Hormonal regulation of spermatogenesis in the hypophysectomized rat: FSH maintenance of cellular viability during pubertal spermatogenesis

The potential for follicle-stimulating hormone (FSH) to promote germ- cell survival and the cellular sites of FSH action were studied using a gonadally maturing (pubertal), hypophysectomized (Hx) rat model in which residual testosterone (T) activity was blocked by injections of an androgen- receptor...

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Publicado: 1998
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01963635_v19_n3_p308_Russell
http://hdl.handle.net/20.500.12110/paper_01963635_v19_n3_p308_Russell
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spelling paper:paper_01963635_v19_n3_p308_Russell2023-06-08T15:20:28Z Hormonal regulation of spermatogenesis in the hypophysectomized rat: FSH maintenance of cellular viability during pubertal spermatogenesis Cell viability Hypohysectomy Testis Testosterone androgen receptor flutamide follitropin recombinant follitropin testosterone adolescent animal cell animal experiment animal tissue article cell viability controlled study germ cell hormonal regulation hormone action hypophysectomy male nonhuman priority journal puberty rat seminiferous tubule sertoli cell spermatocyte spermatogenesis testis weight Androgen Antagonists Animals Body Weight Flutamide Follicle Stimulating Hormone Humans Hypophysectomy Male Models, Biological Organ Size Rats Rats, Sprague-Dawley Seminiferous Tubules Sexual Maturation Sperm Count Spermatogenesis Testis Testosterone The potential for follicle-stimulating hormone (FSH) to promote germ- cell survival and the cellular sites of FSH action were studied using a gonadally maturing (pubertal), hypophysectomized (Hx) rat model in which residual testosterone (T) activity was blocked by injections of an androgen- receptor antagonist, flutamide. Recombinant human FSH was given to androgen- deprived and androgen-blocked male rats at 27 days of age to determine maintenance of individual germ-cell types at 35 days of age. Follicle- stimulating hormone significantly increased testis weights and tubular diameters as compared with Hx and Hx-flutamide controls, although testis weights in FSH-treated animals were significantly lower than in pituitary- intact animals. Morphometric assays to determine ratios of germ cells to Sertoli cells and to determine the number of germ cells present per hour of development showed that the population of type A spermatogonia in the early stages of the cycle was not responsive to FSH. Follicle-stimulating hormone had a marked ability to maintain cell viability in the rapid, successive divisions that begin in the latter part of the cycle and that continue through the next cycle (i.e., from type A1 to A4 and from intermediate spermatogonia to type B spermatogonia to preleptotene spermatocytes to leptotene/zygotene spermatocytes to young pachytene spermatocytes). The data also suggest T responsiveness of these cell types since the Hx-FSH-flutamide group showed lower cell viability at the aforementioned steps when compared with the Hx-FSH group. Too few cell types were present at subsequent phases of spermatogenesis to allow a sensitive determination of FSH activity in the maintenance of cell viability. The data show the potential of FSH in the absence or relative absence of T activity to maintain cell viability. These data support the concept of overlapping and synergistic (or additive) effects of T and FSH in the immature rat and identify the cellular sites of FSH action. 1998 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01963635_v19_n3_p308_Russell http://hdl.handle.net/20.500.12110/paper_01963635_v19_n3_p308_Russell
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Cell viability
Hypohysectomy
Testis
Testosterone
androgen receptor
flutamide
follitropin
recombinant follitropin
testosterone
adolescent
animal cell
animal experiment
animal tissue
article
cell viability
controlled study
germ cell
hormonal regulation
hormone action
hypophysectomy
male
nonhuman
priority journal
puberty
rat
seminiferous tubule
sertoli cell
spermatocyte
spermatogenesis
testis weight
Androgen Antagonists
Animals
Body Weight
Flutamide
Follicle Stimulating Hormone
Humans
Hypophysectomy
Male
Models, Biological
Organ Size
Rats
Rats, Sprague-Dawley
Seminiferous Tubules
Sexual Maturation
Sperm Count
Spermatogenesis
Testis
Testosterone
spellingShingle Cell viability
Hypohysectomy
Testis
Testosterone
androgen receptor
