McClelland I S, Jackson A A
Department of Human Nutrition, University of Southampton.
Br J Nutr. 1996 Aug;76(2):199-209. doi: 10.1079/bjn19960025.
Urea kinetics were measured using prime/intermittent oral doses of [15N15N]urea, on five separate protocols in thirteen normal young women. Each woman underwent either two or three study protocols. Measurements were made at day 12 and day 22 of the menstrual cycle, whilst consuming their habitual protein intake in seven women not taking the contraceptive pill and in six women taking the contraceptive pill. In three women taking the pill, and three not taking the pill, urea kinetics were measured whilst taking a diet in which the intake was restricted to 55 g protein/d. There was no difference in the rate of urea production, urea excretion or urea hydrolysis between the women taking the pill and those not taking the pill at day 22. In the women not taking the pill there was no difference in any measure between day 12 and day 22. In the women taking the pill there was a significant difference in the disposal of urea N to excretion or hydrolysis on day 12 compared with day 22, with a relative decrease in excretion and enhancement of hydrolysis at day 12 compared with day 22. On the restricted diet, an intake of 55 g protein/d represented 77% of the habitual intake and urea production, excretion and hydrolysis were reduced to about 84% of the rate found on the habitual intake. In paired studies the reduction in urea production was statistically significant, and there was a statistically significant linear relationship between urea production and either intake or the sum of intake plus hydrolysis. The within-individual variability for urea production was about 10%, for excretion 15% and for hydrolysis 44%. The between-individual variability for intake was about 17% on the habitual intake. The variability for production, excretion and hydrolysis (14, 13, 36%) was less in the women not taking the contraceptive pill than in those taking the pill 23, 32, 42% respectively). The variability was reduced on the controlled low intake of 55 g protein compared with the habitual intake. These results confirm the wide variability in aspects of urea kinetics between individuals. In women this variability is not, to any large extent, accounted for by changes associated with the menstrual cycle.
在13名正常年轻女性中,采用单次口服[15N15N]尿素的首剂/间歇剂量,按照五个不同方案测量尿素动力学。每名女性接受两到三个研究方案。在月经周期的第12天和第22天进行测量,测量时7名未服用避孕药的女性和6名服用避孕药的女性保持其习惯的蛋白质摄入量。在3名服用避孕药的女性和3名未服用避孕药的女性中,在摄入限制为55克蛋白质/天的饮食期间测量尿素动力学。在第22天,服用避孕药的女性和未服用避孕药的女性之间,尿素生成率、尿素排泄率或尿素水解率没有差异。在未服用避孕药的女性中,第12天和第22天之间的任何测量指标均无差异。在服用避孕药的女性中,与第22天相比,第12天尿素氮排泄或水解的处置存在显著差异,与第22天相比,第12天排泄相对减少,水解增强。在限制饮食中,55克蛋白质/天的摄入量占习惯摄入量的77%,尿素生成、排泄和水解减少至习惯摄入量时所发现速率的约84%。在配对研究中,尿素生成的减少具有统计学意义,并且尿素生成与摄入量或摄入量加水解之和之间存在统计学上显著的线性关系。个体内尿素生成的变异性约为10%,排泄为15%,水解为44%。习惯摄入量时个体间摄入量的变异性约为17%。未服用避孕药的女性中生成、排泄和水解的变异性(分别为14%、13%、36%)低于服用避孕药的女性(分别为23%、32%、42%)。与习惯摄入量相比,在55克蛋白质的受控低摄入量时变异性降低。这些结果证实个体之间尿素动力学各方面存在广泛变异性。在女性中,这种变异性在很大程度上不是由月经周期相关变化引起的。