Suppr超能文献

长时间低温处理后人类玻璃化及复温前卵泡耗氧量的评估

Evaluation of oxygen consumption in human vitrified and warmed pre-antral follicles after prolonged low temperatures.

作者信息

Kyoya Toshihiko, Nakamura Yusuke, Miyatani Shizue, Miyagawa Tomoko, Tomiyama Tatsuhiro, Kyono Koichi

机构信息

Kyono ART Clinic Mitsuiseimei, Sendai Honcho Bldg, 3F, 1-1-1 Honcho, Aoba-ku 980-0014 Sendai Miyagi Japan.

Osaka New ART Clinic Osaka Japan.

出版信息

Reprod Med Biol. 2013 Aug 8;13(1):47-52. doi: 10.1007/s12522-013-0166-9. eCollection 2014 Jan.

Abstract

PURPOSE

The purpose of this study was to evaluate the effect of transportation at prolonged low temperatures on the survival of pre-antral follicles.

METHODS

Ovarian tissue was removed from six women with gender identity disorder. Tissues were stored in an icebox at 4 °C for 6 or 18 h prior to vitrification. After warming, ovarian tissues were cultured for 24 h and follicle survival was assessed via a viability/cytotoxicity kit. Morphological features and oxygen consumption rate (OCR) were evaluated by scanning electrochemical microscopy (SECM).

RESULTS

Survival rate of isolated primordial follicles was 95.7 and 100 %, and that of primary follicles was 91.7 and 81.8 % in the 6- and 18-h groups respectively. There was no difference in morphology between the 6- and 18-h storage groups. In comparison with OCR of vitrified-warmed follicles and OCR of 24-h culture after vitrified-warmed follicles, OCR of 24-h culture after vitrified-warmed primordial follicles was significantly higher in both 6-hour (0.02 ± 0.02 vs 0.07 ± 0.04, < 0.05) and 18-h groups (0.02 ± 0.02 vs 0.11 ± 0.10, < 0.05).

CONCLUSIONS

This strongly suggests that prolonged transportation of ovarian tissue at low temperatures is useful when there are no available local systems for fertility preservation.

摘要

目的

本研究旨在评估长时间低温运输对窦前卵泡存活的影响。

方法

从六名性别认同障碍女性身上取出卵巢组织。在玻璃化之前,将组织在4°C的冰盒中保存6或18小时。复温后,将卵巢组织培养24小时,并通过活力/细胞毒性试剂盒评估卵泡存活率。通过扫描电化学显微镜(SECM)评估形态特征和氧消耗率(OCR)。

结果

在6小时和18小时组中,分离的原始卵泡存活率分别为95.7%和100%,初级卵泡存活率分别为91.7%和81.8%。6小时和18小时储存组之间的形态没有差异。与玻璃化复温卵泡的OCR和玻璃化复温卵泡后24小时培养的OCR相比,玻璃化复温原始卵泡后24小时培养的OCR在6小时组(0.02±0.02对0.07±0.04,<0.05)和18小时组(0.02±0.02对0.11±0.10,<0.05)中均显著更高。

结论

这有力地表明,当没有可用的当地生育力保存系统时,卵巢组织在低温下的长时间运输是有用的。

相似文献

本文引用的文献

5
Preservation of fertility in females with haematological malignancy.血液系统恶性肿瘤患者的生育力保存。
Br J Haematol. 2011 Jul;154(2):175-84. doi: 10.1111/j.1365-2141.2011.08723.x. Epub 2011 May 12.
7
Micro-organ ovarian transplantation enables pregnancy: a case report.卵巢组织微移植实现妊娠:病例报告。
Hum Reprod. 2011 May;26(5):1097-103. doi: 10.1093/humrep/der063. Epub 2011 Mar 18.
8
Cryopreservation of ovarian tissue for a decade in Denmark: a view of the technique.丹麦十年的卵巢组织冷冻保存:技术观察。
Reprod Biomed Online. 2011 Feb;22(2):162-71. doi: 10.1016/j.rbmo.2010.10.015. Epub 2010 Nov 16.
10
Duration of fertility after fresh and frozen ovary transplantation.新鲜和冷冻卵巢移植后的生育持续时间。
Fertil Steril. 2010 Nov;94(6):2191-6. doi: 10.1016/j.fertnstert.2009.12.073. Epub 2010 Feb 19.

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验