Lead Mediated Lipopolysaccharides Exacerbates Fatty Liver Processes in High‐Fat Diets‐Induced Mice

IF 4.4 3区 医学 Q2 ENVIRONMENTAL SCIENCES
Penghui Nie, Liehai Hu, Tao You, Tiantian Jia, Hengyi Xu
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引用次数: 0

Abstract

Obesity leads to a variety of health risks, and lead, which is ranked second in Agency for Toxic Substances and Disease Registry's priority list of harmful substances, may be more harmful to individuals that are obese. C57BL/6 mice were fed a normal diet or a high‐fat diet with or without exposure to 1 g/L lead exposure in drinking water for 8 consecutive weeks. Serum and hepatic biochemistry analysis, histopathological observation, and RT‐qPCR were used to explore the potential mechanism of liver damage in obese individuals after Pb exposure, and fecal microbiota transplantation was performed to investigate the role of the gut microbiota in the progression of fatty liver disease. We found that the progression of fatty liver disease induced by high‐fat diets was accelerated by chronic lead intake. In addition, the occurrences of liver injury in recipient mice suggested the role of the gut microbiota. These findings indicated that the combination of lead and a HFD exacerbated hepatic lipotoxicity by activating LPS‐mediated inflammation, and that gut microbiota disorders and impaired intestinal barrier function play pivotal roles in the progression of fatty liver disease.
铅介导的脂多糖加剧了高脂饮食诱导小鼠的脂肪肝过程
肥胖会导致多种健康风险,而铅,在有毒物质和疾病登记处的有害物质优先清单中排名第二,可能对肥胖的人更有害。C57BL/6小鼠连续8周被喂食正常饮食或高脂肪饮食,并在饮用水中暴露或不暴露于1 g/L铅。通过血清和肝脏生化分析、组织病理学观察和RT - qPCR来探讨Pb暴露后肥胖个体肝损伤的潜在机制,并通过粪便微生物群移植来研究肠道微生物群在脂肪肝疾病进展中的作用。我们发现,慢性铅摄入加速了高脂肪饮食引起的脂肪肝疾病的进展。此外,受体小鼠肝损伤的发生提示了肠道微生物群的作用。这些发现表明,铅和HFD的结合通过激活LPS介导的炎症加剧了肝脏脂肪毒性,肠道微生物群紊乱和肠道屏障功能受损在脂肪肝疾病的进展中起关键作用。
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来源期刊
Environmental Toxicology
Environmental Toxicology 环境科学-毒理学
CiteScore
7.10
自引率
8.90%
发文量
261
审稿时长
4.5 months
期刊介绍: The journal publishes in the areas of toxicity and toxicology of environmental pollutants in air, dust, sediment, soil and water, and natural toxins in the environment.Of particular interest are: Toxic or biologically disruptive impacts of anthropogenic chemicals such as pharmaceuticals, industrial organics, agricultural chemicals, and by-products such as chlorinated compounds from water disinfection and waste incineration; Natural toxins and their impacts; Biotransformation and metabolism of toxigenic compounds, food chains for toxin accumulation or biodegradation; Assays of toxicity, endocrine disruption, mutagenicity, carcinogenicity, ecosystem impact and health hazard; Environmental and public health risk assessment, environmental guidelines, environmental policy for toxicants.
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