Amitriptyline efficacy in decreasing implant‐induced foreign body reaction
Beyond its actions on the nervous system, amitriptyline (AM) has been shown to lower inflammatory, angiogenic, and fibrogenic markers in a few pathological conditions in human and in experimental animal models. However, its effects on foreign body reaction (FBR), a complex adverse healing process, a...
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Veröffentlicht in: | IUBMB life 2023-09, Vol.75 (9), p.732-742 |
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creator | Scheuermann, Karina Viana, Celso Tarso Rodrigues Reis, Diego Carlos Lazari, Marcela Guimarães Takahashi Orellano, Laura Alejandra Ariza Machado, Clara Tolentino Santos, Leticia Cristine Cardoso Ulrich, Henning Capettini, Luciano Santos Aggum Andrade, Silvia Passos Campos, Paula Peixoto |
description | Beyond its actions on the nervous system, amitriptyline (AM) has been shown to lower inflammatory, angiogenic, and fibrogenic markers in a few pathological conditions in human and in experimental animal models. However, its effects on foreign body reaction (FBR), a complex adverse healing process, after biomedical material implantation are not known. We have evaluated the effects of AM on the angiogenic and fibrogenic components on a model of implant‐induced FBR. Sponge disks were implanted subcutaneously in C57BL/6 mice, that were treated daily with oral administration of AM (5 mg/kg) for seven consecutive days in two protocols: treatment was started on the day of surgery and the implants were removed on the seventh day after implantation and treatment started 7 days after implantation and the implants removed 14 after implantation. None of the angiogenic (vessels, Vascular endothelial growth factor (VEGF), and interleukin‐1β (IL‐1β) or fibrogenic parameters (collagen, TGF‐β, and fibrous capsule) and giant cell numbers analyzed were attenuated by AM in 7‐day‐old implants. However, AM was able to downregulate angiogenesis and FBR in 14‐day‐old implants. The effects of AM described here expands its range of actions as a potential agent capable of attenuating fibroproliferative processes that may impair functionality of implantable devices. |
doi_str_mv | 10.1002/iub.2725 |
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However, its effects on foreign body reaction (FBR), a complex adverse healing process, after biomedical material implantation are not known. We have evaluated the effects of AM on the angiogenic and fibrogenic components on a model of implant‐induced FBR. Sponge disks were implanted subcutaneously in C57BL/6 mice, that were treated daily with oral administration of AM (5 mg/kg) for seven consecutive days in two protocols: treatment was started on the day of surgery and the implants were removed on the seventh day after implantation and treatment started 7 days after implantation and the implants removed 14 after implantation. None of the angiogenic (vessels, Vascular endothelial growth factor (VEGF), and interleukin‐1β (IL‐1β) or fibrogenic parameters (collagen, TGF‐β, and fibrous capsule) and giant cell numbers analyzed were attenuated by AM in 7‐day‐old implants. However, AM was able to downregulate angiogenesis and FBR in 14‐day‐old implants. The effects of AM described here expands its range of actions as a potential agent capable of attenuating fibroproliferative processes that may impair functionality of implantable devices.</description><identifier>ISSN: 1521-6543</identifier><identifier>EISSN: 1521-6551</identifier><identifier>DOI: 10.1002/iub.2725</identifier><identifier>PMID: 37086464</identifier><language>eng</language><publisher>Hoboken, USA: John Wiley & Sons, Inc</publisher><subject>Amitriptyline ; Angiogenesis ; Animal models ; Foreign bodies ; foreign body reaction ; Inflammation ; matrix remodeling ; Nervous system ; Oral administration ; sponge model ; Transplants & implants ; Vascular endothelial growth factor</subject><ispartof>IUBMB life, 2023-09, Vol.75 (9), p.732-742</ispartof><rights>2023 International Union of Biochemistry and Molecular Biology.