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口服α-糖苷基异槲皮苷后小鼠、大鼠和猪粪便细菌微生物组的比较。

Comparison of the fecal bacterial microbiota in mice, rats, and pigs after oral administration of alpha-glycosyl isoquercitrin.

机构信息

Laboratory of Veterinary Physiology, Tokyo University of Agriculture and Technology.

Laboratory of Animal Science, Department of Applied Biological Sciences, Setsunan University.

出版信息

J Toxicol Sci. 2024;49(4):151-161. doi: 10.2131/jts.49.151.

DOI:10.2131/jts.49.151
PMID:38556352
Abstract

Alpha-glycosyl isoquercitrin (AGIQ) is composed of isoquercitrin and its glucosylated derivatives and has many biological activities, including anti-inflammatory, antioxidant, and anti-cancer properties. However, the effect of AGIQ administered orally on gut microbiota composition remains unclear. The objective of this study was to evaluate the effect of AGIQ on the gut microbiota of animals in different dose groups. Male rats and mice received different doses of AGIQ (1.5%, 3%, or 5% w/v) in diet for carcinogenic or chronic toxicity studies (rasH2 mice: 6 months; Sprague-Dawley rats: 12 months). Male minipigs received 100, 300, or 1000 mg/kg/day for 28 days. Fecal samples were collected from the different animal species and analyzed using 16S-rRNA gene sequencing. No significant changes were observed in alpha and beta diversity of the gut microbiota. Characteristic bacteria that responded to AGIQ were identified in each animal species, and, interestingly, Kineothrix alysoides, a butyrate-producing bacterium, was commonly detected in all three species, suggesting that it may be related to the biological activities of AGIQ. AGIQ selectively modulated the number of beneficial butyrate-producing commensal bacterium beneficial bacteria without changing the diversity of gut microbiota, which further supports the safe use of AGIQ in food products.

摘要

α-糖苷基异槲皮苷(AGIQ)由异槲皮苷及其葡萄糖苷衍生物组成,具有许多生物活性,包括抗炎、抗氧化和抗癌特性。然而,口服给予 AGIQ 对肠道微生物组成的影响尚不清楚。本研究旨在评估 AGIQ 对不同剂量组动物肠道微生物群的影响。雄性大鼠和小鼠在致癌或慢性毒性研究中接受不同剂量的 AGIQ(1.5%、3%或 5%w/v)饮食(rasH2 小鼠:6 个月;Sprague-Dawley 大鼠:12 个月)。雄性小型猪接受 100、300 或 1000mg/kg/天,共 28 天。收集不同动物物种的粪便样本,并使用 16S-rRNA 基因测序进行分析。肠道微生物群的 alpha 和 beta 多样性未观察到显著变化。在每种动物物种中都鉴定出对 AGIQ 有反应的特征细菌,有趣的是,普遍存在于所有三种物种中的产丁酸菌 Kineothrix alysoides,提示它可能与 AGIQ 的生物活性有关。AGIQ 选择性地调节有益的产丁酸共生菌有益菌的数量,而不改变肠道微生物群的多样性,这进一步支持 AGIQ 在食品中的安全使用。

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