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Donepezil prevents RANK-induced bone loss via inhibition of osteoclast differentiation by downregulating acetylcholinesterase
OBJECTIVE: Donepezil, an inhibitor of acetylcholinesterase (AChE) targeting the brain, is a common medication for Alzheimer's disease. Interestingly, a recent clinical study found that administration of this agent is associated with lower risk of hip fracture independently of falling, suggestin...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4939821/ https://www.ncbi.nlm.nih.gov/pubmed/27441211 http://dx.doi.org/10.1016/j.heliyon.2015.e00013 |
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author | Sato, Tsuyoshi Enoki, Yuichiro Sakamoto, Yasushi Yokota, Kazuhiro Okubo, Masahiko Matsumoto, Masahito Hayashi, Naoki Usui, Michihiko Kokabu, Shoichiro Mimura, Toshihide Nakazato, Yoshihiko Araki, Nobuo Fukuda, Toru Okazaki, Yasushi Suda, Tatsuo Takeda, Shu Yoda, Tetsuya |
author_facet | Sato, Tsuyoshi Enoki, Yuichiro Sakamoto, Yasushi Yokota, Kazuhiro Okubo, Masahiko Matsumoto, Masahito Hayashi, Naoki Usui, Michihiko Kokabu, Shoichiro Mimura, Toshihide Nakazato, Yoshihiko Araki, Nobuo Fukuda, Toru Okazaki, Yasushi Suda, Tatsuo Takeda, Shu Yoda, Tetsuya |
author_sort | Sato, Tsuyoshi |
collection | PubMed |
description | OBJECTIVE: Donepezil, an inhibitor of acetylcholinesterase (AChE) targeting the brain, is a common medication for Alzheimer's disease. Interestingly, a recent clinical study found that administration of this agent is associated with lower risk of hip fracture independently of falling, suggesting its direct effect on bone tissues as well. AChE has been reported to be involved in osteoblast function, but the role of AChE on osteoclastogenesis still remains unclear. We analyzed the effect of AChE and donepezil on osteoclastogenesis in vivo and in vitro. METHODS: Cell-based assays were conducted using osteoclasts generated in cultures of murine bone marrow macrophages (BMMs) with receptor activator of nuclear factor-kappa B ligand (RANKL). The effect of donepezil was also determined in vivo using a mouse model of RANKL-induced bone loss. RESULTS: Recombinant AChE in BMMs cultured with RANKL further promoted RANKL-induced tartrate-resistant acid phosphatase (TRAP)-positive osteoclast differentiation. RANKL also upregulated AChE expression in BMMs. RNA interference-mediated knockdown of AChE significantly inhibited RANKL-induced osteoclast differentiation and suppressed gene expression specific for osteoclasts. AChE upregulated expression of RANK, the receptor of RANKL, in BMMs. Donepezil decreased cathepsin K expression in BMMs and the resorptive function of osteoclasts on dentine slices. Donepezil decreased RANK expression in BMMs, resulting in the inhibition of osteoclast differentiation with downregulation of c-Fos and upregulation of Id2. Moreover, administration of donepezil prevented RANKL-induced bone loss in vivo, which was associated with the inhibition of bone resorption by osteoclasts. CONCLUSIONS: AChE promotes osteoclast differentiation in vitro. Donepezil inhibits osteoclast function in vitro and prevents bone loss by suppressing bone resorption in vivo, suggesting the possibility that donepezil reduces fracture risk in patients with Alzheimer's disease. |
format | Online Article Text |
