Chronic exposure to environmentally relevant levels of simvastatin disrupts zebrafish brain gene signaling involved in energy metabolism

• Published in: Journal of Toxicology and Environmental Health, Part A Part A, 2020-02, Vol.83 (3), p.113-125
• Main Authors: Barros, Susana, Coimbra, Ana M., Alves, Nélson, Pinheiro, Marlene, Quintana, José Benito, Santos, Miguel M., Neuparth, Teresa
• Format: Article
• Language: English
• Subjects: Aquatic organisms; Blood-brain barrier; brain metabolism; Cardiovascular diseases; Central nervous system; Chronic exposure; Danio rerio; Electron transport; Electron transport chain; Energy; Energy metabolism; Exposure; Fatty acids; Gene expression; Gene regulation; gene signaling; Genes; Glucose metabolism; Glucose transport; Glyceraldehyde-3-phosphate dehydrogenase; Lipophilic; low-level exposures; Metabolism; Mitochondria; Oxidation; Signal transduction; Signaling; Simvastatin; Statins; Transcription; Zebrafish
• ISSN: 1528-7394; 1087-2620; 2381-3504
• DOI: 10.1080/15287394.2020.1733722

Simvastatin (SIM), a hypocholesterolaemic drug belonging to the statins group, is a widely prescribed pharmaceutical for prevention of cardiovascular diseases. Several studies showed that lipophilic statins, as SIM, cross the blood-brain barrier and interfere with the energy metabolism of the central nervous system in humans and mammalian models. In fish and other aquatic organisms, the effects of SIM on the brain energy metabolism are unknown, particularly following exposure to low environmentally relevant concentrations. Therefore, the present study aimed at investigating the influence of SIM on gene signaling pathways involved in brain energy metabolism of adult zebrafish (Danio rerio) following chronic exposure (90 days) to environmentally relevant SIM concentrations ranging from 8 ng/L to 1000 ng/L. Real-time PCR was used to determine the transcript levels of several genes involved in different pathways of the brain energy metabolism (glut1b, gapdh, acadm, accα, fasn, idh3a, cox4i1, and cox5aa). The findings here reported integrated well with ecological and biochemical responses obtained in a parallel study. Data demonstrated that SIM modulates transcription of key genes involved in the mitochondrial electron transport chain, in glucose transport and metabolism, in fatty acid synthesis and β-oxidation. Further, SIM exposure led to a sex-dependent transcription profile for some of the studied genes. Overall, the present study demonstrated, for the first time, that SIM modulates gene regulation of key pathways involved in the energy metabolism in fish brain at environmentally relevant concentrations.