SUMMARY1. Twenty 7-week female mice underwent right nephrectomy and twenty others were sham operated. A week later all animals were made pregnant. Pregnancy was repeated five more times consecutively and various renal parameters were assessed in the pups.2. Fractional fresh kidney weight (relative to body weight) was significantly increased in the pups of nephrectomized mothers while percentage renal water and protein content expressed as mg/g kidney weight were not statistically different in the two groups of pups. Thus dry kidney weight and amount of protein per kidney were increased in the experimental group. This was true for the newborns of all six pregnancies.3. Renal morphometric studies performed in newborns of first pregnancies showed that the mean number of glomeruli per microscopic field, mean fractional cumulative glomerular area (relative to microscopic field area) and the mean number of cells per glomerulus were significantly greater in the experimental group. Mean glomerular radius was not statistically different in the two groups.4. The results indicate that: (1) the renotrophic factor(s) crosses the placenta in mice; (2) its activity in maternal circulation following uninephrectomy is sustained for a relatively long period; and (3) fetal response to enhanced maternal renotrophin stimulation consists of increased renal dry weight and renal protein, formation of super-physiological numbers of glomeruli and cellular hyperplasia of the glomeruli.

An animal model with experimental uremia is an important research tool for the study of the sequence of pathophysiological events taking place in the uremic syndrome. An appreciable number of animal models and methods for the induction of chronic uremia have been published. It is surprising that no such method has been reported in the mouse, which is an important laboratory animal. A new method for the induction of chronic uremia in the mouse is described. It consists of unilateral destruction of most of the renal cortex by burns combined with contralateral nephrectomy. This method can be carried out in one or two stages. Follow-up of the experimental animals reveals that significant uremia developed within 4 weeks and remained constant for the rest of the study period, i.e. 10 weeks.

Three hundred 7-week-old Beit Dagan female mice underwent right nephrectomy or sham operation, and either remained virgin or were exposed to six repetitive pregnancies. Fractional kidney weight, dry weight and protein content were determined at ages 9, 10, 11, 17 and 26 weeks corresponding to the ends of the first, second and third trimester of the first pregnancy and completion of the third and sixth pregnancies respectively. In addition histological sections were evaluated morphologically and morphometrically. Renal dry weight and protein content per kidney increased abruptly to maximal values a week after nephrectomy and remained stable thereafter. Repetitive pregnancies were associated with progressive increments in both parameters. The effects of unilateral nephrectomy and repetitive pregnancy were additive. Following unilateral nephrectomy or pregnancy the number of glomeruli per field, as well as fractional glomerular area, increased more rapidly than in sham-operated virgin controls. However, the maximal glomerular number or fractional area attained did not differ from control values. We conclude that (a) in 8-week-old mice pregnancy is associated with renal cell hypertrophy; (b) repetitive pregnancies in these animals produce progressive augmentation in both renal dry weight and protein content; (c) the effects of repetitive pregnancy and unilateral nephrectomy on renal cell hypertrophy are additive; (d) this would indicate that neither manoeuvre exhausts maximal renal capacity for cell hypertrophy, and would suggest some possibilities for the underlying mechanisms.