Amburana cearensis leaf extract maintains survival and promotes in vitro development of ovine secondary follicles

被引:23
作者
Barberino, R. S. [1 ]
Barros, V. R. P. [1 ]
Menezes, V. G. [1 ]
Santos, L. P. [1 ]
Araujo, V. R. [2 ]
Queiroz, M. A. A. [3 ]
Almeida, J. R. G. S. [4 ]
Palheta, R. C., Jr. [5 ]
Matos, M. H. T. [1 ]
机构
[1] Fed Univ San Francisco Valley, Nucleus Biotechnol Appl Ovarian Follicle Dev, Petrolina, PE, Brazil
[2] Univ Estadual Ceara, Lab Manipulat Oocytes & Preantral Follicles, Fac Vet Med, Fortaleza, Ceara, Brazil
[3] Fed Univ San Francisco Valley, Lab Bromatol & Anim Nutr, Petrolina, PE, Brazil
[4] Fed Univ San Francisco Valley, Nucleus Studies & Res Med Plants, Petrolina, PE, Brazil
[5] Fed Univ San Francisco Valley, Pharmacol Lab, Petrolina, PE, Brazil
关键词
Culture; Medicinal plant; Oocyte; Sheep; Umburana; OXIDATIVE STRESS; STIMULATING-HORMONE; PREANTRAL FOLLICLES; ASCORBIC-ACID; GROWTH; IMPROVES; TRANSPORTATION; VIABILITY; ESCULETIN; APOPTOSIS;
D O I
10.1017/S0967199415000179
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The antioxidant properties of Amburana cearensis extract may be a useful substitute for standard cell culture medium. Thus, the aim of this study was to evaluate the effect of this extract, with or without supplementation, on in vitro survival and development of sheep isolated secondary follicles. After collection of the ovaries, secondary follicles were isolated and cultured for 18 days in -MEM+ supplemented with bovine serum albumin, insulin, transferrin, selenium, glutamine, hypoxanthine and ascorbic acid (control medium) or into medium composed of different concentrations of A. cearensis extract without supplements (Amb 0.1; 0.2 or 0.4 mg/ml) or A. cearensis extract supplemented with the same substances described above for alpha-MEM+ supplementation. The A. cearensis supplemented medium was named Amb 0.1(+); 0.2(+) or 0.4(+) mg/ml. There were more morphologically normal follicles in Amb 0.1 or Amb 0.4 mg/ml than in the control medium (alpha-MEM+) after 18 days of culture. Moreover, the percentage of antrum formation was significantly higher in Amb 0.1 or Amb 0.2 mg/ml than in alpha-MEM+ and Amb 0.1(+) mg/ml, and similar to the other treatments. All A. cearensis extract media induced a progressive and significant increase in follicular diameter throughout the culture period. In conclusion, this study showed that 0.1 mg/ml of this extract, without supplementation, maintains follicular survival and promotes the development of ovine isolated secondary follicles in vitro. This extract can be an alternative culture medium for preantral follicle development.
引用
收藏
页码:277 / 285
页数:9
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