Schmeisser · Marine biotechnology (New York, N.Y.) 2021 · comparative animal feeding and transcriptomic study · n=?

Molecular Mechanism Involved in Carotenoid Metabolism in Post-Smolt Atlantic Salmon: Astaxanthin Metabolism During Flesh Pigmentation and Its Antioxidant Properties.

Cited 29 times in the scientific literature.

Level 5 - mechanism / opinion, no new human data

Animal experimental study evaluating tissue transcriptomics (Oxford CEBM level 5).

PubMed 34417678 · doi:10.1007/s10126-021-10055-2 · record verified 2026-08-29

What was done

Post-smolt Atlantic salmon were fed diets either with (+Ax) or without (-Ax) astaxanthin supplementation. A transcriptomic approach was used to evaluate and compare gene expression responses across three tissues: pyloric caeca, liver, and skeletal muscle.

What was found

The abstract reports qualitative pathway and gene-level modulations without numerical data, fold-changes, or exact p-values: - Pyloric caeca exhibited the highest transcriptomic sensitivity to astaxanthin supplementation, particularly among genes governing carotenoid absorption and metabolism (including cd36). - Liver tissue displayed significant modulation of genes associated with upstream regulation of the ferroptosis pathway and cellular lipid peroxidation (including agr2). - Muscle tissue showed fewer transcriptional alterations, limited primarily to genes involved in actin remodeling and glucose homeostasis (including fbp1).

Why it matters

The findings highlight that astaxanthin processing in salmon is driven largely by metabolic activity at the site of absorption in the pyloric caeca and identify potential antioxidant pathways in the liver, aiding aquaculture nutritional strategies aimed at flesh pigmentation.

Limits

The study is restricted to Atlantic salmon post-smolts, limiting generalizability outside aquaculture models. The abstract omits critical experimental parameters, including sample sizes, astaxanthin dosage, feeding duration, and specific quantitative metrics (such as fold-change thresholds or statistical significance levels). Functional verification of antioxidant capacity or protein expression was not detailed in the abstract.

Cited by