# Protective effects of Demethylfuropinnarin on porcine pre-implantation embryos under Tunicamycin-induced oxidative stress and endoplasmic reticulum stress during in vitro culture

## TL;DR

This study shows that Demethylfuropinnarin protects pig embryos from stress during lab culture, improving their survival and development.

## Contribution

This is the first study to demonstrate the protective effects of Demethylfuropinnarin on porcine embryos under oxidative and ER stress.

## Key findings

- DMFP reduced reactive oxygen species and preserved mitochondrial function in embryos.
- DMFP increased Nrf2 expression and antioxidant enzyme activity while decreasing ER stress markers.
- DMFP improved embryo cleavage and blastocyst formation rates and reduced apoptosis.

## Abstract

Assisted Reproductive Technologies (ART) are essential for addressing infertility and improving reproductive outcomes in both humans and animals. In vitro culture (IVC) supports embryo development outside the body but is often compromised by oxidative and endoplasmic reticulum (ER) stress, leading to impaired development and apoptosis. Demethylfuropinnarin (DMFP), a furocoumarin from Notopterygium incisum, has not been previously studied for its biological activity. Given the antioxidant properties of furocoumarins, this study aimed to determine whether DMFP could alleviate tunicamycin (TM)-induced oxidative and ER stress in porcine pre-implantation embryos. Our results show that DMFP significantly reduced reactive oxygen species (ROS) and preserved mitochondrial function. Additionally, DMFP increased Nuclear factor erythroid 2–related factor 2 (Nrf2) expression and decreased Kelch-like ECH-associated protein 1 (Keap1), leading to higher superoxide dismutase (SOD) and catalase (CAT) activity. DMFP treatment also improved cleavage and blastocyst formation rates, reduced apoptosis, and potentially alleviated ER stress, as indicated by lower levels of key ER stress markers. This study concludes that DMFP effectively reduces oxidative stress and may mitigate ER stress, enhancing embryo viability during IVC.

The online version contains supplementary material available at 10.1038/s41598-026-38755-6.