Oxidative stress and protection against reactive oxygen species in the pre-implantation embryo and its surroundings

被引:1098
作者
Guérin, P
El Mouatassim, S
Ménézo, Y
机构
[1] Ecole Natl Vet Lyon, Unite Biol Reprod, F-69280 Marcy Letoile, France
[2] Lab Marcel Merieux, F-69357 Lyon, France
[3] Univ Lyon 1, Fac Med, F-69373 Lyon 08, France
关键词
antioxidant enzymes; embryo culture; non-enzymatic antioxidant defences; oocyte; reactive oxygen species;
D O I
10.1093/humupd/7.2.175
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Oxidative stress is involved in the aetiology of defective embryo development. Reactive oxygen species (ROS) may originate from embryo metabolism and/or embryo surroundings. Embryo metabolism generates ROS via several enzymatic mechanisms. The relative contribution of each source seems different depending on the species, the stage of development, and the culture conditions. Several exogenous factors and culture conditions can enhance the production of ROS by embryos. ROS can alter most types of cellular molecules, and also induce development block and retardation. Multiple mechanisms of embryo protection against ROS exist, and these have complementary actions. External protection, present in follicular and tubal fluids, mainly comprises non-enzymatic antioxidants such as hypotaurine, taurine and ascorbic acid, Internal protection mainly comprises antioxidant enzymes: superoxide dismutase, glutathione peroxidase and gamma -glutamylcysteine synthetase. Transcripts encoding for these enzymes are present in the oocyte, embryo and oviduct. It may be important that these transcripts are stored during oocyte maturation in order to allow the embryo to acquire the aptitude to develop. It is now common to add antioxidant compounds to culture media. Nevertheless, maintaining the pro-oxidant-antioxidant equilibrium in embryos through such supplementation is a complex problem. Further studies are necessary to limit oxidative stress during embryo culture.
引用
收藏
页码:175 / 189
页数:15
相关论文
共 146 条
[1]   REACTIVE OXYGEN SPECIES GENERATION AND HUMAN SPERMATOZOA - THE BALANCE OF BENEFIT AND RISK [J].
AITKEN, J ;
FISHER, H .
BIOESSAYS, 1994, 16 (04) :259-267
[2]  
ALEXIOU M, 1994, J REPROD FERTIL, V101, P151
[3]  
ALEXIOU M, 1992, DEVELOPMENT, V114, P185
[4]   DIFFERENTIAL INCORPORATION OF FATTY-ACIDS INTO AND PEROXIDATIVE LOSS OF FATTY-ACIDS FROM PHOSPHOLIPIDS OF HUMAN SPERMATOZOA [J].
ALVAREZ, JG ;
STOREY, BT .
MOLECULAR REPRODUCTION AND DEVELOPMENT, 1995, 42 (03) :334-346
[5]   TAURINE, HYPOTAURINE, EPINEPHRINE AND ALBUMIN INHIBIT LIPID-PEROXIDATION IN RABBIT SPERMATOZOA AND PROTECT AGAINST LOSS OF MOTILITY [J].
ALVAREZ, JG ;
STOREY, BT .
BIOLOGY OF REPRODUCTION, 1983, 29 (03) :548-555
[6]   The sperm stress test: A novel test that predicts pregnancy in assisted reproductive technologies [J].
Alvarez, JG ;
Minaretzis, D ;
Barrett, CB ;
Mortola, JF ;
Thompson, IE .
FERTILITY AND STERILITY, 1996, 65 (02) :400-405
[7]  
ALVAREZ JG, 1992, J ANDROL, V13, P232
[8]   THE ANTIOXIDANT ACTION OF TAURINE, HYPOTAURINE AND THEIR METABOLIC PRECURSORS [J].
ARUOMA, OI ;
HALLIWELL, B ;
HOEY, BM ;
BUTLER, J .
BIOCHEMICAL JOURNAL, 1988, 256 (01) :251-255
[9]   DNA repair by oocytes [J].
Ashwood-Smith, M. J. ;
Edwards, R. G. .
MOLECULAR HUMAN REPRODUCTION, 1996, 2 (01) :46-51
[10]   HYPOTAURINE REQUIREMENT FOR INVITRO DEVELOPMENT OF GOLDEN-HAMSTER ONE-CELL EMBRYOS INTO MORULAE AND BLASTOCYSTS, AND PRODUCTION OF TERM OFFSPRING FROM INVITRO-FERTILIZED OVA [J].
BARNETT, DK ;
BAVISTER, BD .
BIOLOGY OF REPRODUCTION, 1992, 47 (02) :297-304