Cargando…

Acute Effects of Kisspeptin Administration on Bone Metabolism in Healthy Men

CONTEXT: Osteoporosis results from disturbances in bone formation and resorption. Recent nonhuman data suggest that the reproductive hormone kisspeptin directly stimulates osteoblast differentiation in vitro and thus could have clinical therapeutic potential. However, the effects of kisspeptin on hu...

Descripción completa

Detalles Bibliográficos
Autores principales: Comninos, Alexander N, Hansen, Morten S, Courtney, Alan, Choudhury, Sirazum, Yang, Lisa, Mills, Edouard G, Phylactou, Maria, Busbridge, Mark, Khir, Muaza, Thaventhiran, Thilipan, Bech, Paul, Tan, Tricia, Abbara, Ali, Frost, Morten, Dhillo, Waljit S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9113799/
https://www.ncbi.nlm.nih.gov/pubmed/35244717
http://dx.doi.org/10.1210/clinem/dgac117
_version_ 1784709647250227200
author Comninos, Alexander N
Hansen, Morten S
Courtney, Alan
Choudhury, Sirazum
Yang, Lisa
Mills, Edouard G
Phylactou, Maria
Busbridge, Mark
Khir, Muaza
Thaventhiran, Thilipan
Bech, Paul
Tan, Tricia
Abbara, Ali
Frost, Morten
Dhillo, Waljit S
author_facet Comninos, Alexander N
Hansen, Morten S
Courtney, Alan
Choudhury, Sirazum
Yang, Lisa
Mills, Edouard G
Phylactou, Maria
Busbridge, Mark
Khir, Muaza
Thaventhiran, Thilipan
Bech, Paul
Tan, Tricia
Abbara, Ali
Frost, Morten
Dhillo, Waljit S
author_sort Comninos, Alexander N
collection PubMed
description CONTEXT: Osteoporosis results from disturbances in bone formation and resorption. Recent nonhuman data suggest that the reproductive hormone kisspeptin directly stimulates osteoblast differentiation in vitro and thus could have clinical therapeutic potential. However, the effects of kisspeptin on human bone metabolism are currently unknown. OBJECTIVE: To assess the effects of kisspeptin on human bone metabolism in vitro and in vivo. METHODS: In vitro study: of Mono- and cocultures of human osteoblasts and osteoclasts treated with kisspeptin. Clinical study: Randomized, placebo-controlled, double-blind, 2-way crossover clinical study in 26 men investigating the effects of acute kisspeptin administration (90 minutes) on human bone metabolism, with blood sampling every 30 minutes to +90 minutes. Cells for the in vitro study were from 12 male blood donors and 8 patients undergoing hip replacement surgery. Twenty-six healthy eugonadal men (age 26.8 ± 5.8 years) were included in the clinical study. The intervention was Kisspeptin (vs placebo) administration. The main outcome measures were changes in bone parameters and turnover markers. RESULTS: Incubation with kisspeptin in vitro increased alkaline phosphatase levels in human bone marrow mesenchymal stem cells by 41.1% (P = .0022), and robustly inhibited osteoclastic resorptive activity by up to 53.4% (P < .0001), in a dose-dependent manner. Kisspeptin administration to healthy men increased osteoblast activity, as evidenced by a 20.3% maximal increase in total osteocalcin (P = .021) and 24.3% maximal increase in carboxylated osteocalcin levels (P = .014). CONCLUSION: Collectively, these data provide the first human evidence that kisspeptin promotes osteogenic differentiation of osteoblast progenitors and inhibits bone resorption in vitro. Furthermore, kisspeptin acutely increases the bone formation marker osteocalcin but not resorption markers in healthy men, independent of downstream sex steroid levels. Kisspeptin could therefore have clinical therapeutic application in the treatment of osteoporosis.
format Online
Article
Text
id pubmed-9113799
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-91137992022-05-18 Acute Effects of Kisspeptin Administration on Bone Metabolism in Healthy Men Comninos, Alexander N Hansen, Morten S Courtney, Alan Choudhury, Sirazum Yang, Lisa Mills, Edouard G Phylactou, Maria Busbridge, Mark Khir, Muaza Thaventhiran, Thilipan Bech, Paul Tan, Tricia Abbara, Ali Frost, Morten Dhillo, Waljit S J Clin Endocrinol Metab Clinical Research Article CONTEXT: Osteoporosis results from disturbances in bone formation and resorption. Recent nonhuman data suggest that the reproductive hormone kisspeptin directly stimulates osteoblast differentiation in vitro and thus could have clinical therapeutic potential. However, the effects