Changes In Steroid Concentrations Research Articles

Modeling vitellogenesis in female fish exposed to environmental stressors: predicting the effects of endocrine disturbance due to exposure to a PCB mixture and cadmium

A wide variety of chemical and physical environmental stressors have been shown to alter the reproductive processes in fish by interfering with endocrine function. Most endocrine indicators or biomarkers are static measures from dynamic hormonally-mediated processes, and often do not directly relate to reproductive endpoints of ecological significance. Adequate production of the yolk precursor protein, vitellogenin, is critical for the survival and normal development of the sensitive egg and yolk-sac larval fish life stages. We developed a model that simulates vitellogenesis in a mature female sciaenid fish. The model simulates the major biochemical reactions over a 6-month period from the secretion of gonadotropin (GtH) into the blood to the production of vitellogenin. We simulated the effects of two endocrine disrupting chemicals (EDCs) that have different actions on vitellogenin production: a PCB mixture and cadmium. Predicted changes in steroid concentrations and cumulative vitellogenin production compared favorably with changes reported in laboratory experiments. Simulations illustrate the potential utility of our model for interpreting reproductive endocrine biomarkers measured in fish collected from degraded environments.

Relationship between sex hormones and anterior knee laxity across the menstrual cycle.

To comprehensively quantify through daily, serial measures changes in knee laxity as a function of changing sex-hormone levels across one complete menstrual cycle. Twenty-five females, 18 - 30 yr, body mass index < or = 30, who reported normal menstrual cycles (28-32 d) over the past 6 months participated. Participants were tested daily across one complete menstrual cycle; 5-7 cc of venous blood were withdrawn to assay serum levels of estradiol, progesterone, and testosterone. Knee laxity was measured as the amount of anterior tibial displacement at 133 N, using a standard knee arthrometer. To evaluate the relationship of knee laxity to changes in sex hormone concentrations, a multiple linear regression model with the possibility of a time delay was performed on each individual subject and the group as a whole. Individual regression equations revealed an average of 63% of the variance in knee laxity was explained by the three hormones and their interactions. All three hormones significantly contributed to the prediction equation, and the amount of variance explained was substantially greater when a time delay was considered. On average, knee laxity changed approximately 3, 4, and 4.5 d after changes in estradiol, progesterone, and testosterone, respectively. When females were analyzed as a group, only 8% of the variance in knee laxity was explained by sex-hormones levels. Changes in sex hormones mediate changes in knee laxity across the menstrual cycle. However, the strength of this relationship, the relative contribution of each hormone, and the associated time delay are highly variable between women. This individual variability is consistent with the variability in menstrual cycle characteristics among women.

Relationship between the appearance of preantral follicles in the fetal ovary of Antarctic minke whales (Balaenoptera bonaerensis) and hormone concentrations in the fetal heart, umbilical cord and maternal blood.

The present study aimed to determine the relationship among changes in the number of preantral follicles and concentrations of follicle-stimulating hormone (FSH), luteinizing hormone (LH), progesterone (P4), androstenedione (A) and estradiol-17beta (E2) in the fetal heart, umbilical cord and maternal blood. Primordial follicles had already appeared in a 20 cm fetus and primary follicles were observed in a 50 cm fetus. In a 70 cm fetus, the number of primordial and primary follicles increased rapidly and secondary follicles were present. The concentrations of LH and FSH did not change between 20 cm and 160 cm in fetal length. When the fetal length became > 70 cm, serum levels in the fetus, umbilical cord and mothers, and E2 levels in umbilical cord increased synchronously (p < 0.05). These results showed increases in the number of preantral follicles in the Antarctic minke whale fetal ovary along with fetal growth during the early gestation period. These findings suggest that the change in preantral follicles was associated with changes in the concentration of steroids in early gestation periods. The changes in steroid concentrations in the fetal and umbilical cord blood and the increased number of preantral follicles were coincident at around 70 cm in fetal length, whereas the growth and differentiation of primordial and primary follicles appeared to be independent of FSH and LH.

