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Oral‐bacterial‐induced arterial and venous thrombus in rats: Pathological and immunological studies
OBJECTIVES: Our study investigated the pathological outcome of experimental thrombi that incorporate oral bacteria. MATERIAL AND METHODS: A small artery and vein in the rats' groins were injected with a solution containing periodontal bacteria Porphyromonas gingivalis and followed up for 28 day...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6820577/ https://www.ncbi.nlm.nih.gov/pubmed/31687183 http://dx.doi.org/10.1002/cre2.215 |
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author | Iwai, Takehisa Matsui, Yoshiki Homma, Kaori Takemura, Tamiko Fujiwara, Mutsunori Aoyama, Norio Sato, Hiroki Izumi, Yuichi |
author_facet | Iwai, Takehisa Matsui, Yoshiki Homma, Kaori Takemura, Tamiko Fujiwara, Mutsunori Aoyama, Norio Sato, Hiroki Izumi, Yuichi |
author_sort | Iwai, Takehisa |
collection | PubMed |
description | OBJECTIVES: Our study investigated the pathological outcome of experimental thrombi that incorporate oral bacteria. MATERIAL AND METHODS: A small artery and vein in the rats' groins were injected with a solution containing periodontal bacteria Porphyromonas gingivalis and followed up for 28 days. In all, 18 limbs of nine male rats (500–650 g) were used for the arterial study, and eight limbs of four rats were used for the veins. Two densities of the bacterial solution and two arterial thicknesses sizes were used in the arterial study. Both proximal and distal arteries and veins were ligated loosely using a monofilament nylon suture before bacterial suspensions or control solutions were injected into the ligated vessels. RESULTS: After 7, 14–18, and 28 days, the rats were sacrificed. Pathology and immunohistochemistry were performed. All specimens exhibited thrombus formation and an acute inflammation reaction with granulocytes at 7 days and then settled down to chronic fibrous change with plasma cells or macrophages at 28 days in the arterial thrombus. CD3 (Pan T‐cells), CD79a (Pan B cells in the rats), and IgG were observed in the process of the healing of the arterial thrombus. Venous changes showed relatively clear recanalization that appeared at 7 days, which is slightly different from the artery. Granulocytes were present from 7 to 28 days. CONCLUSIONS: Periodontal bacteria act as an inflammatory core in the vessels, but not as an infectious agent, in our experiments, because of their low ability to invade tissues. |
format | Online Article Text |
id | pubmed-6820577 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-68205772019-11-04 Oral‐bacterial‐induced arterial and venous thrombus in rats: Pathological and immunological studies Iwai, Takehisa Matsui, Yoshiki Homma, Kaori Takemura, Tamiko Fujiwara, Mutsunori Aoyama, Norio Sato, Hiroki Izumi, Yuichi Clin Exp Dent Res Original Articles OBJECTIVES: Our study investigated the pathological outcome of experimental thrombi that incorporate oral bacteria. MATERIAL AND METHODS: A small artery and vein in the rats' groins were injected with a solution containing periodontal bacteria Porphyromonas gingivalis and followed up for 28 days. In all, 18 limbs of nine male rats (500–650 g) were used for the arterial study, and eight limbs of four rats were used for the veins. Two densities of the bacterial solution and two arterial thicknesses sizes were used in the arterial study. Both proximal and distal arteries and veins were ligated loosely using a monofilament nylon suture before bacterial suspensions or control solutions were injected into the ligated vessels. RESULTS: After 7, 14–18, and 28 days, the rats were sacrificed. Pathology and immunohistochemistry were performed. All specimens exhibited thrombus formation and an acute inflammation reaction with granulocytes at 7 days and then settled down to chronic fibrous change with plasma cells or macrophages at 28 days in the arterial thrombus. CD3 (Pan T‐cells), CD79a (Pan B cells in the rats), and IgG were observed in the process of the healing of the arterial thrombus. Venous changes showed relatively clear recanalization that appeared at 7 days, which is slightly different from the artery. Granulocytes were present from 7 to 28 days. CONCLUSIONS: Periodontal bacteria act as an inflammatory core in the vessels, but not as an infectious agent, in our experiments, because of their low ability to invade tissues. John Wiley and Sons Inc. 2019-07-25 /pmc/articles/PMC6820577/ /pubmed/31687183 http://dx.doi.org/10.1002/cre2.215 Text en ©2019 The Authors. Clinical and Experimental Dental Research published by John Wiley & Sons Ltd. This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Iwai, Takehisa Matsui, Yoshiki Homma, Kaori Takemura, Tamiko Fujiwara, Mutsunori Aoyama, Norio Sato, Hiroki Izumi, Yuichi Oral‐bacterial‐induced arterial and venous thrombus in rats: Pathological and immunological studies |
title | Oral‐bacterial‐induced arterial and venous thrombus in rats: Pathological and immunological studies |
title_full | Oral‐bacterial‐induced arterial and venous thrombus in rats: Pathological and immunological studies |
title_fullStr | Oral‐bacterial‐induced arterial and venous thrombus in rats: Pathological and immunological studies |
title_full_unstemmed | Oral‐bacterial‐induced arterial and venous thrombus in rats: Pathological and immunological studies |
title_short | Oral‐bacterial‐induced arterial and venous thrombus in rats: Pathological and immunological studies |
title_sort | oral‐bacterial‐induced arterial and venous thrombus in rats: pathological and immunological studies |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6820577/ https://www.ncbi.nlm.nih.gov/pubmed/31687183 http://dx.doi.org/10.1002/cre2.215 |
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