Long term replacement therapies with testosterone propionate and human chorionic gonadotrophin in hypophysectomized adult male rats

1970 ◽  
Vol 26 (8) ◽  
pp. 911-914
Author(s):  
R. von Berswordt-Wallrabe ◽  
M. Mehring ◽  
E. Richter-Bonacker
Keyword(s):  
Adult Male ◽  
Testosterone Propionate ◽  
Chorionic Gonadotrophin ◽  
Human Chorionic Gonadotrophin ◽  
Male Rats

Adrenal and gonadal function in hypothyroid adult male rats

1997 ◽  
Vol 152 (1) ◽  
pp. 147-154 ◽  
Author(s):  
A Tohei ◽  
M Akai ◽  
T Tomabechi ◽  
M Mamada ◽  
K Taya
Keyword(s):  
Adult Male ◽  
Functional Relationship ◽  
Plasma Concentrations ◽  
Gonadal Hormones ◽  
Chorionic Gonadotrophin ◽  
Human Chorionic Gonadotrophin ◽  
Male Rats ◽  
Plasma Acth ◽  
Corticosterone Release ◽  
Acth Release

Abstract The functional relationship between thyroid, adrenal and gonadal hormones was investigated using adult male rats. Hypothyroidism was produced by the administration of 4-methyl-2-thiouracil (thiouracil) in the drinking water for 2 weeks. Plasma concentrations of TSH dramatically increased, whereas plasma concentrations of tri-iodothyronine and thyroxine decreased in thiouracil-treated rats as compared with euthyroid rats. Hypothyroidism increased basal levels of plasma ACTH and pituitary content of ACTH. The pituitary responsiveness to CRH for ACTH release markedly increased, whereas the adrenal responsiveness to ACTH for corticosterone release decreased. These results indicated that hypothyroidism causes adrenal dysfunction in adult male rats. Pituitary contents of LH and prolactin decreased in hypothyroid rats as compared with euthyroid rats. In addition, hypothyroidism lowered pituitary LH responsiveness to LHRH. Testicular responsiveness to human chorionic gonadotrophin for testosterone release, however, was not different between euthyroid and hypothyroid animals. These results indicated that hypothyroidism causes adrenal dysfunction and results in hypersecretion of ACTH from the pituitary gland. Adrenal dysfunction may contribute to the inhibition of LHRH secretion from the hypothalamus, possibly mediated by excess CRH. Journal of Endocrinology (1997) 152, 147–154

Induction of selective release of FSH in castrated male rats bearing an ovarian transplant by the administration of human chorionic gonadotrophin

1985 ◽  
Vol 106 (1) ◽  
pp. 31-NP ◽  
Author(s):  
G. Watanabe ◽  
K. Taya ◽  
S. Sasamoto
Keyword(s):  
Adult Male ◽  
Sex Differentiation ◽  
Plasma Concentrations ◽  
Chorionic Gonadotrophin ◽  
Human Chorionic Gonadotrophin ◽  
Male Rats ◽  
Corpora Lutea ◽  
Female Rat ◽  
Nacl Solution ◽  
Abrupt Decrease

ABSTRACT The present study was undertaken to determine whether hypothalamic differentiation is involved in the selective release of FSH during the periovulatory period using adult male rats castrated and implanted with an ovary. Adult male rats (70–90 days old) were castrated and an ovary obtained from a prepubertal female rat (26 days old) was immediately grafted subcutaneously. Four weeks later, human chorionic gonadotrophin (hCG, 10 i.u.) was injected i.v. into the experimentally manipulated rats to induce ovulatory changes in the grafted ovaries. Another group of similarly prepared rats was injected with 0·9% (w/v) NaCl solution as controls. After injection of hCG, plasma concentrations of FSH increased significantly by 6 h, reached peak values at 12 h and declined to control levels at 36 h. On the other hand, plasma concentrations of LH were reduced by 6 h and decreased further during the next 36 h. An abrupt fall in plasma concentrations of oestradiol-17β occurred within 3 h of the administration of hCG. Histological examination revealed that ovulatory changes and luteinization of follicles were induced in grafted ovaries by 18 h after the injection of hCG. Thirty-six hours after treatment with hCG, a set of newly formed corpora lutea was observed in grafted ovaries and plasma concentrations of progesterone were raised. Treatment with oestradiol-17β did not inhibit the selective release of FSH after the administration of hCG, suggesting that the abrupt decrease in secretion of oestradiol-17β from the grafted ovary is not involved in the occurrence of the FSH surge. These results indicate that a selective release of FSH can be induced in castrated male rats bearing an ovarian transplant probably due to decreased secretion of inhibin by the luteinized follicles in the grafted ovaries. Sex differentiation of the hypothalamus is not, therefore, involved in the selective surge of FSH. J. Endocr. (1985) 106, 31–36