Endometrial mRNA expression of oestrogen receptor α, progesterone receptor and insulin-like growth factor-I (IGF-I) throughout the bovine oestrous cycle

This study characterized endometrial expression of mRNAs of oestrogen and progesterone receptors (ER, PR) and insulin-like growth factor-I (IGF-I) during the oestrous cycle. Seven Holstein heifers that showed standing oestrus on the same day (day 0) were selected and blood samples for oestradiol (E2) and progesterone (P4) determinations by RIA were taken daily until day 23. Endometrial samples were taken by transcervical biopsies on days 0, 5, 12 and 19 for mRNA determination by solution hybridization. The highest endometrial mRNA levels of ERα and PR were observed at oestrus and a decline was observed already at day 5, which then decreased progressively at the end of the luteal phase. IGF-I mRNA levels were higher at day 0 and 5 than at day 12. At day 19, mRNA levels of ERα, PR and IGF-I were the lowest in heifers that were at the end of their luteal phase ( n=4), but were high again in heifers which P4 levels were basal ( n=3). The temporal changes in mRNA endometrial expression of ERα, PR and IGF-I and their relation to the changes in steroid concentrations during the bovine oestrus cycle are described.

Disruption of male sex hormones with regard to pesticides: pathophysiological and regulatory aspects

Several pesticides used as herbicides, insecticides and fungicides are known to be endocrine disrupting chemicals (EDCs). In three pair-matched studies we found changes in sex hormone concentrations and T-lymphocytes in relation to acute and chronic pesticide exposure. After acute exposure, 1 day later the concentrations of testosterone and especially estradiol decreased. T4- and T8-lymphocytes slightly increased. Effects of chronic occupational pesticide exposure were expressed by a higher level of testosterone and a larger ratio of T4-/T8-lymphocytes in comparison to control persons. Concentrations of LH in exposed men were higher after exposure than before. We assume an inhibition of the aromatase system by testosterone metabolites. The studies show two effects with regard to the duration of exposure: a hormonal and immune suppression after acute exposure and an activation of both systems following chronic exposure.

Direct non-genomic effects of follicular steroids on maturing human oocytes: oestrogen versus androgen antagonism.

Previously published data have suggested that oestradiol exerts direct beneficial effects on human oocytes during in-vitro maturation and that these effects are at least partly due to a non-genomic action of the steroid at the oocyte surface. Here we provide evidence showing that a non-genomic effect of oestradiol is counteracted by androstenedione. In contrast to these results from in-vitro experiments, in which changes in steroid concentrations are abrupt and the non-genomic responses are rapid, the progressively changing follicular steroid concentrations which occur during in-vivo development may rather have permissive or restrictive effects on the events of spontaneous oocyte cytoplasmic maturation. The oocyte is particularly sensitive at the germinal vesicle stage of development to non-genomic steroid actions. Ovarian stimulation protocols should thus be adjusted so as to avoid androgen predominance at the mid-follicular phase. In patients in whom this condition cannot be met, in-vitro maturation of oocytes may be a solution.

Regulation of vascular adaptation during pregnancy and post-partum: effects of nitric oxide inhibition and steroid hormones.

