Luciano Aparecido de Almeida-Junior, Juliana de Lima Gonçalves, Maya Fernanda Manfrin Arnez, Nallery Steysi Rostrán Jimenez, Guido Artemio Marañón-Vasquez, Francisco Wanderley Garcia de Paula-Silva
{"title":"全身和局部给药抗肿瘤坏死因子-α受体-1对小鼠根尖周骨丢失的影响。","authors":"Luciano Aparecido de Almeida-Junior, Juliana de Lima Gonçalves, Maya Fernanda Manfrin Arnez, Nallery Steysi Rostrán Jimenez, Guido Artemio Marañón-Vasquez, Francisco Wanderley Garcia de Paula-Silva","doi":"10.1016/j.joen.2025.05.007","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>The aim of this study was to evaluate whether systemic or topical administration of a monoclonal antibody against tumor necrosis factor-α receptor-1 (TNFR1) could control periapical bone loss in mice.</p><p><strong>Methods: </strong>Thirty C57Bl6 mice were used for induction of periapical lesion through the exposure of the root canals to the oral environment. The root canals remained open to microbial contamination from the oral cavity for 28 days. Then, the animals were randomly assigned to 3 different experimental groups: G1: animals received no medication and periapical lesion followed its natural course up to 42 days; G2: systemic administration of the TNFR1 antibody; G3: intracanal topical administration of the TNFR1 antibody. Healthy teeth were used as controls. At 42 days following periapical lesion induction, the animals were anesthetized then euthanized, and tissues containing bone and teeth were collected for microtomographic, histomorphometry, and quantitative reverse transcriptase polymerase chain reaction analysis. Then groups were compared using one-way analysis of variance followed by Turkey tests (α = 5%).</p><p><strong>Results: </strong>Systemic and topical anti-TNFR1 administered in groups G2 and G3 did not have an impact on the area and volume of periapical lesions when compared to the untreated control group G1 (P > .05). Lower expression of RANKL mRNA was observed in G3 compared to G1 (P < .05) but no change on OPG, MMP-9 or CTSK was detected (P > .05).</p><p><strong>Conclusions: </strong>Under the experimental conditions of this study, systemic or local administration of a TNFR1 antibody was not effective in limiting the expansion of periapical lesions.</p>","PeriodicalId":15703,"journal":{"name":"Journal of endodontics","volume":" ","pages":""},"PeriodicalIF":3.5000,"publicationDate":"2025-05-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Effects of Systemic and Local Anti-tumor Necrosis Factor-α Receptor-1 Administration on Periapical Bone Loss in Mice.\",\"authors\":\"Luciano Aparecido de Almeida-Junior, Juliana de Lima Gonçalves, Maya Fernanda Manfrin Arnez, Nallery Steysi Rostrán Jimenez, Guido Artemio Marañón-Vasquez, Francisco Wanderley Garcia de Paula-Silva\",\"doi\":\"10.1016/j.joen.2025.05.007\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Introduction: </strong>The aim of this study was to evaluate whether systemic or topical administration of a monoclonal antibody against tumor necrosis factor-α receptor-1 (TNFR1) could control periapical bone loss in mice.</p><p><strong>Methods: </strong>Thirty C57Bl6 mice were used for induction of periapical lesion through the exposure of the root canals to the oral environment. The root canals remained open to microbial contamination from the oral cavity for 28 days. Then, the animals were randomly assigned to 3 different experimental groups: G1: animals received no medication and periapical lesion followed its natural course up to 42 days; G2: systemic administration of the TNFR1 antibody; G3: intracanal topical administration of the TNFR1 antibody. Healthy teeth were used as controls. At 42 days following periapical lesion induction, the animals were anesthetized then euthanized, and tissues containing bone and teeth were collected for microtomographic, histomorphometry, and quantitative reverse transcriptase polymerase chain reaction analysis. Then groups were compared using one-way analysis of variance followed by Turkey tests (α = 5%).</p><p><strong>Results: </strong>Systemic and topical anti-TNFR1 administered in groups G2 and G3 did not have an impact on the area and volume of periapical lesions when compared to the untreated control group G1 (P > .05). Lower expression of RANKL mRNA was observed in G3 compared to G1 (P < .05) but no change on OPG, MMP-9 or CTSK was detected (P > .05).</p><p><strong>Conclusions: </strong>Under the experimental conditions of this study, systemic or local administration of a TNFR1 antibody was not effective in limiting the expansion of periapical lesions.</p>\",\"PeriodicalId\":15703,\"journal\":{\"name\":\"Journal of endodontics\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.5000,\"publicationDate\":\"2025-05-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of endodontics\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1016/j.joen.2025.05.007\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"DENTISTRY, ORAL SURGERY & MEDICINE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of endodontics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.joen.2025.05.007","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"DENTISTRY, ORAL SURGERY & MEDICINE","Score":null,"Total":0}
Effects of Systemic and Local Anti-tumor Necrosis Factor-α Receptor-1 Administration on Periapical Bone Loss in Mice.
Introduction: The aim of this study was to evaluate whether systemic or topical administration of a monoclonal antibody against tumor necrosis factor-α receptor-1 (TNFR1) could control periapical bone loss in mice.
Methods: Thirty C57Bl6 mice were used for induction of periapical lesion through the exposure of the root canals to the oral environment. The root canals remained open to microbial contamination from the oral cavity for 28 days. Then, the animals were randomly assigned to 3 different experimental groups: G1: animals received no medication and periapical lesion followed its natural course up to 42 days; G2: systemic administration of the TNFR1 antibody; G3: intracanal topical administration of the TNFR1 antibody. Healthy teeth were used as controls. At 42 days following periapical lesion induction, the animals were anesthetized then euthanized, and tissues containing bone and teeth were collected for microtomographic, histomorphometry, and quantitative reverse transcriptase polymerase chain reaction analysis. Then groups were compared using one-way analysis of variance followed by Turkey tests (α = 5%).
Results: Systemic and topical anti-TNFR1 administered in groups G2 and G3 did not have an impact on the area and volume of periapical lesions when compared to the untreated control group G1 (P > .05). Lower expression of RANKL mRNA was observed in G3 compared to G1 (P < .05) but no change on OPG, MMP-9 or CTSK was detected (P > .05).
Conclusions: Under the experimental conditions of this study, systemic or local administration of a TNFR1 antibody was not effective in limiting the expansion of periapical lesions.
期刊介绍:
The Journal of Endodontics, the official journal of the American Association of Endodontists, publishes scientific articles, case reports and comparison studies evaluating materials and methods of pulp conservation and endodontic treatment. Endodontists and general dentists can learn about new concepts in root canal treatment and the latest advances in techniques and instrumentation in the one journal that helps them keep pace with rapid changes in this field.