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首页> 外文期刊>The Journal of Nutritional Biochemistry >Chronic maternal calcium and 25-hydroxyvitamin D deficiency in Wistar rats programs abnormal hepatic gene expression leading to hepatic steatosis in female offspring
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Chronic maternal calcium and 25-hydroxyvitamin D deficiency in Wistar rats programs abnormal hepatic gene expression leading to hepatic steatosis in female offspring

机译:Wistar大鼠的慢性母体钙和25-羟基维生素D缺乏缺乏症的缺乏程序异常肝基因表达导致女性后代肝脏脂肪变性

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摘要

Importance of calcium and vitamin D deficiency is well established in adult dyslipidemia. We hypothesized that maternal calcium and vitamin D deficiency could alter offspring's lipid metabolism. Our objective was to investigate the effect of maternal dietary calcium and vitamin D deficiency on lipid metabolism and liver function of the F1 generation offspring. intergenerational calcium-deficient (CaD) and vitamin D-deficient (VDD) models were developed by mating normal male rats with deficient females and continuing maternal-deficient diets through pregnancy and lactation. Offspring were fed on control diet post-weaning and studied till 30 weeks. Lipid profile, serum glutamate pyruvate transaminase (SGPT), calcium and vitamin D levels were analyzed. Liver fat deposition, omega-3 fatty acids level and mRNA expression levels of peroxisome proliferator-activated receptor-alpha (PPAR-alpha), sterol regulatory element-binding protein 1c (SREBP-1c), interleukin 6 (IL-6), superoxide dismutase 1 (SOD-1) and uncoupling protein 2 (UCP2) were determined. Low serum vitamin D levels with an increase in SGPT and TG levels in CaD and VDD female offspring were observed. Severe liver steatosis with down-regulation of PPAR-alpha and UCP2 and up regulation of SREBP-1c, IL-6 and SOD-1 was observed in the female offspring born to deficient dams. CaD and VDD male offspring showed mild steatosis and down-regulation of UCP2 and SOD-1. We conclude that maternal calcium and vitamin D deficiency programs abnormal lipid metabolism and hepatic gene expression in the F1 generation female offspring leading to hepatic steatosis, despite feeding them on control diet post-weaning. (C) 2017 Elsevier Inc. All rights reserved.
机译:钙和维生素D缺乏的重要性在成人血脂血症中得到了很好的成熟。我们假设母体钙和维生素D缺乏可能会改变后代的脂质代谢。我们的目标是探讨母体膳食钙和维生素D缺乏缺乏对F1代后代的脂质代谢和肝功能的影响。通过将常规雄性大鼠配合缺乏的女性和持续的孕妇饮食通过妊娠和哺乳期通过孕母大鼠开发代际钙缺陷(CAD)和维生素D缺陷(VDD)模型。后代被喂食治疗饮食后断奶后,并研究到30周。分析了脂质型材,血清谷氨酸丙酮酸转氨酶(SGPT),钙和维生素D水平。肝脏脂肪沉积,过氧化物体增殖物激活受体-α(PPAR-α),甾醇调节元素结合蛋白1C(Srebp-1C),白细胞介素6(IL-6),超氧化物的肝脂肪酸水平和mRNA表达水平。测定歧化酶1(SOD-1)和解偶联蛋白2(UCP2)。观察到低血清维生素D水平,CAD和VDD雌性后代的SGPT和TG水平增加。严重的肝脏脂肪变性与PPAR-α和UCP2的下调及SREBP-1C,IL-6和SOD-1的调节,在缺乏漏洞的女性后代观察到。 CAD和VDD雄性后代显示出轻微的脂肪变性和UCP2和SOD-1的下调。我们得出结论,母体钙和维生素D缺乏症的脂质代谢和肝基因表达在F1代雌性后代,尽管喂养了对照饮食后饲养后的肝脏脂肪变性。 (c)2017年Elsevier Inc.保留所有权利。

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