Treatment of pregnant rats with the nitric oxide synthase inhibitor NG-nitro-L-arginine methyl ester (L-NAME), has been shown to produce symptoms similar to pre-eclampsia (i.e. elevated blood pressure, proteinuria and fetal growth retardation). After L-NAME infusion is initiated on day 17 or 18 of gestation, the blood pressure proceeds in a biphasic pattern (immediate rise, followed by a decline, then increasing again in the post-partum period). The blood pressure actually begins to rise prior to delivery on days 21-22, i.e. after progesterone withdrawal occurs, suggesting that these responses may be regulated by changes in steroid hormone concentrations during pregnancy. Therefore, we evaluated the effects of the different steroid hormones: progestins (progesterone, promegestone, levonorgestrel), antiprogestins (mifepristone), 17 beta-oestradiol or androgens (testosterone, dihydrotestosterone) on systolic blood pressure in pregnant, non-pregnant female and normal male rats with and without L-NAME treatment and spontaneously hypertensive male rats. The animals received continuous infusions of L-NAME (150 mg/kg/day) or vehicle through osmotic mini-pumps and daily s.c. injections of steroid hormones. In pregnant rats the pump was inserted on day 17 or 18 of gestation and steroid hormone injections were started on the first day following delivery at term and continued daily until post-partum day 10. In non-pregnant female or male rats steroid hormone injections were initiated 5 days after the L-NAME pump was inserted. Systolic blood pressure was measured daily from the tail with a pneumatic tail-cuff device. R5020 (1.5 mg/kg/day) significantly attenuated the blood pressure elevation induced by L-NAME during the post-partum period. Similarly, it lowered blood pressure in L-NAME treated non-pregnant female rats or male rats. R5020 also lowered blood pressure in spontaneously hypertensive male rats. Progesterone (6 mg/kg/day) had similar effects on blood pressure in the post-partum period, although it also lowered the blood pressure in control animals. Interestingly, administration of two different doses of levonorgestrel (0.3 and 1.5 mg/kg/day) did not decrease the blood pressure in either L-NAME-infused rats or controls. Mifepristone (RU486, 30 mg/kg/day) further increased blood pressure in L-NAME-treated rats post-partum. 17 beta-oestradiol (30 micrograms/kg/day) had no effect on blood pressure in either L-NAME infused rats in the post-partum period or controls, whereas both testosterone (0.3 mg/kg/day) and dihydrotestosterone (0.3 mg/kg/day) significantly attenuated the blood pressure increase after L-NAME, while raising the blood pressure in vehicle-infused animals. These results suggest that the control of systemic blood pressure during pregnancy may be modulated by steroid hormones. Progesterone may be the steroid hormone with the major action on vascular tension during pregnancy.

Normal human follicle development: an evaluation of correlations with oestradiol, androstenedione and progesterone levels in individual follicles.

The mechanism of dominant follicle selection remains obscure. We have investigated the association between follicle diameter and follicular steroid levels in individual human ovarian follicles throughout the menstrual cycle. Fluid from ovarian follicles (n = 326) was obtained in vivo during surgery from 55 regularly cycling women with proven fertility. Follicles were divided into dominant (diameter >9 mm, n = 45) and non-dominant (diameter < or = 9 mm, n = 281) based on ultrasound measurements. Fluid was assayed for oestradiol (E2), androstenedione (AD), and progesterone (P). Median P and E2 levels were significantly lower (P < 0.0001) and AD levels significantly higher (P = 0.03) in non-dominant as compared to dominant follicles. In non-dominant follicles AD (r = 0.14, P = 0.02), but not P and E2, levels were correlated to follicular diameter, and significant changes in steroid concentrations across the menstrual cycle were absent. In dominant follicles, diameter was positively correlated with P and E2 (P < 0.001) levels, and inversely correlated with AD concentrations (P = 0.01). Results indicate that (1) intrafollicular oestradiol concentrations rise only in follicles exceeding 9 mm in diameter and correlate with the diameter of these dominant follicles, suggesting that significant increase in aromatase enzyme activity occurs only in the dominant follicle (2) a cycle-independent accumulation of androstenedione with size occurs in non-dominant follicles, and (3) progesterone production occurs in the largest dominant follicles only, suggesting a limited, if any, role for progesterone during follicle development.

