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GnRHa/Stanozolol Combined Therapy Maintains Normal Bone Growth in Central Precocious Puberty
BACKGROUND: Gonadotropin-releasing hormone agonist (GnRHa) is the gold standard in the treatment of Central Precocious Puberty (CPP) with progressive puberty and accelerative growth. However, GnRHa treatment is reported to result in growth deceleration and prevents growth plate development which lea...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8221533/ https://www.ncbi.nlm.nih.gov/pubmed/34177807 http://dx.doi.org/10.3389/fendo.2021.678797 |
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author | Zhu, Shunye Long, Lingli Hu, Yue Tuo, Ying Li, Yubin Yu, Zhenhua |
author_facet | Zhu, Shunye Long, Lingli Hu, Yue Tuo, Ying Li, Yubin Yu, Zhenhua |
author_sort | Zhu, Shunye |
collection | PubMed |
description | BACKGROUND: Gonadotropin-releasing hormone agonist (GnRHa) is the gold standard in the treatment of Central Precocious Puberty (CPP) with progressive puberty and accelerative growth. However, GnRHa treatment is reported to result in growth deceleration and prevents growth plate development which leads to a reduction in height velocity. Stanozolol (ST) has been used to stimulate growth in patients with delayed growth and puberty, nevertheless, the effects and mechanisms of ST on CPP with GnRHa treatment are currently unclear. METHODS AND RESULTS: In the current study, we recorded the following vital observations that provided insights into ST induced chondrogenic differentiation and the maintenance of normal growth plate development: (1) ST efficiently prevented growth deceleration and maintained normal growth plate development in rats undergoing GnRHa treatment; (2) ST suppressed the inhibitory effect of GnRHa to promote chondrogenic differentiation; (3) ST induced chondrogenic differentiation through the activation of the JNK/c-Jun/Sox9 signaling pathway; (4) ST promoted chondrogenic differentiation and growth plate development through the JNK/Sox9 signaling pathway in vivo. CONCLUSIONS: ST mitigated the inhibitory effects of GnRHa and promoted growth plate development in rats. ST induced the differentiation of chondrocytes and maintained normal growth plate development through the activation of JNK/c-Jun/Sox9 signaling. These novel findings indicated that ST could be a potential agent for maintaining normal bone growth in cases of CPP undergoing GnRHa treatment. |
format | Online Article Text |
id | pubmed-8221533 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-82215332021-06-24 GnRHa/Stanozolol Combined Therapy Maintains Normal Bone Growth in Central Precocious Puberty Zhu, Shunye Long, Lingli Hu, Yue Tuo, Ying Li, Yubin Yu, Zhenhua Front Endocrinol (Lausanne) Endocrinology BACKGROUND: Gonadotropin-releasing hormone agonist (GnRHa) is the gold standard in the treatment of Central Precocious Puberty (CPP) with progressive puberty and accelerative growth. However, GnRHa treatment is reported to result in growth deceleration and prevents growth plate development which leads to a reduction in height velocity. Stanozolol (ST) has been used to stimulate growth in patients with delayed growth and puberty, nevertheless, the effects and mechanisms of ST on CPP with GnRHa treatment are currently unclear. METHODS AND RESULTS: In the current study, we recorded the following vital observations that provided insights into ST induced chondrogenic differentiation and the maintenance of normal growth plate development: (1) ST efficiently prevented growth deceleration and maintained normal growth plate development in rats undergoing GnRHa treatment; (2) ST suppressed the inhibitory effect of GnRHa to promote chondrogenic differentiation; (3) ST induced chondrogenic differentiation through the activation of the JNK/c-Jun/Sox9 signaling pathway; (4) ST promoted chondrogenic differentiation and growth plate development through the JNK/Sox9 signaling pathway in vivo. CONCLUSIONS: ST mitigated the inhibitory effects of GnRHa and promoted growth plate development in rats. ST induced the differentiation of chondrocytes and maintained normal growth plate development through the activation of JNK/c-Jun/Sox9 signaling. These novel findings indicated that ST could be a potential agent for maintaining normal bone growth in cases of CPP undergoing GnRHa treatment. Frontiers Media S.A. 2021-06-09 /pmc/articles/PMC8221533/ /pubmed/34177807 http://dx.doi.org/10.3389/fendo.2021.678797 Text en Copyright © 2021 Zhu, Long, Hu, Tuo, Li and Yu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology Zhu, Shunye Long, Lingli Hu, Yue Tuo, Ying Li, Yubin Yu, Zhenhua GnRHa/Stanozolol Combined Therapy Maintains Normal Bone Growth in Central Precocious Puberty |
title | GnRHa/Stanozolol Combined Therapy Maintains Normal Bone Growth in Central Precocious Puberty |
title_full | GnRHa/Stanozolol Combined Therapy Maintains Normal Bone Growth in Central Precocious Puberty |
title_fullStr | GnRHa/Stanozolol Combined Therapy Maintains Normal Bone Growth in Central Precocious Puberty |
title_full_unstemmed | GnRHa/Stanozolol Combined Therapy Maintains Normal Bone Growth in Central Precocious Puberty |
title_short | GnRHa/Stanozolol Combined Therapy Maintains Normal Bone Growth in Central Precocious Puberty |
title_sort | gnrha/stanozolol combined therapy maintains normal bone growth in central precocious puberty |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8221533/ https://www.ncbi.nlm.nih.gov/pubmed/34177807 http://dx.doi.org/10.3389/fendo.2021.678797 |
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