Understanding the molecular basis
of sexual dimorphism in the cardiovascular
system may contribute to the improvement of the outcome in biological,
pharmacological, and toxicological studies as well as on the development
of sex-based drugs and therapeutic approaches. Label-free protein
quantification using high-resolution mass spectrometry was applied
to detect sex-based proteome differences in the heart of zebrafish Danio rerio. Out of almost 3000 unique identified
proteins in the heart, 79 showed significant abundance differences
between male and female fish. The functional differences were mapped
using enrichment analyses. Our results suggest that a large amount
of materials needed for reproduction (e.g., sugars, lipids, proteins,
etc.) may impose extra pressure on blood, vessels, and heart on their
way toward the ovaries. In the present study, the female’s
heart shows a clear sexual dimorphism by changing abundance levels
of numerous proteins, which could be a way to safely overcome material-induced
elevated pressures. These proteins belong to the immune system, oxidative
stress response, drug metabolization, detoxification, energy, metabolism,
and so on. In conclusion, we showed that sex can induce dimorphism
at the molecular level in nonsexual organs such as heart and must
be considered as an important factor in cardiovascular research. Data
are available via ProteomeXchange with identifier PXD023506.