Dietary methylmercury and fatty acids affect the lipid metabolism of adipose tissue and liver in rainbow trout.


Journal

Aquatic toxicology (Amsterdam, Netherlands)
ISSN: 1879-1514
Titre abrégé: Aquat Toxicol
Pays: Netherlands
ID NLM: 8500246

Informations de publication

Date de publication:
Oct 2023
Historique:
received: 28 06 2023
revised: 24 08 2023
accepted: 25 08 2023
medline: 10 10 2023
pubmed: 6 9 2023
entrez: 5 9 2023
Statut: ppublish

Résumé

Methylmercury (MeHg) is a pervasive environmental contaminant in aquatic ecosystems that can reach elevated concentrations in fish of high trophic levels, such as salmonids. The present study aims at investigating the individual and combined impacts of dietary MeHg and fatty acids on lipid metabolism in juvenile rainbow trout (Oncorhynchus mykiss) with a focus on two key organs, adipose tissue and liver. MeHg and fatty acids are both known to act on energy homeostasis although little is known about their interplay on lipid metabolism in fish. Fish were fed diets enriched in linoleic acid (LA, 18:2 n-6), α-linolenic acid (ALA, 18:3 n-3), eicosapentaenoic acid (EPA, 20:5 n-3) or docosahexaenoic acid (DHA, 22:6 n-3) for ten weeks, with the addition of MeHg to the diets during the last six weeks (0, 2.4 or 5.5 mg MeHg/kg dry matter). LA and ALA are polyunsaturated fatty acids (PUFA) typical of plant-derived oils whereas EPA and DHA are n-3 long chain PUFA largely found in fish oil, all used in feed formulation in aquaculture. The results showed that the LA-enriched diet induced a higher whole-body lipid content compared to the three other diets. On the contrary, the addition of MeHg led to a significant reduction of the whole-body lipid content, regardless of the diet. Interestingly, the adipocytes were larger both in presence of LA, compared to EPA and DHA, or MeHg, indicating a lipogenic effect of these two compounds. No effect was, however, observed on lipid accumulation per gram of adipose tissue. The fatty acid composition of adipose tissue and liver was significantly modified by the dietary lipids, reflecting both the fatty acid composition of the diets and the high bioconversion capacity of the rainbow trout. Exposure to MeHg selectively led to a release of n-6 PUFA from the hepatic membranes of fish fed the LA-enriched diet, showing a disruption of the pathways using n-6 PUFA. This study highlights the significant impact of MeHg exposure and dietary fatty acids on lipid metabolism in fish. Further investigation is needed to elucidate the underlying mechanisms and to explore the potential involvement of other organs.

Identifiants

pubmed: 37669601
pii: S0166-445X(23)00275-8
doi: 10.1016/j.aquatox.2023.106673
pii:
doi:

Substances chimiques

Fatty Acids 0
Methylmercury Compounds 0
Water Pollutants, Chemical 0
Docosahexaenoic Acids 25167-62-8

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

106673

Informations de copyright

Copyright © 2023. Published by Elsevier B.V.

Déclaration de conflit d'intérêts

Declaration of Competing Interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper.

Auteurs

Gilles Tinant (G)

Louvain Institute of Biomolecular Science and Technology (LIBST), Université catholique de Louvain, Croix du Sud 4-5/L7.07.03, 1348 Louvain-la-Neuve, Belgium. Electronic address: gilles.tinant@uclouvain.be.

Mélusine Van Larebeke (M)

Louvain Institute of Biomolecular Science and Technology (LIBST), Université catholique de Louvain, Croix du Sud 4-5/L7.07.03, 1348 Louvain-la-Neuve, Belgium.

Benjamin Lemaire (B)

Louvain Institute of Biomolecular Science and Technology (LIBST), Université catholique de Louvain, Croix du Sud 4-5/L7.07.03, 1348 Louvain-la-Neuve, Belgium.

Marine Courteille (M)

Louvain Institute of Biomolecular Science and Technology (LIBST), Université catholique de Louvain, Croix du Sud 4-5/L7.07.03, 1348 Louvain-la-Neuve, Belgium.

Cécile Gardin (C)

Louvain Institute of Biomolecular Science and Technology (LIBST), Université catholique de Louvain, Croix du Sud 4-5/L7.07.03, 1348 Louvain-la-Neuve, Belgium.

Ineke Neefs (I)

Louvain Institute of Biomolecular Science and Technology (LIBST), Université catholique de Louvain, Croix du Sud 4-5/L7.07.03, 1348 Louvain-la-Neuve, Belgium.

Krishna Das (K)

Laboratory of Oceanology, Université de Liège, 11 Allée du 6 Août, B6C, 4000 Liège, Belgium.

Melissa M Page (MM)

Louvain Institute of Biomolecular Science and Technology (LIBST), Université catholique de Louvain, Croix du Sud 4-5/L7.07.03, 1348 Louvain-la-Neuve, Belgium.

Jean-François Rees (JF)

Louvain Institute of Biomolecular Science and Technology (LIBST), Université catholique de Louvain, Croix du Sud 4-5/L7.07.03, 1348 Louvain-la-Neuve, Belgium.

Yvan Larondelle (Y)

Louvain Institute of Biomolecular Science and Technology (LIBST), Université catholique de Louvain, Croix du Sud 4-5/L7.07.03, 1348 Louvain-la-Neuve, Belgium.

Cathy Debier (C)

Louvain Institute of Biomolecular Science and Technology (LIBST), Université catholique de Louvain, Croix du Sud 4-5/L7.07.03, 1348 Louvain-la-Neuve, Belgium. Electronic address: cathy.debier@uclouvain.be.

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Classifications MeSH