Synaptonemal complex studies in male mice treated with cyproterone acetate or with testosterone

1993 ◽  
Vol 303 (2) ◽  
pp. 45-53 ◽  
Author(s):  
Mungo B. Masumbuko ◽  
Roger De Meyer ◽  
Maria M. Freund
Chromosoma ◽  
1982 ◽  
Vol 87 (2) ◽  
pp. 149-164 ◽  
Author(s):  
Terry Ashley ◽  
Liane B. Russell ◽  
N. L. A. Cacheiro

1988 ◽  
Vol 119 (2) ◽  
pp. 263-268
Author(s):  
G. Veyssiére ◽  
Ch. Gallon ◽  
M. Berger ◽  
Ch. Jean-Faucher ◽  
M. de Turckheim ◽  
...  

Abstract. To determine whether neonatal endogenous androgens influence adult renal androgen binding, newborn male mice were injected from 1 to 10 days of age with cyproterone acetate and newborn females with testosterone from 1 to 10 days and from 20 to 40 days of age. In controls, at adulthood, the total cellular androgen receptor content was significantly higher in males (1700 200 receptors per cell) than in females (1060 ± 50) and, as expected, the nuclear receptor content was 12-fold higher in males. While the total number of receptors (1650 ± 220 per cell) was unchanged in adult males neonatally treated with cyproterone acetate, their distribution between cytosol and nucleus was similar to that in control females despite normal circulating and renal testosterone levels. The nuclear receptors represented 50, 7 and 11% of the total receptors in control males, control females and cyproterone acetate-treated males, respectively. The very low levels of nuclear receptors present in the kidney of cyproterone acetate-treated males probably explain the decreased sensitivity of this organ to testosterone. The nuclear receptor accumulation measured in adult animals after a single injection of testosterone did not seem to be affected by neonatal hormonal manipulations.


1987 ◽  
Vol 115 (2) ◽  
pp. 241-246 ◽  
Author(s):  
Ch. Jean-Faucher ◽  
M. Berger ◽  
Ch. Gallon ◽  
M. de Turckheim ◽  
G. Veyssière ◽  
...  

ABSTRACT Kidneys of adult male mice are larger than those of females because of both cellular hyperplasia and hypertrophy. Administration of testosterone to adult female mice induced cellular hypertrophy but not hyperplasia, so that the weight of the kidney remained smaller than in male mice. The sexual dimorphism in kidney size is not congenital but programmed by neonatal endogenous androgens and expressed between 30 and 40 days of age. Treatment of newborn males with cyproterone acetate and of newborn females with testosterone induced female and male patterns of renal growth respectively. It appears that neonatal endogenous androgens are required to induce the characteristic cellular hyperplasia of the kidneys of male mice. Manipulation of androgen levels during neonatal and prepubertal life was found to affect the growth response of the kidney to androgens in adult male and female mice. J. Endocr. (1987) 115, 241–246


Genes ◽  
2010 ◽  
Vol 1 (3) ◽  
pp. 505-520 ◽  
Author(s):  
Neil M. Vranis ◽  
Godfried W. Van der Heijden ◽  
Safia Malki ◽  
Alex Bortvin

1970 ◽  
Vol 46 (4) ◽  
pp. 477-481 ◽  
Author(s):  
D. A. EDWARDS

SUMMARY Cyproterone acetate exerted strong anti-androgenic effects on the seminal vesicles of mice, but failed to affect androgen-dependent aggressive behaviour in mice. Groups of adult castrated male mice were treated with (1) testosterone propionate (TP); (2) TP plus cyproterone acetate; or (3) neither TP nor cyproterone acetate, for 5 weeks and given weekly tests for aggressive behaviour. The seminal vesicles were removed after the last test for aggression. Although treatment of mice with cyproterone acetate in combination with TP almost totally suppressed the stimulatory effect of TP on seminal vesicle weight, aggressive behaviour was not affected by cyproterone acetate. It was concluded that cyproterone acetate probably does not influence central nervous tissue and non-neural tissue in the same manner.


Chromosoma ◽  
1983 ◽  
Vol 88 (3) ◽  
pp. 171-177 ◽  
Author(s):  
Terry Ashley ◽  
L. B. Russell ◽  
N. L. A. Cacheiro

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