Acute Effects of Kisspeptin Administration on Bone Metabolism in Healthy Men

Author:

Comninos Alexander N123ORCID,Hansen Morten S45,Courtney Alan6,Choudhury Sirazum16ORCID,Yang Lisa1,Mills Edouard G1,Phylactou Maria1,Busbridge Mark6,Khir Muaza6,Thaventhiran Thilipan1,Bech Paul16,Tan Tricia16ORCID,Abbara Ali12ORCID,Frost Morten457,Dhillo Waljit S12ORCID

Affiliation:

1. Division of Diabetes, Endocrinology and Metabolism, Imperial College London, London, UK

2. Department of Endocrinology, Imperial College Healthcare NHS Trust, London, UK

3. Endocrine Bone Unit, Imperial College Healthcare NHS Trust, London, UK

4. KMEB Molecular Endocrinology Laboratory, Department of Endocrinology, Odense University Hospital, Denmark

5. Department of Clinical Research, University of Southern Denmark, Denmark

6. Department of Clinical Biochemistry, Imperial College Healthcare NHS Trust, London, UK

7. Steno Diabetes Centre, Odense University Hospital, Denmark

Abstract

Abstract 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.

Funder

MRC

NIHR

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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