共查询到20条相似文献,搜索用时 187 毫秒
1.
目前 ,动物腔前卵泡的体外培养正日益受到重视 ,并已取得了较大进展 ,已建立的培养体系可成功地使腔前卵泡发育到有腔阶段 ,猪、山羊等已可实现腔前卵泡卵母细胞体外成熟 ,体外受精并发育至囊胚阶段。但有关腔前卵泡体外成熟的机制仍不明了。本文通过对体内发育与体外培养之卵泡及其卵母细胞超微结构进行比较 ,从微细结构上客观评定体外培养卵泡的形态、活力、代谢状况及功能完整性 ,界定体外生长卵泡所处发育阶段 ,从而为确立和完善腔前卵泡体外培养体系并最终选择高质量的卵母细胞进行体外受精提供可靠的理论依据。1 体内发育卵泡及其卵… 相似文献
2.
3.
近20年来,胚胎移植、体外受精、核移植、转基因等胚胎工程技术在理论和生产应用上已取得了很大进展.然而,所有这些技术是建立在具有完全发育能力的卵母细胞的基础之上的.大量卵母细胞的体外成熟培养是这些技术的限速步骤之一.目前采用的有腔卵泡卵母细胞的体外成熟和超数排卵,不能提供充足的卵母细胞以支撑胚胎工程技术的进一步发展.此外,卵巢中的卵母细胞绝大多数以无腔的形式存在于卵巢皮质内,有腔卵泡所占比例不到1%,屠宰场屠宰羊只后的卵巢内含有大量的腔前卵泡.如果建立腔前卵泡的体外培养体系,获得大量的具有成熟和受精能力的卵母细胞,一方面将会最大限度地挖掘保存卵巢上遗传资源;另一方面将极大的促进胚胎工程技术的研究与应用,还有利于研究卵泡和卵母细胞的生长和发育规律. 相似文献
4.
5.
6.
7.
8.
9.
用改良的McCoy’s 5a无血清培养液 (含 3mML -谷氨酰胺、0 1%BSA、2 0ng/ml睾酮、2 5 μg/ml转铁蛋白、10 0ng/ml胰岛素和 4ng/ml硒 ) ,在 96孔培养板中 ,每孔 2 5 0 μl培养液的条件下 ,研究了维生素C和维生素E对腔前卵泡体外发育的影响。结果表明 :在培养液中添加 90 μM的维生素C有利于维持腔前卵泡体外生长时结构的完整性 ,显著提高牛腔前卵泡体外培养 10天的存活率 (P <0 0 5 ) ,但并没有发现对腔前卵泡的生长、发育和成腔有促进作用 (P >0 0 5 ) ;在培养液中添加3 0 μM的维生素E对Φ >13 0 μm的腔前卵泡及其卵母细胞有促进发育和促进卵泡腔形成的趋势 (P >0 0 5 ) ;在培养液中联合添加 12 μM维生素E和 96μM维生素C ,能显著提高牛腔前卵泡体外培养 10天的存活率 (P <0 0 5 ) ,并对牛腔前卵泡的生长和发育有一定的促进作用 ,但差异不显著 (P >0 0 5 )。 相似文献
10.
11.
哺乳动物卵巢中绝大多数卵母细胞以无腔形式存在,有腔卵泡所占比例很少。通过建立腔前卵泡的培养体系,获取大量的具有成熟和受精能力的卵母细胞,将极大地促进体外受精、核移植等胚胎工程技术的发展,并有利于研究卵泡和卵母细胞的发育规律。 相似文献
12.
猪腔前卵泡机械分离研究 总被引:1,自引:0,他引:1
本研究以分离到的卵泡数量、分离时间和卵泡在体外培养3 d后的存活率为指标比较了两种机械方法分离猪腔前卵泡的效果。结果表明:用针刮法分离猪腔前卵泡的数量(Φ<50μm:203600±59000;50μm≤Φ≤150μm:29.40±10.34;Φ>150μm:9.30±3.29)极显著(P<0.01)高于剪碎法(Φ<50μm:18900±12000;50μm≤Φ≤150μm:13.95±3.70;Φ>150μm:4.95±1.61),而且针刮法16.16±1.43 min分离时间比剪碎法(20.30±1.48)min短,(P<0.01)。体外培养3 d后,腔前卵泡存活率在两种方法之间没有明显差异。说明应用针刮法分离猪腔前卵泡能有效保护卵母细胞和颗粒细胞的正常形态以及基膜的完整性,从而使分离到的猪腔前卵泡维持正常的生理活性。 相似文献
13.
