Effect of carvacrol antioxidant capacity on oocyte maturation and embryo production in cattle

被引:5
作者
Morais, A. N. P. [1 ]
Lima, L. F. [1 ]
Silva, A. F. B. [1 ]
Lienou, L. L. [2 ]
Ferreira, A. C. A. [1 ]
Watanabe, Y. F. [3 ]
Joaquim, D. C. [3 ]
Alves, B. G. [4 ]
Pereira, A. F. [5 ]
Alves, D. R. [6 ]
Oliveira, A. C. [7 ]
Morais, S. M. [6 ]
Magalhaes-Padilha, D. M. [8 ]
Figueiredo, J. R. [1 ]
Gastal, E. L. [9 ]
机构
[1] Univ Estadual Ceara, Fac Vet, Lab Manipulat Oocytes & Preantral Follicles, Fortaleza, CE, Brazil
[2] Univ Douala, Fac Sci, Lab Biochem, Douala, Cameroon
[3] Vitrogen YVF Biotech, Cravinhos, SP, Brazil
[4] Univ Fed Goias, Postgrad Programme Anim Biosci, Jatai, GO, Brazil
[5] Fed Rural Univ Semiarid, Lab Anim Biotechnol, Mossoro, RN, Brazil
[6] Univ Estadual Ceara, Anim Hlth Res Ctr, Postgrad Programme Nat Sci, Nat Prod Chem Lab, Fortaleza, CE, Brazil
[7] Univ Estadual Ceara, Super Inst Biomed Sci, Fortaleza, CE, Brazil
[8] Univ Potiguar, Laureate Int Univ, Postgrad Biotechnol, Natal, RN, Brazil
[9] Southern Illinois Univ, Sch Agr Sci, Anim Sci, Carbondale, IL 62901 USA
关键词
Antioxidant capacity; Carvacrol; In vitro embryo production; Oocyte; Oxidative stress; IN-VITRO MATURATION; REACTIVE OXYGEN; BOVINE OOCYTES; OXIDATIVE STRESS; SUPPLEMENTATION; LYCOPENE; THYMOL; CELLS; IVM;
D O I
10.1017/S0967199422000673
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Carvacrol (C10H14O), an efficient phenolic antioxidant substance for several cell types, may become a useful antioxidant for female germ cells and embryo culture. This study investigates the effects of carvacrol supplementation on bovine oocytes in in vitro maturation (IVM) and embryo production. In total, 1222 cumulus-oocyte complexes were cultured in TCM-199(+) alone (control treatment) or supplemented with carvacrol at the concentrations of 3 mu M (Carv-3), 12.5 mu M (Carv-12.5), or 25 mu M (Carv-25). After IVM, the oocytes were subjected to in vitro fertilization and embryo production, and the spent medium post-IVM was used for evaluating the levels of reactive oxygen species and the antioxidant capacity (2,2-diphenyl-1-picryl-hydrazyl-hydrate and 2,2 '-azinobis-3-ethyl-benzothiozoline-6-sulphonic acid quantification). A greater (P < 0.05) antioxidant potential was observed in the spent medium of all carvacrol-treated groups compared with the control medium. Moreover, the addition of carvacrol to the maturation medium did not affect (P > 0.05) blastocyst production on days 7 and 10 of culture; however, the total number of cells per blastocyst was reduced (P < 0.05) in two carvacrol-treated groups (Carv-3 and Carv-25). In conclusion, carvacrol demonstrated a high antioxidant capacity in the spent medium after oocyte maturation; however, although embryo production was not affected, in general, carvacrol addition to IVM medium reduced the total number of cells per blastocyst. Therefore, due to the high antioxidant capacity of carvacrol, new experiments are warranted to investigate the beneficial effects of lower concentrations of carvacrol on embryo production in cattle and other species.
引用
收藏
页码:173 / 179
页数:7
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