Literature DB >> 15725436

Low oxygen tension during in vitro maturation of porcine follicular oocytes improves parthenogenetic activation and subsequent development to the blastocyst stage.

Masaki Iwamoto1, Akira Onishi, Dai-Ichiro Fuchimoto, Tamas Somfai, Kumiko Takeda, Takahiro Tagami, Hirofumi Hanada, Junko Noguchi, Hiroyuki Kaneko, Takashi Nagai, Kazuhiro Kikuchi.   

Abstract

To establish a reliable in vitro maturation system for activation and subsequent development as nuclear recipients for the effective production of pig clones, we assessed maturation, activation and parthenogenetic development in response to the following: (1) type of immature oocytes (cumulus-oocyte complexes (COCs) or parietal granulosa plus cumulus-oocyte complexes (GCOCs)); (2) oxygen (O(2)) tension (5 or 20%); and (3) maturation period (36-60 h). The rate of nuclear maturation to metaphase-II (M-II) in the GCOC group (73.0 +/- 3.1%) was higher than that in the COC group (P < 0.05, 60.6 +/- 3.5%), but the rates did not differ between the 5 and 20% O(2) tension groups. M-II rate increased (P < 0.05) to about 70% after 42 h and then remained constant until 60 h of culture. When oocytes were matured under 5% O(2) tension and stimulated, the rate of normal oocyte activation (a female pronucleus formation and emission of the second polar body) was higher (P < 0.05, 38.5 +/- 3.9%) than when oocytes were matured under 20% O(2) tension (24.5 +/- 3.9%). On the other hand, the rate of normal activation was not significantly different between the COC and GCOC groups, and the highest (P < 0.05) normal activation rate was obtained in oocytes cultured for 48 and 54 h (48.4 +/- 5.5% and 47.9 +/- 8.2%, respectively). When COC and GCOC matured for 48 h under 5 and 20% O(2) tension were stimulated and subsequently cultured in vitro for 6 days, the rate of blastocyst formation did not differ between the oocyte types nor between the O(2) tension groups. However, blastocyst quality, as measured by mean total cell number, was significantly higher in the 5% O(2) group (P < 0.05, 34.6 +/- 2.0 for COC; 33.8 +/- 1.8 for GCOC) compared with the 20% O(2) group (25.9 +/- 1.8 for COC; 27.0 +/- 2.0 for GCOC). In conclusion, low O(2) tension (5%) during in vitro maturation of porcine oocytes promoted their ability to be activated normally and improved the quality of parthenogenetic blastocysts developed in vitro in modified NCSU-37 solutions. This knowledge may be applicable for preparation of in vitro matured oocytes with good quality as recipient oocytes for generating pig clones.

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Year:  2005        PMID: 15725436     DOI: 10.1016/j.theriogenology.2004.05.024

Source DB:  PubMed          Journal:  Theriogenology        ISSN: 0093-691X            Impact factor:   2.740


  5 in total

Review 1.  Could oxidative stress influence the in-vitro maturation of oocytes?

Authors:  Catherine M H Combelles; Sajal Gupta; Ashok Agarwal
Journal:  Reprod Biomed Online       Date:  2009-06       Impact factor: 3.828

2.  Dynamic oxygen enhances oocyte maturation in long-term follicle culture.

Authors:  Matthew K Heise; Richard Koepsel; Elizabeth A McGee; Alan J Russell
Journal:  Tissue Eng Part C Methods       Date:  2009-09       Impact factor: 3.056

3.  Secondary follicle growth and oocyte maturation during encapsulated three-dimensional culture in rhesus monkeys: effects of gonadotrophins, oxygen and fetuin.

Authors:  J Xu; M S Lawson; R R Yeoman; K Y Pau; S L Barrett; M B Zelinski; R L Stouffer
Journal:  Hum Reprod       Date:  2011-02-28       Impact factor: 6.918

4.  Human exhaled air can efficiently support in vitro maturation of porcine oocytes and subsequent early embryonic development.

Authors:  Zubing Cao; Di Gao; Tengteng Xu; Xu Tong; Yiqing Wang; Yunsheng Li; Fugui Fang; Jianping Ding; Xiaorong Zhang; Yunhai Zhang
Journal:  Anim Reprod       Date:  2018-08-16       Impact factor: 1.807

5.  Quercetin improves the in vitro development of porcine oocytes by decreasing reactive oxygen species levels.

Authors:  Jung-Taek Kang; Dae-Kee Kwon; Sol-Ji Park; Su-Jin Kim; Joon-Ho Moon; Ok-Jae Koo; Goo Jang; Byeong-Chun Lee
Journal:  J Vet Sci       Date:  2013-02-05       Impact factor: 1.672

  5 in total

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