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母鼠胚胎着床前低蛋白饮食可导致子代血管功能障碍和肾素-血管紧张素系统平衡改变。

Maternal low-protein diet during mouse pre-implantation development induces vascular dysfunction and altered renin-angiotensin-system homeostasis in the offspring.

机构信息

School of Biological Sciences, University of Southampton, Bassett Crescent East, Southampton, UK.

出版信息

Br J Nutr. 2010 Jun;103(12):1762-70. doi: 10.1017/S0007114509993783. Epub 2010 Feb 4.

Abstract

Environmental perturbations during early mammalian development can affect aspects of offspring growth and cardiovascular health. We have demonstrated previously that maternal gestational dietary protein restriction in mice significantly elevated adult offspring systolic blood pressure. Therefore, the present study investigates the key mechanisms of blood pressure regulation in these mice. Following mating, female MF-1 mice were assigned to either a normal-protein diet (NPD; 18 % casein) or an isocaloric low-protein diet throughout gestation (LPD; 9 % casein), or fed the LPD exclusively during the pre-implantation period (3.5 d) before returning to the NPD for the remainder of gestation (Emb-LPD). All offspring received standard chow. At 22 weeks, isolated mesenteric arteries from LPD and Emb-LPD males displayed significantly attenuated vasodilatation to isoprenaline (P = 0.04 and P = 0.025, respectively), when compared with NPD arteries. At 28 weeks, stereological analysis of glomerular number in female left kidneys revealed no significant difference between the groups. Real-time RT-PCR analysis of type 1a angiotensin II receptor, Na+/K+ ATPase transporter subunits and glucocorticoid receptor expression in male and female left kidneys revealed no significant differences between the groups. LPD females displayed elevated serum angiotensin-converting enzyme (ACE) activity (P = 0.044), whilst Emb-LPD males had elevated lung ACE activity (P = 0.001), when compared with NPD offspring. These data demonstrate that elevated offspring systolic blood pressure following maternal gestational protein undernutrition is associated with impaired arterial vasodilatation in male offspring, elevated serum and lung ACE activity in female and male offspring, respectively, but kidney glomerular number in females and kidney gene expression in male and female offspring appear unaffected.

摘要

哺乳动物胚胎发育早期的环境干扰会影响后代生长和心血管健康的多个方面。我们之前已经证明,母鼠妊娠期的饮食蛋白质限制会显著升高成年后代的收缩压。因此,本研究旨在探讨这些小鼠血压调节的关键机制。在交配后,MF-1 雌性小鼠被分配到正常蛋白饮食(NPD;18%酪蛋白)或等热量低蛋白饮食(LPD;9%酪蛋白)中,或仅在着床前(3.5d)期间给予 LPD,然后在其余妊娠期返回 NPD。所有后代均给予标准饮食。在 22 周时,与 NPD 动脉相比,LPD 和 Emb-LPD 雄性的肠系膜动脉对异丙肾上腺素的血管舒张作用明显减弱(P=0.04 和 P=0.025)。在 28 周时,雌性左肾肾小球数量的体视学分析显示各组间无显著差异。对雄性和雌性左肾 1a 型血管紧张素 II 受体、Na+/K+ATP 酶转运体亚基和糖皮质激素受体表达的实时 RT-PCR 分析显示各组间无显著差异。与 NPD 后代相比,LPD 雌性的血清血管紧张素转换酶(ACE)活性升高(P=0.044),而 Emb-LPD 雄性的肺 ACE 活性升高(P=0.001)。这些数据表明,母鼠妊娠期蛋白质营养不良导致后代收缩压升高与雄性后代的动脉血管舒张功能受损有关,分别与雌性和雄性后代的血清和肺 ACE 活性升高以及雌性后代的肾小球数量以及雄性和雌性后代的肾脏基因表达无关。

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