Liliya Sokalchuk Sokalchuk

Ms. Liliya Sokalchuk Sokalchuk


Research Focus & Metrics

Academic Career Length

1Year (2026-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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19 October 2026 in Preprints.org
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AJAlba Julià-López
Alba Julià-López
MGMarta González-Manso
Marta González-Manso
LSLiliya Sokalchuk Sokalchuk
Liliya Sokalchuk Sokalchuk
Laia Navarro-MartinLaia Navarro-Martin
Laia Navarro-Martin
Carlos BarataCarlos Barata
Carlos Barata
Bisphenol A (BPA) is one of the most extensively studied endocrine-disrupting chemicals, but its increasing replacement by alternative bisphenols has raised concerns about the safety of these substitutes. In the present study, we compared the effects of BPA, bisphenol F (BPF), bisphenol S (BPS), bisphenol Z (BPZ), bisphenol AP (BPAP) and bisphenol A diglycidyl ether (BADGE) in Daphnia magna, focusing on lipid storage, feeding activity, photomotor behaviour and molecular biomarkers related to lipid metabolism and endocrine regulation. The tested compounds produced distinct biological responses. BPA increased neutral lipid accumulation, whereas exposure to BPF, BPS, BPZ, BPAP and BADGE generally resulted in reduced lipid reserves. Several compounds also decreased feeding activity, suggesting that altered energy intake may contribute to the observed changes in lipid storage. Behavioural analyses revealed significant effects on photomotor responses, particularly after exposure to BPA, BPF, BPS and BADGE. At the molecular level, bisphenol exposure modified the expression of genes involved in lipid metabolism, lipid transport and endocrine-related pathways. BPA induced the expression of genes associated with lipid synthesis and storage, while compounds causing lipid depletion more frequently affected genes involved in lipid mobilization and fatty acid metabolism. Marked effects were also observed for endocrine biomarkers. BADGE increased the expression of neverland, a key gene in ecdysteroid biosynthesis, while reducing the expression of the juvenoid-responsive gene hb2 and vitellogenin. In contrast, BPF significantly increased hb2 transcription. Correlation analyses further supported links between metabolic, behavioural and endocrine responses. Overall, the results show that bisphenol analogues differ substantially in their mode of action and biological effects. While BPA displayed clear obesogenic properties, most replacement bisphenols reduced lipid stores and altered endocrine-regulated pathways. These findings indicate that BPA substitutes cannot be assumed to represent safer alternatives and highlight the need for a broader evaluation of their ecological impacts in aquatic organisms.