Investigational parathyroid hormone receptor analogs for the treatment of osteoporosis
- PMID: 25316089
- DOI: 10.1517/13543784.2015.973021
Investigational parathyroid hormone receptor analogs for the treatment of osteoporosis
Abstract
Introduction: Intermittent parathyroid hormone (PTH) administration, acting through multiple signaling pathways, exerts an osteoanabolic effect on the skeleton that surpasses the effect of other antiosteoporotic agents. However, its efficacy is limited by the coupling effect and relatively common adverse events. Thus, the development of more sophisticated PTH receptor analogs seems imperative.
Areas covered: In this review, the authors summarize the role of PTH signaling pathway in bone remodeling. The authors also summarize investigational analogs targeting this pathway, which may be potential treatments for osteoporosis.
Expert opinion: β-arrestins are multifunctional cytoplasmic molecules that are decisive for regulating intracellular PTH signaling. Recently, in preclinical studies, arrestin analogs have achieved the anabolic bone effect of PTH without an accompanying increase in bone resorption. However, it is not yet known whether these analogs have adverse effects and there are no clinical data for their efficacy to date. On the other hand, several molecules derived either from PTH and PTH-related protein (PTHrP) molecules have been developed. Alternative routes of PTH 1 - 34 delivery (oral, transdermal), the PTH analog ostabolin and the N-terminal PTHrP analogs PTHrP 1 - 36 and abaloparatide, have recently been or are currently being tested in clinical trials and are more likely to become available for use in the near future.
Keywords: arrestin; osteoanabolic; osteoporosis; parathyroid hormone; parathyroid hormone-related peptide; treatment.
Similar articles
-
Current perspectives on parathyroid hormone (PTH) and PTH-related protein (PTHrP) as bone anabolic therapies.Biochem Pharmacol. 2013 May 15;85(10):1417-23. doi: 10.1016/j.bcp.2013.03.002. Epub 2013 Mar 13. Biochem Pharmacol. 2013. PMID: 23500550 Review.
-
Parathyroid hormone (PTH) and PTH-related peptide domains contributing to activation of different PTH receptor-mediated signaling pathways.J Pharmacol Exp Ther. 2013 Jun;345(3):404-18. doi: 10.1124/jpet.112.199752. Epub 2013 Mar 20. J Pharmacol Exp Ther. 2013. PMID: 23516330
-
β-Arrestin-biased signaling of PTH analogs of the type 1 parathyroid hormone receptor.Cell Signal. 2013 Feb;25(2):527-38. doi: 10.1016/j.cellsig.2012.11.012. Epub 2012 Nov 15. Cell Signal. 2013. PMID: 23159578
-
β-arrestin-biased agonism at the parathyroid hormone receptor uncouples bone formation from bone resorption.Endocr Metab Immune Disord Drug Targets. 2011 Jun;11(2):112-9. doi: 10.2174/187153011795564151. Endocr Metab Immune Disord Drug Targets. 2011. PMID: 21476967 Review.
-
Arrestins in bone.Prog Mol Biol Transl Sci. 2013;118:335-58. doi: 10.1016/B978-0-12-394440-5.00013-9. Prog Mol Biol Transl Sci. 2013. PMID: 23764060 Review.
Cited by
-
Prolonged Pharmacokinetic and Pharmacodynamic Actions of a Pegylated Parathyroid Hormone (1-34) Peptide Fragment.J Bone Miner Res. 2017 Jan;32(1):86-98. doi: 10.1002/jbmr.2917. Epub 2016 Sep 9. J Bone Miner Res. 2017. PMID: 27428040 Free PMC article.
-
Abaloparatide.Clin Cases Miner Bone Metab. 2016 May-Aug;13(2):106-109. doi: 10.11138/ccmbm/2016.13.2.106. Epub 2016 Oct 5. Clin Cases Miner Bone Metab. 2016. PMID: 27920805 Free PMC article. Review.
-
Chronic kidney disease and the skeleton.Bone Res. 2014 Dec 23;2:14044. doi: 10.1038/boneres.2014.44. eCollection 2014. Bone Res. 2014. PMID: 26273531 Free PMC article. Review.
-
Attenuation of Alzheimer's brain pathology in 5XFAD mice by PTH1-34, a peptide of parathyroid hormone.Alzheimers Res Ther. 2023 Mar 14;15(1):53. doi: 10.1186/s13195-023-01202-z. Alzheimers Res Ther. 2023. PMID: 36918976 Free PMC article.
-
PTH receptor-1 signalling-mechanistic insights and therapeutic prospects.Nat Rev Endocrinol. 2015 Dec;11(12):712-24. doi: 10.1038/nrendo.2015.139. Epub 2015 Aug 25. Nat Rev Endocrinol. 2015. PMID: 26303600 Free PMC article. Review.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
Research Materials