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Aberrant maternal inflammation as a cause of pregnancy complications: A potential therapeutic target?
被引:79
|作者:
Cotechini, T.
[1
]
Graham, C. H.
[1
]
机构:
[1] Queens Univ, Dept Biomed & Mol Sci, Kingston, ON K7L 3N6, Canada
来源:
基金:
加拿大健康研究院;
关键词:
Inflammation;
Fetal growth restriction;
Pre-eclampsia;
Fetal death;
Pre-term labour;
Placenta;
Utero-placental perfusion;
Tumour necrosis factor;
Vasoconstriction;
Spiral artery remodelling;
Hemostasis;
Oxidative stress;
Nitric oxide;
Nitroglycerin;
TUMOR-NECROSIS-FACTOR;
FETAL-GROWTH RESTRICTION;
NITRIC-OXIDE SYNTHASE;
LOW-DOSE ENDOTOXIN;
ALPHA-INDUCED HYPERTENSION;
SOLUBLE GUANYLYL CYCLASE;
ACTIVATED PROTEIN-C;
FACTOR-V-LEIDEN;
TNF-ALPHA;
SEVERE PREECLAMPSIA;
D O I:
10.1016/j.placenta.2015.05.016
中图分类号:
Q [生物科学];
学科分类号:
07 ;
0710 ;
09 ;
摘要:
Pre-eclampsia (PE), fetal growth restriction (FGR), pre-term labour and fetal death are common complications of pregnancy often associated with abnormal maternal inflammation. Though the precise causes of these complications remain obscure, altered maternal blood flow to the placenta is an underlying hallmark, especially with respect to the pathogenesis of PE, FGR and fetal demise. Furthermore, deficient trophoblast-mediated spiral artery remodelling is often cited as the primary cause of impaired utero-placental perfusion. Considerably less attention has been directed towards investigating other factors, including maternal vasoconstriction or hemostatic alterations, as contributors to poor utero-placental perfusion. This review provides a rationale for investigating the role of abnormal maternal inflammation in the pathophysiology of pregnancy complications including PE, FGR and fetal demise. In particular, the association between aberrant maternal inflammation and inadequate utero-placental perfusion is considered in the context of inflammation-associated alterations in maternal hemostasis and vasoconstriction. Finally, the role of aberrant maternal inflammation as a cause of local oxidative/nitrosative stress is examined and the possibility of targeting deficient nitric oxide signalling as a therapeutic intervention for the treatment of inflammation-associated pregnancy complications is discussed. (C) 2015 Published by Elsevier Ltd.
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页码:960 / 966
页数:7
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