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首页> 外文期刊>The Journal of Nutritional Biochemistry >Postnatal high-fat diet sex-specifically exacerbates prenatal dexamethasone-induced hypertension: Mass spectrometry-based quantitative proteomic approach
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Postnatal high-fat diet sex-specifically exacerbates prenatal dexamethasone-induced hypertension: Mass spectrometry-based quantitative proteomic approach

机译:产后高脂饮食性别 - 特异性加剧产前地塞米松诱导的高血压:基于质谱的定量蛋白质组学方法

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Hypertension can originate from pre- and post-natal insults. High-fat (HF) diet and prenatal dexamethasone (DEX) exposure are both involved in hypertension of developmental origins We examined whether postnatal HF diet sex-specifically increases the vulnerability to prenatal DEX exposure-induced programmed hypertension in adult offspring. Additionally, we sought to identify candidate proteins involved in programmed hypertension through a mass spectrometry-based quantitative proteomic approach. Male and female offspring were studied separately: control, DEX, HF, and DEX + HF (n=8/group). Pregnant Sprague-Dawley rats received dexamethasone (0.1 mg/kg body weight) or vesicle from gestational day 16-22. Offspring received high-fat diet (D12331, Research Diets) or regular diet from weaning to 4 months of age. Rats were sacrificed at 4 months of age. We found that postnatal HF diet increased vulnerability of prenatal DEX-induced hypertension in male but not in female adult offspring Additionally, HF and DEX elicited renal programming in a sex-specific fashion. In males, DEX + HF increased renal parvalbumin (PVALB) and carbonic anhydrase III (CA III) protein levels. While prenatal DEX down-regulated PVALB and CA III protein abundance in female offspring kidneys. Moreover, DEX + HF increased renal protein level of type 3 sodium hydrogen exchanger (NHE3) in males but not in females. In conclusion, postnatal HF diet and prenatal DEX exposure synergistically induced programmed hypertension in male-only offspring. DEX + HF induced sex-specific alterations of protein profiles in offspring kidneys. By identifying candidate proteins underlying sex-specific mechanisms, our results could lead to novel offspring sex-specific interventions to prevent hypertension induced by antenatal corticosteroids and postnatal HF intake in both sexes. (C) 2018 Elsevier Inc. All rights reserved.
机译:高血压可以源自生一个侮辱前和后期的侮辱。高脂肪(HF)饮食和产前地塞米松(DEX)曝光均涉及发育起源的高血压,我们检查后产后性能是否饮食性别 - 特异性增加了成人后代对产前DEX暴露诱导的编程性高血压的脆弱性。另外,我们试图通过基于质谱的定量蛋白质组学方法识别参与编程的高血压的候选蛋白。分别研究雄性和女性后代:对照,DEX,HF和DEX + HF(n = 8 /组)。怀孕的Sprague-Dawley大鼠从妊娠第16-22天接受了地塞米松(0.1mg / kg体重)或囊泡。后代接受了高脂饮食(D12331,研究饮食)或常规饮食从断奶到4个月。大鼠在4个月的年龄处死。我们发现产前的HF饮食增加了产前Dex诱导的男性高血压的脆弱性,但不在女性成人后代,HF和DEX以性别特异性的方式引发肾脏编程。在雄性中,DE​​X + HF增加肾帕瓦蛋白(PVALB)和碳酸酐酶III(CA III)蛋白质水平。而prenatal dex下调的pvalb和ca III蛋白质在女性后代肾脏中的丰富。此外,DEX + HF在雄性中增加3型氢气交换机(NHE3)的肾蛋白水平,但不在女性中。总之,产后HF饮食和产前DEX暴露协同诱导男性后代的编程高血压。 DEX + HF在后代肾脏中诱导蛋白质谱的特异性改变。通过确定性别特异性机制的候选蛋白质,我们的结果可能导致新的后代性别特异性干预措施,以预防产前皮质类固醇诱导的高血压和两性的后期HF摄入量。 (c)2018年Elsevier Inc.保留所有权利。

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