Acute changes in plasma testosterone levels and their relation to measures of sexual behaviour in the male house mouse (Mus musculus)

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.

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Effects of oestradiol benzoate (OeB) and human chorionic gonadotrophin (hCG) on the testes and accessory sex glands of the rat

Acta Endocrinologica ◽

10.1530/acta.0.0960273 ◽

1981 ◽

Vol 96 (2) ◽

pp. 273-280 ◽

Cited By ~ 1

Author(s):

Mridula Chowdhury ◽

Robert Tcholakian ◽

Emil Steinberger

Keyword(s):

Treated Group ◽

Inhibitory Effect ◽

Male Rats ◽

Plasma Testosterone ◽

Control Group ◽

Intact Male ◽

Intact Control ◽

Testosterone Levels ◽

Oestradiol Benzoate ◽

Direct Inhibitory Effect

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.

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Early Cold Exposure: Effects on Behavioral and Physiological Thermoregulation in the House Mouse, Mus musculus

Physiological Zoology ◽

10.1086/physzool.49.2.30152539 ◽

1976 ◽

Vol 49 (2) ◽

pp. 191-199 ◽

Cited By ~ 15

Author(s):

G. Robert Lynch ◽

Carol Becker Lynch ◽

Marjory Dube ◽

Cynthia Allen

Keyword(s):

House Mouse ◽

Cold Exposure ◽

Mus Musculus

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The Immediate Effect of HCG Upon Plasma Testosterone Levels in the Bull

Acta Veterinaria Scandinavica ◽

10.1186/bf03548665 ◽

1981 ◽

Vol 22 (3-4) ◽

pp. 403-408 ◽

Cited By ~ 1

Author(s):

A. Sundby

Keyword(s):

Plasma Testosterone ◽

Testosterone Levels

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Insights into mammalian biology from the wild house mouse Mus musculus

eLife ◽

10.7554/elife.05959 ◽

2015 ◽

Vol 4 ◽

Cited By ~ 45

Author(s):

Megan Phifer-Rixey ◽

Michael W Nachman

Keyword(s):

House Mouse ◽

Mus Musculus ◽

Genetic Model ◽

Inbred Strains ◽

Mendelian Inheritance ◽

Model Organisms ◽

House Mice ◽

Small Subset ◽

Wild Mice ◽

Wide Range

The house mouse, Mus musculus, was established in the early 1900s as one of the first genetic model organisms owing to its short generation time, comparatively large litters, ease of husbandry, and visible phenotypic variants. For these reasons and because they are mammals, house mice are well suited to serve as models for human phenotypes and disease. House mice in the wild consist of at least three distinct subspecies and harbor extensive genetic and phenotypic variation both within and between these subspecies. Wild mice have been used to study a wide range of biological processes, including immunity, cancer, male sterility, adaptive evolution, and non-Mendelian inheritance. Despite the extensive variation that exists among wild mice, classical laboratory strains are derived from a limited set of founders and thus contain only a small subset of this variation. Continued efforts to study wild house mice and to create new inbred strains from wild populations have the potential to strengthen house mice as a model system.

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