Gene expression of nitric oxide synthase and heme oxygenase in placental villi during pregnancy with and without intrauterine growth restriction

被引:0
作者
Muta, K
Masuzaki, H
Urata, Y
Goto, S
Ishimaru, T
Kondo, T [1 ]
机构
[1] Nagasaki Univ, Sch Med, Dept Biochem & Mol Biol Dis, Atom Bomb Dis Inst, Nagasaki 8528523, Japan
[2] Nagasaki Univ, Sch Med, Dept Obstet & Gynecol, Nagasaki 8528501, Japan
关键词
nitric oxide; carbon monoxide; nitric oxide synthase; heme oxygenase; intrauterine growth restriction;
D O I
暂无
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
It is commonly accepted that the intrauterine growth restriction (IUGR) is correlated with an impairment of utero-placental blood flow. This blood flow is regulated by prostaglandins and nitric oxide (NO), which regulate vascular tone in placental villi. The factors that regulate utero-placental blood flow play different functions independently, and their functions differ according to the gestational stage. To evaluate the influence of NO and carbon monoxide (CO) on the feto-maternal circulation, we quantified endothelial NO synthase (eNOS) and heme oxygenase (HO) type 1 (HO-1) mRNAs in the placental villi. Forty-three placental samples were employed. We measured both eNOS and HO-1 mRNAs by Northern blot hybridization. The eNOS mRNA expression in the first trimester (relative intensity, 3.741+/-0.679, mean+/-SEM) was higher than that after the first trimester (0.500+/-0.038, p<0.0001). The HO-1 mRNA expression in the third trimester was higher than that before the third trimester (2.648+/-0.409 and 1.122+/-0.182, respectively, p<0.005). There was no difference in the expression of eNOS and HO-1 mRNAs between pregnancies with or without IUGR. Independent expression of eNOS and HO-1 mRNAs suggests that eNOS is important in placentation at early gestation, whereas HO-1 is important in maintenance of pregnancy for the term.
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页码:11 / 21
页数:11
相关论文
共 37 条
[1]   Hemeoxygenase-1 inhibits human myometrial contractility via carbon monoxide and is upregulated by progesterone during pregnancy [J].
Acevedo, CH ;
Ahmed, A .
JOURNAL OF CLINICAL INVESTIGATION, 1998, 101 (05) :949-955
[2]   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
[3]   Vascular endothelial growth factor up-regulates nitric oxide synthase expression in endothelial cells [J].
Bouloumié, A ;
Schini-Kerth, VB ;
Busse, R .
CARDIOVASCULAR RESEARCH, 1999, 41 (03) :773-780
[4]   Effects of transdermal nitroglycerin on impedance to flow in the uterine, umbilical, and fetal middle cerebral arteries in pregnancies complicated by preeclampsia and intrauterine growth retardation [J].
Cacciatore, B ;
Halmesmaki, E ;
Kaaja, R ;
Teramo, K ;
Ylikorkala, O .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1998, 179 (01) :140-145
[5]  
Cai QH, 2001, SCH INT ENT UMWEL, V2, P21
[6]   Transcriptional and posttranscriptional regulation of endothelial nitric oxide synthase expression by hydrogen peroxide [J].
Drummond, GR ;
Cai, H ;
Davis, ME ;
Ramasamy, S ;
Harrison, DG .
CIRCULATION RESEARCH, 2000, 86 (03) :347-354
[7]   Heme oxygenase: Recent advances in understanding its regulation and role [J].
Elbirt, KK ;
Bonkovsky, HL .
PROCEEDINGS OF THE ASSOCIATION OF AMERICAN PHYSICIANS, 1999, 111 (05) :438-447
[8]   Thrombin suppresses endothelial nitric oxide synthase and upregulates endothelin-converting enzyme-1 expression by distinct pathways -: Role of Rho/ROCK and mitogen-activated protein kinase [J].
Eto, M ;
Barandiér, C ;
Rathgeb, L ;
Kozai, T ;
Joch, H ;
Yang, ZH ;
Lüscher, TF .
CIRCULATION RESEARCH, 2001, 89 (07) :583-590
[9]   Vascular endothelial growth factor signals endothelial cell production of nitric oxide and prostacyclin through Flk-1/KDR activation of c-Src [J].
He, H ;
Venema, VJ ;
Guo, XL ;
Venema, RC ;
Marrero, MB ;
Caldwell, RB .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (35) :25130-25135
[10]   L-Arginine reverses the adverse pregnancy changes induced by nitric oxide synthase inhibition in the rat [J].
Helmbrecht, GD ;
Farhat, MY ;
Lochbaum, L ;
Brown, HE ;
Yadgarova, KT ;
Eglinton, GS ;
Ramwell, PW .
AMERICAN JOURNAL OF OBSTETRICS AND GYNECOLOGY, 1996, 175 (04) :800-805