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首页> 外文期刊>The British Journal of Nutrition >Emergence of ageing-related changes in insulin secretion by pancreatic islets of male rat offspring of mothers fed a low-protein diet.
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Emergence of ageing-related changes in insulin secretion by pancreatic islets of male rat offspring of mothers fed a low-protein diet.

机译:饲喂低蛋白饮食的母亲的雄性大鼠后代的胰岛会出现与年龄相关的胰岛素分泌变化。

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摘要

Maternal low-protein (LP) diets programme beta-cell secretion, potentially altering the emergence of ageing of offspring pancreatic function. We hypothesised that isolated pancreatic islet beta-cell secretory responses are blunted in offspring exposed to LP during development and age-related reduction is influenced by the developmental stage of exposure to decreased nutrition. We studied male offspring of rats fed control (C) or LP protein (R) diets in pregnancy, first letter and/or lactation second letter of CC, RR, CR or RC groups. Serum glucose, insulin and homeostatic model assessment (HOMA) were measured. Pancreatic islets were isolated and in vitro insulin secretion quantified in low (LG - 5mM) or high glucose (HG - 11mM). Body weight and serum values between groups were similar at all ages. Insulin and HOMA rose with age and were highest at postnatal day (PND) 450 in all groups. At PND 36, insulin secretion was greatest in RR and RC. Only CC increased insulin secretion to HG. By PND 110, restricted groups responded less to LG but increased secretion to HG. By PND 450, CC offspring alone increased secretion to HG. Despite minimal differences in circulating insulin and glucose, reduced maternal protein intake affected insulin secretion at all ages. In addition, ageing reduced function in all R groups compared with CC by PND 110 and further by PND 450 most markedly in RC. We conclude that maternal LP diet during pregnancy and/or lactation impairs offspring insulin secretory response to a glucose challenge and alters the trajectory of ageing of pancreatic insulin secretion. Copyright copyright The Authors 2011.
机译:母体低蛋白(LP)饮食可设定β细胞分泌,从而可能改变后代胰腺功能衰老的出现。我们假设,在发育过程中暴露于LP的后代中孤立的胰岛β细胞分泌反应减弱,而与年龄相关的减少受暴露于减少营养的发育阶段的影响。我们研究了在妊娠,CC,RR,CR或RC组的第一个字母和/或泌乳第二个字母喂养对照(C)或LP蛋白(R)饮食的大鼠的雄性后代。测量血清葡萄糖,胰岛素和稳态模型评估(HOMA)。分离胰岛并以低(LG-5mM)或高葡萄糖(HG-11mM)定量体外胰岛素分泌。两组之间的体重和血清值在所有年龄段都是相似的。胰岛素和HOMA随年龄增长而上升,在所有组中,出生后第450天最高。在PND 36时,RR和RC中的胰岛素分泌最大。仅CC增加胰岛素分泌至HG。通过PND 110,受限群体对LG的反应较少,但对HG的分泌增加。通过PND 450,仅CC后代增加了对HG的分泌。尽管循环胰岛素和葡萄糖的差异很小,但降低母体蛋白质摄入量会影响各个年龄段的胰岛素分泌。此外,与PND 110的CC和RC的PND 450相比,与CC相比,所有R组的衰老功能均降低。我们得出的结论是,孕期和/或哺乳期的孕妇LP饮食会损害后代胰岛素对葡萄糖激发的分泌反应,并改变胰腺胰岛素分泌的衰老轨迹。版权版权所有The Authors 2011。

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