High seasonal variation of plasma testosterone levels for a tropical grassland bird resembles patterns of temperate birds

Author(s):  
Leonardo Esteves Lopes ◽  
João Paulo Gusmão Teixeira ◽  
Ricardo Camargos Meireles ◽  
Daniel Silva Sena Bastos ◽  
Leandro Licursi de Oliveira ◽  
...  
1979 ◽  
Vol 27 (6) ◽  
pp. 939 ◽  
Author(s):  
PC Catling

Eastern Highlands and Central Australian dingoes housed in Canberra do not have a testicular cycle. They are spermatogenically active and capable of mating with oestrous females and fathering young all year. They do exhibit a breeding season (April-June) but this is entirely governed by the female. During the breeding season testosterone levels rise; this is thought to be influenced by the presence of an oestrous female and copulation. There are indications that captive dingoes in Central Australia may have a testicular cycle. Colony dingoes showed little interest in and do not mate with an oestrous domestic female at times other than January-July. They also become almost aspermous outside the breeding season. In contrast, Central Australian dingoes housed in Canberra are spermatogenically active and capable of successful matings all year.


2013 ◽  
Vol 12 (48) ◽  
pp. 6785-6790
Author(s):  
Amrane A. Ait ◽  
S. M. Hammoudi ◽  
B. T. Belhamiti ◽  
S. M. A. Selles ◽  
A. R. Benia ◽  
...  

1973 ◽  
Vol 51 (6) ◽  
pp. 651-658 ◽  
Author(s):  
P. E. Whitehead ◽  
E. H. McEwan

Plasma testosterone levels of reindeer increased from 1 ng/cm3 in August to 30–60 ng/cm3 in mid-September. By late October, when rutting activity had almost ceased, the testosterone concentration had declined to barely detectable levels. The seasonal pattern exhibited by caribou was similar except the peak levels associated with rutting occurred about 1 month later than reindeer. The seasonal changes in plasma testosterone levels of two hybrid calves were studied. Peak testosterone levels of 5 and 3.8 ng/cm3 were attained in late October.The influence of the endocrine glands on antler renewal and casting, and the rhythmic growth pattern exhibited by caribou and reindeer are discussed.


1971 ◽  
Vol 68 (3) ◽  
pp. 576-584 ◽  
Author(s):  
K. O. Nilsson ◽  
B. Hökfelt

ABSTRACT Metyrapone was administered either orally, 750 mg every four h, in a total of six doses, or intravenously 30 mg per kg body weight as a four h infusion. In three males with normal endocrine functions, metyrapone given orally or intravenously induced a fall in plasma testosterone and an elevation of androstenedione within 2–8 h. When metyrapone was administered to a patient given dexamethasone to suppress endogenous ACTH production, the androstenedione levels did not alter whereas the testosterone levels showed a slight, transient decrease. In two normal females metyrapone administration was followed by a marked increase in plasma androstenedione whereas testosterone showed only a minor, gradual increase. In one male patient with Addison's disease the basal plasma testosterone was normal whereas the level of androstenedione was low. Following metyrapone intravenously, there was a slight suppression of plasma testosterone but no change in the androstenedione concentration. In one patient with primary hypogonadism, two with secondary hypogonadism and two with Klinefelter's syndrome the plasma testosterone was low under basal conditions and did not change following metyrapone. Basal plasma androstenedione was within the range for normal males and increased markedly following metyrapone in all the cases.


1981 ◽  
Vol 96 (2) ◽  
pp. 273-280 ◽  
Author(s):  
Mridula Chowdhury ◽  
Robert Tcholakian ◽  
Emil Steinberger

Abstract. It has been suggested that treatment of intact male rats with oestradiol benzoate (OeB) causes an interference with testosterone (T) production by the testes by a direct inhibitory effect on steroidogenesis. To test this hypothesis, different doses (5, 10 or 25 IU) of hCG were administered concomitantly with 50 μg of OeB to adult intact or hypophysectomized male rats. The testicular and plasma testosterone, and serum hCG levels were determined. The sex accessory weights were recorded. In the intact OeB-treated group of animals, hCG stimulated both the secondary sex organs and plasma testosterone levels above the intact control group. However, in hypophysectomized animals, although plasma testosterone levels increased above that of intact controls, their secondary sex organ weights did not. Moreover, inspite of high circulating hCG levels, the testicular testosterone content and concentration remained suppressed in OeB-treated animals. The reason for such dichotomy of hCG action on OeB-treated animals is not clear at present.


2005 ◽  
Vol 12 (2) ◽  
pp. 135-141 ◽  
Author(s):  
Ilma Simoni Brum ◽  
Poli Mara Spritzer ◽  
Franyoise Paris ◽  
Maria Augusta Maturana ◽  
Franyoise Audran ◽  
...  

1991 ◽  
Vol 124 (4) ◽  
pp. 399-404 ◽  
Author(s):  
Wieland Kiess ◽  
Linda L. Liu ◽  
Nicholas R. Hall

Abstract. Sex-related differences in immune responsiveness are mediated at least in part by sex steroid hormones. Lymphocyte subset distribution in peripheral blood and natural killer cell function both have been reported to be under hormonal control. In order to gain more insight into sex steroid hormone action on the immune system, we have measured the lymphocyte subset distribution and natural killer cell activity in 18 men with idiopathic hypogonadotropic hypogonadism before treatment, and after hormonal treatment had normalized plasma testosterone levels. In untreated patients, the mean plasma testosterone concentrations were significantly lower than those in the treated men (3.0 ± 0.5 nmol/l vs 16 ± 1.7 nmol/l, p < 0.001). The percentage of peripheral CD3+ lymphocytes, CD8+ cells, the CD4+/CD8+ ratio, and the natural killer cell activity of peripheral mononuclear cells measured in a 51Cr release assay against target K 562 cells did not differ between patients with idiopathic hypogonadotropic hypogonadism and healthy adults, and most importantly, did not change during hormonal treatment which normalized plasma testosterone levels in the patients. In contrast, the percentage of peripheral CD4+ cells was significantly higher in untreated patients compared with normal adult subjects or patients with idiopathic hypogonadotropic hypogonadism after hormonal treatment that resulted in normal plasma testosterone levels (53 ± 2 vs 47 ± 2, p < 0.05). It should be noted that the percentage of peripheral CD 16+ cells was significantly lower in untreated men with low plasma testosterone levels than in normal controls. The percentage of CD16+ cells in peripheral venous blood rose significantly after hormonal treatment restored plasma testosterone levels to normal (6 ± 1 vs 11 ± 1, p < 0.001). In addition, the percentage of peripheral CD16+ cells correlated significantly with the plasma testosterone levels measured in men with idiopathic hypogonadotropic hypogonadism (r = 0.534, p < 0.001). In conclusion, both the percentage of peripheral CD4+ cells (T-helper lymphocytes) and peripheral CD16+ cells (non-T-non-B cells) are related to the plasma testosterone levels in men with idiopathic hypogonadotropic hypogonadism. These data suggest that in vivo human immune cells are under the regulatory influence of endogenous sex steroids.


1991 ◽  
Vol 6 (1-2) ◽  
pp. 185-191 ◽  
Author(s):  
P.S.P. Gupta ◽  
P.C. Sanwal ◽  
V.P. Varshney

Oecologia ◽  
2021 ◽  
Author(s):  
Martin Těšický ◽  
Tereza Krajzingrová ◽  
Jiří Eliáš ◽  
Hana Velová ◽  
Jana Svobodová ◽  
...  

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