PUBLICATION

Combined western diet and bisphenol A exposure induces an oxidative stress-based paraoxonase 1 response in larval zebrafish

Authors
van den Boom, R., Vergauwen, L., Koedijk, N., da Silva, K.M., Covaci, A., Knapen, D.
ID
ZDB-PUB-231002-136
Date
2023
Source
Comparative biochemistry and physiology. Toxicology & pharmacology : CBP   274: 109758109758 (Journal)
Registered Authors
Knapen, Dries, Vergauwen, Lucia
Keywords
Antioxidant, Bisphenol A, Lipid metabolism, Metabolic disorders, Metabolism, Western diet
MeSH Terms
none
PubMed
37757927 Full text @ Comp. Biochem. Physiol. C Toxicol. Pharmacol.
Abstract
Paraoxonase 1 (PON1) is an antioxidant enzyme linked to metabolic disorders by genome-wide association studies in humans. Exposure to metabolic disrupting chemicals (MDCs) such as bisphenol A (BPA), together with genetic and dietary factors, can increase the risk of metabolic disorders. The objective of this study was to investigate how PON1 responds to the metabolic changes and oxidative stress caused by a western diet, and whether exposure to BPA alters the metabolic and PON1 responses. Zebrafish larvae at 14 days post fertilization were fed a custom-made western diet with and without aquatic exposure to two concentrations of BPA for 5 days. A combination of western diet and 150 μg/L BPA exposure resulted in a stepwise increase in weight, length and oxidative stress, suggesting that BPA amplifies the western diet-induced metabolic shift. PON1 arylesterase activity was increased in all western diet and BPA exposure groups and PON1 lactonase activity was increased when western diet was combined with exposure to 1800 μg/L BPA. Both PON1 activities were positively correlated to oxidative stress. Based on our observations we hypothesize that a western diet caused a shift towards fatty acid-based metabolism, which was increased by BPA exposure. This shift resulted in increased oxidative stress, which in turn was associated with a PON1 activity increase as an antioxidant response. This is the first exploration of PON1 responses to metabolic challenges in zebrafish, and the first study of PON1 in the context of MDC exposure in vertebrates.
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