The role and modulation of the oxidative balance in pregnancy

被引:43
作者
Biondi, C
Pavan, B
Lunghi, L
Florini, S
Vesce, F
机构
[1] Univ Ferrara, Sect Obstet & Gynecol, Dept Biomed Sci & Adv Therapy, I-44100 Ferrara, Italy
[2] Univ Ferrara, Sect Gen Physiol, Dept Biol, I-44100 Ferrara, Italy
关键词
reactive oxygen species; reactive nitrogen species; antioxidants; pregnancy; preeclampsia and premature labour;
D O I
10.2174/1381612054065747
中图分类号
R9 [药学];
学科分类号
1007 [药学];
摘要
Oxidative processes exert a fundamental regulatory function during pregnancy. It depends on the influence of oxygen, nitric oxide, reactive oxygen species and reactive nitrogen species metabolic pathways upon the vascular changes in the maternal organism, as well as on the regulation of uterine and cervical tone throughout gestation and delivery. These functions are strictly linked with the mediators of the inflammatory pathway. At the beginning of pregnancy, when a certain grade of inflammatory change is necessary to the trophoblast invasion of maternal tissue, the activation of the process by nitric oxide and reactive nitrogen species is welcome. Indeed, these products modulate the metalloproteinases, which are responsible for the remodelling of uterine extracellular matrix. At this stage estrogens are involved as well in the regulation of the delicate balance of pro-oxidant and anti-oxidant effects. Furthermore, reactive oxygen and nitrogen species appear to play an important role both in normal and pathologic embryogenesis. During advanced pregnancy, a derangement of the oxidative balance can lead to the improper activation of inflammatory changes, thus triggering premature labour as well as other complications, such as foetal growth restriction and preeclampsia. Although a number of pro- and anti-oxidant agents are available to influence the above-mentioned processes, there is no way to adequately measure the oxidative needs in single cases, in order to modulate the oxidative balance in clinical practice. Pharmacological research should be addressed to the development of new drugs, as well as to selective methods of delivery to the gestational tissues.
引用
收藏
页码:2075 / 2089
页数:15
相关论文
共 169 条
[1]
OXIDATIVE INFLUENCE ON DEVELOPMENT AND DIFFERENTIATION - AN OVERVIEW OF A FREE-RADICAL THEORY OF DEVELOPMENT [J].
ALLEN, RG ;
BALIN, AK .
FREE RADICAL BIOLOGY AND MEDICINE, 1989, 6 (06) :631-661
[2]
Presence of uterine peroxidase activity in the rat early pregnancy [J].
Baiza-Gutman, LA ;
Flores-Sánchez, MM ;
Díaz-Flores, M ;
Hicks, JJ .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2000, 32 (02) :255-262
[3]
Decline in myometrial nitric oxide synthase expression is associated with labor and delivery [J].
Bansal, RK ;
Goldsmith, PC ;
He, YP ;
Zaloudek, CJ ;
Ecker, JL ;
Riemer, RK .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (10) :2502-2508
[4]
The role of ROS and RNS in regulating life and death of blood monocytes [J].
Baran, CP ;
Zeigler, MM ;
Tridandapani, S ;
Marsh, CB .
CURRENT PHARMACEUTICAL DESIGN, 2004, 10 (08) :855-866
[5]
Hemoxygenase and nitric oxide synthase do not maintain human uterine quiescence during pregnancy [J].
Barber, A ;
Robson, SC ;
Lyall, F .
AMERICAN JOURNAL OF PATHOLOGY, 1999, 155 (03) :831-840
[6]
Antioxidant vitamin levels in term and preterm infants and their relation to maternal vitamin status [J].
Baydas, G ;
Karatas, F ;
Gursu, MF ;
Bozkurt, HA ;
Ilhan, N ;
Yasar, A ;
Canatan, H .
ARCHIVES OF MEDICAL RESEARCH, 2002, 33 (03) :276-280
[7]
Interactions between the nitric oxide and prostaglandin E2 biosynthetic pathways in human amnion-like WISH cells [J].
Biondi, C ;
Fiorini, S ;
Pavan, B ;
Ferretti, ME ;
Barion, P ;
Vesce, F .
JOURNAL OF REPRODUCTIVE IMMUNOLOGY, 2003, 60 (01) :35-52
[8]
Effect of nitric oxide on arachidonic acid release from human amnion-like WISH cells [J].
Biondi, C ;
Fiorini, S ;
Boarini, I ;
Barbin, L ;
Cervellati, F ;
Ferretti, ME ;
Vesce, F .
PLACENTA, 2002, 23 (8-9) :575-583
[9]
Bohles H, 1997, INT J VITAM NUTR RES, V67, P321
[10]
Antenatal supplementation of antioxidant vitamins to reduce the oxidative stress at delivery - a pilot study [J].
Bolisetty, S ;
Naidoo, D ;
Lui, K ;
Koh, THHG ;
Watson, D ;
Whitehall, J .
EARLY HUMAN DEVELOPMENT, 2002, 67 (1-2) :47-53