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Research article2024Peer reviewed

Effect of an endothelial regulatory module on plasma proteomics in exercising horses

Amiri, Roudbar, M.; Rosengren, M.K.; Mousavi, S.F.; Fegraeus, K.; Naboulsi, R.; Meadows, J.R.S.; Lindgren, G.

Abstract

Elite performing exercise requires an intricate modulation of the blood pressure to support the working muscles with oxygen. We have previously identified a genomic regulatory module that associates with differences in blood pressures of importance for elite performance in racehorses. This study aimed to determine the effect of the regulatory module on the protein repertoire. We sampled plasma from 12 Coldblooded trotters divided into two endothelial regulatory module haplotype groups, a sub-elite performing haplotype (SPH) and an elite performing haplotype (EPH), each at rest and exercise. The haplotype groups and their interaction were interrogated in two analyses, i) individual paired ratio analysis for identifying differentially abundant proteins of exercise (DAPE) and interaction (DAPI) between haplotype and exercise, and ii) unpaired ratio analysis for identifying differentially abundant protein of haplotype (DAPH). The proteomics analyses revealed a widespread change in plasma protein content during exercise, with a decreased tendency in protein abundance that is mainly related to lung function, tissue fluids, metabolism, calcium ion pathway and cellular energy metabolism. Furthermore, we provide the first investigation of the proteome variation due to the interaction between exercise and related blood pressure haplotypes, which this difference was related to a faster switch to the lipoprotein and lipid metabolism during exercise for EPH. The molecular signatures identified in the present study contribute to an improved understanding of exercise-related blood pressure regulation.

Keywords

Horse; Plasma proteins; Proteomics; Secretomics; Training

Published in

Comparative Biochemistry and Physiology - Part D: Genomics and Proteomics
2024, Volume: 52, article number: 101265Publisher: Elsevier Inc.