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首页> 外文期刊>Theriogenology >In vitro maturation of bitch oocytes from advanced preantral follicles in synthetic oviduct fluid medium: serum is not essential
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In vitro maturation of bitch oocytes from advanced preantral follicles in synthetic oviduct fluid medium: serum is not essential

机译:合成输卵管液培养基中高级前窦卵泡对母体卵母细胞的体外成熟:血清不是必需的

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The ability of oocytes from preantral follicles to mature in vitro was assessed using a synthetic oviduct fluid (SOF) medium. Advanced preantral follicles (approximately 210 pm diameter) were isolated from the ovaries of domestic bitches and assigned to one of four treatment groups: (1) SOF (n = 230); (2) SOF + 3 mg/ml bovine serum albumin (+BSA, n = 220); (3) SOF + 20% fetal bovine serum (+FBS, n = 227); or (4) SOF + 3 mg/ml BSA + 20% FBS (+BSA+FBS, n = 232), then cultured for up to 72 h. A group of control follicles was not cultured (n = 103). The percentages of oocytes reaching metaphase I to metaphase II stages (MI to MII) did not differ between treatments at each culture period. Within treatments, the percentages of oocytes at MI to MII stages did not differ with duration of culture. However, when compared to the control group (0.97%) the percentages of oocytes at MI to MII increased (P < 0.05) in the SOF group after 48 h (10.0%) and 72 h (12.2%) of culture. In the +BSA (10.1%) and +FBS (9.7%) groups, the percentages of oocytes at MI to MII increased (P < 0.05) above control values only after 72 It of culture. The percentage of oocytes at MI to MII did not significantly increase in the +BSA+FBS group (3.9, 6.6 and 7.6% at 24,48 and 72 h of culture, respectively) compared to the control group. These results indicate that under the described conditions supplementation of culture medium with BSA or FBS is not essential, and the simple medium SOF can support nuclear maturation of a small proportion of bitch oocytes in vitro.
机译:使用合成输卵管液(SOF)培养基评估了窦前卵泡卵母细胞体外成熟的能力。从家中雌性卵巢中分离出高级的窦前卵泡(直径约210 pm),并分为四个治疗组之一:(1)SOF(n = 230); (2)SOF + 3 mg / ml牛血清白蛋白(+ BSA,n = 220); (3)SOF + 20%胎牛血清(+ FBS,n = 227);或(4)SOF + 3 mg / ml BSA + 20%FBS(+ BSA + FBS,n = 232),然后培养长达72小时。未培养一组对照卵泡(n = 103)。在每个培养期的处理之间,达到I期至II期(MI至MII)的卵母细胞百分比没有差异。在处理过程中,MI至MII阶段的卵母细胞百分比与培养持续时间没有差异。但是,与对照组相比(0.97%),在培养48 h(10.0%)和72 h(12.2%)后,SOF组中MI至MII的卵母细胞百分比增加(P <0.05)。在+ BSA(10.1%)和+ FBS(9.7%)组中,MI至MII的卵母细胞百分比仅在培养72 It后才高于对照值(P <0.05)。与对照组相比,+ BSA + FBS组中MI至MII的卵母细胞百分比没有显着增加(分别在培养24,48和72 h时分别为3.9、6.6和7.6%)。这些结果表明,在所述条件下,补充BSA或FBS的培养基不是必需的,并且简单的培养基SOF可以在体外支持小比例的母卵母细胞的核成熟。

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