Exploring Metabolic and Gut Microbiome Responses to Paraquat Administration in Male Wistar Rats: Implications for Oxidative Stress

Author:

Hernandez-Baixauli Julia12ORCID,Chomiciute Gertruda1,Tracey Harry134ORCID,Mora Ignasi5ORCID,Cortés-Espinar Antonio J.6ORCID,Ávila-Román Javier7ORCID,Abasolo Nerea8,Palacios-Jordan Hector8ORCID,Foguet-Romero Elisabet8,Suñol David9,Galofré Mar9,Alcaide-Hidalgo Juan María1ORCID,Baselga-Escudero Laura1,del Bas Josep M.10ORCID,Mulero Miquel6ORCID

Affiliation:

1. Eurecat, Centre Tecnològic de Catalunya, Unitat de Nutrició i Salut, 43204 Reus, Spain

2. Laboratory of Metabolism and Obesity, Vall d’Hebron-Institut de Recerca, Universitat Autònoma de Barcelona, 08035 Barcelona, Spain

3. Department of Medical Sciences, School of Medicine, University of Girona, 17004 Girona, Spain

4. School of Science, RMIT University, Bundoora, VIC 3000, Australia

5. Brudy Technology S.L., 08006 Barcelona, Spain

6. Nutrigenomics Research Group, Department of Biochemistry and Biotechnology, Universitat Rovira i Virgili, 43007 Tarragona, Spain

7. Molecular and Applied Pharmacology Group (FARMOLAP), Department of Pharmacology, Universidad de Sevilla, 41012 Sevilla, Spain

8. Eurecat, Centre Tecnològic de Catalunya, Centre for Omic Sciences (COS), Joint Unit Universitat Rovira i Virgili-EURECAT, 43204 Reus, Spain

9. Eurecat, Centre Tecnològic de Catalunya, Digital Health, 08005 Barcelona, Spain

10. Eurecat, Centre Tecnològic de Catalunya, Àrea Biotecnologia, 43204 Reus, Spain

Abstract

In this study, we examined the metabolic and gut microbiome responses to paraquat (PQ) in male Wistar rats, focusing on oxidative stress effects. Rats received a single intraperitoneal injection of PQ at 15 and 30 mg/kg, and various oxidative stress parameters (i.e., MDA, SOD, ROS, 8-isoprostanes) were assessed after three days. To explore the omic profile, GC-qTOF and UHPLC-qTOF were performed to assess the plasma metabolome; 1H-NMR was used to assess the urine metabolome; and shotgun metagenomics sequencing was performed to study the gut microbiome. Our results revealed reductions in body weight and tissue changes, particularly in the liver, were observed, suggesting a systemic effect of PQ. Elevated lipid peroxidation and reactive oxygen species levels in the liver and plasma indicated the induction of oxidative stress. Metabolic profiling revealed changes in the tricarboxylic acid cycle, accumulation of ketone body, and altered levels of key metabolites, such as 3-hydroxybutyric acid and serine, suggesting intricate links between energy metabolism and redox reactions. Plasma metabolomic analysis revealed alterations in mitochondrial metabolism, nicotinamide metabolism, and tryptophan degradation. The gut microbiome showed shifts, with higher PQ doses influencing microbial populations (e.g., Escherichia coli and Akkermansia muciniphila) and metagenomic functions (pyruvate metabolism, fermentation, nucleotide and amino acid biosynthesis). Overall, this study provides comprehensive insights into the complex interplay between PQ exposure, metabolic responses, and gut microbiome dynamics. These findings enhance our understanding of the mechanisms behind oxidative stress-induced metabolic alterations and underscore the connections between xenobiotic exposure, gut microbiota, and host metabolism.

Funder

Catalan Government

Centre for the Development of Industrial Technology (CDTI) of the Spanish Ministry of Science and Innovation

European Union’s Horizon 2020 research and innovation program

Agència de Gestió d’Ajuts Universitaris i de Recerca (AGAUR) of the Catalan Government

Vicente Lopez fellowship

Publisher

MDPI AG

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