将辣木叶的酸化提取物作为绵羊前胚乳卵泡体外培养基的补充物的效果

Valéria da Silva Guimarães, Regina Lucia dos Santos Silva, Ricássio de Souza Barberino, Istefani Moreira Mota, Joisyleide Gonçalves Costa Pinto, Maria Lilian Gomes Loiola Torres, Naiane Darklei do Santos Silva, Mário Adriano Ávila Queiroz, Maria Helena Tavares de Matos, Alane Pains Oliveira do Monte
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引用次数: 0

摘要

本研究旨在评估油橄榄叶酸化提取物作为绵羊离体次级卵泡体外培养基础培养基补充物的效果。在添加或不添加 0.1、0.2 或 0.4 mg/ml 油橄榄叶酸化提取物的 α-MEM+(添加牛血清白蛋白、胰岛素、谷氨酰胺、次黄嘌呤、转铁蛋白、硒和抗坏血酸)培养基中分离卵泡并培养 12 天。对卵泡形态、前腔形成、卵泡和卵母细胞直径、谷胱甘肽(GSH)浓度、线粒体活性和减数分裂恢复情况进行了评估。培养 12 天后,各处理在卵泡形态、前腔形成、直径和线粒体活性方面没有显著差异。然而,与含有油橄榄提取物的培养基相比,在 α-MEM+ 中培养的卵泡卵母细胞显示出更高的 GSH 浓度。此外,与其他处理相比,浓度为 0.4 mg/ml 的油橄榄提取物能显著提高完全成熟卵母细胞(≥ 110 µm)的百分比。总之,浓度为 0.4 毫克/毫升的油橄榄提取物作为培养基的补充物,可维持卵母细胞的存活率,并提高完全成熟卵母细胞的比例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of the acidified extract of Moringa oleifera leaves as a supplement in the in vitro culture medium of sheep preantral follicles
This study was conducted to evaluate the effects of the acidified extract of M. oleifera leaves as a supplement into the base medium for in vitro culture of sheep isolated secondary follicles. Follicles were isolated and cultured for 12 days in α-MEM+(supplemented with bovine serum albumin, insulin, glutamine, hypoxanthine, transferrin, selenium, and ascorbic acid) with or without 0.1; 0.2 or 0.4 mg/ml of the acidified extract of M. oleifera. Follicle morphology, antral cavity formation, follicular and oocyte diameter, glutathione (GSH) concentration, mitochondrial activity and meiotic resumption were evaluated. After 12 days of culture, there was no significant difference among treatments in relation to follicular morphology, antral cavity formation, diameter and mitochondrial activity. Nevertheless, oocytes from follicles cultured in α-MEM+ showed greater GSH concentration than media containing M. oleifera extract. Furthermore, the concentration of 0.4 mg/ml M. oleifera extract significantly increased the percentage of fully grown oocyte (≥ 110 µm) when compared to the other treatments. In conclusion, the concentration of 0.4 mg/ml M. oleifera extract as a supplement of the culture medium, maintained the survival, and increased the percentage of fully grown oocytes.
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