scholarly journals Prepubertal PTU treatment in rat increases Sertoli cell number and sperm production

Reproduction ◽  
2019 ◽  
Vol 158 (2) ◽  
pp. 201-211 ◽  
Author(s):  
André F A Figueiredo ◽  
Natália Teixeira Wnuk ◽  
Amanda O Tavares ◽  
José Rafael Miranda ◽  
Rex A Hess ◽  
...  
Keyword(s):  
Mitotic Activity ◽  
Transition Region ◽  
Sertoli Cells ◽  
Cell Number ◽  
Rete Testis ◽  
Neonatal Rat ◽  
Testis Weight ◽  
Sperm Production ◽  
Neonatal Hypothyroidism ◽  
Male Wistar Rats

The number of Sertoli cells (SCs) ultimately determines the upper limit of sperm production in the testis. Previous studies have shown that thyroid hormones (TH) receptors are abundantly expressed in developing SCs; therefore, it was highly significant to discover that transient neonatal hypothyroidism induced by the goitrogen 6-n-propyl-2-thiouracil (PTU) can extend SCs proliferation beyond the first 2 weeks postnatal and increase testis weight and sperm production. Further studies concluded that treatment must begin before day 8 post birth in rats. Recent studies, however, showed that SCs present in the transition region at the rete testis exhibit a more immature phenotype and have prolonged mitotic activity, which led to the hypothesis that SCs in this region will retain the capacity to respond to PTU treatment over a longer period of time. In the present study, male Wistar rats were treated with PTU from days 21 to 40 and were evaluated at 40 and 160 days of age. Similar to neonatal rat SCs, it was demonstrated that prepubertal SCs in the transition region have a high mitotic activity and are highly sensitive to TH levels. This delayed, transient hypothyroidism resulted in significantly increased testis weight, SCs number and daily sperm production. The results demonstrate for the first time that Sertoli cells showing plasticity in the transition region can be stimulated to increase proliferation and contribute to a late stage surge in testis weight and sperm output.

Endocrinological and histological changes induced by flutamide treatment on the hypothalamo-hypophyseal testicular axis of the adult male rat and their incidences on fertility

1983 ◽  
Vol 104 (2) ◽  
pp. 246-252 ◽  
Author(s):  
M. C. Viguier-Martinez ◽  
M. T. Hochereau de Reviers ◽  
B. Barenton ◽  
C. Perreau
Keyword(s):  
Adult Male ◽  
Cell Number ◽  
Male Rat ◽  
Plasma Testosterone ◽  
Seminiferous Tubules ◽  
Testis Weight ◽  
Accessory Glands ◽  
Accessory Sex Organs ◽  
Adult Male Rat ◽  
Male Wistar Rats

Abstract. Adult male Wistar rats were treated with flutamide from 90 to 105 days of age. In a first experiment, testis and accessory sex organs were weighed. In the same animals, hypothalamic LRH content, pituitary gonadotrophin concentrations, plasma LH, FSH, prolactin and testosterone levels, and testicular gonadotrophin receptors were evaluated. In a second experiment, fertility was tested at the end of the treatment, and histology of the testis was performed. All the results were compared to those obtained in control animals of the same age. Accessory glands of genital tract were significantly lower in flutamide-treated animals (P < 0.01). Hypothalamic LRH, pituitary and plasma FSH, and prolactin concentrations were unchanged, while pituitary and plasma LH level and especially plasma testosterone concentration were increased (P < 0.001). Flutamide therefore exerted a strong inhibition on testosterone-dependent organs, and blocked the negative feedback of testosterone on the hypothalamo-pituitary axis, increasing the LH levels. Testis weight, intertubular tissue volume, total number and total volume of Leydig cells/testis, as well as total length and diameter of seminiferous tubules were unchanged in flutamide treated rats. However number of LH receptors/Leydig cell, nuclear area of Sertoli cells, number of FSH receptors/Sertoli cell, number of leptotene spermatocytes and of round spermatids per cross section, and yield of spermatogonial divisions were decreased after treatment. Flutamide treatment also decreased fertility by 48% (P < 0.05). This lowered fertility is likely the result of impaired spermatogenesis and/or a dysfunction of accessory sex organs.

