Gold Nanoparticles Elevate Plasma Testosterone Levels in Male Mice without Affecting Fertility

Small ◽  
2012 ◽  
Vol 9 (9-10) ◽  
pp. 1708-1714 ◽  
Author(s):  
Wen-Qing Li ◽  
Feng Wang ◽  
Zhi-Min Liu ◽  
Yu-Cai Wang ◽  
Jun Wang ◽  
...  
1994 ◽  
Vol 82 (1-2) ◽  
pp. 185-192 ◽  
Author(s):  
J.C. Compaan ◽  
J.B. Hutchison ◽  
A. Wozniak ◽  
A.J.H. de Ruiter ◽  
J.M. Koolhaas

1974 ◽  
Vol 60 (1) ◽  
pp. 145-148 ◽  
Author(s):  
A. BARTKE

SUMMARY In male mice of the C57BL/10J (C57) strain the testicular weight, sex drive and aggression are low compared with a number of other strains, indicating androgen deficiency. In contrast, DBA/2J (DBA) males were 'normal' in all studied parameters of testicular function. The weight of the seminal vesicles is similar in both strains. Plasma testosterone levels, and the responsiveness of the seminal vesicles to injected testosterone propionate in C57 and DBA animals were compared. Plasma testosterone levels were 1·3 ± 0·4 ng/ml in C57 and 4·6 ± 1·0 ng/ml in DBA mice. The increase in weight of the seminal vesicles after administration of testosterone propionate to castrated male mice was, however, considerably greater in C57 than in DBA mice. In order to restore the weight of the seminal vesicles to normal it was necessary to administer twice as much testosterone propionate to DBA than to C57 males.


1978 ◽  
Vol 89 (4) ◽  
pp. 780-788 ◽  
Author(s):  
Ch. Jean-Faucher ◽  
M. Berger ◽  
M. de Turckheim ◽  
G. Veyssiere ◽  
Cl. Jean

ABSTRACT Male mice were raised in cohabitation with females from birth to 90 days. Testosterone was measured every 10 days in plasma and testes. Sex difference in body weight was related to the pre-pubertal increase of testosterone levels in males. The weight of the seminal vesicle was positively correlated with circulating testosterone levels between 1 and 40 days but not between 50 and 90 days Testosterone concentrations in the plasma and testes were high at birth: 630 pg/ml and 58.0 ± 17.7 ng/100 mg; they subsequently decreased during the first days of life and remained low until day 20: 240 ± 110 pg/ml and 0.1 ± 0.03 ng/100 mg. The testosterone levels then increased rapidly between days 20 and 30 and especially between 30 and 40 reaching their maxima: 5770 ± 1720 pg/ml and 123.7 ± 18.3 ng/100 mg testis. This increase was transitory and testosterone levels fell after day 40. By 90 days, the testosterone levels, 440 ± 65 pg/ml and 43.2 ± 5.5 ng/100 mg testis, were comparable to those measured at birth. Plasma testosterone and age were positively correlated between 1 and 40 days, and negatively between 50 and 90 days. The first fertile matings occurred at age 40 days.


Animals ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 2135
Author(s):  
Roger Grífols ◽  
Carolina Zamora ◽  
Iván Ortega-Saez ◽  
Garikoitz Azkona

Rearing laboratory mice in groups is important since social isolation after weaning induces brain alterations, which entails behavioral abnormalities in adulthood. Age is an important factor when grouping males of different litters due to inter-male aggressiveness. The aim of this study was to determine whether newly weaned mice could safely be grouped with late juvenile or early and late pubescent mice, and whether cage cleaning, the number of the hosting group members and testosterone plasma levels have any influence. Newly weaned C57BL/6J, CD1, and SCID Beige male mice were systematically grouped with same strain late juvenile, early or late pubescent male mice in clean or dirty cages of 1, 2 or 3 hosting members. We also analyzed plasma testosterone levels at different postnatal days. Our result showed that only strain and hosting male’s age influence agonistic behavior toward newly weaned mice. Thus, in order not to house a recently weaned male alone, we would recommend grouping it with late juvenile same strain mice in all studied strains. In the same way, CD1 and SCID Beige pubescent mice will admit a newly weaned mouse in their group. However, we would not recommend grouping newly weaned and pubescent C57BL/6J males.


Science ◽  
1975 ◽  
Vol 189 (4208) ◽  
pp. 1104-1106 ◽  
Author(s):  
F Macrides ◽  
A Bartke ◽  
S Dalterio

2009 ◽  
Vol 297 (2) ◽  
pp. E375-E383 ◽  
Author(s):  
Ayala Luria ◽  
Christophe Morisseau ◽  
Hsing-Ju Tsai ◽  
Jun Yang ◽  
Bora Inceoglu ◽  
...  

Soluble epoxide hydrolase ( Ephx2, sEH) is a bifunctional enzyme with COOH-terminal hydrolase and NH2-terminal phosphatase activities. sEH converts epoxyeicosatrienoic acids (EETs) to dihydroxyeicosatrienoic acids (DHETs), and the phosphatase activity is suggested to be involved in cholesterol metabolism. EETs participate in a wide range of biological functions, including regulation of vascular tone, renal tubular transport, cardiac contractility, and inflammation. Inhibition of sEH is a potential approach for enhancing the biological activity of EETs. Therefore, disruption of sEH activity is becoming an attractive therapeutic target for both cardiovascular and inflammatory diseases. To define the physiological role of sEH, we characterized a knockout mouse colony lacking expression of the Ephx2 gene. Lack of sEH enzyme is characterized by elevation of EET to DHET ratios in both the linoleate and arachidonate series in plasma and tissues of both female and male mice. In male mice, this lack of expression was also associated with decreased plasma testosterone levels, sperm count, and testicular size. However, this genotype was still able to sire litters. Plasma cholesterol levels also declined in this genotype. Behavior tests such as anxiety-like behavior and hedonic response were also examined in Ephx2-null and WT mice, as all can be related to hormonal changes. Null mice showed a level of anxiety with a decreased hedonic response. In conclusion, this study provides a broad biochemical, physiological, and behavioral characterization of the Ephx2-null mouse colony and suggests a mechanism by which sEH and its substrates may regulate circulating levels of testosterone through cholesterol biosynthesis and metabolism.


1981 ◽  
Vol 90 (3) ◽  
pp. 397-402 ◽  
Author(s):  
CH. JEAN-FAUCHER ◽  
M. BERGER ◽  
M. DE TURCKHEIM ◽  
G. VEYSSIERE ◽  
CL. JEAN

Male mice were raised in populations of two different sizes from birth to adulthood: six animals (three of each sex) or 30 animals (15 of each sex) being maintained in cages of the same dimensions. Animals were killed every 10 days from weaning to 60 days and at 90 days. Increased population size induced decreased body and seminal vesicle weights; testicular, pituitary and adrenal weights were little affected. Plasma testosterone levels were lowered by increasing population size over the period from weaning to 50 days but they were increased at 60 and 90 days. The age at which first fertile matings occurred was not affected. These results indicate that the endocrine function of the testis, as determined by the measures used here, was specifically affected by this differential housing.


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.


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