Durlej M Knapczyk-Stwora K Duda M Kopera-Sobota I Hejmej A Bilinska B Slomczynska M 《Domestic animal endocrinology》2011,40(1):19-29
Connexin 43 (Cx43) is the predominant gap junction protein within porcine ovary and is required for proper follicle and corpus luteum (CL) development. Recent research suggests maternally or neonatally mediated effects of antiandrogens on reproductive function during adulthood, notably those dependent on gap junctional communication. The current study was conducted to determine whether late gestational or neonatal exposure to the antiandrogen flutamide influences Cx43 gene expression in the adult porcine ovary. Flutamide was injected into pregnant gilts between days 80 and 88 of gestation and into female piglets between days 2 and 10 posnatally. After animals reached sexual maturity, the ovaries were collected from treated and nontreated (control) pigs. Expression of Cx43 mRNA and protein was determined for preantral and antral follicles and for CLs. In addition, 3β-hydroxysteroid dehydrogenase (3β-HSD) expression and progesterone concentration were determined for luteal tissues. In preantral follicles, Cx43 mRNA was down-regulated (P < 0.01) following maternal and neonatal flutamide exposure. In large antral follicles, Cx43 mRNA was up-regulated (P < 0.01) after neonatal flutamide administration. Immunofluorescence showed that Cx43 expression decreased (P < 0.001) in preantral follicles and increased (P < 0.001) in large antral follicles following flutamide exposure. In luteal tissues, Cx43 and 3β-HSD expression and progesterone concentration decreased (P < 0.01) after postnatal flutamide treatment. Overall, these results suggest the involvement of androgens in the regulation of Cx43 expression in pig ovary. Moreover, alteration of Cx43 expression by the administration of flutamide during particular prenatal and neonatal time periods may affect porcine follicle development, as well as CL formation and function. 相似文献
14.
D. Phoophitphong S. Srisuwatanasagul P. Tummaruk 《Anatomia, histologia, embryologia》2017,46(4):334-341
This study aimed to investigate leptin immuno‐staining of the porcine ovary in different reproductive stages. Ovaries from 21 gilts were collected from slaughterhouses. The ovarian tissue sections were incubated with a polyclonal anti‐leptin as a primary antibody. The immuno‐staining in ovarian tissue compartments was calculated using imaging software. Leptin immuno‐staining was found in primordial, primary, preantral and antral follicles. Leptin immuno‐staining was expressed in the oocyte and granulosa and theca interna layers in both preantral and antral follicles. In the corpora lutea, leptin immuno‐staining was found in the cytoplasm of the luteal cells. The leptin immuno‐staining in the granulosa cell layer of preantral follicles did not differ compared to antral follicles (90.7 and 91.3%, respectively, P > 0.05). However, the leptin immuno‐staining in the theca interna layer of preantral follicles was lower than antral follicles (49.4 and 74.3%, respectively, P < 0.001). There was no difference in leptin immuno‐staining in the granulosa cell layer between follicular and luteal phases (92.4 and 89.7%, respectively, P > 0.05). However, the leptin immuno‐staining in the theca interna layer of follicular phase was greater than that in the luteal phase (72.7 and 51.0%, respectively, P < 0.001). These findings indicated that leptin exists in different compartments of the porcine ovary, including the oocyte, granulosa cells, theca interna cells, corpus luteum, blood vessel and smooth muscles. Therefore, this morphological study confirmed a close relationship between leptin and ovarian function in the pig. 相似文献
15.
In this study, the expressions of VEGF in dog follicles were detected by immunohistochemistry and the effects of VEGF treatment on the primordial to primary follicle transition and on subsequent follicle progression were examined using a dog ovary organ culture system. The frozen‐thawed canine ovarian follicles within slices of ovarian cortical tissue were cultured for 7 and 14 days in presence or absence of VEGF. After culture, the ovaries were fixed, sectioned, stained and counted for morphologic analysis. The results showed that VEGF was expressed in the theca cells of antral follicles and in the granulosa cells nearest the oocyte in preantral follicle but not in granulosa cells of primordial and primary follicles; however, the VEGF protein was expressed in CL. After in vitro culture, VEGF caused a decrease in the number of primordial follicles and concomitant increase in the number of primary follicles that showed growth initiation and reached the secondary and preantral stages of development after 7 and 14 days. Follicular viability was also improved in the presence of VEGF after 7 and 14 days in culture. In conclusion, treatment with VEGF was found to promote the activation of primordial follicle development that could provide an alternative approach to stimulate early follicle development in dogs. 相似文献
16.
