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The Protective Effects of Astaxanthin on Pre-Antral Follicle Degeneration in Ovine Vitrified/Warmed Ovarian Tissue Publisher Pubmed



Afzali A1 ; Nazari H2 ; Ahmadi E2 ; Davoodian N2 ; Amidi F3 ; Taheri F1, 4 ; Bashiri Z5, 6 ; Kadivar A7 ; Nemati Dehkordi M8
Authors
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Authors Affiliations
  1. 1. Faculty of Medical Sciences, Shahrekord University of Medical Sciences, Shahrekord, Iran
  2. 2. Research Institute of Animal Embryo Technology, Shahrekord University, Shahrekord, Iran
  3. 3. Department of Anatomy, Faculty of Medicine, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Department of Anatomy, Faculty of Medicine, Shahrekord University of Medical Sciences, Shahrekord, Iran
  5. 5. Department of Anatomy, Faculty of Medicine, Iran University of Medical Sciences, Tehran, Iran
  6. 6. Omid Fertility and Infertility Clinic, Hamedan, Iran
  7. 7. Department of Clinical Sciences, Faculty of Veterinary Medicine, Shahrekord University, Shahrekord, Iran
  8. 8. Department of Gynecology and Obstetrics, Shahrekord University of Medical Sciences, Shahrekord, Iran

Source: Cryobiology Published:2023


Abstract

This study assesses the protective effects of astaxanthin (AST) against vitrification/warming-induced cryoinjuries of ovarian tissue slices in sheep. Cortical slices of slaughterhouse acquired-ovine ovaries were randomly distributed in different groups: fresh, toxicity, and five vitrification groups including vitrification in presence of 0 (control group), 1, 10 and 100 μM astaxanthin or 100 μM vitamin E. After vitrification/warming and 24 h culturing, the samples were subjected to histological studies, antioxidant evaluation by TAC and TBAR assays, and assessment of relative expression of BMP4, BMP15, GDF9 and KITLG genes related to folliculogenesis and follicular growth regulation. According to the results, vitrification reduced the percentage of morphologically intact follicles compared to the fresh and toxicity groups (p < 0.05). In vitrification groups, vitamin E and all three concentrations of AST increased the percentage of intact pre-antral follicles and antioxidant activity relative to the vitrified control (p < 0.05). This enhancement significantly occurred in 10 μM AST group more than vitamin E (p < 0.05). Also, 10 μM concentration of AST enhanced the expression of all the examined genes compared to the control (p < 0.05), while the expression of BMP4, BMP15 and KITLG was higher in the AST than vitamin E (p < 0.05). The latter could increase only the expression of GDF9 compared to the control group (p = 0.011). In conclusion, AST is a highly effective antioxidant for maintaining the survival of pre-antral follicles, retaining cell density, increasing total antioxidant capacity, and increasing the expression of some genes related to follicular development after short-term culture of vitrified/warmed ovarian tissue slices. © 2023 Elsevier Inc.