作用。在Caco-2细胞中,PSE肠道生物利用度仅限于(+)-儿茶素、槲皮素、原花青素A2,暂定为原花青素A1。Caco-2细胞代谢PSE多酚,包括a型原花青素二聚体的甲基化。因此,这些基于细胞的研究表明,生花生皮含有肠道生物可利用的多酚,具有潜在的抗白血病特性。PSE多酚,包括a型原花青素,被肠细胞代谢。因此,PSE多酚的抗白血病活性是由a型原花青素的生物利用度和代谢调节的。生花生皮含有丰富的多酚类物质,包括a型原花青素。花生皮提取物抑制培养白血病细胞的生长,花生a型原花青素与这种作用有关。花生皮通常不会在食品加工中被保留,因此需要进一步的研究和开发来回收或保留这些化合物,并在人体研究中记录它们的健康促进活动。
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来源期刊
Journal of Food Science
Journal of Food Science 工程技术-食品科技
CiteScore
7.10
自引率
2.60%
发文量
412
审稿时长
3.1 months
期刊介绍: The goal of the Journal of Food Science is to offer scientists, researchers, and other food professionals the opportunity to share knowledge of scientific advancements in the myriad disciplines affecting their work, through a respected peer-reviewed publication. The Journal of Food Science serves as an international forum for vital research and developments in food science. The range of topics covered in the journal include: -Concise Reviews and Hypotheses in Food Science -New Horizons in Food Research -Integrated Food Science -Food Chemistry -Food Engineering, Materials Science, and Nanotechnology -Food Microbiology and Safety -Sensory and Consumer Sciences -Health, Nutrition, and Food -Toxicology and Chemical Food Safety The Journal of Food Science publishes peer-reviewed articles that cover all aspects of food science, including safety and nutrition. Reviews should be 15 to 50 typewritten pages (including tables, figures, and references), should provide in-depth coverage of a narrowly defined topic, and should embody careful evaluation (weaknesses, strengths, explanation of discrepancies in results among similar studies) of all pertinent studies, so that insightful interpretations and conclusions can be presented. Hypothesis papers are especially appropriate in pioneering areas of research or important areas that are afflicted by scientific controversy.
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