EFFECT OF GONADOTROPHINS ON THE SECRETION OF OESTRADIOL-17β AND TESTOSTERONE BY THE RAT TESTIS

1973 ◽  
Vol 57 (2) ◽  
pp. 277-284 ◽  
Author(s):  
F. H. DE JONG ◽  
A. H. HEY ◽  
H. J. van der MOLEN
Keyword(s):  
Intravenous Administration ◽  
Adult Male ◽  
Follicle Stimulating Hormone ◽  
Chorionic Gonadotrophin ◽  
Human Chorionic Gonadotrophin ◽  
Male Rats ◽  
Testosterone Concentration ◽  
Peripheral Plasma ◽  
Before And After ◽  
Venous Plasma

SUMMARY Concentrations of oestradiol-17β and testosterone were estimated in peripheral venous plasma and testicular venous plasma of adult male rats before and after administration of human chorionic gonadotrophin (HCG) or follicle-stimulating hormone (FSH). The concentration of oestradiol-17β in peripheral plasma, as measured with a radioimmunological technique, was 2·0 ± 0·9 (s.d.) pg/ml (n = 12). Peripheral testosterone concentrations were 2·4 ± 1·8 (s.d.) ng/ml (n = 21). Concentrations of oestradiol-17β and testosterone in testicular venous plasma were significantly higher than those in peripheral plasma. After intravenous administration of HCG (100 i.u.), oestradiol-17β and testosterone concentrations in testicular venous plasma increased significantly. After prolonged s.c. administration of HCG (5 days) the concentration of oestradiol-17β in testicular venous plasma did not change significantly, although the concentration of testosterone increased more than ten times. Intravenous administration of HCG after 5 days of pretreatment with HCG caused a significant increase in oestradiol-17β concentrations in testicular venous plasma. The increase in testosterone concentration was not significant under these conditions. Intravenous administration of FSH did not change oestradiol-17β or testosterone concentrations in testicular venous plasma.

Long-term exposure to a continuous 900 MHz electromagnetic field disrupts cerebellar morphology in young adult male rats

2017 ◽  
Vol 92 (5) ◽  
pp. 324-330 ◽  
Author(s):  
A Aslan ◽  
A İkinci ◽  
O Baş ◽  
OF Sönmez ◽  
H Kaya ◽  
...  
Keyword(s):  
Electromagnetic Field ◽  
Young Adult ◽  
Adult Male ◽  
Male Rats ◽  
Young Adult Male ◽  
900 Mhz Electromagnetic Field

scholarly journals Altered sexual differentiation of hepatic uridine diphosphate glucuronyltransferase by neonatal hormone treatment in rats

1979 ◽  
Vol 180 (2) ◽  
pp. 313-318 ◽  
Author(s):  
Coral A. Lamartiniere ◽  
Cindy S. Dieringer ◽  
Etsuko Kita ◽  
George W. Lucier
Keyword(s):  
Enzyme Activity ◽  
Adult Male ◽  
Sexual Differentiation ◽  
Reproductive Tract ◽  
Testosterone Propionate ◽  
Hormone Treatment ◽  
Male Rats ◽  
Ventral Prostate ◽  
Uridine Diphosphate ◽  
Neonatal Administration

The hepatic microsomal enzyme UDP-glucuronyltransferase undergoes a complex developmental pattern in which enzyme activity is first detectable on the 18th day of gestation in rats. Prepubertal activities are similar for males and females. However, postpubertal sexual differentiation of enzyme activity occurs in which male activities are twice those of females. Neonatal administration of testosterone propionate or diethylstilboestrol to intact animals resulted in lowered UDP-glucuronyltransferase activity in liver microsomal fractions of adult male rats, whereas no changes were observed in the adult females and prepubertal male and female animals. Neonatal administration of testosterone propionate and diethylstilboestrol adversely affected male reproductive-tract development as evidenced by decreased weights of testes, seminal vesicles and ventral prostate. Diethylstilboestrol also markedly decreased spermatogenesis. Hypophysectomy of adult male rats resulted in negative modulation of microsomal UDP-glucuronyltransferase and prevented the sexual differentiation of enzyme activity. In contrast hypophysectomy had no effect on female UDP-glucuronyltransferase activity. A pituitary transplant under the kidney capsule was not capable of reversing the enzyme effects of hypophysectomy, therefore suggesting that the male pituitary factor(s) responsible for positive modulation of UDP-glucuronyltransferase might be under hypothalamic control in the form of a releasing factor. Neonatal testosterone propionate and diethylstilboestrol administration apparently interfered with the normal sequence of postpubertal UDP-glucuronyltransferase sexual differentiation.

