Efficient Cryopreservation of Porcine Blastocysts produced by In Vitro Fertilization
(주)코리아스칼라
- 최초 등록일
- 2016.09.03
- 최종 저작일
- 2016.03
- 8페이지/
어도비 PDF
- 가격 4,000원
![할인쿠폰받기](/images/v4/document/ico_det_coupon.gif)
* 본 문서는 배포용으로 복사 및 편집이 불가합니다.
서지정보
ㆍ발행기관 : 한국수정란이식학회
ㆍ수록지정보 : Journal of Embryo Transfer / 31권 / 1호
ㆍ저자명 : Sung-Hun Min, Hak Jun Jeong, Deog-Bon Koo
목차
INTRODUCTION
MATERIALS AND METHODS
1. Chemicals
2. In Vitro Production of Porcine Embryos
3. FBC of Blastocysts Cavity
4. Vitrification Procedure
5. TUNEL Assay
6. Measurement of ROS Levels
7. Statistical Analysis
RESULTS
1. FBC/FBS Enhances the Rates of Survival in Cryopreserved ExpandedPorcine Blastocysts
2. Total Cell Numbers and Apoptosis in Blastocysts derived fromGroup A~D of Cryopreserved Porcine Expanded Blastocysts
3. Effects of FBC/FBS Treatment on Expression Levels of ROS inCryopreserved Porcine Expanded Blastocysts
DISCUSSION
REFERENCES
영어 초록
Cryopreservation has been applied successfully in many mammalian species. Nevertheless, pig embryos, because of their greater susceptibility to cryoinjuries, have shown a reduced developmental competence. The aim of this study was to evaluate the survival status of vitrified-warmed porcine embryos. Forced blastocoele collapse (FBC) and non-FBC blastocysts are vitrified and concomitantly cultured in culture media which were supplemented with/without fetal bovine serum (FBS). Porcine vitrified-warmed embryos were examined in four different methods: group A, non- FBC without FBS; group B, non-FBC with FBS; group C, FBC without FBS; group D, FBC with FBS. After culture, differences in survival rates of blastocysts derived from vitrified-warmed porcine embryos were found in group A∼D (39.5 (A) vs 52.5 (B) and 54.8 (C) vs 66.7% (D), respectively, p<0.05). Reactive oxygen species (ROS) level of survived blastocysts was lower in group D than that of another groups (p<0.05). Moreover, total cell number of survived blastocysts was higher in group D than that of other groups (p<0.05). Otherwise, group D showed significantly lower number of apoptotic cells than other groups (2.0±1.5 vs 3.2±2.1, 2.8±1.9, and 2.7±1.6, respectively, p<0.05). Taken together, these results showed that FBS/FBC improves the developmental competence of vitrified porcine embryos by modulating intracellular levels of ROS and the apoptotic index during the vitrification/warming procedure. Therefore, we suggest that FBS and FBC are effective treatment techniques during the vitrification/warming procedures of porcine blastocysts.
참고 자료
없음
"Journal of Embryo Transfer"의 다른 논문
더보기 (4/9)