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Differential Growth of the Reproductive Organs during the Peripubertal Period in Male Rats

In mammals, puberty is a process of acquiring reproductive competence, triggering by activation of hypothalamic kisspeptin (KiSS)-gonadotropin releasing hormone (GnRH) neuronal circuit. During peripubertal period, not only the external genitalia but the internal reproductive organs have to be mature...

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Autores principales: Han, Seung Hee, Lee, Sung-Ho
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Developmental Biology 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4382944/
https://www.ncbi.nlm.nih.gov/pubmed/25949164
http://dx.doi.org/10.12717/DR.2013.17.4.469
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author Han, Seung Hee
Lee, Sung-Ho
author_facet Han, Seung Hee
Lee, Sung-Ho
author_sort Han, Seung Hee
collection PubMed
description In mammals, puberty is a process of acquiring reproductive competence, triggering by activation of hypothalamic kisspeptin (KiSS)-gonadotropin releasing hormone (GnRH) neuronal circuit. During peripubertal period, not only the external genitalia but the internal reproductive organs have to be matured in response to the hormonal signals from hypothalamic-pituitary-gonadal (H-P-G) axis. In the present study, we evaluated the maturation of male rat accessory sex organs during the peripubertal period using tissue weight measurement, histological analysis and RT-PCR assay. Male rats were sacrificed at 25, 30, 35, 40, 45, 50, and 70 postnatal days (PND). The rat accessory sex organs exhibited differential growth patterns compared to those of non-reproductive organs. The growth rate of the accessory sex organs were much higher than the those of non-reproductive organs. Also, the growth spurts occurred differentially even among the accessory sex organs; the order of prepubertal organ growth spurts is testis = epididymis > seminal vesicle = prostate. Histological study revealed that the presence of sperms in seminiferous tubules and epididymal ducts at day 50, indicating the puberty onset. The number of duct and the volume of duct in epididymis and prostate were inversely correlated during the experimental period. Our RT-PCR revealed that the levels of hypothalamic GnRH transcript were increased significantly on PND 40, suggesting the activation of hypothalamic GnRH pulse-generator before puberty onset. Studies on the peripubertal male accessory sex organs will provide useful references on the growth regulation mechanism which is differentially regulated during the period in andevrepogen-sensitive organs. The detailed references will render easier development of endocrine disruption assay.
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spelling pubmed-43829442015-05-06 Differential Growth of the Reproductive Organs during the Peripubertal Period in Male Rats Han, Seung Hee Lee, Sung-Ho Dev Reprod Article In mammals, puberty is a process of acquiring reproductive competence, triggering by activation of hypothalamic kisspeptin (KiSS)-gonadotropin releasing hormone (GnRH) neuronal circuit. During peripubertal period, not only the external genitalia but the internal reproductive organs have to be matured in response to the hormonal signals from hypothalamic-pituitary-gonadal (H-P-G) axis. In the present study, we evaluated the maturation of male rat accessory sex organs during the peripubertal period using tissue weight measurement, histological analysis and RT-PCR assay. Male rats were sacrificed at 25, 30, 35, 40, 45, 50, and 70 postnatal days (PND). The rat accessory sex organs exhibited differential growth patterns compared to those of non-reproductive organs. The growth rate of the accessory sex organs were much higher than the those of non-reproductive organs. Also, the growth spurts occurred differentially even among the accessory sex organs; the order of prepubertal organ growth spurts is testis = epididymis > seminal vesicle = prostate. Histological study revealed that the presence of sperms in seminiferous tubules and epididymal ducts at day 50, indicating the puberty onset. The number of duct and the volume of duct in epididymis and prostate were inversely correlated during the experimental period. Our RT-PCR revealed that the levels of hypothalamic GnRH transcript were increased significantly on PND 40, suggesting the activation of hypothalamic GnRH pulse-generator before puberty onset. Studies on the peripubertal male accessory sex organs will provide useful references on the growth regulation mechanism which is differentially regulated during the period in andevrepogen-sensitive organs. The detailed references will render easier development of endocrine disruption assay. Korean Society of Developmental Biology 2013-12 /pmc/articles/PMC4382944/ /pubmed/25949164 http://dx.doi.org/10.12717/DR.2013.17.4.469 Text en © Copyright A Official Journal of the Korean Society of Developmental Biology. All Rights Reserved. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Article
Han, Seung Hee
Lee, Sung-Ho
Differential Growth of the Reproductive Organs during the Peripubertal Period in Male Rats
title Differential Growth of the Reproductive Organs during the Peripubertal Period in Male Rats
title_full Differential Growth of the Reproductive Organs during the Peripubertal Period in Male Rats
title_fullStr Differential Growth of the Reproductive Organs during the Peripubertal Period in Male Rats
title_full_unstemmed Differential Growth of the Reproductive Organs during the Peripubertal Period in Male Rats
title_short Differential Growth of the Reproductive Organs during the Peripubertal Period in Male Rats
title_sort differential growth of the reproductive organs during the peripubertal period in male rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4382944/
https://www.ncbi.nlm.nih.gov/pubmed/25949164
http://dx.doi.org/10.12717/DR.2013.17.4.469
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