Detrimental effects of oxidative stress in bovine oocytes during intracytoplasmic sperm injection (ICSI)

被引:18
作者
Ashibe, Shiori [1 ,2 ]
Miyamoto, Rui [2 ]
Kato, Yoku [2 ]
Nagao, Yoshikazu [1 ,2 ]
机构
[1] Tokyo Univ Agr & Technol, United Grad Sch Agr Sci, Dept Anim Prod Sci, Fuchu, Tokyo 1838509, Japan
[2] Utsunomiya Univ, Fac Agr, Univ Farm, 443 Shimokomoriya, Mohka, Tochigi 3214415, Japan
关键词
Intracytoplasmic sperm injection(ICSI); Oxidative stress; Antioxidants; DNA fragmentation; IN-VITRO DEVELOPMENT; INVITRO FERTILIZATION; BETA-MERCAPTOETHANOL; OXYGEN CONCENTRATION; DEPENDENT OXIDATION; GLUTATHIONE CONTENT; PORCINE OOCYTES; CUMULUS CELLS; PIG OOCYTES; DNA-DAMAGE;
D O I
10.1016/j.theriogenology.2019.04.012
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Intracytoplasmic sperm injection (ICSI) is an essential technology in animal and human reproduction. However, the developmental competence and pregnancy rate of embryos derived from ICSI are still lower than that from the conventional in vitro fertilization technique. In this report, we focused on reactive oxygen species (ROS) as a potential detrimental factor for ICSI. Experiment 1 was conducted to evaluate the effect of oxidative stress by two different oxygen concentrations (20%: control vs. 5%) in ICSI on the developmental competence (blastocyst rate: day 7, DNA fragmentation rate: day 4) and, ROS concentration and mitochondrial membrane potential of oocytes in ICSI. In the 5% O-2 group, the blastocyst rate (29.5%) was higher and DNA fragmentation rate (4.8 +/- 1.0%) was lower than those in the control group significantly (12.7% and 18.2 +/- 2.4%, respectively, P < 0.05). Also, ROS concentration in the 5% O-2 group (12.8 +/- 0.7) was significantly lower than that in the control group (47.8 +/- 6.9, P < 0.05). In experiment 2, we examined the supplementation of media with reduced glutathione (GSH) during ICSI procedure in an attempt to reduce the oxidative stress. The addition of GSH to the culture medium improved the blastocyst rate (17.6% vs. 30.4%, P < 0.05), and decreased the ROS levels in the oocytes (70.0 +/- 7.4 vs. 23.9 +/- 4.0, P < 0.05). In conclusion, our present study revealed that oocytes are under oxidative stress in ICSI procedure. Reduction of the oxygen concentration to 5% in the culture environment, or the addition of GSH in to the medium during ICSI procedure can promote the normal embryo development following the ICSI. (C) 2019 Elsevier Inc. All rights reserved.
引用
收藏
页码:71 / 78
页数:8
相关论文
共 52 条
[1]   Presence of β-mercaptoethanol can increase the glutathione content of pig oocytes matured in vitro and the rate of blastocyst development after in vitro fertilization [J].
Abeydeera, LR ;
Wang, WH ;
Cantley, TC ;
Prather, RS ;
Day, BN .
THERIOGENOLOGY, 1998, 50 (05) :747-756
[2]   Apoptosis and DNA damage in human spermatozoa [J].
Aitken, R. John ;
Koppers, Adam J. .
ASIAN JOURNAL OF ANDROLOGY, 2011, 13 (01) :36-42
[3]  
AVISSAR N, 1989, J BIOL CHEM, V264, P15850
[4]   Permanent embryo arrest: molecular and cellular concepts [J].
Betts, D. H. ;
Madan, P. .
MOLECULAR HUMAN REPRODUCTION, 2008, 14 (08) :445-453
[5]   1ST CELL-CYCLE OF ZYGOTES OF THE MOUSE DERIVED FROM OOCYTES AGED POSTOVULATION INVIVO AND FERTILIZED INVIVO [J].
BOERJAN, ML ;
DEBOER, P .
MOLECULAR REPRODUCTION AND DEVELOPMENT, 1990, 25 (02) :155-163
[6]   CAPACITATION OF RABBIT SPERMATOZOA INVITRO [J].
BRACKETT, BG ;
OLIPHANT, G .
BIOLOGY OF REPRODUCTION, 1975, 12 (02) :260-274
[7]  
BRINSTER RL, 1968, J REPROD FERTIL, V17, P521, DOI 10.1530/jrf.0.0170521
[8]   Influence of reactive oxygen species on human sperm functions and fertilizing capacity including therapeutical approaches [J].
Chen, Shu-jian ;
Allam, Jean-Pierre ;
Duan, Yong-gang ;
Haidl, Gerhard .
ARCHIVES OF GYNECOLOGY AND OBSTETRICS, 2013, 288 (01) :191-199
[9]   EFFECT OF SUPEROXIDE-DISMUTASE ON THE DEVELOPMENT OF PREIMPLANTATION MOUSE EMBRYOS [J].
CHUN, YS ;
KIM, JH ;
LEE, HT ;
CHUNG, KS .
THERIOGENOLOGY, 1994, 41 (02) :511-520
[10]   THIOL DEPENDENT OXIDATION OF ENZYMES - THE LAST CHANCE AGAINST OXIDATIVE STRESS [J].
DELCORSO, A ;
CAPPIELLO, M ;
MURA, U .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY, 1994, 26 (06) :745-750