Breath of Life: Heart Disease Link to Developmental Hypoxia

被引:49
作者
Giussani, Dino A. [1 ,2 ,3 ,4 ]
机构
[1] Univ Cambridge, Dept Physiol Dev & Neurosci, Downing St, Cambridge CB2 3EG, England
[2] Univ Cambridge, Barcroft Ctr, Cambridge, England
[3] Univ Cambridge, Cambridge Cardiovasc British Heart Fdn Ctr Res Ex, Cambridge, England
[4] Univ Cambridge, Cambridge Strateg Res Initiat Reprod, Cambridge, England
基金
英国医学研究理事会;
关键词
fetus; hypoxia; mitochondria; oxidative stress; FETAL CARDIOVASCULAR DEFENSE; INTRAUTERINE GROWTH RESTRICTION; AORTIC-WALL THICKNESS; HIGH-ALTITUDE HYPOXIA; ACUTE HYPOXEMIA; NEUROPEPTIDE-Y; BLOOD-FLOW; SYMPATHETIC HYPERINNERVATION; GESTATIONAL HYPOXIA; ENDOCRINE RESPONSES;
D O I
10.1161/CIRCULATIONAHA.121.054689
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Heart disease remains one of the greatest killers. In addition to genetics and traditional lifestyle risk factors, we now understand that adverse conditions during pregnancy can also increase susceptibility to cardiovascular disease in the offspring. Therefore, the mechanisms by which this occurs and possible preventative therapies are of significant contemporary interest to the cardiovascular community. A common suboptimal pregnancy condition is a sustained reduction in fetal oxygenation. Chronic fetal hypoxia results from any pregnancy with increased placental vascular resistance, such as in preeclampsia, placental infection, or maternal obesity. Chronic fetal hypoxia may also arise during pregnancy at high altitude or because of maternal respiratory disease. This article reviews the short- and long-term effects of hypoxia on the fetal cardiovascular system, and the importance of chronic fetal hypoxia in triggering a developmental origin of future heart disease in the adult progeny. The work summarizes evidence derived from human studies as well as from rodent, avian, and ovine models. There is a focus on the discovery of the molecular link between prenatal hypoxia, oxidative stress, and increased cardiovascular risk in adult offspring. Discussion of mitochondria-targeted antioxidant therapy offers potential targets for clinical intervention in human pregnancy complicated by chronic fetal hypoxia.
引用
收藏
页码:1429 / 1443
页数:15
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