EFFECTS OF TESTOSTERONE AND PROLACTIN OR GROWTH HORMONE ON THE ACCESSORY SEX ORGANS OF CASTRATED MICE

1975 ◽  
Vol 64 (1) ◽  
pp. 111-115 ◽  
Author(s):  
E. J. KEENAN ◽  
J. A. THOMAS

SUMMARY In 5-day experiments, neither bovine prolactin (300 or 600 i.u./kg) nor ovine growth hormone (25 i.u./kg) alone significantly enhanced accessory sex organ weights in the castrated mouse. Seminal vesicle weights, and to a lesser extent anterior prostate gland weights, were augmented by the simultaneous injection of testosterone (1·5 mg/kg) daily plus prolactin or growth hormone. The effect was greater than that produced by testosterone alone. The levels of fructose in accessory sex organs used to indicate androgenic activity were similar in castrated mice receiving testosterone alone or in combination with prolactin or growth hormone. Prolactin alone did not influence uptake of [3H]testosterone by the seminal vesicles or anterior prostate gland over a 5 min period in vivo.

1981 ◽  
Vol 90 (3) ◽  
pp. 323-330 ◽  
Author(s):  
E. J. KEENAN ◽  
P. A. KLASE ◽  
J. A. THOMAS

Treatment of adult male mice with varying doses of prolactin increased the weights of the seminal vesicles and the anterior prostate gland. Only in the seminal vesicles were these increases in organ weights associated with increased levels of DNA. In castrated mice, prolactin alone failed to alter the weights of the accessory sex organs or DNA content. However, the simultaneous administration of prolactin and testosterone resulted in enhanced androgenic stimulation of seminal vesicle weights and their DNA content. Prostatic weights, but not DNA content, were augmented by treatment with prolactin and testosterone. Although the kidneys exhibited androgen sensitivity, prolactin failed to enhance the effect of testosterone upon the kidney. Augmentation of androgen action in the accessory sex organs was observed only after treatment with prolactin or growth hormone. Prolactin also enhanced the effects of dihydrotestosterone and 5α-androstane-3α, 17β-diol, but not of 5α-androstane-3β,17β-diol. These studies revealed that prolactin enhances the proliferative actions of androgens in mouse seminal vesicles, but not in the anterior prostate glands or the kidneys.


2001 ◽  
Vol 125 (1) ◽  
pp. 141-145
Author(s):  
Rajal B. Shah ◽  
Min W. Lee ◽  
Alvaro A. Giraldo ◽  
Mahul B. Amin

Abstract Context.—We have observed intraluminal crystalloid morphology in seminal vesicles that is superficially similar to that seen in prostate neoplasia, but found little information on such morphology in the literature. Design.—Two hundred fifty-three prostate specimens (163 needle biopsies, 75 radical prostatectomies with prostate carcinoma, 11 prostates from autopsy, and 4 cystoprostatectomies without prostate carcinoma) were examined for seminal vesicle secretions, which were categorized as (a) dense platelike inspissated, (b) fluidlike, (c) crystalloid morphology, and (d) absent. Histochemical stains (periodic acid–Schiff with and without diastase, Alcian blue at pH 2.5, and mucicarmine) were performed to characterize the nature of secretions. Results.—Proteinaceous secretions were identified in 82% of seminal vesicles examined. Of these, 61% had predominantly dense, platelike, inspissated secretions, 15% had predominantly fluidlike secretions, and 24% had predominantly crystalloid morphology. Although in some cases the crystalloid morphology resembled that of prostatic intraluminal crystalloids, the seminal vesicle crystalloids differed in that they were invariably multiple, had curved edges, and had varied forms (elliptical, cylindrical, rodlike, and rectangular). Seventy-one percent of seminal vesicle crystalloids were associated with dense, platelike, inspissated secretions and appeared to be created by fracturing within platelike secretions. There was no relationship between seminal vesicle crystalloid morphology and associated malignancy in the prostate gland, as it was seen in 24% of cases with prostate carcinoma and 25% of cases without prostate carcinoma (P = 1.0000). Fluidlike secretions were positive for Alcian blue (pH 2.5) and mucicarmine, whereas dense platelike secretions and crystalloid morphology were negative for Alcian blue (pH 2.5) and mucicarmine. Conclusions.—Seminal vesicle secretions are fairly common and, when fluidlike, are composed of acid mucopolysaccharides. Inspissation of secretions appears to be associated with loss of acidity, presumably resulting in dense platelike secretions and crystallization. Awareness of both the crystalloid morphology in seminal vesicle tissue and the distinguishing features from prostatic crystalloids may be important while interpreting prostate needle biopsies in which seminal vesicle epithelium may be confused for prostate carcinoma because of a small acinar morphology with accompanying cytologic atypia and crystalloid morphology.


