The Metabolic Homeostasis of Harpagoside and Taurine Sustains Postovulatory Oocyte Quality

Balanced metabolic homeostasis is critical for maintaining high-quality oocytes. Growing evidence suggests that metabolic dysregulation induced by postovulatory aging severely compromises oocyte quality. However, the metabolic signatures of postovulatory aged oocyte remain poorly characterized. In this study, we employed metabolomic sequencing to delineate the distinctive metabolic alterations in postovulatory aged (PostOA) oocytes. Notably, we identified that Harpagoside accumulation in PostOA oocytes leads to reduced nitric oxide (NO) levels, resulting in spindle/chromosome instability and DNA damage. Furthermore, we demonstrated that Taurine plays a crucial role in preserving the quality of PostOA oocytes. Exogenous Taurine supplementation significantly rescued meiotic defects in PostOA oocytes, primarily by restoring mitochondrial function and enhancing developmental competence. Collectively, our findings provide a valuable resource for understanding metabolic remodeling during postovulatory aging and highlight potential therapeutic strategies to mitigate aging-related oocyte deterioration.

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Publication Details

Journal
The FASEB Journal
Published
2026-03-17
DOI
https://doi.org/10.1096/fj.202504163r
Primary Topic
Aldose Reductase and Taurine
Type
article
Field-Weighted Citation Impact
0.00
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article

The Metabolic Homeostasis of Harpagoside and Taurine Sustains Postovulatory Oocyte Quality

T. L. Zhang, Y. Z. Zhou, Yongbin Liu, Zengyou Ma et al.
The FASEB Journal
Aldose Reductase and Taurine
article

The Metabolic Homeostasis of Harpagoside and Taurine Sustains Postovulatory Oocyte Quality

T. L. Zhang, Y. Z. Zhou, Yongbin Liu, Zengyou Ma, Li Kong, Mengjiao Yuan
article en

Abstract

Balanced metabolic homeostasis is critical for maintaining high-quality oocytes. Growing evidence suggests that metabolic dysregulation induced by postovulatory aging severely compromises oocyte quality. However, the metabolic signatures of postovulatory aged oocyte remain poorly characterized. In this study, we employed metabolomic sequencing to delineate the distinctive metabolic alterations in postovulatory aged (PostOA) oocytes. Notably, we identified that Harpagoside accumulation in PostOA oocytes leads to reduced nitric oxide (NO) levels, resulting in spindle/chromosome instability and DNA damage. Furthermore, we demonstrated that Taurine plays a crucial role in preserving the quality of PostOA oocytes. Exogenous Taurine supplementation significantly rescued meiotic defects in PostOA oocytes, primarily by restoring mitochondrial function and enhancing developmental competence. Collectively, our findings provide a valuable resource for understanding metabolic remodeling during postovulatory aging and highlight potential therapeutic strategies to mitigate aging-related oocyte deterioration.

The FASEB JournalVol. 40(6)
Inner Mongolia Agricultural University (CN), Inner Mongolia University (CN)
Responsible consumption and production
Openalex Percentile: Top 20%
Aldose Reductase and Taurine
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