</rights><rights>2023 International Union of Biochemistry and Molecular Biology</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3495-ea89fc0985472e016fe6b5bbe603870789297d5bb45a2aca57990c444167da3a3</citedby><cites>FETCH-LOGICAL-c3495-ea89fc0985472e016fe6b5bbe603870789297d5bb45a2aca57990c444167da3a3</cites><orcidid>0000-0002-2114-3815</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fiub.2725$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fiub.2725$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,1427,27901,27902,45550,45551,46384,46808</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37086464$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Scheuermann, Karina</creatorcontrib><creatorcontrib>Viana, Celso Tarso Rodrigues</creatorcontrib><creatorcontrib>Reis, Diego Carlos</creatorcontrib><creatorcontrib>Lazari, Marcela Guimarães Takahashi</creatorcontrib><creatorcontrib>Orellano, Laura Alejandra Ariza</creatorcontrib><creatorcontrib>Machado, Clara Tolentino</creatorcontrib><creatorcontrib>Santos, Leticia Cristine Cardoso</creatorcontrib><creatorcontrib>Ulrich, Henning</creatorcontrib><creatorcontrib>Capettini, Luciano Santos Aggum</creatorcontrib><creatorcontrib>Andrade, Silvia Passos</creatorcontrib><creatorcontrib>Campos, Paula Peixoto</creatorcontrib><title>Amitriptyline efficacy in decreasing implant‐induced foreign body reaction</title><title>IUBMB life</title><addtitle>IUBMB Life</addtitle><description>Beyond its actions on the nervous system, amitriptyline (AM) has been shown to lower inflammatory, angiogenic, and fibrogenic markers in a few pathological conditions in human and in experimental animal models. However, its effects on foreign body reaction (FBR), a complex adverse healing process, after biomedical material implantation are not known. We have evaluated the effects of AM on the angiogenic and fibrogenic components on a model of implant‐induced FBR. Sponge disks were implanted subcutaneously in C57BL/6 mice, that were treated daily with oral administration of AM (5 mg/kg) for seven consecutive days in two protocols: treatment was started on the day of surgery and the implants were removed on the seventh day after implantation and treatment started 7 days after implantation and the implants removed 14 after implantation. None of the angiogenic (vessels, Vascular endothelial growth factor (VEGF), and interleukin‐1β (IL‐1β) or fibrogenic parameters (collagen, TGF‐β, and fibrous capsule) and giant cell numbers analyzed were attenuated by AM in 7‐day‐old implants. However, AM was able to downregulate angiogenesis and FBR in 14‐day‐old implants. The effects of AM described here expands its range of actions as a potential agent capable of attenuating fibroproliferative processes that may impair functionality of implantable devices.</description><subject>Amitriptyline</subject><subject>Angiogenesis</subject><subject>Animal models</subject><subject>Foreign bodies</subject><subject>foreign body reaction</subject><subject>Inflammation</subject><subject>matrix remodeling</subject><subject>Nervous system</subject><subject>Oral administration</subject><subject>sponge model</subject><subject>Transplants & implants</subject><subject>Vascular endothelial growth factor</subject><issn>1521-6543</issn><issn>1521-6551</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp1kM1Kw0AQxxdRbK2CTyABL15Sdzf7kRxr8aNQ8GLPYbOZlC35cjdBcvMRfEafxK2tFQTnMsPw4zfDH6FLgqcEY3pr-mxKJeVHaEw4JaHgnBwfZhaN0JlzG-xL4uQUjSKJY8EEG6PlrDKdNW03lKaGAIrCaKWHwNRBDtqCcqZeB6ZqS1V3n-8fps57DXlQNBbMug6yJh8Cj-nONPU5OilU6eBi3ydo9XD_Mn8Kl8-Pi_lsGeqIJTwEFSeFxknMmaSAiShAZDzLQOAolljGCU1k7heMK6q04jJJsGaMESFzFalogm523tY2rz24Lq2M01D6H6HpXUpjzDHlMmIevf6Dbpre1v47T3F_WxAa_wq1bZyzUKStNZWyQ0pwuk049Qmn24Q9erUX9lkF-QH8idQD4Q54MyUM_4rSxeruW_gF_-eEiQ</recordid><startdate>202309</startdate><enddate>202309</enddate><creator>Scheuermann, Karina</creator><creator>Viana, Celso Tarso Rodrigues</creator><creator>Reis, Diego Carlos</creator><creator>Lazari, Marcela Guimarães Takahashi</creator><creator>Orellano, Laura Alejandra Ariza</creator><creator>Machado, Clara Tolentino</creator><creator>Santos, Leticia Cristine Cardoso</creator><creator>Ulrich, Henning</creator><creator>Capettini, Luciano Santos Aggum</creator><creator>Andrade, Silvia Passos</creator><creator>Campos, Paula Peixoto</creator><general>John Wiley & Sons, Inc</general><general>Wiley Subscription Services, Inc</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-2114-3815</orcidid></search><sort><creationdate>202309</creationdate><title>Amitriptyline efficacy in decreasing implant‐induced foreign body