Journal of Animal Science and Technology
Korean Society of Animal Science and Technology
Research Article

Comparative Effects of Deoxynivalenol and Deepoxy-Deoxynivalenol on Porcine Oocyte Maturation and Embryonic Development, and the Partial Protective Role of Resveratrol

Hoyong Choi1, JaeHyeok Yoon1, Junghui Jo1, Xiang Zhang1, Kukbin Ji1, Inchul Choi3, Jeongwoong Lee4, Minkyu Kim1,2,*
134134, Korea.
234134, Korea.
334134, Korea.
434134, Korea.
*Corresponding Author: Minkyu Kim, Department of Animal Science and Biotechnology, College of Agriculture and Life Science, Chungnam National University, Daejeon, South Korea, Daejeon 34134, Korea, Republic of. Phone: +82-42-821-5773. E-mail: kminkyu@cnu.ac.kr.

© Copyright 2026 Korean Society of Animal Science and Technology. This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.

Received: Feb 11, 2026; Revised: Mar 26, 2026; Accepted: Mar 27, 2026

Published Online: Apr 23, 2026

Abstract

Mycotoxin contamination of animal feed is a major threat to livestock reproduction. Deoxynivalenol (DON), a trichothecene mycotoxin, disrupts cellular function by binding to ribosomes and inducing ribotoxic stress, oxidative imbalance, and apoptosis. Its primary microbial metabolite, deepoxy-deoxynivalenol (DOM-1), is thought to be less toxic, but its reproductive effects remain unclear. Here, we evaluated the effects of DON (250, 500, 1000 ng/mL) and DOM-1 (250, 500, 1000 ng/mL) on porcine oocyte maturation and embryonic development in vitro, and examined whether resveratrol (Res, 2 μM) could mitigate DON-induced toxicity. DON exposure reduced cumulus expansion, decreased maturation rates, and impaired developmental competence in a dose-dependent manner, with complete developmental arrest at 1000 ng/mL. DON-treated oocytes showed elevated ROS, reduced GSH, and upregulation of ER stress– and apoptosis-related genes (ATF4, XBP1, CHOP, BAX), alongside downregulation of the anti-apoptotic gene BCL2. In contrast, DOM-1 had no significant effects compared with controls, except for a modest reduction in blastocyst rate at the highest concentration. Resveratrol did not restore cumulus expansion or nuclear maturation but attenuated DON-induced ER stress markers, stabilized BCL2 expression, and enabled some DON-exposed oocytes to develop to blastocysts. These findings demonstrate that DON exerts dose-dependent toxicity on porcine oocytes through oxidative stress and ER stress–mediated apoptosis, whereas DOM-1 is largely non-toxic. Resveratrol provides partial protection, suggesting its potential as a dietary intervention to reduce reproductive losses caused by DON.

Keywords: reproduction, oocyte; mycotoxin; deoxynivalenol; deepoxy-deoxynivalenol; ER stress