Hashimoto S Ohsumi K Tsuji Y Harauma N Miyata Y Fukuda A Hosoi Y Iritani A Morimoto Y 《The Journal of reproduction and development》2007,53(2):379-384
The aim of this study was to establish a culture system to improve the meiotic competence of porcine oocyte-granulosa cell complexes (OGCs) obtained from preantral or early antral follicles. Porcine OGCs were recovered from follicles with diameters of 230-300 (preantral follicles), 300-500, and 500-700 mum (early antral follicles) using scalpels. The OGCs were cultured for 2 weeks in culture medium. We examined the effects of the sizes of the follicles from which OGCs were recovered, the concentrations of polyvinylpyrrolidone (PVP, 0-8%) in the culture medium, and 2 types of culture dish (Falcon 3002 vs 1007) on formation of the antrum of OGCs. After culture, the oocytes were matured for 44 h to assess their meiotic competence. OGCs recovered from small follicles (230-500 microm) required longer (P<0.05) than larger follicles to form the antrum structure. The percentage of OGCs forming the antrum structure that were cultured in 2% PVP (31%) was higher (P<0.05) than for those cultured in other PVP concentrations (0-11%). The percentages of antrum-structure formation for OGCs cultured on Falcon 3002 (83% for 2% PVP and 60% for 4% PVP) were higher (P<0.05) than those cultured on Falcon 1007 (47% for 2% PVP and 9% for 4% PVP). Furthermore, all of the intact oocytes that were obtained from culture of OGCs and that formed an antrum were in the GV stage (n=28). When these immature oocytes were cultured for 44 h, the percentage of oocytes that reached the metaphase II stage (25%, n=68) was higher (P<0.0001) than that of oocytes matured without culture (0.7%, n=137). The results of the present study show that porcine OGCs obtained from preantral or early antral follicles acquire meiotic competence in vitro. 相似文献
17.
卵巢大小及发育状况与牛腔前卵泡采集数量的关系 总被引:3,自引:1,他引:2
用简单机械分离法处理了 12 7枚成年牛卵巢。结果显示 ,在外观正常的卵巢中 ,腔前卵泡的采集数量与卵巢的大小成正相关关系 ,而有无黄体与腔前卵泡的采集数量无明显关系 ;卵巢上不同大小的可见卵泡的数量和分布与腔前卵泡的采集量有关。卵巢上可见卵泡分布均衡 ,大、中、小卵泡均有分布 ,小卵泡不过多以及无大卵泡 ,但中、小卵泡较多的 ,无论是否有黄体存在 ,均可获得较多腔前卵泡。而卵巢表面脂肪化、卵巢充血、有弥散性片状黄体及幼稚卵巢的 ,则腔前卵泡分离很少或几乎分离不到 相似文献
18.
Effects of long-term grafting on follicular growth in porcine ovarian cortical grafts xenoplanted to severe combined immunodeficient (SCID) mice 总被引:2,自引:0,他引:2
To establish a tool for the study of follicular growth and development, we xenotransplanted small pieces (approximately 1 mm3) of porcine ovarian cortical tissues containing only primordial follicles and small preantral follicles under the capsules of kidneys of severe combined immunodeficient (SCID) mice (8-10 weeks old). The changes in cell proliferation and cell death/apoptosis, and vascularization in xenotransplanted follicles during follicular growth and development were analyzed histochemically at 1-26 weeks after operation. Follicles in grafted ovarian tissues grew rapidly forming an antral cavity (a hallmark of tertiary follicles) at 1 week after grafting. The diameter of the follicles in transplanted tissues ranged from 0.5 to 1.5 mm, from 0.5 to 2.0 mm and from 0.5 to 3.0 mm at 1, 2 and 26 weeks after the operation, respectively. Histological observation of ovarian tissues at 26 weeks after grafting revealed that all grafts had abundant capillary vessels, which invaded from murine organs and surrounded the growing follicles. Grafted small preantral follicles developed to the antral stages at 1 week after grafting and growing antral follicles survived at 26 weeks after grafting. The oocytes in the growing follicles were easily recovered for evaluating the quality. Our simple xenografting system is easy to use and a good experimental tool for the study of folliclular growth and development in porcine ovaries. 相似文献
19.
Amanda Michelle torres Panta Ana Flvia Bezerra da Silva Rodrigo Tenrio Padilha Hudson Henrique Vieira Correia Davide Rondina Jos Ricardo Figueiredo Deborah de Melo Magalhes Padilha 《Reproduction in domestic animals》2019,54(3):480-485
This study aimed to examine the in vitro culture of secondary preantral follicles, using reused ovaries, to compare both the 2D and 3D methods of in vitro culture of preantral follicles, and the system of medium replacement. Twenty‐five pairs of ovaries from mixed‐breed goats were used for the experiment. Follicular puncture of antral follicles was performed for in vitro production. After this procedure, the secondary preantral follicles were submitted to a microdissection procedure. The isolated preantral follicles were randomly divided into three treatments: (a) Two‐dimensional culture with partial replacement of medium during culture (2D PR), (b) Three‐dimensional culture with addition of medium during culture (3D AD) and (c) Three‐dimensional culture with partial replacement of medium (3D PR). The culture period was 18 days. All treatments at the end of the in vitro culture period (18 days) presented a follicular survival rate which ranged from 59% to 70%, demonstrating that it was possible to perform an experiment with preantral follicles using ovaries that had previously been used in another reproductive biotechnique. The 3D AD treatment showed a survival percentage and follicular diameter higher than the 2D PR treatment, however, it did not differ from the 3D PR treatment. In conclusion, experiments employing the use of preantral follicles can be performed with success after the ovaries have been used for experiments with antral follicles. Moreover, the three‐dimensional system with the addition of medium is recommended for in vitro culture of preantral follicles, since this system is more practical and financially feasible. 相似文献