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March 3, 2026Cell Communication and Signaling2 citationsOpen Access

Integrated metabolomic and proteomic analyses reveal global reprogramming of oocyte metabolism following AFB1 exposure

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YXYue XiongNanjing Agricultural UniversityMGMing GaoNanjing Agricultural UniversityYMYixin MaNanjing Agricultural University

Key Points

  • AFB1 exposure leads to metabolic reprogramming in oocytes, particularly affecting fatty acid β-oxidation and nucleotide metabolism.
  • Metabolomic and proteomic analyses show significant changes in oocyte metabolism after chronic AFB1 exposure.
  • Functional assays indicate that taurine supplementation could alleviate meiotic defects and metabolic dysfunction caused by AFB1.
  • Findings suggest that taurine may mitigate reproductive toxicity from mycotoxin exposure, highlighting a potential therapeutic pathway.

Abstract

Aflatoxin B1 (AFB1) is a potent mycotoxin that impairs reproductive health, yet its impact on oocyte metabolism remains unclear. Our study aimed to characterize the metabolic profile of mouse oocytes exposed to AFB1.Using a murine model of chronic AFB1 exposure, we performed integrated metabolomic and proteomic analyses of oocytes. AFB1 exposure induced profound metabolic reprogramming, characterized by excessive activation of fatty acid β-oxidation (FAO) and one-carbon metabolism, and suppressed nucleotide metabolism. Functional assays further demonstrated that exogenous taurine supplementation improved quality of AFB1-exposed oocytes, specifically, alleviating meiotic defects and metabolic dysfunction. Collectively, these findings provide novel mechanistic insight into AFB1-induced metabolic perturbations in oocytes and highlight taurine as a promising intervention to mitigate mycotoxin-associated reproductive toxicity.

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Cite This Study

Xiong et al. (2026) studied this question.

synapsesocial.com/papers/69a7674fbadf0bb9e87e06b2https://doi.org/10.1186/s12964-026-02711-8
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