The effects of altered suckling intensity, boar exposure in lactation and gonadotropins on endocrine changes, fertility and the incidence of lactational oestrus in multiparous sows

AbstractOne of the more promising techniques for the improvement of sow productivity has been the use of partial weaning or the separation of the sow and litter for periods of between 3 to 12 h/day towards the end of lactation. The purpose of the present study was to examine changes in steroid hormone concentrations, oestrus and fertility responses in lactating sows subjected to altered sucking, boar exposure and gonadotropins in mid lactation and at weaning. Thirty-two crossbred sows were allocated at random to one of four experimental treatments. Treatment 1 sows (no. = 8) were separated from their respective litters for 3 h/day from 12 days post partum through until weaning which was carried out at 21 days post partum. Treatment 1 sows were also given in-pen boar exposure for 1 h/day between day 12 post partum and weaning. Treatment 2 sows (no. = 8) were given the same protocol of litter separation (LS) and boar exposure (BE) as in treatment 1 and they were also given a combination of gonadotropins (Gn) on day 17 of lactation. Treatment 3 sows (no. = 8) were given LS + BE as above and the sows were injected with Gn on the day of weaning. Treatment 4 sows were controls given no LS, BE or Gn (no. = 8). During lactation, treatment 1 sows exhibited significantly (P &lt; 0·05) reduced progesterone concentrations compared with treatment 2 sows. There were no other significant effects of treatment for any of the periods considered. The separation of sows from their piglets with or without gonadotropic treatment did not result in lactational oestrus in any treated sows. No significant treatment differences were found in the subsequent litter size (piglets born alive or total number of piglets). In conclusion, the present results have demonstrated no significant effects of LS, BE and Gn treatment during lactation on sow and litter performance. This was associated with low levels of peripheral plasma progesterone in all lactating sows.

The influence of food intake and allyl trenbolone administration during lactation on plasma steroid concentrations and the reproductive performance of multiparous sows

AbstractAn experiment was made to examine the effects of food intake and an orally active progestagen on plasma steroid concentrations and subsequent reproductive performance of multiparous sows. Thirty-five multiparous Landrace × Large White sows were assigned to one of four treatments immediately after parturition. Treatment H-AT sows were offered a high level of food intake throughout lactation: 3·5 kg of a diet containing 160 g/kg dry matter (DM) of crude protein and 13 MJ digestible energy per kg DM given twice daily. Treatment H+AT sows were offered the same food intake as H-AT sows and in addition they were given 20 mglday of allyl trenbolone (AT) mixed with the morning feed. Treatment L-AT sows were given 1·5 kg of the same diet offered twice daily during lactation and treatment L+AT sows were also offered this lower level of food intake and given AT. The respective levels of food intake were offered to sows from the 1st day of lactation onwards until weaning at 21 days post partum. Litter weights at weaning were influenced significantly by feeding level (P&lt; 0·001) and also by AT administration (P&lt;0·05). Sows on the high level of feeding had the heaviest litters and food-restricted sows had the lightest litters. AT treatment depressed litter weight at weaning. There was no effect of food level or AT on the plasma concentrations of progesterone or oestrogens during lactation. There was a highly significant (P&lt;0·001) difference in mean plasma oestrogen concentration between high (H-AT and H+AT) and low (L-AT and L+AT) fed groups during early pregnancy in the subsequent cycle. Sows given a combination of high energy in lactation and AT (H+AT) exhibited shorter intervals from weaning to oestrus than both groups of food-restricted (L-AT and L+AT) sows fP&lt;0·01) but treatment had no significant effect on either the farrowing rate or on the subsequent litter size. It is concluded that despite significant changes in the live weight and condition of sows and changes in steroid hormone concentrations due to food intake and the administration of allyl trenbolone, there were no significant effects on reproductive performance.

Anthropometric-hormonal correlation patterns in fertile and post-menopausal women from Austria.

