Division of Women's Health, Women's Health Academic Centre, King's College London and King's Health Partners, London, UK.
Acta Physiol (Oxf). 2014 Mar;210(3):508-23. doi: 10.1111/apha.12223.
Mother-child cohort studies have established that both pre-pregnancy body mass index (BMI) and gestational weight gain are independently associated with cardio-metabolic risk factors in young adult offspring, including systolic and diastolic blood pressure. Animal models in sheep and non-human primates provide further evidence for the influence of maternal obesity on offspring cardiovascular function, whilst recent studies in rodents suggest that perinatal exposure to the metabolic milieu of maternal obesity may permanently change the central regulatory pathways involved in blood pressure regulation. Leptin plays an important role in the central control of appetite, is also involved in activation of efferent sympathetic pathways to both thermogenic and non-thermogenic tissues, such as the kidney, and is therefore implicated in obesity-related hypertension. Leptin is also thought to have a neurotrophic role in the development of the hypothalamus, and altered neonatal leptin profiles secondary to maternal obesity are associated with permanently altered hypothalamic structure and function. In rodent studies, maternal obesity confers persistent sympathoexcitatory hyper-responsiveness and hypertension acquired in the early stages of development. Experimental neonatal hyperleptinaemia in naive rat pups provides further evidence of heightened sympathetic tone and proof of principle that hyperleptinaemia during a critical window of hypothalamic development may directly lead to adulthood hypertension. Insight from these animal models raises the possibility that early-life exposure to leptin in humans may lead to early onset essential hypertension. Ongoing mother-child cohort and intervention studies in obese pregnant women provide a unique opportunity to address associations between maternal obesity and offspring cardiovascular function. The goal of the review is to highlight the potential importance of leptin in the developmental programming of hypertension in obese pregnancy.
母婴队列研究已经证实,孕前体重指数(BMI)和妊娠期体重增加均与成年子女的心血管代谢危险因素独立相关,包括收缩压和舒张压。绵羊和非人类灵长类动物的动物模型为母体肥胖对后代心血管功能的影响提供了进一步的证据,而最近在啮齿动物中的研究表明,围产期暴露于母体肥胖的代谢环境可能会永久性地改变参与血压调节的中枢调节途径。瘦素在食欲的中枢控制中起着重要作用,还参与激活向产热和非产热组织(如肾脏)的传出交感神经通路,因此与肥胖相关的高血压有关。瘦素也被认为在下丘脑的发育中具有神经营养作用,而由于母体肥胖导致的新生儿瘦素谱改变与永久性改变下丘脑结构和功能有关。在啮齿动物研究中,母体肥胖赋予持久的交感神经兴奋亢进和在早期发育阶段获得的高血压。在新生大鼠幼仔中进行的实验性新生儿高瘦素血症提供了进一步的证据,证明交感神经张力升高,并且证明在下丘脑发育的关键窗口期内高瘦素血症可能直接导致成年期高血压。这些动物模型提供的见解提出了这样一种可能性,即人类生命早期暴露于瘦素可能导致原发性高血压的早期发病。正在进行的肥胖孕妇母婴队列和干预研究为解决母体肥胖与后代心血管功能之间的关联提供了独特的机会。综述的目的是强调瘦素在肥胖妊娠中高血压发育编程中的潜在重要性。