of kisspeptin on human bone metabolism are currently unknown. OBJECTIVE: To assess the effects of kisspeptin on human bone metabolism in vitro and in vivo. METHODS: In vitro study: of Mono- and cocultures of human osteoblasts and osteoclasts treated with kisspeptin. Clinical study: Randomized, placebo-controlled, double-blind, 2-way crossover clinical study in 26 men investigating the effects of acute kisspeptin administration (90 minutes) on human bone metabolism, with blood sampling every 30 minutes to +90 minutes. Cells for the in vitro study were from 12 male blood donors and 8 patients undergoing hip replacement surgery. Twenty-six healthy eugonadal men (age 26.8 ± 5.8 years) were included in the clinical study. The intervention was Kisspeptin (vs placebo) administration. The main outcome measures were changes in bone parameters and turnover markers. RESULTS: Incubation with kisspeptin in vitro increased alkaline phosphatase levels in human bone marrow mesenchymal stem cells by 41.1% (P = .0022), and robustly inhibited osteoclastic resorptive activity by up to 53.4% (P < .0001), in a dose-dependent manner. Kisspeptin administration to healthy men increased osteoblast activity, as evidenced by a 20.3% maximal increase in total osteocalcin (P = .021) and 24.3% maximal increase in carboxylated osteocalcin levels (P = .014). CONCLUSION: Collectively, these data provide the first human evidence that kisspeptin promotes osteogenic differentiation of osteoblast progenitors and inhibits bone resorption in vitro. Furthermore, kisspeptin acutely increases the bone formation marker osteocalcin but not resorption markers in healthy men, independent of downstream sex steroid levels. Kisspeptin could therefore have clinical therapeutic application in the treatment of osteoporosis. Oxford University Press 2022-03-04 /pmc/articles/PMC9113799/ /pubmed/35244717 http://dx.doi.org/10.1210/clinem/dgac117 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Clinical Research Article
Comninos, Alexander N
Hansen, Morten S
Courtney, Alan
Choudhury, Sirazum
Yang, Lisa
Mills, Edouard G
Phylactou, Maria
Busbridge, Mark
Khir, Muaza
Thaventhiran, Thilipan
Bech, Paul
Tan, Tricia
Abbara, Ali
Frost, Morten
Dhillo, Waljit S
Acute Effects of Kisspeptin Administration on Bone Metabolism in Healthy Men
title Acute Effects of Kisspeptin Administration on Bone Metabolism in Healthy Men
title_full Acute Effects of Kisspeptin Administration on Bone Metabolism in Healthy Men
title_fullStr Acute Effects of Kisspeptin Administration on Bone Metabolism in Healthy Men
title_full_unstemmed Acute Effects of Kisspeptin Administration on Bone Metabolism in Healthy Men
title_short Acute Effects of Kisspeptin Administration on Bone Metabolism in Healthy Men
title_sort acute effects of kisspeptin administration on bone metabolism in healthy men
topic Clinical Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9113799/
https://www.ncbi.nlm.nih.gov/pubmed/35244717
http://dx.doi.org/10.1210/clinem/dgac117
work_keys_str_mv AT comninosalexandern acuteeffectsofkisspeptinadministrationonbonemetabolisminhealthymen
AT hansenmortens acuteeffectsofkisspeptinadministrationonbonemetabolisminhealthymen
AT courtneyalan acuteeffectsofkisspeptinadministrationonbonemetabolisminhealthymen
AT choudhurysirazum acuteeffectsofkisspeptinadministrationonbonemetabolisminhealthymen
AT yanglisa acuteeffectsofkisspeptinadministrationonbonemetabolisminhealthymen
AT millsedouardg acuteeffectsofkisspeptinadministrationonbonemetabolisminhealthymen
AT phylactoumaria acuteeffectsofkisspeptinadministrationonbonemetabolisminhealthymen
AT busbridgemark acuteeffectsofkisspeptinadministrationonbonemetabolisminhealthymen
AT khirmuaza acuteeffectsofkisspeptinadministrationonbonemetabolisminhealthymen
AT thaventhiranthilipan acuteeffectsofkisspeptinadministrationonbonemetabolisminhealthymen
AT bechpaul acuteeffectsofkisspeptinadministrationonbonemetabolisminhealthymen
AT tantricia acuteeffectsofkisspeptinadministrationonbonemetabolisminhealthymen
AT abbaraali acuteeffectsofkisspeptinadministrationonbonemetabolisminhealthymen
AT frostmorten acuteeffectsofkisspeptinadministrationonbonemetabolisminhealthymen
AT dhillowaljits acuteeffectsofkisspeptinadministrationonbonemetabolisminhealthymen