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February 28, 2026Journal of Hazardous Materials3 citationsOpen Access

Melatonin safeguards against butylparaben-induced oxidative stress, DNA damage, microtubule instability, and organelle dysfunction during porcine oocyte maturation

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PJPil-Soo JeongSJSe-Been JeonHKHyo-Gu Kang

Key Points

  • To examine the effects of butylparaben on female reproduction and assess melatonin as a protective agent.
  • Investigated the effects of butylparaben on porcine oocytes during maturation.
  • Assessed cytoplasmic and nuclear maturation, microtubule stability, and organelle function.
  • Evaluated the role of melatonin in preventing butylparaben-induced defects.
  • Butylparaben exposure leads to impaired oocyte maturation and embryonic development.
  • Microtubule structure and organelle function are disrupted due to butylparaben exposure.
  • Oxidative stress from butylparaben induces DNA damage and increases early cell death.
  • Melatonin supplementation rescues oocyte maturity and developmental defects caused by butylparaben.
  • Melatonin offers a protective strategy for enhancing oocyte quality in the presence of endocrine disruptors.

Abstract

Butylparaben (BP) is widely used in food, beverage containers, personal care products, and cosmetics, resulting in high human exposure. Previous studies reported a potential link between BP and adverse effects on human health, but its effects on female reproduction and the underlying mechanisms remain to be fully elucidated. This study examined the molecular mechanisms of BP-induced female reproductive damage and a potential therapeutic strategy. BP exposure was found to impair cumulus cell expansion, oocyte nuclear maturation, and subsequent embryonic development. BP-exposed oocytes exhibited abnormalities in microtubule structure, stability, and actin-mediated cytoskeleton dynamics. BP exposure also induced cytoplasmic maturation defects by disrupting mitochondria, the endoplasmic reticulum, and lipid metabolism. In addition, BP exposure induces oxidative stress, which interferes with DNA double-strand break repair, causes DNA damage, and ultimately leads to cell death. However, melatonin (MLT) supplementation ameliorated BP-induced meiotic and developmental defects in porcine oocytes. These results suggest that MLT plays a protective role in BP-exposed oocytes by preventing meiotic failure due to impaired nuclear and cytoplasmic maturation. MLT supplementation, therefore, offers a strategy to improve oocyte quality, fertility, and subsequent embryonic development. Our findings regarding the toxicological effects of endocrine disruptors on female reproduction suggest a novel approach for preserving female fertility. • BP exposure disrupts oocyte maturation and embryonic development • BP alters microtubule structure, cytoskeleton dynamics, and organelle function • BP-induced oxidative stress causes DNA damage and early apoptosis • MLT supplementation effectively rescues BP-induced meiotic and developmental defects • MLT offers a protective strategy to preserve female fertility against EDCs toxicity

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Cite This Study

Jeong et al. (2026) studied this question.

synapsesocial.com/papers/69a2878e0a974eb0d3c034d6https://doi.org/10.1016/j.jhazmat.2026.141621
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