Harrison Matthew, Langley-Evans Simon C
University of Nottingham, School of Biosciences, Sutton Bonington, Loughborough LE12 5RD, UK.
Br J Nutr. 2009 Apr;101(7):1020-30. doi: 10.1017/S0007114508057607. Epub 2008 Sep 9.
Associations between birth weight and CVD in adult life are supported by experiments showing that undernutrition in fetal life programmes blood pressure. In rats, the feeding of a maternal low-protein (MLP) diet during gestation programmes hypertension. The present study aimed to assess the potential for a nutritional insult to impact across several generations. Pregnant female Wistar (F0) rats were fed a control (CON; n 10) or MLP (n 10) diet throughout gestation. At delivery all animals were fed a standard laboratory chow diet. At 10 weeks of age, F1 generation offspring were mated to produce a second generation (F2) without any further dietary change. The same procedure produced an F3 generation. Blood pressure in all generations was determined at 4, 6 and 8 weeks of age and nephron number was determined at 10 weeks of age. F1 generation MLP-exposed offspring exhibited raised (P < 0.001) systolic blood pressure (male 143 (sem 4) mmHg; female 141 (sem 4) mmHg) compared with CON animals (male 132 (sem 3) mmHg; female 134 (sem 4) mmHg). Raised blood pressure and reduced nephron number was also noted in the F2 generation (P < 0.001) and this intergenerational transmission occurred via both the maternal and paternal lines, as all three possible offspring crosses (MLP x CON, CON x MLP and MLP x MLP) were hypertensive (132 (sem 3) mmHg) compared with CON animals (CON x CON; 123 (sem 2) mmHg). No effect was noted in the F3 generation. It is concluded that fetal protein restriction may play a critical role in determining blood pressure and overall disease risk in a subsequent generation.
出生体重与成年后心血管疾病(CVD)之间的关联得到了实验的支持,这些实验表明胎儿期营养不良会影响血压。在大鼠中,孕期给予母体低蛋白(MLP)饮食会导致高血压。本研究旨在评估营养损伤对多代产生影响的可能性。怀孕的雌性Wistar(F0)大鼠在整个孕期被喂食对照(CON;n = 10)或MLP(n = 10)饮食。分娩时,所有动物均喂食标准实验室饲料。在10周龄时,F1代后代进行交配以产生第二代(F2),且不再进行任何饮食改变。同样的程序产生了F3代。在4、6和8周龄时测定所有代的血压,并在10周龄时测定肾单位数量。与CON组动物(雄性132(标准误3)mmHg;雌性134(标准误4)mmHg)相比,F1代暴露于MLP的后代收缩压升高(P < 0.001)(雄性143(标准误4)mmHg;雌性141(标准误4)mmHg)。F2代也出现了血压升高和肾单位数量减少(P < 0.001),并且这种代际传递通过母系和父系发生,因为所有三种可能的后代杂交组合(MLP×CON、CON×MLP和MLP×MLP)均为高血压(132(标准误3)mmHg),而CON组动物(CON×CON;123(标准误2)mmHg)则不是。F3代未观察到影响。结论是,胎儿期蛋白质限制可能在决定后代的血压和总体疾病风险方面起关键作用。