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Local administration of WP9QY (W9) peptide promotes bone formation in a rat femur delayed-union model
The WP9QY peptide (W9) consists of nine amino acids. It binds to RANKL and blocks RANKL-induced increases in bone resorption and osteoclastogenesis. W9 has a unique effect on the coupling mechanism between osteoclasts and osteoblasts, which promotes bone formation while working to suppress bone reso...
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Published in: | Journal of bone and mineral metabolism 2018-07, Vol.36 (4), p.383-391 |
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container_title | Journal of bone and mineral metabolism |
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creator | Sawa, Mikiya Wakitani, Shigeyuki Kamei, Naosuke Kotaka, Shinji Adachi, Nobuo Ochi, Mitsuo |
description | The WP9QY peptide (W9) consists of nine amino acids. It binds to RANKL and blocks RANKL-induced increases in bone resorption and osteoclastogenesis. W9 has a unique effect on the coupling mechanism between osteoclasts and osteoblasts, which promotes bone formation while working to suppress bone resorption. In this study, with the aim of clinical application of W9 for fracture treatment, we aimed to clarify the bone repair-promoting effect of W9 when administered locally to a rat femur model of delayed union. Using Sprague–Dawley rats, a model of delayed union was created in the right femur by cauterizing the periosteum. Injection of W9 (1 mg in 100 μl) or phosphate-buffered saline (PBS) (100 μl) at the fracture site was performed at the operation and every week thereafter until death (sacrifice). The bone union rate was 14% in the PBS group and 57% in the W9 group at 8 weeks postoperatively. The X-ray score of the W9 group was significantly higher than that of the PBS group at 8 weeks postoperatively. When bone morphometry was analyzed by micro-computed tomography (CT), total callus volume (TV) and mineralized callus bone volume (BV) were measured. TV showed no significant difference between the two groups, but BV/TV was significantly higher in the W9 group. This finding suggests that local administration of W9 can promote bone maturation from callus and can be considered to contribute to fracture healing. These results reveal that W9 has an effect on fractures of promoting healing and could be applied as a fracture treatment. |
doi_str_mv | 10.1007/s00774-017-0852-5 |
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It binds to RANKL and blocks RANKL-induced increases in bone resorption and osteoclastogenesis. W9 has a unique effect on the coupling mechanism between osteoclasts and osteoblasts, which promotes bone formation while working to suppress bone resorption. In this study, with the aim of clinical application of W9 for fracture treatment, we aimed to clarify the bone repair-promoting effect of W9 when administered locally to a rat femur model of delayed union. Using Sprague–Dawley rats, a model of delayed union was created in the right femur by cauterizing the periosteum. Injection of W9 (1 mg in 100 μl) or phosphate-buffered saline (PBS) (100 μl) at the fracture site was performed at the operation and every week thereafter until death (sacrifice). The bone union rate was 14% in the PBS group and 57% in the W9 group at 8 weeks postoperatively. The X-ray score of the W9 group was significantly higher than that of the PBS group at 8 weeks postoperatively. When bone morphometry was analyzed by micro-computed tomography (CT), total callus volume (TV) and mineralized callus bone volume (BV) were measured. TV showed no significant difference between the two groups, but BV/TV was significantly higher in the W9 group. This finding suggests that local administration of W9 can promote bone maturation from callus and can be considered to contribute to fracture healing. These results reveal that W9 has an effect on fractures of promoting healing and could be applied as a fracture treatment.</description><identifier>ISSN: 0914-8779</identifier><identifier>EISSN: 1435-5604</identifier><identifier>DOI: 10.1007/s00774-017-0852-5</identifier><identifier>PMID: 28660377</identifier><language>eng</language><publisher>Tokyo: Springer Japan</publisher><subject>Bone growth ; Bone healing ; Bone resorption ; Callus ; Computed tomography ; Femur ; Fractures ; Medicine ; Medicine & Public Health ; Metabolic Diseases ; Morphometry ; Original Article ; Orthopedics ; Osteoblasts ; Osteoclastogenesis ; Osteoclasts ; Osteogenesis ; Periosteum ; TRANCE protein</subject><ispartof>Journal of bone and mineral metabolism, 2018-07, Vol.36 (4), p.383-391</ispartof><rights>The Japanese Society for Bone and Mineral Research and Springer Japan KK 2017</rights><rights>Journal of Bone and Mineral Metabolism is a copyright of Springer, (2017). