全氟辛烷磺酸诱导发育中的斑马鱼血脂异常和胆碱能神经传递受损:对其机制的深入了解。

IF 2.6 3区 医学 Q3 NEUROSCIENCES Neurotoxicology and teratology Pub Date : 2023-10-05 DOI:10.1016/j.ntt.2023.107304
Archisman Mahapatra , Priya Gupta , Anjali Suman, Shubhendu Shekhar Ray, Rahul Kumar Singh
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引用次数: 0

摘要

全氟辛烷磺酸(PFOS)是一种持久性有机污染物,已在环境中广泛检测到,已知会在包括人类在内的生物体中积累。在这项研究中,我们研究了全氟辛烷磺酸暴露对脂质代谢和神经毒性的影响,以及它们在斑马鱼胚胎发育中的相关性。结果表明,全氟辛烷磺酸暴露导致总脂质、甘油三酯、总胆固醇和低密度脂蛋白以浓度依赖的方式显著增加,而高密度脂蛋白胆固醇水平显著降低。此外,全氟辛烷磺酸暴露导致血糖水平显著下降。该研究还揭示了参与脂质代谢的基因表达的改变,包括fasn、acaca和hmgcr的上调和ldlr、pparα和abca1的下调,以及脂蛋白脂酶降低和脂肪酸合成酶活性增加。此外,全氟辛烷磺酸暴露导致乙酰胆碱酯酶和Na+/K+-ATP酶活性受到抑制,分别表明胆碱能神经传递和离子稳态受到破坏。总的来说,这项研究为全氟辛烷磺酸暴露带来的潜在健康风险提供了重要见解,包括血脂异常、心血管疾病、糖代谢受损和神经毒性。需要进一步研究,以充分阐明全氟辛烷磺酸暴露的潜在机制和潜在的长期影响。
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PFOS-induced dyslipidemia and impaired cholinergic neurotransmission in developing zebrafish: Insight into its mechanisms

Perfluorooctane sulfonate (PFOS) is a persistent organic pollutant that has been widely detected in the environment and is known to accumulate in organisms, including humans. The study investigated dose-dependent mortality, hatching rates, malformations, lipid accumulation, lipid metabolism alterations, and impacts on cholinergic neurotransmission. Increasing PFOS concentration led to higher mortality, hindered hatching, and caused concentration-dependent malformations, indicating severe abnormalities in developing zebrafish. The results also demonstrated that PFOS exposure led to a significant increase in total lipids, triglycerides, total cholesterol, and LDL in a concentration-dependent manner, while HDL cholesterol levels were significantly decreased. Additionally, PFOS exposure led to a significant decrease in glucose levels. The study identified TGs, TCHO, and glucose as the most sensitive biomarkers in assessing lipid metabolism alterations. The study also revealed altered expression of genes involved in lipid metabolism, including upregulation of fasn, acaca, and hmgcr and downregulation of ldlr, pparα, and abca1, as well as decreased lipoprotein lipase (LPL) and increased fatty acid synthase (FAS) activity,suggesting an impact on fatty acid synthesis, cholesterol uptake, and lipid transport. Additionally, PFOS exposure led to impaired cholinergic neurotransmission, evidenced by a concentration-dependent inhibition of acetylcholinesterase activity, altered gene expressions related to neural development and function, and reduced Na+/K+-ATPase activity. STRING network analysis highlighted two distinct gene clusters related to lipid metabolism and cholinergic neurotransmission, with potential interactions through the pparα-creb1 pathway. Overall, this study provide important insights into the potential health risks associated with PFOS exposure, including dyslipidemia, cardiovascular disease, impaired glucose metabolism, and neurotoxicity. Further research is needed to fully elucidate the underlying mechanisms and potential long-term effects of PFOS exposure.

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来源期刊
CiteScore
5.60
自引率
10.30%
发文量
48
审稿时长
58 days
期刊介绍: Neurotoxicology and Teratology provides a forum for publishing new information regarding the effects of chemical and physical agents on the developing, adult or aging nervous system. In this context, the fields of neurotoxicology and teratology include studies of agent-induced alterations of nervous system function, with a focus on behavioral outcomes and their underlying physiological and neurochemical mechanisms. The Journal publishes original, peer-reviewed Research Reports of experimental, clinical, and epidemiological studies that address the neurotoxicity and/or functional teratology of pesticides, solvents, heavy metals, nanomaterials, organometals, industrial compounds, mixtures, drugs of abuse, pharmaceuticals, animal and plant toxins, atmospheric reaction products, and physical agents such as radiation and noise. These reports include traditional mammalian neurotoxicology experiments, human studies, studies using non-mammalian animal models, and mechanistic studies in vivo or in vitro. Special Issues, Reviews, Commentaries, Meeting Reports, and Symposium Papers provide timely updates on areas that have reached a critical point of synthesis, on aspects of a scientific field undergoing rapid change, or on areas that present special methodological or interpretive problems. Theoretical Articles address concepts and potential mechanisms underlying actions of agents of interest in the nervous system. The Journal also publishes Brief Communications that concisely describe a new method, technique, apparatus, or experimental result.
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