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增加细胞外基质中的胶原蛋白纤维和牛卵巢皮质组织中过氧化物酶 6 的 mRNA 表达。

increases collagen fibres in extracellular matrix and mRNA expression of peroxiredoxin-6 in bovine ovarian cortical tissues cultured .

机构信息

Postgraduate Program in Biotechnology, Laboratory of Biotechnology and Physiology of Reproduction (LABIREP), Federal University of Ceará, Sobral, CE, Brazil.

出版信息

Zygote. 2022 Jun;30(3):365-372. doi: 10.1017/S0967199421000824. Epub 2021 Dec 1.

Abstract

In vitro culture of ovarian tissue containing primordial follicles is an important tool to study the initiation of follicular populations and to develop efficient culture systems to support in vitro follicle growth. Considering that in vitro culture favours oxidative stress, it is very important to supplement culture medium with antioxidant substances such as Aloe vera extract. This study aims to evaluate the effects of different concentrations of Aloe vera on the distribution of collagen fibres in the extracellular matrix, follicular activation, development and survival in bovine ovarian cortical tissues cultured in vitro, as well as on expression of mRNAs for antioxidant enzymes [superoxide dismutase (SOD), catalase (CAT), peroxiredoxin 6 (PRDX6) and glutathione peroxidase 1 (GPX1)]. To this end, ovarian cortical tissues were cultured for 6 days in α-MEM alone or supplemented with different concentrations of Aloe vera extract (1.0, 5.0, 10.0 or 50.0%). After culture, fragments were fixed and processed histologically to evaluate follicular morphology and activation, as well as the extracellular matrix by staining with picrosirius red. The levels of mRNA for SOD, CAT, PRDX6 and GPX1 in cultured ovarian tissues were evaluated by real-time polymerase chain reaction (PCR). Ovarian tissues cultured with 10.0 or 50.0% Aloe vera had higher percentages of collagen fibres than tissues cultured in control medium. A significant increase in developing follicles was observed in ovarian tissues cultured in α-MEM alone or supplemented with 10% Aloe vera when compared with fresh control or tissues cultured with 1.0% Aloe vera. Presence of Aloe vera did not influence the percentage of morphologically normal follicles when compared with control medium. Ovarian tissues cultured with 50.0% Aloe vera had higher percentages of morphologically normal follicles than those cultured with 10.0% Aloe vera. Furthermore, 10% Aloe vera significantly increased mRNA levels for PRDX6. In conclusion, 10.0% Aloe vera improves extracellular matrix distribution in cultured tissues and increases the expression of mRNA for PRDX6 after 6 days in vitro.

摘要

体外培养含有原始卵泡的卵巢组织是研究卵泡群体启动和开发支持体外卵泡生长的有效培养系统的重要工具。考虑到体外培养有利于氧化应激,因此向培养基中补充抗氧化物质如芦荟提取物非常重要。本研究旨在评估不同浓度的芦荟对牛卵巢皮质组织体外培养中细胞外基质中胶原纤维分布、卵泡激活、发育和存活以及抗氧化酶[超氧化物歧化酶 (SOD)、过氧化氢酶 (CAT)、过氧化物酶 6 (PRDX6) 和谷胱甘肽过氧化物酶 1 (GPX1)]mRNA 表达的影响。为此,将卵巢皮质组织在 α-MEM 中单独培养或添加不同浓度的芦荟提取物 (1.0、5.0、10.0 或 50.0%) 培养 6 天。培养后,通过番红 O 染色固定和处理组织学片段以评估卵泡形态和激活以及细胞外基质。通过实时聚合酶链反应 (PCR) 评估培养卵巢组织中 SOD、CAT、PRDX6 和 GPX1 的 mRNA 水平。与对照培养基培养的组织相比,用 10.0%或 50.0%芦荟培养的卵巢组织中的胶原纤维百分比更高。与新鲜对照或用 1.0%芦荟培养的组织相比,在 α-MEM 中单独培养或添加 10%芦荟培养的卵巢组织中发育中的卵泡数量显著增加。与对照培养基相比,芦荟的存在对形态正常卵泡的百分比没有影响。用 50.0%芦荟培养的卵巢组织中的形态正常卵泡百分比高于用 10.0%芦荟培养的组织。此外,10%芦荟显著增加了 PRDX6 的 mRNA 水平。综上所述,10%芦荟可改善培养组织中细胞外基质的分布,并在体外培养 6 天后增加 PRDX6 的 mRNA 表达。

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