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Bone healing response in cyclically loaded implants: Comparing zero, one, and two loading sessions per day

When bone implants are loaded, they are inevitably subjected to displacement relative to bone. Such micro-motion generates stress/strain states at the interface that can cause beneficial or detrimental sequels. The objective of this study is to better understand the mechanobiology of bone healing at...

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Autores principales: Bueno, Renan de Barros e Lima, Dias, Ana Paula, Ponce, Katia J., Wazen, Rima, Brunski, John B., Nanci, Antonio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6035061/
https://www.ncbi.nlm.nih.gov/pubmed/29894930
http://dx.doi.org/10.1016/j.jmbbm.2018.05.044
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author Bueno, Renan de Barros e Lima
Dias, Ana Paula
Ponce, Katia J.
Wazen, Rima
Brunski, John B.
Nanci, Antonio
author_facet Bueno, Renan de Barros e Lima
Dias, Ana Paula
Ponce, Katia J.
Wazen, Rima
Brunski, John B.
Nanci, Antonio
author_sort Bueno, Renan de Barros e Lima
collection PubMed
description When bone implants are loaded, they are inevitably subjected to displacement relative to bone. Such micro-motion generates stress/strain states at the interface that can cause beneficial or detrimental sequels. The objective of this study is to better understand the mechanobiology of bone healing at the tissue-implant interface during repeated loading. Machined screw shaped Ti implants were placed in rat tibiae in a hole slightly bigger than the implant diameter. Implants were held stable by a specially-designed bone plate that permits controlled loading. Three loading regimens were applied, (a) zero loading, (b) one daily loading session of 60 cycles with an axial force of 1.5 N/cycle for 7 days, and (c) two such daily sessions with the same axial force also for 7 days. Finite element analysis was used to characterize the mechanobiological conditions produced by the loading sessions. After 7 days, the implants with surrounding interfacial tissue were harvested and processed for histological, histomorphometric and DNA microarray analyses. Histomorphometric analyses revealed that the group subjected to repeated loading sessions exhibited a significant decrease in bone-implant contact and increase in bone-implant distance, as compared to unloaded implants and those subjected to only one loading session. Gene expression profiles differed during osseointegration between all groups mainly with respect to inflammatory and unidentified gene categories. The results indicate that increasing the daily cyclic loading of implants induces deleterious changes in the bone healing response, most likely due to the accumulation of tissue damage and associated inflammatory reaction at the bone-implant interface.
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spelling pubmed-60350612019-09-01 Bone healing response in cyclically loaded implants: Comparing zero, one, and two loading sessions per day Bueno, Renan de Barros e Lima Dias, Ana Paula Ponce, Katia J. Wazen, Rima Brunski, John B. Nanci, Antonio J Mech Behav Biomed Mater Article When bone implants are loaded, they are inevitably subjected to displacement relative to bone. Such micro-motion generates stress/strain states at the interface that can cause beneficial or detrimental sequels. The objective of this study is to better understand the mechanobiology of bone healing at the tissue-implant interface during repeated loading. Machined screw shaped Ti implants were placed in rat tibiae in a hole slightly bigger than the implant diameter. Implants were held stable by a specially-designed bone plate that permits controlled loading. Three loading regimens were applied, (a) zero loading, (b) one daily loading session of 60 cycles with an axial force of 1.5 N/cycle for 7 days, and (c) two such daily sessions with the same axial force also for 7 days. Finite element analysis was used to characterize the mechanobiological conditions produced by the loading sessions. After 7 days, the implants with surrounding interfacial tissue were harvested and processed for histological, histomorphometric and DNA microarray analyses. Histomorphometric analyses revealed that the group subjected to repeated loading sessions exhibited a significant decrease in bone-implant contact and increase in bone-implant distance, as compared to unloaded implants and those subjected to only one loading session. Gene expression profiles differed during osseointegration between all groups mainly with respect to inflammatory and unidentified gene categories. The results indicate that increasing the daily cyclic loading of implants induces deleterious changes in the bone healing response, most likely due to the accumulation of tissue damage and associated inflammatory reaction at the bone-implant interface. 2018-05-31 2018-09 /pmc/articles/PMC6035061/ /pubmed/29894930 http://dx.doi.org/10.1016/j.jmbbm.2018.05.044 Text en https://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/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Article
Bueno, Renan de Barros e Lima
Dias, Ana Paula
Ponce, Katia J.
Wazen, Rima
Brunski, John B.
Nanci, Antonio
Bone healing response in cyclically loaded implants: Comparing zero, one, and two loading sessions per day
title Bone healing response in cyclically loaded implants: Comparing zero, one, and two loading sessions per day
title_full Bone healing response in cyclically loaded implants: Comparing zero, one, and two loading sessions per day
title_fullStr Bone healing response in cyclically loaded implants: Comparing zero, one, and two loading sessions per day
title_full_unstemmed Bone healing response in cyclically loaded implants: Comparing zero, one, and two loading sessions per day
title_short Bone healing response in cyclically loaded implants: Comparing zero, one, and two loading sessions per day
title_sort bone healing response in cyclically loaded implants: comparing zero, one, and two loading sessions per day
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6035061/
https://www.ncbi.nlm.nih.gov/pubmed/29894930
http://dx.doi.org/10.1016/j.jmbbm.2018.05.044
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