Alpha lipoic acid controls degeneration and ensures follicular development in ovine ovarian tissue cultured in vitro

被引:0
|
作者
Naupas, L. V. S. [1 ]
Gomes, F. D. R. [1 ]
Ferreira, A. C. A. [1 ]
Morais, S. M. [2 ]
Alves, D. R. [2 ]
Teixeira, D. I. A. [3 ]
Alves, B. G. [4 ]
Watanabe, Y. [5 ]
Figueiredo, J. R. [1 ]
Tetaping, G. M. [1 ]
Rodrigues, A. P. R. [1 ,6 ]
机构
[1] Univ Estadual Ceara, Fac Vet Med, Lab Manipulat Oocytes & Ovarian Preantral Follicle, Fortaleza, CE, Brazil
[2] Univ Estadual Ceara, Fac Vet Med, Lab Nat Prod Chem, Fortaleza, CE, Brazil
[3] Univ Estadual Ceara, Fac Vet Med, Lab Image Diag Appl Anim Reprod, Fortaleza, CE, Brazil
[4] Ovid Res Co, Berkeley, CA USA
[5] Vitrogen YVF Biotech, Cravinhos, SP, Brazil
[6] Univ Estadual Ceara, Lab Manipulat Oocyte & Ovarian Preantral Follicles, Av Dr Silas Munguba 1700,Campus Itaperi, Fortaleza, CE, Brazil
关键词
Ovary. cryopreservation. preantral follicles; steroidogenesis. oxidative stress. sheep; ENDOPLASMIC-RETICULUM STRESS; PRIMORDIAL FOLLICLES; PREANTRAL FOLLICLES; MOUSE OOCYTES; MATURATION; GROWTH; CELLS; GOAT; CRYOPRESERVATION; VITRIFICATION;
D O I
10.1016/j.theriogenology.2024.05.024
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
This study aims to evaluate the effects of adding alpha lipoic acid (ALA) to the in vitro ovarian tissue culture medium, either fresh or after vitrification/warming. For this purpose, 10 ovaries from five adult sheep were used. Each pair of ovaries gave rise to 16 fragments and were randomly distributed into two groups: fresh (n = 8) and vitrified (n = 8). Two fresh fragments were fixed immediately and considered the control, while another six were cultured in vitro for 14 days in the absence; presence of a constant (100 mu M/0-14 day) or dynamic (50 mu M/day 0-7 and 100 mu M/day 8-14) concentration of ALA. As for the vitrified fragments, two were fixed and the other six were cultured in vitro under the same conditions described for the fresh group. All the fragments were subjected to morphological evaluation, follicular development and stromal density (classical histology), DNA fragmentation (TUNEL), senescence (Sudan Black), fibrosis (Masson's Trichome), and endoplasmic reticulum stress (immunofluorescence). Measurements of the antioxidant capacity against the free radicals 2,2 '-azino-bis (3ethylbenzothiazoline-6-sulfonic acid) (ABTS) and 2,2-diphenyl-1-picryl-hydrazyl-hydrate (DPPH) and estradiol (E2) levels in the culture medium was performed. The results showed that in the absence of ALA, in vitro culture of vitrified ovarian fragments showed a significant reduction (P < 0.05) in follicular morphology and increased the presence of senescence and tissue fibrosis (P < 0.05). Dynamic ALA maintained E2 levels unchanged (P > 0.05) until the end of vitrified ovarian tissue culture and controlled the levels of ABTS and DPPH radicals in fresh or vitrified cultures. Therefore, it is concluded that ALA should be added to the vitrified ovarian tissue in vitro culture medium to reduce the damage that leads to loss of ovarian function. To ensure steroidogenesis during in vitro culture, ALA should be added dynamically (different concentrations throughout culture).
引用
收藏
页码:55 / 66
页数:12
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