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Effect of dietary phosphorus intake and age on intestinal phosphorus absorption efficiency and phosphorus balance in male rats

机译:饮食中磷的摄入量和年龄对雄性大鼠肠道磷吸收效率和磷平衡的影响

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摘要

Intestinal phosphorus absorption is an important component of whole-body phosphorus metabolism, and limiting dietary phosphorus absorption is particularly of interest as a therapeutic target in patients with chronic kidney disease to manage mineral bone disorders. Yet, mechanisms and regulation of intestinal phosphorus absorption have not been adequately studied and discrepancies in findings exist based on the absorption assessment technique used. In vitro techniques show rather consistent effects of dietary phosphorus intake level and age on intestinal sodium-dependent phosphate transport. But, the few studies that have used in vivo techniques conflict with these in vitro studies. Therefore, we aimed to investigate the effects of dietary phosphorus intake level on phosphorus absorption using the in situ ligated loop technique in three different aged rats. Male Sprague-Dawley rats (n = 72), were studied at 10-, 20-, and 30-weeks-of-age on a low (0.1%), normal (0.6%), or high (1.2%) phosphorus diet in a 3x3 factorial design (n = 8/group). Rats were fed their assigned diet for 2-weeks prior to absorption testing by jejunal ligated loop as a non-survival procedure, utilizing 33P radioisotope. Metabolic cages were used for determination of calcium and phosphorus balance over the final four days prior to sacrifice, and blood was collected at the time of sacrifice for biochemistries. Our results show that phosphorus absorption was higher in 10-week-old rats compared with 20- and 30-week-olds and this corresponded to higher gene expression of the major phosphate transporter, NaPi-2b, as well as higher whole-body phosphorus balance and net phosphorus absorption. Dietary phosphorus intake level did not affect jejunal phosphorus absorption or NaPi-2b gene expression. Our results contrast with studies utilizing in vitro techniques, but corroborate results of other rodent studies utilizing in situ or in vivo methods. Thus, there is need for additional studies that employ more physiological methods of phosphorus absorption assessment.
机译:肠道磷的吸收是全身磷代谢的重要组成部分,限制饮食中磷的吸收作为慢性肾脏疾病患者管理矿物质骨疾病的治疗目标尤其令人关注。然而,尚未充分研究肠道磷吸收的机制和调节,并且根据所采用的吸收评估技术,发现存在差异。体外技术显示饮食磷摄入水平和年龄对肠钠依赖性磷酸盐转运的影响相当一致。但是,很少使用体内技术的研究与这些体外研究相冲突。因此,我们的目的是使用原位结扎环技术研究三只不同年龄大鼠的饮食中磷摄入量对磷吸收的影响。研究了Sprague-Dawley雄性大鼠(n = 72),分别在其低(0.1%),正常(0.6%)或高(1.2%)磷饮食的10、20和30周龄时进行了研究采用3x3阶乘设计(n = 8 /组)。用 33 P放射性同位素通过空肠结扎环作为非存活方法,对大鼠喂食指定的饮食2周,然后进行空肠结扎环吸收测试。在处死前的最后四天,使用代谢笼测定钙和磷的平衡,并在处死时收集血液用于生物化学。我们的研究结果表明,与20和30周龄相比,10周龄大鼠的磷吸收更高,这与主要磷酸盐转运蛋白NaPi-2b的基因表达较高以及全身磷含量更高相对应。平衡和净磷吸收。饮食中的磷摄入量不影响空肠磷吸收或NaPi-2b基因表达。我们的结果与利用体外技术的研究形成对比,但证实了其他利用原位或体内方法进行啮齿动物研究的结果。因此,需要采用更多的生理学方法进行磷吸收评估的附加研究。

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