1991 ◽  
Vol 3 (3) ◽  
pp. 313 ◽  
Author(s):  
S Sujarit ◽  
RC Jones

The uptake of [3H]thymidine by the epididymis, ventral prostate gland and seminal vesicles was determined in vivo for rats aged 15, 20, 25, 30, 35, 45 and 55 days. The pattern of uptake varied considerably between organs and generally was different from patterns of growth measured as mass or ratio of mass of DNA:tissue. The 'initial segment' of the epididymis and caput and corpus epididymidis showed a similar pattern of [3H]thymidine uptake, being greatest in 15-day-old animals and declining thereafter. On Day 15 the cauda epididymidis had a lower uptake than more proximal regions of the epididymis, but it subsequently showed two significant peaks of increased uptake on Days 25-30 and Day 45. The uptake by the seminal vesicles was high on Day 15, fell to low levels on Day 20, increased considerably from Days 20 to 35, then gradually decreased from Day 35 to 55. The uptake by the prostate gland was a little lower than by the seminal vesicles on Days 15 and 20, then reduced to about the same level as non-reproductive tissues.


1970 ◽  
Vol 63 (2) ◽  
pp. 207-215 ◽  
Author(s):  
Kjell J. Tveter

ABSTRACT The distribution of radioactive material in the prostate gland and the seminal vesicles has been studied by autoradiography after intramuscular administration of [1,2-3H] testosterone in vivo to adult castrated male rats. Positive autoradiographs were obtained from 7½ min to 8 h after the administration. As early as after 15 min, there appeared to be a selective localization of radioactivity in the epithelial cells, with much of the labelling associated with the nuclei; the stromal labelling was markedly less. This picture was even more significant ½, 1 and 2 h after the injection, when the autoradiographs demonstrated a preferential labelling of the nuclei of the epithelial cells. A distinct labelling of the epithelial cells was also found 8 h after the injection. The same qualitative pattern of distribution of radioactivity was seen in the four prostatic lobes and the seminal vesicles. No significant labelling of the secretions in the glandular lumina was observed.


1960 ◽  
Vol XXXIV (III) ◽  
pp. 344-352 ◽  
Author(s):  
Jerome A. Grunt ◽  
Joseph E. Walker

ABSTRACT The responses of several seminal vesicle in vivo microscopic characteristics, seminal vesicle contractions, seminal vesicle, kidney and adrenal weights and seminal vesicle histology have been compared following the administration of testosterone propionate (T. P.) and norethandrolone (19-NT) to castrated male rats. Fourteen days after castration 35 male Osborne-Mendel rats were divided into 5 groups each containing 6 to 8 animals and given daily subcutaneous injections of 0.1 ml sesame oil with or without added steroids. The groups were: I – sesame oil; II – 100 μg 19-NT; III – 500 μg 19-NT; IV – 100 μg T.P.; V – 500 μg T. P. After 7 days of injections, seminal vesicles were studied by the transillumination method of Knisely. The seminal vesicles, adrenals and kidneys were then removed and weighed and the vesicles were prepared for routine histological examination. The adrenal and kidney weights, as well as the seminal vesicle contractions, responded to both steroids in a similar manner, however, seminal vesicle weight and histology and in vivo characteristics differed greatly. 19-NT appeared to have very little effect on vesicle weight, in vivo characteristics and histology although contractions were inhibited in 13 of 14 animals so treated. Therefore, when used as the end-point in hormonal reactions, seminal vesicle contractions should not be considered comparable to the usual secondary sexual organ reactivity to hormones.


1983 ◽  
Vol 96 (3) ◽  
pp. 457-464 ◽  
Author(s):  
W. D. Booth

Minces of the prostate and seminal vesicles of the mature boar were incubated with the following major testicular steroids of the pig: [3H]dehydroepiandrosterone, [3H]5-androstene-3β,17β-diol, [3H]oestrone, [3H]oestradiol-17β and their respective sulphate conjugates (excluding oestradiol-17β). Incubations were also carried out with [3H]testosterone, [3H]5α-dihydrotestosterone and [3H]5α-androstanediols. Minces of the epididymides were incubated with [3H]dehydroepiandrosterone and [3H]oestrone sulphates. The prostate and seminal vesicles converted dehydroepiandrosterone predominantly to weak androgens, whereas 5-androstene-3β,17β-diol was primarily converted to testosterone; testosterone and its 5α-reduced metabolites were metabolized in a manner typical of androgen end target organs. Unconjugated oestrone and oestradiol-17β were interconverted by the prostate and seminal vesicles. The metabolism of C19 steroid sulphates was < 1% in all incubations; some oestrone sulphate, however, was converted to unconjugated oestrone and oestradiol, particularly by the caput epididymidis. The significance of these results is discussed in relation to recent studies in vivo.


