Modulation of Apoptosis and Autophagy by Melatonin in Juglone-Exposed Bovine Oocytes

Author:

El-Sheikh Marwa1ORCID,Mesalam Ahmed Atef2ORCID,Kang Seon-Min3,Joo Myeong-Don3,Soliman Seham Samir4ORCID,Khalil Atif Ali Khan5ORCID,Ahn Mi-Jeong6ORCID,Kong Il-Keun378ORCID

Affiliation:

1. Department of Microbial Biotechnology, Biotechnology Research Institute, National Research Centre (NRC), Dokki, Cairo 12622, Egypt

2. Department of Therapeutic Chemistry, Pharmaceutical and Drug Industries Research Institute, National Research Centre (NRC), Dokki, Cairo 12622, Egypt

3. Division of Applied Life Science (BK21 Four), Gyeongsang National University, Jinju 52828, Republic of Korea

4. Department of Animal Reproduction and Artificial Insemination, Veterinary Research Institute, National Research Centre (NRC), Dokki, Cairo 12622, Egypt

5. Department of Pharmacognosy, Faculty of Pharmaceutical and Allied Health Sciences, Lahore College for Women University, Lahore 54000, Pakistan

6. College of Pharmacy and Research Institute of Pharmaceutical Sciences, Gyeongsang National University, Jinju 52828, Republic of Korea

7. Institute of Agriculture and Life Science, Gyeongsang National University, Jinju 52828, Republic of Korea

8. The King Kong Corp. Ltd., Gyeongsang National University, Jinju 52828, Republic of Korea

Abstract

Melatonin, an antioxidant hormone secreted by the pineal gland, has been recognized as a regulator for numerous biological events. The deleterious effects of juglone, a polyphenolic extract of walnut trees, on embryo development has been previously reported. In the current study, we aimed to display the impact of melatonin administrated during in vitro oocyte maturation (IVM) on juglone-treated oocytes. Thus, in vitro matured oocytes were collected after 24 h post incubation with juglone in the presence or absence of melatonin. Reactive oxygen species (ROS), glutathione (GSH) content, mitochondrial distribution, and the relative abundance of mRNA transcription levels were assessed in oocytes, in addition, oocytes were in vitro fertilized to check the competency levels of oocytes to generate embryos. We found that administration of melatonin during the maturation of oocytes under juglone stress significantly improved the cleavage rate, 8-16 cell-stage embryos and day-8 blastocysts when compared to the sole juglone treatment. In addition, the fluorescence intensity of ROS increased, whereas the GSH decreased in juglone-treated oocytes compared to melatonin–juglone co-treated and untreated ones. Additionally, a significant increase in the mitochondrial aberrant pattern, the pattern that was normalized following melatonin supplementation, was observed following juglone administration. The mRNA analysis using RT-qPCR revealed a significant upregulation of autophagy and oxidative-stress-specific markers in the juglone-treated group compared to the co-treatment and control. In conclusion, the study reveals, for the first time, a protective effect of melatonin against the oxidative stress initiated following juglone treatment during the in vitro maturation of oocytes.

Funder

National Research Foundation of Korea

Korean Ministry of Education

Publisher

MDPI AG

Subject

General Veterinary,Animal Science and Zoology

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