Correlations between sex-hormone levels and body dimensions were investigated in a group of women from Vienna. Since sex-hormone concentrations in women are subject to dramatic changes with increasing age, both 124 fertile and 142 postmenopausal women were examined. Twenty-nine anthropometric traits were correlated with oestradiol, the gonadotrophins luteinizing hormone (LH) and follicle-stimulating hormone (FSH), the gestagens progesterone, 17-hydroxyprogesterone and prolactin, and the androgens testosterone, androstenedione and DHEA-S, as well as with the transport protein, sex-hormone binding globulin. It was also found that oestradiol concentration was related to levels of gonadotrophins, prolactin, progesterone and androgens and was equally correlated with metric traits. Statistically significant correlations could be observed between all sex-hormone concentrations and the 29 anthropometric traits. The most striking result is the change in direction of correlations between metric traits and oestrogen, gonadotrophin, prolactin and gestagen levels between both proband groups, which is probably due to changes in sex-hormone concentrations in women after menopause. The direction of correlations with androgens remained the same. In post-menopausal women the great impact of fat tissue for sufficient synthesis of oestrogen is shown by a positive correlation between oestradiol and circumference measures.

Ovarian follicular changes after weaning in sows.

Three experiments investigated ovarian follicular development in sows whose litters were weaned at 28 to 31 d of lactation. Unilateral ovariectomy near the time of weaning was used to assess early follicular characteristics and to identify those sows that would not return to estrus within 10 d after weaning. This allowed segregation of and exclusion from the study those sows that had a prolonged interval from weaning to first estrus. In Exp. 1, 82 and 72% of the large follicles that were marked at 48 or 72 h after weaning (10 sows per time point) were subsequently identified as corpora lutea. In Exp. 2, sows (seven to nine per time point) were unilaterally ovariectomized at 0, 6, 12, 18, 24, or 48 h after weaning, and follicular fluid was evaluated for changes in steroid concentrations. Progesterone concentrations in fluid from medium-sized (4 to 6 mm) follicles increased by 6 h after weaning and then declined through 24 h concomitant with increases in testosterone and estradiol. For Exp. 3, follicular fluid and granulosa cells from individual follicles were obtained from sows (seven to nine per time point) at 0, 6, and 24 h after weaning. In follicular fluid, insulin-like growth factor I (IGF-I) concentrations were not correlated (P greater than .05) with concentrations of progesterone, testosterone, or estradiol, or with granulosa cell production of estradiol during culture in androstenedione-supplemented medium.(ABSTRACT TRUNCATED AT 250 WORDS)

Evidence for Changes in Adrenal and Testicular Steroids During HIV Infection

The serum levels of cortisol, progesterone, 17 alpha-hydroxyprogesterone, dehydroepiandrosterone (DHEA), DHEA sulfate, androstenedione (delta 4), testosterone (T), estrone, and estradiol of HIV+ men and HIV- men were determined by radioimmunoassay. The cortisol, 17 alpha-hydroxyprogesterone, and estrone levels of all HIV+ subjects were 35-55% (p less than 0.01), 25-90% (p less than 0.01), and 30-50% (p less than 0.01) higher, respectively, than those of controls. Androgen levels were very high in Centers for Disease Control (CDC) groups II and III of HIV infection (DHEA, 85%, p less than 0.01; delta 4, 60%, p less than 0.01; T, 30%, p less than 0.05), but much lower in group IVC1 and IVC2. The estradiol levels were significantly elevated only in group IVD (50%, p less than 0.01) and group IVC2 (25%, NS). These results indicate that serum hormone levels are correlated with HIV infection group. The changes in steroid hormone concentrations during the development of HIV infection may have important implications for the immune response of patients. The high cortisol and estrone levels of all groups, the elevated androgen levels in asymptomatic groups, and the low androgens in AIDS patients may form part of the complex network of immunomodulatory factors.

