Glyphosate exposure impairs glucose and lipid metabolism by disturbing the circadian clock system in mice liver

IF 3.9 3区 医学 Q2 FOOD SCIENCE & TECHNOLOGY
Bonan Xiao , Haizhen Jiang , Hao Dong , Chao Li , Haisen Zhang , Dengke Gao , Aihua Wang , Yaping Jin , Huatao Chen
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Abstract

Glyphosate, the most extensively applied organophosphonate herbicide, poses risks to aquatic ecosystems and potentially compromises human health via dietary exposure. Although toxicological assessments have confirmed glyphosate-induced hepatotoxicity in mammalian systems, the cellular pathogenesis involving metabolic disruption warrants further mechanistic investigation. This study aimed to elucidate the effect of glyphosate exposure on hepatic glucose/lipid metabolism and its association with circadian clock disruption using murine hepatocytes (AML12) and mice models. Time-course analysis revealed that glyphosate exposure significantly suppressed core circadian and metabolic transcripts in AML12 hepatocytes, with corresponding reduction in NR1D1 protein level. Longitudinal locomotor activity monitoring revealed that glyphosate exposure caused photophase-specific hyperlocomotion and circadian period elongation in mice. Glyphosate exposure elicited marked depletion of hepatic glycogen reserves and serum total cholesterol concentrations. Notably, glyphosate also disrupted the expression of hepatic metabolic genes, paralleled by alterations of circadian clock genes expression at both mRNA and protein levels in mice. Additionally, Hmgcr and Glut2 mRNA levels were significantly decreased in Bmal1−/− AML12 cells compared to their control groups, no further significant reduction was detected in Bmal1−/− AML12 cells with glyphosate exposure. Collectively, the current study demonstrated that glyphosate exposure impairs glucose and lipid metabolism by disturbing the circadian clock system.

Abstract Image

草甘膦暴露通过扰乱小鼠肝脏生物钟系统损害糖脂代谢
草甘膦是应用最广泛的有机膦酸盐除草剂,对水生生态系统构成风险,并可能通过饮食接触损害人类健康。尽管毒理学评估已证实草甘膦会在哺乳动物系统中诱发肝脏毒性,但涉及代谢紊乱的细胞发病机制还需要进一步的机理研究。本研究旨在利用小鼠肝细胞(AML12)和小鼠模型,阐明草甘膦暴露对肝脏葡萄糖/脂质代谢的影响及其与昼夜节律紊乱的关系。时程分析表明,草甘膦暴露会显著抑制 AML12 肝细胞中的核心昼夜节律和代谢转录本,并相应降低 NR1D1 蛋白水平。纵向运动活动监测显示,草甘膦暴露会导致小鼠光相特异性过度运动和昼夜节律周期延长。接触草甘膦会导致肝糖原储备和血清总胆固醇浓度明显下降。值得注意的是,草甘膦还破坏了肝脏代谢基因的表达,同时改变了小鼠昼夜节律钟基因在 mRNA 和蛋白质水平上的表达。此外,与对照组相比,Bmal1-/- AML12细胞中的Hmgcr和Glut2 mRNA水平显著降低,但草甘膦暴露后,Bmal1-/- AML12细胞中的Hmgcr和Glut2 mRNA水平没有进一步显著降低。总之,目前的研究表明,草甘膦暴露通过干扰昼夜节律时钟系统损害葡萄糖和脂质代谢。
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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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