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c589t-82eae53e0634c188836910ec8e02f18698a6e20f82fa95106c9c597da6c6aa783</citedby><cites>FETCH-LOGICAL-c589t-82eae53e0634c188836910ec8e02f18698a6e20f82fa95106c9c597da6c6aa783</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28660377$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sawa, Mikiya</creatorcontrib><creatorcontrib>Wakitani, Shigeyuki</creatorcontrib><creatorcontrib>Kamei, Naosuke</creatorcontrib><creatorcontrib>Kotaka, Shinji</creatorcontrib><creatorcontrib>Adachi, Nobuo</creatorcontrib><creatorcontrib>Ochi, Mitsuo</creatorcontrib><title>Local administration of WP9QY (W9) peptide promotes bone formation in a rat femur delayed-union model</title><title>Journal of bone and mineral metabolism</title><addtitle>J Bone Miner Metab</addtitle><addtitle>J Bone Miner Metab</addtitle><description>The WP9QY peptide (W9) consists of nine amino acids. It binds to RANKL and blocks RANKL-induced increases in bone resorption and osteoclastogenesis. W9 has a unique effect on the coupling mechanism between osteoclasts and osteoblasts, which promotes bone formation while working to suppress bone resorption. In this study, with the aim of clinical application of W9 for fracture treatment, we aimed to clarify the bone repair-promoting effect of W9 when administered locally to a rat femur model of delayed union. Using Sprague–Dawley rats, a model of delayed union was created in the right femur by cauterizing the periosteum. Injection of W9 (1 mg in 100 μl) or phosphate-buffered saline (PBS) (100 μl) at the fracture site was performed at the operation and every week thereafter until death (sacrifice). The bone union rate was 14% in the PBS group and 57% in the W9 group at 8 weeks postoperatively. The X-ray score of the W9 group was significantly higher than that of the PBS group at 8 weeks postoperatively. When bone morphometry was analyzed by micro-computed tomography (CT), total callus volume (TV) and mineralized callus bone volume (BV) were measured. TV showed no significant difference between the two groups, but BV/TV was significantly higher in the W9 group. This finding suggests that local administration of W9 can promote bone maturation from callus and can be considered to contribute to fracture healing. These results reveal that W9 has an effect on fractures of promoting healing and could be applied as a fracture treatment.</description><subject>Bone growth</subject><subject>Bone healing</subject><subject>Bone resorption</subject><subject>Callus</subject><subject>Computed tomography</subject><subject>Femur</subject><subject>Fractures</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metabolic Diseases</subject><subject>Morphometry</subject><subject>Original Article</subject><subject>Orthopedics</subject><subject>Osteoblasts</subject><subject>Osteoclastogenesis</subject><subject>Osteoclasts</subject><subject>Osteogenesis</subject><subject>Periosteum</subject><subject>TRANCE protein</subject><issn>0914-8779</issn><issn>1435-5604</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kUtr3DAUhUVpaCaPH9BNEXSTLJReydZrWUKbBAaSQMOQlVDk6-JgW1PJXuTfR4OnLQSykRD3O0eXcwj5zOGCA-hvuRy6ZsA1AyMFkx_IiteVZFJB_ZGswPKaGa3tITnK-RkKKDX_RA6FUQoqrVcE1zH4nvpm6MYuT8lPXRxpbOnmzt4_0rONPadb3E5dg3Sb4hAnzPQpjkjbmIaF7kbqaVHSFoc50QZ7_4INm8fdcIjlfUIOWt9nPN3fx-Th549fl9dsfXt1c_l9zYI0dmJGoEdZIaiqDtwYUynLAYNBEC03yhqvUEBrROut5KCCDdLqxqugvNemOiZni29Z9c-MeXJDlwP2vR8xztnxEoiRAKIq6Nc36HOc01i2cwJUCUooqQvFFyqkmHPC1m1TN_j04ji4XQdu6cCVaN2uAyeL5sveeX4asPmn-Bt6AcQC5DIaf2P6__X7rq84po_Y</recordid><startdate>20180701</startdate><enddate>20180701</enddate><creator>Sawa, Mikiya</creator><creator>Wakitani, Shigeyuki</creator><creator>Kamei, Naosuke</creator><creator>Kotaka, Shinji</creator><creator>Adachi, Nobuo</creator><creator>Ochi, Mitsuo</creator><general>Springer Japan</general><general>Springer Nature B.V</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20180701</creationdate><title>Local administration of WP9QY (W9) peptide promotes bone formation in a rat femur delayed-union model</title><author>Sawa, Mikiya ; 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subjects | Bone growth Bone healing Bone resorption Callus Computed tomography Femur Fractures Medicine Medicine & Public Health Metabolic Diseases Morphometry Original Article Orthopedics Osteoblasts Osteoclastogenesis Osteoclasts Osteogenesis Periosteum TRANCE protein |
title | Local administration of WP9QY (W9) peptide promotes bone formation in a rat femur delayed-union model |
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