4.7 Article

Exposure to acute waterborne cadmium caused severe damage on lipid metabolism of freshwater fish, revealed by nuclear lipid droplet deposition in hepatocytes of rare minnow

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AQUATIC TOXICOLOGY
卷 257, 期 -, 页码 -

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ELSEVIER
DOI: 10.1016/j.aquatox.2023.106433

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Lipid droplet; Lipid transport; Liver; Heavy metal; Freshwater fish; Metabolic toxicology

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This study aimed to investigate the effects of cadmium on lipid metabolism in freshwater fish using rare minnows (Gobiocypris rarus) as the model species. The results showed that exposure to high concentrations of cadmium led to severe damage in the form of lipid droplet accumulation, abnormal rough endoplasmic reticulum lamellae, and hepatocyte necrosis. Furthermore, hepatic and serum lipids were significantly increased, while the mRNA transcripts of certain genes related to lipid oxidation, synthesis, and transport were altered. These findings suggest that disrupted lipid transport may play a key role in the accumulation of hepatic lipid droplets.
Cadmium (Cd) is a widely distributed aquatic toxic heavy metal with the potential to disrupt fish metabolism; however, more research is needed to clarify the underlying mechanisms. In the present study, rare minnows (Gobiocypris rarus) were used to detect the effects of cadmium on freshwater fish lipid metabolism and its underlying mechanism by histopathological observation, measurement of serum and liver biochemical indexes, and analysis of gene expression in terms of lipid oxidation, synthesis and transport. Here, severe damage, such as cytoplasmic lipid droplet (LD) accumulation, ectopic deposition of LDs, and the appearance of nuclear LDs (nLDs), was detected after exposure to 2.0 mg/L or higher concentrations (2.5 and 2.8 mg/L CdCl2) for 96 h. Other damage included abnormal increases in rough endoplasmic reticulum (RER) lamellae in a fingerprint or concentric circle pattern and necrosis of hepatocytes, and which was observed in the livers of fish exposed to 2.0 mg/L CdCl2.. Both hepatic and serum lipids, such as triglycerides and total cholesterol, were significantly increased after exposure to 2.0 mg/L CdCl2, as was serum lipase (LPS). Hepatic lipase and lipoprotein lipase remained unchanged, in accordance with the unchanged hepatic mRNA transcripts of PPARalpha. Furthermore, the mRNA transcripts of both SCD and SQLE were significantly decreased. Moreover, hepatic and serum low-density and high-density lipoprotein cholesterol showed significant changes, which were accompanied by a significant increase and decrease in hepatic APOAI and APOB100 mRNA levels, respectively. All the results indicate the presence of severe damage to hepatic lipid metabolism and that disrupted lipid transport may play a key role in the accumulation of hepatic LDs. In addition, the hepatic nLDs of nonmammalian vertebrates and their location across the nuclear envelope are intriguing, suggesting that large-size nLDs are a common marker for severe liver damage.

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