scholarly journals Conversion of Testosterone to Estradiol is Necessary for the Development of Long‐term Facilitation in Adult Male Rats

2021 ◽  
Vol 35 (S1) ◽  
Author(s):  
Jessica Grittner ◽  
Shawn Miller ◽  
Brendan Dougherty
Keyword(s):  
Adult Male ◽  
Male Rats ◽  
Long Term Facilitation

SHORT-TERM EFFECTS OF COPULATION, HUMAN CHORIONIC GONADOTROPHIN INJECTION AND NON-TACTILE ASSOCIATION WITH A FEMALE ON TESTOSTERONE LEVELS IN THE MALE RAT

1974 ◽  
Vol 60 (3) ◽  
pp. 429-439 ◽  
Author(s):  
K. PURVIS ◽  
N. B. HAYNES
Keyword(s):  
Chorionic Gonadotrophin ◽  
Human Chorionic Gonadotrophin ◽  
Physical Contact ◽  
Male Rats ◽  
Male Rat ◽  
Plasma Testosterone ◽  
Short Term ◽  
Testosterone Levels ◽  
Peripheral Plasma ◽  
First Contact

SUMMARY Peripheral plasma testosterone levels in the male rat were increased above control levels 5 min after the first intromission with an oestrous female, or 8–10 min after first contact with the female. The levels remained raised for at least 30 min if copulation was allowed to continue. Intravenous injection of human chorionic gonadotrophin resulted in an increased peripheral concentration of plasma testosterone after 10–15 min and an increase of testosterone content of the testis 5–10 min after injection, indicating that the rat testis has a potential to respond rapidly to gonadotrophin. The results suggested that if the testosterone surge during copulation was gonadotrophin-dependent, it was initiated before the first intromission. Indeed, plasma testosterone levels were raised in male rats 5 min after being placed in the proximity of oestrous females but not allowed physical contact.

Long-term (6-wk) hindlimb suspension inhibits spermatogenesis in adult male rats

2002 ◽  
Vol 92 (3) ◽  
pp. 1191-1198 ◽  
Author(s):  
Joseph S. Tash ◽  
Donald C. Johnson ◽  
George C. Enders
Keyword(s):  
Adult Male ◽  
Inguinal Canal ◽  
Space Station ◽  
Male Rats ◽  
Hindlimb Suspension ◽  
Spermatogenic Cells ◽  
Cage Floor ◽  
Seminal Vesicle Weight ◽  
The Impact

The International Space Station will allow extended habitation in space and long-term exposure to microgravity (μG). A concern is the impact of long-term μG exposure on the ability of species to reproduce. The model often used to simulate μG is rat hindlimb suspension (HLS), where the hindlimbs are elevated above the cage floor with a tail harness. Experiments described here are the first to examine the effect of long-term HLS on testicular function in adult male rats. Free-roaming (controls), animals with only the tail harnessed but hindlimbs in contact with the cage floor (TO), and HLS animals were tested for 6 wk. Cryptorchidism was prevented in TO and HLS animals by partial constriction of the inguinal canal with sutures. All parameters were compared at the end of the 6-wk experiment. Testicular weights and spermatogenesis were significantly reduced by HLS, such that no spermatogenic cells beyond round spermatids were present and epididymides were devoid of mature sperm. In many tubules, loss of all germ cells, except a few spermatogonia, resulting in histopathology similar to the Sertoli cell, was observed. Spermatogenesis appeared unaffected in control and TO animals. Sertoli and Leydig cell appearance, testosterone, luteinizing hormone, and follicle-stimulating hormone levels, and epididymal and seminal vesicle weight were unchanged by HLS. Cortisone was not elevated by HLS; thus stress may not be a factor. These results demonstrate that spermatogenesis is severely inhibited by long-term HLS, whereas testicular androgen production is not. These results have significant implications regarding serious effects of long-term exposure to μG on the reproductive capability of scrotal mammals, including humans.

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