Long-term administration of gonadotropin-releasing hormone agonist and dexamethasone: assessment of the adrenal role in ovarian dysfunction

To examine the possible impact of abnormal adrenal steroidogenesis on the ovarian dysfunction seen in polycystic ovarian disease (PCOD). Prospective analysis of blood sampling monthly for 6 months, then three times weekly for 90 days. Tertiary institutional outpatient care. Six anovulatory women with a diagnosis of PCOD. Six-month suppression with gonadotropin-releasing hormone agonist (GnRH-a) followed by suppression with dexamethasone (DEX) for 90 days. Serum levels of testosterone (T), androstenedione (A), dehydroepiandrosterone (DHEA), dehydroepiandrosterone sulfate (DHEAS), cortisol, estradiol (E2), progesterone (P), follicle-stimulating hormone (FSH), luteinizing hormone (LH) and bioactive LH. Gonadotropin-releasing hormone agonist administration suppressed greater than 60% of the circulating levels of T and A, suggesting an ovarian origin. Minimal changes of DHEA, DHEAS, and cortisol were seen. With the addition of DEX, there was greater than 90% suppression of the total circulating A, T, DHEA, DHEAS, and cortisol, supporting the adrenal origin of the non-GnRH-a suppressible androgens. Excessive ovarian T and A secretion returned during the 90-day recovery study period in spite of rises of FSH concentrations that changed the ratio of FSH to LH in all subjects. Four of the six women failed to ovulate. In comparison of the women who did and did not ovulate during recovery, no differences in absolute levels or changes in concentrations of steroids or gonadotropins could be detected. Using sequential and simultaneous administration of GnRH-a and DEX, we were able to delineate the contributions of the ovaries and adrenals to the abnormal steroidogenesis seen in PCOD. Despite prolonged suppression of ovarian and then adrenal steroidogenesis, ovarian dysfunction, evidenced by abnormal androgen production, returned with cessation of agonist administration.

Sex hormones in postmenopausal women with primary biliary cirrhosis

To evaluate serum sex hormone profiles in nonalcoholic postmenopausal women with liver disease, 25 women with primary biliary cirrhosis (11 in cirrhotic stage) and 46 healthy controls were studied. The patients had significantly (p <0.05) elevated serum concentrations of estrone and androstenedione and significantly (p <0.05) lower concentrations of estrone sulfate, dehydroepiandrosterone sulfate and 5α-dihydrotestosterone compared with the 46 controls. Serum concentrations of sex hormone binding globulin, testosterone, non-sex hormone binding globulin-bound testosterone and non-protein-bound testosterone did not differ significantly (p> 0.05) between primary biliary cirrhosis patients and controls. Patients in the cirrhotic stage had significantly (p < 0.05) higher concentrations of sex hormone binding globulin than did controls. Patients in the cirrhotic stage had significantly (p < 0.05) higher sex hormone binding globulin and estrone sulfate levels compared with noncirrhotic patients with primary biliary cirrhosis. Otherwise, no significant differences were observed between cirrhotic and noncirrhotic patients. The observed changes in steroid concentrations may be a consequence of hepatic dysfunction. (HEPATOLOGY 1991;13:865–869.)

Sex hormones in postmenopausal women with primary biliary cirrhosis

To evaluate serum sex hormone profiles in nonalcoholic postmenopausal women with liver disease, 25 women with primary biliary cirrhosis (11 in cirrhotic stage) and 46 healthy controls were studied. The patients had significantly (p less than 0.05) elevated serum concentrations of estrone and androstenedione and significantly (p less than 0.05) lower concentrations of estrone sulfate, dehydroepiandrosterone sulfate and 5 alpha-dihydrotestosterone compared with the 46 controls. Serum concentrations of sex hormone binding globulin, testosterone, non-sex hormone binding globulin-bound testosterone and non-protein-bound testosterone did not differ significantly (p greater than 0.05) between primary biliary cirrhosis patients and controls. Patients in the cirrhotic stage had significantly (p less than 0.05) higher concentrations of sex hormone binding globulin than did controls. Patients in the cirrhotic stage had significantly (p less than 0.05) higher sex hormone binding globulin and estrone sulfate levels compared with noncirrhotic patients with primary biliary cirrhosis. Otherwise, no significant differences were observed between cirrhotic and noncirrhotic patients. The observed changes in steroid concentrations may be a consequence of hepatic dysfunction.

