Aviv A, Kobayashi T, Higashino H, Bauman J W, Yu S S
Am J Physiol. 1982 Apr;242(4):E241-7. doi: 10.1152/ajpendo.1982.242.4.E241.
The impact of chronic low-sodium intake during early development on body sodium homeostasis is not sufficiently known. To explore this effect, we have investigated the influence of chronic sodium deficit during the rapid growth period of rats (first phase, age 3-7 wk) and the short-term effect of sodium repletion (second phase, age 8-9 wk) on parameters such as growth rate, urinary aldosterone excretion, 22Na volume of distribution (space), and various renal functions. Three groups were studied: group I (control) and groups II and III. During the first phase the respective sodium intake values for these groups were 8.9, 3.1, and 1.5 meq.kg body wt-1.day-1. During the second phase, all groups had sodium intake of 8.7-8.8 meq.kg body wt-1.day-1. At the end of the first phase, group II showed weight gain and 22Na space values similar to those of group I. Group III demonstrated severe growth retardation and reduced 22Na space. During the second phase, both groups II and III demonstrated expansion of the 22Na space and persistently elevated urinary "acid-labile" aldosterone excretions. Despite the 2 wk of sodium repletion, group III failed to catch up with the body weight of groups I and II. It is concluded that chronic sodium deficit during early development transition is made to a higher sodium intake.
早期发育过程中慢性低钠摄入对机体钠稳态的影响尚不清楚。为探究这种影响,我们研究了大鼠快速生长期(第一阶段,3 - 7周龄)慢性缺钠的影响以及钠补充(第二阶段,8 - 9周龄)对生长速率、尿醛固酮排泄、22Na分布容积(空间)和各种肾功能等参数的短期影响。研究了三组:第一组(对照组)以及第二组和第三组。在第一阶段,这些组各自的钠摄入量分别为8.9、3.1和1.5 meq·kg体重-1·天-1。在第二阶段,所有组的钠摄入量为8.7 - 8.8 meq·kg体重-1·天-1。在第一阶段结束时,第二组的体重增加和22Na空间值与第一组相似。第三组表现出严重的生长迟缓且22Na空间减小。在第二阶段,第二组和第三组均表现出22Na空间扩大以及尿“酸不稳定”醛固酮排泄持续升高。尽管进行了2周的钠补充,第三组仍未能赶上第一组和第二组的体重。得出的结论是,早期发育过程中的慢性缺钠在转变为较高钠摄入时……(原文最后一句不完整)