Mean Plasma Concentrations Of Testosterone Research Articles

Growth and reproductive development of red deer calves (Cervus elaphus) born out-of-season

AbstractSince the productivity of farmed red deer is constrained by their inherent seasonal biology, the potential advantages of breeding out-of-season following melatonin administration were investigated. Calves born in February (F; no. = 8) were heavier at weaning in September of the same year than calves born with normal birth dates in June (}; no. = 8) (73·2 v. 441 (s.e.d. 3·59) kg; P < 0·001) and at the end of April of the next year (88·0 v. 67·6 (s.e.d. 6·44) kg; P < 0·02) although their suckled live-weight gain to 100 days of age was lower (304 v. 361 (s.e.d. 21·4) g/day; P < 0·05). After weaning, F calves had higher voluntary food intake than / calves (g dry matter per head per day) from September to November (1643 v. 2224 (s.e.d. 92·6); P < 0·002), November to February (1435 v. 926 (s.e.d. 67·9); P < 0·002), and February to April (1487 v. 2059 (s.e.d. 115·5); P < 0·02).Unlike J calves, F calves showed puberty in their first autumn. F male calves (no. = 3) grew antlers which hardened in November, whereas J males (no. = 3) did not, and F males, aged 8 months, had significantly higher mean plasma concentrations of testosterone than J males, aged 4 months (1·35 v. 0·28 (s.e.d. 0·154) fj.g/1, P < 0·001). Oestrous cyclicity was observed in 3/5 group F females, aged 9 months, but in 0/5 group ] females, aged 5 months. Although the dams of F and ] calves had similar live weights at mating, birth and 100 days pos t partum, F dams were heavier (P < 0·05) at weaning. Following parturition, F dams had a mean voluntary food intake of 2700 (s.e. 110) g dry matter per head per day from February to April.

Reproductive cycles of male and female tuatara (Sphenodon punctatus) on Stephens Island, New Zealand

Cycles in gonadal activity and plasma sex steroid concentrations were investigated in wild female and male tuatara on Stephens Island, New Zealand. Females nest once every four years on average. Vitellogenesis is spread over the first three years, and mating, ovulation and nesting occur in the fourth. Oviducal eggs are carried for6–8 months before nesting. Although the length of this ovarian cycle is unparalleled among oviparous reptiles, the associated cycles in plasma concentrations of sex steroids are similar to those in other reptiles. Mean plasma concentrations of oestradiol increase during vitellogenesis, peak at mating, fall rapidly before or around ovulation, are low during most of gravidity, and rise slightly during late gravidity‐nesting. Plasma concentrations of testosterone show a similarcycle. Mean plasma concentrations of progesterone are low during vitellogenesis and peak around ovulation. This periovulatory surge falls within1–2 months, and mean concentrations are low during the final 5–6 months of gravidity. Male tuatara show an annual, pre‐nuptial reproductive cycle. Mean plasma concentrations of testosterone are low during winter, rise during spring, peak during midsummer‐early autumn, when pre‐nuptial displays and mating occur, and fall in mid autumn. Limited histological data indicate that spermiogenesis occurs during midsummer‐early autumn, and also support a previous study suggesting that there may be no period of complete testicular and epididymal regression. In comparison with the pre‐nuptial cycles of other temperate‐zone reptiles, the cycle in male tuatara shows a more prolonged duration of testicular activity and of rising or elevated plasma testosterone concentrations. The prolonged reproductive cycles of male and female tuatara may be adaptations to a temperate environment with cool summers and cool, but not freezing, winters.

PLASMA CONCENTRATIONS OF TESTOSTERONE, ANDROSTENEDIONE, DIHYDROTESTOSTERONE, 5α-ANDROSTANE-3α, 17β-DIOL, 5α-ANDROSTANE-3β, 17β-DIOL, AND ANDROSTERONE IN BULL CALVES: RESPONSE TO hCG

Plasma androgen concentrations were measured in bull calves sampled weekly from birth to 30 wk of age and in calves sampled every 30 min for 8 h at 6, 14, 22 and 30 wk of age, before and after administration of hCG (5 IU kg−1, i.v.). Mean plasma concentrations of testosterone rose to 20 wk of age and then fell, but were variable. Mean plasma concentrations of androstenedione rose to 14 wk of age and then declined. Mean plasma concentrations of 5α-androstane-3α, 17β-diol and 5α-androstane-3β,17β-diol did not change with age, but dihydrotestosterone and androsterone were elevated at 14 and 22 wk of age, respectively. The overall means were 0.9 ± 0.08 ng mL−1 for testosterone, and 0.6 ± 0.07 ng mL−1 for dihydrotestosterone. Other androgens were present at concentrations of < 0.3 ng mL−1. However, the total concentration of the 5α-reduced androgens exceeded that of testosterone in bull calves from birth to 28 wk of age. Changes in mean androgen concentration with age and in response to hCG appeared to be reflected primarily in changes in the amplitude of pulses in plasma androgen concentration. Significant increases in pulse amplitude for testosterone and androstenedione occurred in response to hCG in 14-, 22- and 30-wk-old bull calves and for 5α-androstane-3α,17β-diol in 30-wk-old calves. The developing bull calf differs from laboratory rodents in that there is no period of time during reproductive development when individual 5α-reduced androgens circulate in concentrations greater than testosterone. Key words: Bull calf, sexual maturation, androgens

Annual variations in plasma levels of testosterone and luteininzing hormone in the laboratory male mongrel dog.

Blood samples, drawn every 15 days (September 1975-September 1976) from four laboratory-housed male mongrel dogs, were assayed by radioimmunoassay for levels of testosterone and LH in the plasma. The mean plasma concentrations of testosterone remained relatively constant for most of the year with the exception of a significant rise in late August and early September. Mean plasma levels of LH showed a cyclic pattern throughout the year which could be represented by a cosine function curve. However, this cyclic pattern of LH was not accompanied by cyclic changes in plasma levels of testosterone and there was no relationship between these two hormones during the period of 1 year. As the cyclic pattern of LH was altered, the plasma level of testosterone began to rise and reached its highest concentration. Since this alteration of the LH cycle occurred before the increased concentrations of testosterone, and since there was no relationship between these two hormones for the period of a year, we have concluded that there may be another hormone(s) involved which either alters the sensitivity of the canine testis to LH or alters the Lh synthesis/release mechanism of the pituitary gland.

Endocrine Studies in a Phenotypic Girl with XY Gonadal Agenesis

An 18-year-old phenotypic girl with XY gonadal agenesis had endocrine studies. The patient had a small amount of sexual hair, a slightly enlarged clitoris, normal labia and no posterior fusion. Her vagina was of normal length, but no cervix was palpable. At laparoscopy, no gonads, uterus or fallopian tubes were identified. The buccal smear was chromatin negative and the karyotype was 46XY. The 24 h LH plasma pattern was qualitatively similar to that found in normal late pubertal subjects, but the values were in the castrate range. The 24h mean plasma concentrations of testosterone and dihydrotestosterone were 16.4 ng/dl and 14.2 ng/dl, respectively. Urinary estrogen excretion was 15 and 19 mug/day. These clinical and endocrine findings suggest that the patient was a genetic male in whom Mullerian regression occurred normally; however, the testes probably ceased functioning early in gestation preventing normal development of the Wolffian system. This set of events resulted in agenesis of the gonaductal system and female external genitalia. The patient represents the second example of this variation of male pseudohermaphroditism associated with XY gonadal agenesis.