Health Care ◽  
2014 ◽  
Vol 2 (2) ◽  
pp. 47
Author(s):  
Popoola Oladele Biliamin ◽  
Ajayi Ruth Taiwo ◽  
Akinyemi Raphael Akinsola ◽  
Oguntoye Shemilore Gbenga ◽  
Huthman Ibrahim Oluwaseun

1989 ◽  
Vol 121 (1) ◽  
pp. 121-128 ◽  
Author(s):  
G. Veyssiere ◽  
Ch. Jean-Faucher ◽  
M. Berger ◽  
Cl. Jean

Abstract. Studies were conducted to evaluate the effects of neonatal administration of supraphysiological doses of testosterone on the growth, hormone responsiveness, DNA and protein content, and protein profiles of the epididymis, vas deferens and seminal vesicles in adult mice. Results indicate that in androgenized males, testicular growth (DNA and protein content), circulating and organ androgen levels, and fertility were significantly depressed. The weights of the epididymis, vas deferens, seminal vesicle and kidney, but not that of the spleen, were significantly diminished subsequently to a reduction of protein (all organs) and DNA (epididymis, vas deferens) content. The efficacy of testosterone in promoting accessory sex organs and kidney growth, in adult castrated males, was persistently reduced in neonatally androgenized males. When assessed by DNA content, the response of all organs (except the seminal vesicle) was similar to that of controls, but it was significantly reduced from 16 to 43% when measured in terms of protein content. The protein profiles from seminal vesicles and vas deferens analysed by polyacrylamide gel electrophoresis, showed reproducible persistent alterations which could be reversed by adult androgen therapy.


1964 ◽  
Vol 30 (2) ◽  
pp. 225-233 ◽  
Author(s):  
ILSE LASNITZKI

SUMMARY The effect of hydrocortisone was studied in organ cultures of the ventral and anterior prostate gland of young rats grown in natural and semi-defined medium and the action of hydrocortisone on the ventral gland was compared with that of testosterone. In natural medium the ventral prostates showed a reduction of the number of alveoli, a lowering of the epithelium and a striking increase of the stroma. In the semi-defined medium the changes were confined to a lowering of the epithelium and a reduction of secretory activity. Hydrocortisone counteracted this regression in all cultures to which it had been added. In natural medium it preserved the number of alveoli, maintained epithelial height and suppressed the proliferation of the stroma. In the semi-defined medium the hormone preserved the height and function of the epithelium. Testosterone added to natural medium inhibited stromal growth and partially maintained the epithelium; in semi-defined medium it maintained the epithelium but the cells were better preserved by hydrocortisone. The anterior prostate gland showed epithelial hyperplasia and increase of connective tissue in both media; hydrocortisone inhibited both changes and produced cultures that resembled the organ in vivo.


1971 ◽  
Vol 51 (4) ◽  
pp. 707-NP ◽  
Author(s):  
T. MANN ◽  
L. E. A. ROWSON ◽  
S. BARONOS ◽  
A. KARAGIANNIDIS

SUMMARY The androgenic effects of testosterone and dihydrotestosterone on the bovine seminal vesicles have been evaluated by (i) introducing the steroid directly into one seminal vesicle in situ, while retaining the other vesicle as a control or for the introduction of another steroid, or (ii) injecting the steroid subcutaneously into a whole animal, and examining the seminal vesicles after autopsy. When introduced directly into a seminal vesicle dihydrotestosterone oenanthate stimulated growth and the formation of fructose and citric acid, but the magnitude of the effect was not greater than that of a similar dose of testosterone oenanthate. When twin calves were injected subcutaneously, one with dihydrotestosterone propionate, and the other with the same dose of testosterone propionate, only the latter responded with increased output of fructose, citric acid and α-mannosidase in electro-ejaculated semen. But the seminal vesicles grew to approximately the same size in both twins. Parenterally administered bovine growth hormone produced a sudden but transient burst of secretory activity in the seminal vesicles, resulting in the appearance of fructose and citric acid in electro-ejaculated semen.


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