Mangiferin improves early porcine embryonic development by reducing oxidative stress

Author:

Ji He‐Wei1,Wang Chao‐Rui1,Yuan Xiu‐Wen1,Wang Jing2,Wang Lin3,Cao Qi‐Long3,Li Ying‐Hua1ORCID,Xu Yong‐Nan1,Kim Nam‐Hyung1ORCID

Affiliation:

1. Guangdong Provincial Key Laboratory of Large Animal Models for Biomedicine, School of Pharmacy and Food Engineering Wuyi University Jiangmen China

2. College of Life and Health Hainan University Haikou China

3. Qingdao Haier Biotechnology Co., Ltd. Qingdao China

Abstract

AbstractMangiferin (MGN) is primarily found in the fruits, leaves, and bark of plants of the Anacardiaceae family, including mangoes. MGN exhibits various pharmacological effects, such as protection of the liver and gallbladder, anti‐lipid peroxidation, and cancer prevention. This study aimed to investigate the effects of MGN supplementation during in vitro culture (IVC) on the antioxidant capacity of early porcine embryos and the underlying mechanisms involved. Porcine parthenotes in the IVC medium were exposed to different concentrations of MGN (0, 0.01, 0.1, and 1 μM). The addition of 0.1 μM MGN significantly increased the blastocyst formation rate of porcine embryos while reducing the apoptotic index and autophagy. Furthermore, the expression of antioxidation‐related (SOD2, GPX1, NRF2, UCHL1), cell pluripotency (SOX2, NANOG), and mitochondria‐related (TFAM, PGC1α) genes was upregulated. In contrast, the expression of apoptosis‐related (CAS3, BAX) and autophagy‐related (LC3B, ATG5) genes decreased after MGN supplementation. These findings suggest that MGN improves early porcine embryonic development by reducing oxidative stress‐related genes.

Publisher

Wiley

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