Functional properties of developing rat Leydig cells after treatment with ethylene dimethanesulphonate (EDS)

The development of a new population of Leydig cells after specific elimination of existing Leydig cells in mature rats by ethylene dimethanesulphonate (EDS) was characterized by investigating the testicular activities of 5 alpha-reductase and non-specific esterase, the serum concentrations of 3 alpha-androstanediol and testosterone and the Leydig cell morphology. Plasma concentrations of both androgens were strongly reduced up to 15 days after administration of EDS. Thereafter, in contrast to the gradual and continuous increase of serum testosterone values, the changes in serum 3 alpha-androstanediol were transient, with the highest level on Day 35. The temporal pattern of testicular 5 alpha-reductase activity was almost similar to that of serum 3 alpha-androstanediol. The testicular esterase activity increased gradually from Day 25 until Day 76. The temporal changes in steroid concentrations and enzyme activities after EDS administration indicate that the development of the Leydig cells in EDS-treated rats occurs in a fashion similar to that in pubertal rats. However, the numerous lipid droplets and large nuclei in these Leydig cells indicate that these cells may also be classified as fetal cells. It is concluded that, after treatment with EDS, fetal and pubertal characteristics are present in Leydig cells. It is, however, unknown whether both characteristics are present in one or in two distinct cell populations.

Changes in steroid concentrations during sexual ontogenesis in tilapia

Testosterone, estradiol and 11-ketotestosterone were determined by radioimmunoassay in whole body extracts of tilapia at various stages of ontogenesis: before, during and after sexual differentiation. The study was conducted on Tilapia nilotica (= Oreochromis niloticus), T. mossambica (= O. mossambicus) and T. hornorum in a series of intraspecific and interspecific spawn combinations. The concentrations of testosterone and estradiol measured in homogenates prepared from groups of individuals just after fertilization were relatively high (c. 1 ng/individual) and declined to undetectable levels in 3–4-week-old fry. In older fry (4–6 weeks), the concentrations of both steroids started to increase; however, the testosterone increase was tenfold that of estradiol. In 6–8-week-old fry measured individually, the testosterone concentrations in intraspecific spawns showed a clear tendency toward two peaks of distribution. This bimodality in testosterone concentrations probably reflects the presence of males and females with different testosterone contents in the population. In interspecific crosses characterized by 100% male progeny, the distribution pattern of testosterone was unimodal, which would be expected in a monoxexual population. Estradiol and 11-ketotestosterone concentrations in the young differentiated fry at this age were low in all cases. It is suggested, therefore, that, of the steroids examined in tilapia at the age of 6–8 weeks, only testosterone reflects the processes of sex differentiation.

Seasonal changes of steroid concentrations in seminal plasma of a European wild boar.

The influence of season on testicular steroid production as a parameter of testicular function has been studied in a wild boar. Semen was collected once weekly while it served the dummy. In seminal plasma concentrations of the following steroids were determined by radioimmunoassay: unconjugated testosterone, conjugated testosterone, unconjugated total oestrogens, conjugated total oestrogens and 5 alpha-androst-16-en-3-one ('boar-taint steroid'). All steroids showed a clear seasonal pattern with highest concentrations in autumn and early winter and low levels from January to July. Maxima during the rutting season were 10-25 times greater than average values out of season. During a 2-month-period (mid-July until mid-September) libido was abolished and the wild boar refused to mount the dummy. These results indicate that the seasonal variation in testicular steroid production by the wild boar, regulated by photoperiod, are similar to those of the domestic boar.

Direct effect of the luteinizing hormone releasing hormone analog D-Trp 6-Pro 9-Net-LHRH on rat testicular steroidogenesis

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