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Results for “testosterone secretion”

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PubMed1978

Plasma testosterone profiles in male macropodid marsupials.

Serial blood samples were collected over a 3.5-8 h period from ten adult male macropodid marsupials belonging to five different species to study the pattern of testosterone secretion. The concentration of testosterone in the plasma ranged from 0.5 to 9.5 ng/ml, and in each animal the levels declined progressively during the study; this effect was attributed to the stress effects of handling. Injection of 5 microgram synthetic luteinizing hormone releasing hormone induced a rapid and substantial increase in the level of testosterone.

Animals↗
PubMed2006

[The culture and identification of rat testis Leydig cell].

OBJECTIVE: To establish a primary culture method of rat testis Leydig cell. METHODS: The primary rat Leydig cells were treated with or without 4 U/ml human chorionic gonadotropin (hCG), and testosterone in culture medium was detected by radioimmunoassay. The morphology and biological characteristics of Leydig cell were observed. RESULTS: The culture cells were highly homogeneous, proliferative and had a high differentiation rate. The high purified Leydig cells were verified by their dynamic morphological changes and 3beta-hydroxysteroid dehydrogenase delta4-delta5 isomerase (3beta-HSD) histochemical staining. The testosterone secretion induced by hCG significantly increased (P < 0.05) 24 hours after inoculation than that induced without hCG in the control. CONCLUSION: It suggests that the Leydig cell cultured in vitro may secrete high concentration of testosterone, and this study laid the basis of androgen replacement therapy for partial androgen deficiency in aging male.

3-Hydroxysteroid Dehydrogenases↗
PubMed2005

In vitro effects of diethylstilbestrol, genistein, 4-tert-butylphenol, and 4-tert-octylphenol on steroidogenic activity of isolated immature rat ovarian follicles.

Isolated rat ovarian follicles grow and produce steroid hormones in vitro and so provide a good model for studying the effects of hormonally active compounds on follicular steroidogenesis. We have evaluated the effects of diethylstilbestrol (DES), genistein (GEN) and two alkylphenols, 4-tert-butylphenol (BP) and 4-tert-octylphenol (OP) on the growth, survival, and steroid hormone and cAMP production by isolated 14-day-old rat (Sprague-Dawley) ovarian follicles. During a 5-day culture, FSH was obligatory for follicle growth and increased estradiol and testosterone secretion in a dose-dependent manner. DES (10(-6) M) caused the strongest decline in estradiol and testosterone levels but did not have detectable effects on either cAMP production or aromatase enzyme activity. GEN caused a prominent decrease in cAMP and testosterone levels without significant changes in secreted estradiol. The latter, apparently, was due to a dose-dependent stimulation of aromatase enzyme activity in the presence of genistein. Both BP and OP decreased estradiol and testosterone secretion in a dose-dependent manner while no effect on aromatase activity was observed. OP, unlike BP, decreased forskolin-induced cAMP levels. Xenoestrogens at the used concentrations did not interfere with the growth and survival of the follicles. The results indicate that isolated ovarian follicles representing intact morphological and functional units offer a sensitive model system for elucidating the female-specific reproductive effects of environmental chemicals.

Animals↗
PubMed1984

Direct effect of the luteinizing hormone releasing hormone analog D-Trp6-Pro9-Net-LHRH on rat testicular steroidogenesis.

The luteinizing hormone releasing hormone analog D-Trp6-Pro9-Net-LHRH (LHRHa) inhibits rat testicular testosterone secretion. To determine whether LHRHa decreases serum testosterone concentrations solely by inhibiting gonadotropin secretion or, in addition, by influencing directly testicular testosterone biosynthesis, we examined the effects of LHRHa on the activities of 5 key testicular steroidogenic enzymes. Thirty hypophysectomized, hOG treated rats were given either LHRHa (1 micrograms sc/day) or saline during 7 days. The LHRHa treated animals exhibited a significant decrease of serum testosterone when compared to the control group (498 +/- 37 ng/dl vs 2044 +/- 105 ng/dl, mean +/- SEM, P less than 0.001). 17-Hydroxyprogesterone serum levels were also decreased in the LHRHa treated rats (61 +/- 6 ng/dl vs 93 +/- 7 ng/dl, P less than 0.005), while serum progesterone levels were similar in both groups of animals. These changes in steroid concentrations were associated with decreases in the microsomal enzyme activities of 17-hydroxylase (37 +/- 9 vs 654 +/- 41 pmol/mg protein/min, P less than 0.001), 17,20-desmolase (103 +/- 9 vs 522 +/- 47 pmol/mg protein/min, P less than 0.001), 3 beta-hydroxysteroid dehydrogenase (1.7 +/- 0.02 vs 4.1 +/- 0.1 nmol/mg protein/min, P less than 0.001), aromatase (95 +/- 7 vs 228 +/- 6 pmol/mg protein/min, P less than 0.001) and 17-ketosteroid reductase (167 +/- 9 vs 290 +/- 18 pmol/mg protein/min, P less than 0.01) in the LHRHa treated animals. These findings indicate that LHRHa can inhibit directly rat testicular testosterone biosynthesis.

17-alpha-Hydroxyprogesterone↗
PubMed2003

The effect of intraperitoneal melatonin supplementation on the release of thyroid hormones and testosterone in rats with hyperthyroid.

OBJECTIVE: Melatonin has a general inhibitory effect on the reproductive system and thyroid functions. Testosterone secretion increases in parallel to thyroid hormones in hyperthyroidism. The aim of this study was to investigate the effects of melatonin application on total T3, T4 and testosterone in hyperthyroid rats. METHODS: This study was performed on 4 groups each consisted of 6 male Spraque Dawley rats. Control group (G1); sham group (G2); applied 0.5 ml/day of serum physiologic intraperitoneally for 2 weeks, hyperthyroid group (G3); applied 0.3 mg/kg/day thyroxine intraperitoneally for 2 weeks, and hyperthyroid and melatonin supplemented group (G4); applied 0.3 mg/kg/day thyroxine and 3 mg/kg/day melatonin. Blood samples taken by way of decapitation were analysed for total T3, T4 and testosterone by RIA. RESULTS: Serum total T3 and total testosterone levels were the highest in hyperthyroid group (G3), whereas in hyperthyroid and melatonin supplemented group (G4) were the lowest (P<0.001). Total T4 levels were higher in group 3 than group 1, 2 and 4 (P<0.001). CONCLUSION: Results revealed that melatonin supplementation in hyperthyroidism suppress secretion of thyroid hormones and testosterone secretion.

Animals↗