Segovia Stephanie A, Vickers Mark H, Harrison Claudia J, Patel Rachna, Gray Clint, Reynolds Clare M
Liggins Institute, University of Auckland, Auckland, New Zealand.
Front Nutr. 2018 Mar 7;5:1. doi: 10.3389/fnut.2018.00001. eCollection 2018.
Maternal high-fat or high-salt diets can independently program adverse cardiometabolic outcomes in offspring. However, there is a paucity of evidence examining their effects in combination on metabolic function in adult offspring. Female Sprague Dawley rats were randomly assigned to either: control (CD; 10% kcal from fat, 1% NaCl), high-salt (SD; 10% kcal from fat, 4% NaCl), high-fat (HF; 45% kcal from fat, 1% NaCl) or high-fat and salt (HFSD; 45% kcal from fat, 4% NaCl) diets 21 days prior to mating and throughout pregnancy and lactation. Male offspring were weaned onto a standard chow diet and were culled on postnatal day 130 for plasma and tissue collection. Adipocyte histology and adipose tissue, liver, and gut gene expression were examined in adult male offspring. HF offspring had significantly greater body weight, impaired insulin sensitivity and hyperleptinemia compared to CD offspring, but these increases were blunted in HFSD offspring. HF offspring had moderate adipocyte hypertrophy and increased expression of the pre-adipocyte marker . There was a significant effect of maternal salt with increased hepatic expression of and . Gut expression of inflammatory (, and ) and renin-angiotensin system () markers was significantly reduced in HFSD offspring compared to HF offspring. Therefore, salt mitigates some adverse offspring outcomes associated with a maternal HF diet, which may be mediated by altered adipose tissue morphology and gut inflammatory and renin-angiotensin regulation.
母体高脂或高盐饮食可独立地使后代出现不良的心脏代谢结局。然而,关于它们联合作用对成年后代代谢功能影响的证据却很少。将雌性斯普拉格-道利大鼠在交配前21天以及整个怀孕和哺乳期随机分为以下几组:对照组(CD;10%的热量来自脂肪,1%氯化钠)、高盐组(SD;10%的热量来自脂肪,4%氯化钠)、高脂组(HF;45%的热量来自脂肪,1%氯化钠)或高脂高盐组(HFSD;45%的热量来自脂肪,4%氯化钠)。雄性后代断奶后采用标准饲料喂养,并在出生后第130天处死以收集血浆和组织。对成年雄性后代的脂肪细胞组织学以及脂肪组织、肝脏和肠道的基因表达进行了检测。与CD组后代相比,HF组后代体重显著增加、胰岛素敏感性受损且瘦素血症更为严重,但这些增加在HFSD组后代中有所减弱。HF组后代有中度的脂肪细胞肥大,且前脂肪细胞标志物的表达增加。母体盐摄入对肝脏中[具体基因1]和[具体基因2]的表达增加有显著影响。与HF组后代相比,HFSD组后代肠道中炎症标志物([具体炎症基因1]、[具体炎症基因2]和[具体炎症基因3])和肾素-血管紧张素系统([具体肾素-血管紧张素基因])标志物的表达显著降低。因此,盐可减轻一些与母体高脂饮食相关的后代不良结局,这可能是由脂肪组织形态改变以及肠道炎症和肾素-血管紧张素调节改变介导的。