reaction</title><author>Scheuermann, Karina ; Viana, Celso Tarso Rodrigues ; Reis, Diego Carlos ; Lazari, Marcela Guimarães Takahashi ; Orellano, Laura Alejandra Ariza ; Machado, Clara Tolentino ; Santos, Leticia Cristine Cardoso ; Ulrich, Henning ; Capettini, Luciano Santos Aggum ; Andrade, Silvia Passos ; Campos, Paula Peixoto</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3495-ea89fc0985472e016fe6b5bbe603870789297d5bb45a2aca57990c444167da3a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Amitriptyline</topic><topic>Angiogenesis</topic><topic>Animal models</topic><topic>Foreign bodies</topic><topic>foreign body reaction</topic><topic>Inflammation</topic><topic>matrix remodeling</topic><topic>Nervous system</topic><topic>Oral administration</topic><topic>sponge model</topic><topic>Transplants & implants</topic><topic>Vascular endothelial growth factor</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Scheuermann, Karina</creatorcontrib><creatorcontrib>Viana, Celso Tarso Rodrigues</creatorcontrib><creatorcontrib>Reis, Diego Carlos</creatorcontrib><creatorcontrib>Lazari, Marcela Guimarães Takahashi</creatorcontrib><creatorcontrib>Orellano, Laura Alejandra Ariza</creatorcontrib><creatorcontrib>Machado, Clara Tolentino</creatorcontrib><creatorcontrib>Santos, Leticia Cristine Cardoso</creatorcontrib><creatorcontrib>Ulrich, Henning</creatorcontrib><creatorcontrib>Capettini, Luciano Santos Aggum</creatorcontrib><creatorcontrib>Andrade, Silvia Passos</creatorcontrib><creatorcontrib>Campos, Paula Peixoto</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>IUBMB life</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Scheuermann, Karina</au><au>Viana, Celso Tarso Rodrigues</au><au>Reis, Diego Carlos</au><au>Lazari, Marcela Guimarães Takahashi</au><au>Orellano, Laura Alejandra Ariza</au><au>Machado, Clara Tolentino</au><au>Santos, Leticia Cristine Cardoso</au><au>Ulrich, Henning</au><au>Capettini, Luciano Santos Aggum</au><au>Andrade, Silvia Passos</au><au>Campos, Paula Peixoto</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Amitriptyline efficacy in decreasing implant‐induced foreign body reaction</atitle><jtitle>IUBMB life</jtitle><addtitle>IUBMB Life</addtitle><date>2023-09</date><risdate>2023</risdate><volume>75</volume><issue>9</issue><spage>732</spage><epage>742</epage><pages>732-742</pages><issn>1521-6543</issn><eissn>1521-6551</eissn><abstract>Beyond its actions on the nervous system, amitriptyline (AM) has been shown to lower inflammatory, angiogenic, and fibrogenic markers in a few pathological conditions in human and in experimental animal models. However, its effects on foreign body reaction (FBR), a complex adverse healing process, after biomedical material implantation are not known. We have evaluated the effects of AM on the angiogenic and fibrogenic components on a model of implant‐induced FBR. Sponge disks were implanted subcutaneously in C57BL/6 mice, that were treated daily with oral administration of AM (5 mg/kg) for seven consecutive days in two protocols: treatment was started on the day of surgery and the implants were removed on the seventh day after implantation and treatment started 7 days after implantation and the implants removed 14 after implantation. None of the angiogenic (vessels, Vascular endothelial growth factor (VEGF), and interleukin‐1β (IL‐1β) or fibrogenic parameters (collagen, TGF‐β, and fibrous capsule) and giant cell numbers analyzed were attenuated by AM in 7‐day‐old implants. However, AM was able to downregulate angiogenesis and FBR in 14‐day‐old implants. The effects of AM described here expands its range of actions as a potential agent capable of attenuating fibroproliferative processes that may impair functionality of implantable devices.</abstract><cop>Hoboken, USA</cop><pub>John Wiley & Sons, Inc</pub><pmid>37086464</pmid><doi>10.1002/iub.2725</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0002-2114-3815</orcidid></addata></record> |
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subjects | Amitriptyline Angiogenesis Animal models Foreign bodies foreign body reaction Inflammation matrix remodeling Nervous system Oral administration sponge model Transplants & implants Vascular endothelial growth factor |
title | Amitriptyline efficacy in decreasing implant‐induced foreign body reaction |
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