4.8 Article

The Use of Non-targeted Lipidomics and Histopathology to Characterize the Neurotoxicity of Bifenthrin to Juvenile Rainbow Trout (Oncorhynchus mykiss)

期刊

ENVIRONMENTAL SCIENCE & TECHNOLOGY
卷 56, 期 16, 页码 11482-11492

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.est.2c01542

关键词

pyrethroid; salmonid; neurotoxic; brain; histology; adverse outcome

资金

  1. California Department of Fish and Wildlife Proposition 1 Restoration Grant Program
  2. [P1896015]

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Exposure to bifenthrin resulted in concentration-dependent alterations in lipid metabolism in juvenile rainbow trout, with decreased levels of triglycerides and significant changes in phosphatidylcholines and phosphatidylethanolamines. Histopathological insults, such as focal hemorrhages and blood vessel congestion, were observed in the brains of bifenthrin-treated animals, indicating a potential association between altered lipid metabolism and neuronal cell structure and integrity.
Due to the detection frequencies and measured concentrations in surface water, the type I pyrethroid insecticide, bifenthrin, has been of particular concern within the Sacramento-San Joaquin Delta in California. Concentrations have been detected above levels previously reported to impair neuroendocrine function and induce neurotoxicity to several species of salmonids. Metabolomic and transcriptomic studies indicated impairment of cellular signaling within the brain of exposed animals and potential alteration of lipid metabolism. To better understand the potential impacts of bifenthrin on brain lipids, juvenile rainbow trout (Oncorhynchus mykiss) were exposed to mean bifenthrin concentrations of 28 or 48 ng/L for 14 days, and non-targeted lipidomic profiling in the brain was conducted. Brain tissue sections were also assessed for histopathological insult following bifenthrin treatment. Bifenthrin-exposed trout had a concentration-dependent decrease in the relative abundance of triglycerides (TGs) with levels of phosphatidylcholines (PCs) and phosphatidylethanolamines (PEs) significantly altered following 48 ng/L bifenthrin exposure. An increased incidence of histopathological lesions, such as focal hemorrhages and congestion of blood vessels, was noted in the brains of bifenthrin-treated animals, suggesting an association between altered lipid metabolism and neuronal cell structure and integrity.

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