id | pubmed-4939821 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-49398212016-07-20 Donepezil prevents RANK-induced bone loss via inhibition of osteoclast differentiation by downregulating acetylcholinesterase Sato, Tsuyoshi Enoki, Yuichiro Sakamoto, Yasushi Yokota, Kazuhiro Okubo, Masahiko Matsumoto, Masahito Hayashi, Naoki Usui, Michihiko Kokabu, Shoichiro Mimura, Toshihide Nakazato, Yoshihiko Araki, Nobuo Fukuda, Toru Okazaki, Yasushi Suda, Tatsuo Takeda, Shu Yoda, Tetsuya Heliyon Article OBJECTIVE: Donepezil, an inhibitor of acetylcholinesterase (AChE) targeting the brain, is a common medication for Alzheimer's disease. Interestingly, a recent clinical study found that administration of this agent is associated with lower risk of hip fracture independently of falling, suggesting its direct effect on bone tissues as well. AChE has been reported to be involved in osteoblast function, but the role of AChE on osteoclastogenesis still remains unclear. We analyzed the effect of AChE and donepezil on osteoclastogenesis in vivo and in vitro. METHODS: Cell-based assays were conducted using osteoclasts generated in cultures of murine bone marrow macrophages (BMMs) with receptor activator of nuclear factor-kappa B ligand (RANKL). The effect of donepezil was also determined in vivo using a mouse model of RANKL-induced bone loss. RESULTS: Recombinant AChE in BMMs cultured with RANKL further promoted RANKL-induced tartrate-resistant acid phosphatase (TRAP)-positive osteoclast differentiation. RANKL also upregulated AChE expression in BMMs. RNA interference-mediated knockdown of AChE significantly inhibited RANKL-induced osteoclast differentiation and suppressed gene expression specific for osteoclasts. AChE upregulated expression of RANK, the receptor of RANKL, in BMMs. Donepezil decreased cathepsin K expression in BMMs and the resorptive function of osteoclasts on dentine slices. Donepezil decreased RANK expression in BMMs, resulting in the inhibition of osteoclast differentiation with downregulation of c-Fos and upregulation of Id2. Moreover, administration of donepezil prevented RANKL-induced bone loss in vivo, which was associated with the inhibition of bone resorption by osteoclasts. CONCLUSIONS: AChE promotes osteoclast differentiation in vitro. Donepezil inhibits osteoclast function in vitro and prevents bone loss by suppressing bone resorption in vivo, suggesting the possibility that donepezil reduces fracture risk in patients with Alzheimer's disease. Elsevier 2015-09-21 /pmc/articles/PMC4939821/ /pubmed/27441211 http://dx.doi.org/10.1016/j.heliyon.2015.e00013 Text en © 2015 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Sato, Tsuyoshi Enoki, Yuichiro Sakamoto, Yasushi Yokota, Kazuhiro Okubo, Masahiko Matsumoto, Masahito Hayashi, Naoki Usui, Michihiko Kokabu, Shoichiro Mimura, Toshihide Nakazato, Yoshihiko Araki, Nobuo Fukuda, Toru Okazaki, Yasushi Suda, Tatsuo Takeda, Shu Yoda, Tetsuya Donepezil prevents RANK-induced bone loss via inhibition of osteoclast differentiation by downregulating acetylcholinesterase |
title | Donepezil prevents RANK-induced bone loss via inhibition of osteoclast differentiation by downregulating acetylcholinesterase |
title_full | Donepezil prevents RANK-induced bone loss via inhibition of osteoclast differentiation by downregulating acetylcholinesterase |
title_fullStr | Donepezil prevents RANK-induced bone loss via inhibition of osteoclast differentiation by downregulating acetylcholinesterase |
title_full_unstemmed | Donepezil prevents RANK-induced bone loss via inhibition of osteoclast differentiation by downregulating acetylcholinesterase |
title_short | Donepezil prevents RANK-induced bone loss via inhibition of osteoclast differentiation by downregulating acetylcholinesterase |
title_sort | donepezil prevents rank-induced bone loss via inhibition of osteoclast differentiation by downregulating acetylcholinesterase |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4939821/ https://www.ncbi.nlm.nih.gov/pubmed/27441211 http://dx.doi.org/10.1016/j.heliyon.2015.e00013 |
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