Woods Lori L
Division of Nephrology and Hypertension, Oregon Health & Science University, Portland, OR 97239-3098, USA.
Curr Drug Targets. 2007 Aug;8(8):906-13. doi: 10.2174/138945007781386875.
Although it is well-accepted that size at birth is inversely related to adult blood pressure and cardiovascular risk in humans, the majority of information available with regard to maternal nutrition, prenatal growth, and subsequent renal disease comes from animal models. Restriction of food or protein during specific windows of pregnancy leads to hypertension in adult offspring. Depending on the degree of maternal restriction, nephron number and renal function in the offspring may be reduced, and proteinuria and histological signs of renal disease are present. All of these abnormalities appear to worsen with age. Female gender is relatively protective against these prenatal insults, but with more severe maternal dietary restriction female offspring are also affected. In addition to macronutrients, roles for several micronutrients have been identified in fetal programming for hypertension and renal disease. Ongoing investigations into the roles of sex hormones, the renin-angiotensin system, and vitamin A in these developmental processes may lead to strategies for prevention of dietary programming for hypertension and renal disease in humans.
尽管人们普遍认为出生时的体型与成人血压及心血管疾病风险呈负相关,但关于母体营养、产前生长以及后续肾脏疾病的大多数现有信息都来自动物模型。孕期特定阶段限制食物或蛋白质摄入会导致成年后代患高血压。根据母体限制的程度,后代的肾单位数量和肾功能可能会降低,并且会出现蛋白尿和肾脏疾病的组织学迹象。所有这些异常情况似乎都会随着年龄的增长而恶化。女性性别对这些产前损伤具有相对的保护作用,但如果母体饮食限制更为严重,雌性后代也会受到影响。除了常量营养素外,几种微量营养素在胎儿高血压和肾脏疾病编程中的作用也已得到确认。对性激素、肾素 - 血管紧张素系统和维生素A在这些发育过程中的作用进行的持续研究,可能会带来预防人类高血压和肾脏疾病饮食编程的策略。