Insights into differentiation and function of the transition region between the seminiferous tubule and rete testis

2021 ◽  
Author(s):  
A.F.A. Figueiredo ◽  
Rex A. Hess ◽  
S.R. Batlouni ◽  
N.T. Wnuk ◽  
A.O. Tavares ◽  
...  
Keyword(s):  
Transition Region ◽  
Seminiferous Tubule ◽  
Rete Testis ◽  
And Function

scholarly journals Number and function of Sertoli cells, number and yield of spermatogonia, and daily sperm production in three breeds of boar

Reproduction ◽  
1996 ◽  
Vol 107 (1) ◽  
pp. 137-149 ◽  
Author(s):  
O. E. Okwun ◽  
G. Igboeli ◽  
J. J. Ford ◽  
D. D. Lunstra ◽  
L. Johnson
Keyword(s):  
Sertoli Cells ◽  
Sperm Production ◽  
And Function ◽  
Daily Sperm Production

A novel epithelial cell from neonatal rat lung: isolation and differentiated phenotype

1990 ◽  
Vol 259 (6) ◽  
pp. L415-L425 ◽  
Author(s):  
P. E. Roberts ◽  
D. M. Phillips ◽  
J. P. Mather
Keyword(s):  
Epithelial Cell ◽  
Molecular Mechanisms ◽  
Basal Medium ◽  
Fold Increase ◽  
Cell Types ◽  
Cell Number ◽  
Neonatal Rat ◽  
Rat Lung ◽  
Cell Type

A novel epithelial cell from normal neonatal rat lung has been isolated, established, and maintained for multiple passages in the absence of serum, without undergoing crisis or senescence. By careful manipulation of the nutrition/hormonal microenvironment, we have been able to select, from a heterogeneous population, a single epithelial cell type that can maintain highly differentiated features in vitro. This cell type has characteristics of bronchiolar epithelial cells. A clonal line, RL-65, has been selected and observed for greater than 2 yr in continuous culture. It has been characterized by ultrastructural, morphological, and biochemical criteria. The basal medium for this cell line is Ham's F12/Dulbecco's modified Eagle's (DME) medium plus insulin (1 micrograms/ml), human transferrin (10 micrograms/ml), ethanolamine (10(-4) M), phosphoethanolamine (10(-4) M), selenium (2.5 x 10(-8) M), hydrocortisone (2.5 x 10(-7) M), and forskolin (5 microM). The addition of 150 micrograms/ml of bovine pituitary extract to the defined basal medium stimulates a greater than 10-fold increase in cell number and a 50- to 100-fold increase in thymidine incorporation. The addition of retinoic acid results in further enhancement of cell growth and complete inhibition of keratinization. We have demonstrated a strategy that may be applicable to isolating other cell types from the lung and maintaining their differentiated characteristics for long-term culture in vitro. Such a culture system promises to be a useful model in which to study cellular events associated with differentiation and proliferation in the lung and to better understand the molecular mechanisms involved in these events.

scholarly journals Effect of Vincristine on Steroidogenic Pathway of Male Wistar Rat

2016 ◽  
Vol 3 (2) ◽  
Author(s):  
Tareeka Sonawane ◽  
Hersharan Nischal ◽  
Shalini Rao ◽  
Liji Thayil ◽  
Dayanand Bhiwgade
Keyword(s):  
Reproductive Toxicity ◽  
Physiological Saline ◽  
Wistar Rat ◽  
Testis Weight ◽  
Testosterone Production ◽  
Expression Studies ◽  
End Of Treatment ◽  
Major Player ◽  
Male Wistar Rats ◽  
Steroidogenic Acute Regulatory

Vincristine is major player in front line combination chemotherapy for treatment of cancer and shows decrease in testosterone after treatment contributing to reproductive toxicity. Hence, the present research was aimed to study the effect of vincristine on steroidogenic pathway which is responsible for testosterone production in males. Vincristine was intraperitoneally injected to adult male Wistar rats of proven fertility with a dose of 40μg/kg/day dissolved in 0.5 ml of physiological saline for 30 days. Animals were sacrificed at the end of treatment period; their testes were removed and used for further studies. No significant changes were observed in body weight, testis weight and mean relative testis weight. Expression studies of enzymes involved in steroidogenic pathway showed that there was decrease in expression of Steroidogenic acute regulatory (StAR) protein which might be responsible for altered testosterone production.