flutamide
follitropin
recombinant follitropin
testosterone
adolescent
animal cell
animal experiment
animal tissue
article
cell viability
controlled study
germ cell
hormonal regulation
hormone action
hypophysectomy
male
nonhuman
priority journal
puberty
rat
seminiferous tubule
sertoli cell
spermatocyte
spermatogenesis
testis weight
Androgen Antagonists
Animals
Body Weight
Flutamide
Follicle Stimulating Hormone
Humans
Hypophysectomy
Male
Models, Biological
Organ Size
Rats
Rats, Sprague-Dawley
Seminiferous Tubules
Sexual Maturation
Sperm Count
Spermatogenesis
Testis
Testosterone
Hormonal regulation of spermatogenesis in the hypophysectomized rat: FSH maintenance of cellular viability during pubertal spermatogenesis
topic_facet Cell viability
Hypohysectomy
Testis
Testosterone
androgen receptor
flutamide
follitropin
recombinant follitropin
testosterone
adolescent
animal cell
animal experiment
animal tissue
article
cell viability
controlled study
germ cell
hormonal regulation
hormone action
hypophysectomy
male
nonhuman
priority journal
puberty
rat
seminiferous tubule
sertoli cell
spermatocyte
spermatogenesis
testis weight
Androgen Antagonists
Animals
Body Weight
Flutamide
Follicle Stimulating Hormone
Humans
Hypophysectomy
Male
Models, Biological
Organ Size
Rats
Rats, Sprague-Dawley
Seminiferous Tubules
Sexual Maturation
Sperm Count
Spermatogenesis
Testis
Testosterone
description The potential for follicle-stimulating hormone (FSH) to promote germ- cell survival and the cellular sites of FSH action were studied using a gonadally maturing (pubertal), hypophysectomized (Hx) rat model in which residual testosterone (T) activity was blocked by injections of an androgen- receptor antagonist, flutamide. Recombinant human FSH was given to androgen- deprived and androgen-blocked male rats at 27 days of age to determine maintenance of individual germ-cell types at 35 days of age. Follicle- stimulating hormone significantly increased testis weights and tubular diameters as compared with Hx and Hx-flutamide controls, although testis weights in FSH-treated animals were significantly lower than in pituitary- intact animals. Morphometric assays to determine ratios of germ cells to Sertoli cells and to determine the number of germ cells present per hour of development showed that the population of type A spermatogonia in the early stages of the cycle was not responsive to FSH. Follicle-stimulating hormone had a marked ability to maintain cell viability in the rapid, successive divisions that begin in the latter part of the cycle and that continue through the next cycle (i.e., from type A1 to A4 and from intermediate spermatogonia to type B spermatogonia to preleptotene spermatocytes to leptotene/zygotene spermatocytes to young pachytene spermatocytes). The data also suggest T responsiveness of these cell types since the Hx-FSH-flutamide group showed lower cell viability at the aforementioned steps when compared with the Hx-FSH group. Too few cell types were present at subsequent phases of spermatogenesis to allow a sensitive determination of FSH activity in the maintenance of cell viability. The data show the potential of FSH in the absence or relative absence of T activity to maintain cell viability. These data support the concept of overlapping and synergistic (or additive) effects of T and FSH in the immature rat and identify the cellular sites of FSH action.
title Hormonal regulation of spermatogenesis in the hypophysectomized rat: FSH maintenance of cellular viability during pubertal spermatogenesis
title_short Hormonal regulation of spermatogenesis in the hypophysectomized rat: FSH maintenance of cellular viability during pubertal spermatogenesis
title_full Hormonal regulation of spermatogenesis in the hypophysectomized rat: FSH maintenance of cellular viability during pubertal spermatogenesis
title_fullStr Hormonal regulation of spermatogenesis in the hypophysectomized rat: FSH maintenance of cellular viability during pubertal spermatogenesis
title_full_unstemmed Hormonal regulation of spermatogenesis in the hypophysectomized rat: FSH maintenance of cellular viability during pubertal spermatogenesis
title_sort hormonal regulation of spermatogenesis in the hypophysectomized rat: fsh maintenance of cellular viability during pubertal spermatogenesis
publishDate 1998
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_01963635_v19_n3_p308_Russell
http://hdl.handle.net/20.500.12110/paper_01963635_v19_n3_p308_Russell
_version_ 1768543990258335744