环境氟暴露与肠道微生物的相互作用:对人类氟中毒发展的潜在影响。

IF 3.9 3区 医学 Q2 FOOD SCIENCE & TECHNOLOGY
Neha Rawat , Saravanadevi Sivanesan , Gajanan Sitaramji Kanade , Amit Bafana
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引用次数: 0

摘要

氟接触主要通过受污染的水发生,并导致氟中毒,这是一个全球性的健康问题。摄入后,氟化物通过胃肠道被吸收,在那里它与肠道微生物群相互作用。虽然动物研究已经探索了氟化物对肠道微生物群的影响,但尚未进行人体研究。大多数研究强调宏基因组的多样性,而忽略了纯培养物的分离和特性以供进一步应用。此外,在氟化物暴露人群中,肠道微生物群与氟中毒结果之间的关系尚未得到探讨。本研究对氟暴露人群中(有症状的,II组)或无(无症状的,I组)氟骨症症状的可培养肠道微生物群与未暴露对照组(III组)进行了特征和比较。I组富厚菌门丰度较高(58.58%),II组以变形菌门为主(61.25%),III组Proteobacteria丰度相似(50.38%)和厚壁菌门(49.51%)。短链脂肪酸(SCFA)谱分析显示,ⅰ组菌株产生的异丁酸(1.31±0.9 mM)高于ⅱ组(0.71±0.35 mM),异戊酸(0.8±0.41 mM)高于ⅰ组(0.61±0.08 mM) (p < 0.05)。这些发现表明,肠道微生物群和SCFAs的改变可能影响骨代谢,影响氟中毒的进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Interaction of environmental fluoride exposure and gut microbes: Potential implication in the development of fluorosis in human subjects

Interaction of environmental fluoride exposure and gut microbes: Potential implication in the development of fluorosis in human subjects
Fluoride exposure primarily occurs through contaminated water and leads to fluorosis, which is a global health concern. After ingestion, fluoride is absorbed via gastrointestinal tract, where it interacts with the gut microbiota. While animal studies have explored fluoride's effects on gut microbiota, no human studies have yet been conducted. Most research emphasizes metagenomic diversity, neglecting isolation and characterization of pure cultures for further applications. Additionally, the association between gut microbiota with fluorosis outcomes in fluoride-exposed populations is unexplored. This study characterizes and compares the cultivable gut microbiota in the fluoride-exposed population with (symptomatic, group II) or without (asymptomatic, group I) signs of skeletal fluorosis along with unexposed control (group III). Group I displayed higher abundance of Firmicutes (58.58 %), group II had predominance of Proteobacteria (61.25 %) while group III showed similar abundance of Proteobacteria (50.38 %) and Firmicutes (49.51 %). On analyzing short-chain fatty acid (SCFA) profiles, group I isolates produced higher isobutyric acid (1.31 ± 0.9 mM) than group II (0.71 ± 0.35 mM), while group II produced more isovaleric acid (0.8 ± 0.41 mM) than group I (0.61 ± 0.08 mM) (p < 0.05). These findings suggest that gut microbiota and SCFAs alteration may influence bone metabolism, affecting the fluorosis progression.
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来源期刊
Food and Chemical Toxicology
Food and Chemical Toxicology 工程技术-毒理学
CiteScore
10.90
自引率
4.70%
发文量
651
审稿时长
31 days
期刊介绍: Food and Chemical Toxicology (FCT), an internationally renowned journal, that publishes original research articles and reviews on toxic effects, in animals and humans, of natural or synthetic chemicals occurring in the human environment with particular emphasis on food, drugs, and chemicals, including agricultural and industrial safety, and consumer product safety. Areas such as safety evaluation of novel foods and ingredients, biotechnologically-derived products, and nanomaterials are included in the scope of the journal. FCT also encourages submission of papers on inter-relationships between nutrition and toxicology and on in vitro techniques, particularly those fostering the 3 Rs. The principal aim of the journal is to publish high impact, scholarly work and to serve as a multidisciplinary forum for research in toxicology. Papers submitted will be judged on the basis of scientific originality and contribution to the field, quality and subject matter. Studies should address at least one of the following: -Adverse physiological/biochemical, or pathological changes induced by specific defined substances -New techniques for assessing potential toxicity, including molecular biology -Mechanisms underlying toxic phenomena -Toxicological examinations of specific chemicals or consumer products, both those showing adverse effects and those demonstrating safety, that meet current standards of scientific acceptability. Authors must clearly and briefly identify what novel toxic effect (s) or toxic mechanism (s) of the chemical are being reported and what their significance is in the abstract. Furthermore, sufficient doses should be included in order to provide information on NOAEL/LOAEL values.
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