The murine seminiferous epithelial cycle is pre-figured in the Sertoli cells of the embryonic testis

Development ◽  
2002 ◽  
Vol 129 (3) ◽  
pp. 635-647 ◽  
Author(s):  
Paula M. Timmons ◽  
Peter W. J. Rigby ◽  
Françoise Poirier
Keyword(s):  
Germ Cell ◽  
Sertoli Cells ◽  
Cell Function ◽  
Seminiferous Epithelium ◽  
Developmental Origins ◽  
Sperm Production ◽  
Functional Heterogeneity ◽  
Adult Testis ◽  
Germ Cell Apoptosis ◽  
Cell Lineages

The seminiferous epithelial cycle and spermatogenic wave are conserved features of vertebrate spermatogenic organisation that reflect the need for the rigorous maintenance of sperm production. Although the cycle and the wave of the adult seminiferous epithelium have been well characterised, particularly in rodent species, their developmental origins are unknown. We show that the Sertoli cells of the pre-pubertal mouse, including those of the germ cell-deficient XXSxra mutant, exhibit coordinated, cyclical patterns of gene expression, presaging the situation in the adult testis, where Sertoli cell function is coupled to the spermatogenic cycle. In the case of the galectin 1 gene (Lgals1), localised differential expression in the Sertoli cells can be traced back to neonatal and embryonic stages, making this the earliest known molecular marker of functional heterogeneity in mammalian testis cords. In addition, the timing of germ cell apoptosis in normal pre-pubertal testes is linked to the temporal cycle of the Sertoli cells. These data show that the cycle and wave of the murine seminiferous epithelium originate at a much earlier stage in development than was previously known, and that their maintenance in the early postnatal cords depends exclusively on the somatic cell lineages.

scholarly journals Bovine fetal testicular development in the Nellore breed

2017 ◽  
Vol 38 (4Supl1) ◽  
pp. 2551
Author(s):  
Juliana Stephany de Souza ◽  
Maria Carolina Villani Miguel ◽  
Marcos Antônio Maioli ◽  
Arthur Nelson Trali Neto ◽  
David Giraldo Arana ◽  
...  
Keyword(s):  
Germ Cells ◽  
Sertoli Cells ◽  
Leydig Cells ◽  
Principal Component ◽  
Gonadal Development ◽  
Cell Number ◽  
Testicular Development ◽  
Testosterone Concentration ◽  
Testicular Weight ◽  
Bovine Fetuses

The study of gonadal development improves the understanding of factors that can influence the reproductive development process. This study aims to characterize bovine fetal testicular development and the testosterone level in the Nellore breed. For the study, 162 bovine fetuses aged between 3 and 8 months were collected from Nellore cows at a local abattoir. The fetal age was estimated by DP=8.4+0.087L+5.46?L, where DP is the estimated pregnancy day and L represents fetal length. The fetal gonadal weight (g), width (cm), and thickness (cm) were measured. Thereafter, the gonads were submitted to classic histology processes in 3-µm-thick slices cut at 210 µm intervals. The Sertoli cells, Leydig cells, and germ cells were counted. Blood samples were collected from umbilical cords for testosterone levels. The data were analyzed using the Spearman correlation test followed by Principal Component Analysis and one-way ANOVA to compare the averages between months. The testicular weight and volume were found to have a positive correlation with the numbers of Sertoli cells (r = 0.84; p < 0.0001 and r = 0.92; p < 0.0001, respectively), Leydig cells (r = 0.80; p < 0.0001 and r = 0.90; p < 0.0001, respectively), and germ cells (r = 0.84; p < 0.0001 and r = 0.93; p < 0.0001, respectively) and to be negatively correlated with testosterone plasmatic concentration (r = -0.31; p = 0.0001 and r = -0.22; p = 0.006, respectively) during pregnancy. After the fifth month, the numbers of Sertoli cells, Leydig cells and germ cells differed (p < 0.0001) from the following gestational months. The highest testosterone concentration (p = 0.007) was observed in the fifth month of gestation and was followed by a concentration decrease in the seventh and eighth months. The increase in cell quantity was responsible for the increase in testicular weight and volume during fetal development. On the other hand, the testosterone concentration followed the increase in testicular weight and volume until the 7th month of gestation and regressed during the 8th and 9th months, in addition to the increase in cell number.

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