Influence of neonatal injections of testosterone propionate on sexual behavior and plasma testosterone levels in the male house mouse

1979 ◽  
Vol 12 (3) ◽  
pp. 231-238 ◽  
Author(s):  
Jennifer Batty
1974 ◽  
Vol 60 (1) ◽  
pp. 145-148 ◽  
Author(s):  
A. BARTKE

SUMMARY In male mice of the C57BL/10J (C57) strain the testicular weight, sex drive and aggression are low compared with a number of other strains, indicating androgen deficiency. In contrast, DBA/2J (DBA) males were 'normal' in all studied parameters of testicular function. The weight of the seminal vesicles is similar in both strains. Plasma testosterone levels, and the responsiveness of the seminal vesicles to injected testosterone propionate in C57 and DBA animals were compared. Plasma testosterone levels were 1·3 ± 0·4 ng/ml in C57 and 4·6 ± 1·0 ng/ml in DBA mice. The increase in weight of the seminal vesicles after administration of testosterone propionate to castrated male mice was, however, considerably greater in C57 than in DBA mice. In order to restore the weight of the seminal vesicles to normal it was necessary to administer twice as much testosterone propionate to DBA than to C57 males.


1983 ◽  
Vol 98 (3) ◽  
pp. 365-371 ◽  
Author(s):  
E. M. Sommerville ◽  
M. F. Tarttelin

Testosterone propionate (TP) was administered, by means of subcutaneous implanted silicone elastomer capsules, into adult and neonatal (aged 3 days) female rats. In the adult rats a dose-dependent increase in plasma testosterone was measured for capsules of three different sizes (5, 10 and 20 mm crystal length). Testosterone levels reached a peak 4–8 h after insertion (5 mm, 24·6±1·4 (s.e.m.) nmol/l; 10 mm, 34·0 ± 3±8; 20 mm, 44·4 ± 3·1) and returned to control levels within 4 h after removal: the calculated half-life of testosterone was 1 h for all sizes of capsule. In neonates, a capsule of 2·5 mm crystal length was removed after 4 h subcutaneous implantation (at day 3 of age) and produced peak testosterone levels of 126·2± 11·8 nmol/l: the calculated half-life was 8·6 h which compared with a half-life of 48 h after a subcutaneous injection of 312 μmol TP (in 0·05 ml arachis oil) which produced peak levels of testosterone in 4–8 h of 84·6 ±11·8 nmol/l. Chronic implants of TP-filled capsules (2·5 mm crystal length) at 3 days of age and left in situ for 15 weeks gave a half-life of 69 h. Removable silicone elastomer capsules were found to be a versatile vehicle for the administration of TP to rats of all ages where precise hormone treatment for a known period or prolonged administration is required. The duration and magnitude of plasma hormone levels should be established by assay in an in-vivo situation.


1971 ◽  
Vol 68 (3) ◽  
pp. 576-584 ◽  
Author(s):  
K. O. Nilsson ◽  
B. Hökfelt

ABSTRACT Metyrapone was administered either orally, 750 mg every four h, in a total of six doses, or intravenously 30 mg per kg body weight as a four h infusion. In three males with normal endocrine functions, metyrapone given orally or intravenously induced a fall in plasma testosterone and an elevation of androstenedione within 2–8 h. When metyrapone was administered to a patient given dexamethasone to suppress endogenous ACTH production, the androstenedione levels did not alter whereas the testosterone levels showed a slight, transient decrease. In two normal females metyrapone administration was followed by a marked increase in plasma androstenedione whereas testosterone showed only a minor, gradual increase. In one male patient with Addison's disease the basal plasma testosterone was normal whereas the level of androstenedione was low. Following metyrapone intravenously, there was a slight suppression of plasma testosterone but no change in the androstenedione concentration. In one patient with primary hypogonadism, two with secondary hypogonadism and two with Klinefelter's syndrome the plasma testosterone was low under basal conditions and did not change following metyrapone. Basal plasma androstenedione was within the range for normal males and increased markedly following metyrapone in all the cases.


1981 ◽  
Vol 96 (2) ◽  
pp. 273-280 ◽  
Author(s):  
Mridula Chowdhury ◽  
Robert Tcholakian ◽  
Emil Steinberger

Abstract. It has been suggested that treatment of intact male rats with oestradiol benzoate (OeB) causes an interference with testosterone (T) production by the testes by a direct inhibitory effect on steroidogenesis. To test this hypothesis, different doses (5, 10 or 25 IU) of hCG were administered concomitantly with 50 μg of OeB to adult intact or hypophysectomized male rats. The testicular and plasma testosterone, and serum hCG levels were determined. The sex accessory weights were recorded. In the intact OeB-treated group of animals, hCG stimulated both the secondary sex organs and plasma testosterone levels above the intact control group. However, in hypophysectomized animals, although plasma testosterone levels increased above that of intact controls, their secondary sex organ weights did not. Moreover, inspite of high circulating hCG levels, the testicular testosterone content and concentration remained suppressed in OeB-treated animals. The reason for such dichotomy of hCG action on OeB-treated animals is not clear at present.


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