An Involvement of Granulocyte Medullasin in Phenytoin-Induced Gingival Overgrowth in Rats
To investigate the relationship between histological changes and distributions of medullasin, a neutrophil elastase-like serine proteinase, in phenytoin-induced gingival overgrowth, we established a rat model of gingival overgrowth. Thirty-two, 20-day-old male Fischer 344 rats were fed a diet contai...
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Published in | Japanese Journal of Pharmacology Vol. 89; no. 3; pp. 235 - 241 |
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Language | English |
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2002
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Abstract | To investigate the relationship between histological changes and distributions of medullasin, a neutrophil elastase-like serine proteinase, in phenytoin-induced gingival overgrowth, we established a rat model of gingival overgrowth. Thirty-two, 20-day-old male Fischer 344 rats were fed a diet containing phenytoin and sacrificed at 1, 2, 4 and 8 weeks. Control rats (n = 40) were fed the same diet, but without the drug and killed at the same weeks as experimental rats (n = 32) and 0 week (n = 8). The mandible specimens were resected and sectioned bucco-lingually between the first and second molars. A marked inflammatory-cell infiltration and elongated rete pegs were seen in the phenytoin-treated group. The extent of the overgrowth assessed by computer image analysis and the density of medullasin-positive cells by immuno-histochemistry in the approximal gingiva showed a significant increase in the phenytoin-treated group compared to the control group. A marked infiltration of the positive cells in experimental rats was observed as early as 2 weeks when gingival overgrowth was not fully established. Medullasin-positive cells were mostly neutrophils and partly macrophage-like cells. These findings suggest that medullasin may be involved in mainly host defense and secondarily collagen metabolism in the phenytoin-induced rat model of gingival overgrowth. |
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AbstractList | To investigate the relationship between histological changes and distributions of medullasin, a neutrophil elastase-like serine proteinase, in phenytoin-induced gingival overgrowth, we established a rat model of gingival overgrowth. Thirty-two, 20-day-old male Fischer 344 rats were fed a diet containing phenytoin and sacrificed at 1, 2, 4 and 8 weeks. Control rats (n = 40) were fed the same diet, but without the drug and killed at the same weeks as experimental rats (n = 32) and 0 week (n = 8). The mandible specimens were resected and sectioned bucco-lingually between the first and second molars. A marked inflammatory-cell infiltration and elongated rete pegs were seen in the phenytoin-treated group. The extent of the overgrowth assessed by computer image analysis and the density of medullasin-positive cells by immunohistochemistry in the approximal gingiva showed a significant increase in the phenytoin-treated group compared to the control group. A marked infiltration of the positive cells in experimental rats was observed as early as 2 weeks when gingival overgrowth was not fully established. Medullasin-positive cells were mostly neutrophils and partly macrophage-like cells. These findings suggest that medullasin may be involved in mainly host defense and secondarily collagen metabolism in the phenytoin-induced rat model of gingival overgrowth. To investigate the relationship between histological changes and distributions of medullasin, a neutrophil elastase-like serine proteinase, in phenytoin-induced gingival overgrowth, we established a rat model of gingival overgrowth. Thirty-two, 20-day-old male Fischer 344 rats were fed a diet containing phenytoin and sacrificed at 1, 2, 4 and 8 weeks. Control rats (n = 40) were fed the same diet, but without the drug and killed at the same weeks as experimental rats (n = 32) and 0 week (n = 8). The mandible specimens were resected and sectioned bucco-lingually between the first and second molars. A marked inflammatory-cell infiltration and elongated rete pegs were seen in the phenytoin-treated group. The extent of the overgrowth assessed by computer image analysis and the density of medullasin-positive cells by immuno-histochemistry in the approximal gingiva showed a significant increase in the phenytoin-treated group compared to the control group. A marked infiltration of the positive cells in experimental rats was observed as early as 2 weeks when gingival overgrowth was not fully established. Medullasin-positive cells were mostly neutrophils and partly macrophage-like cells. These findings suggest that medullasin may be involved in mainly host defense and secondarily collagen metabolism in the phenytoin-induced rat model of gingival overgrowth. To investigate the relationship between histological changes and distributions of medullasin, a neutrophil elastase-like serine proteinase, in phenytoin-induced gingival overgrowth, we established a rat model of gingival overgrowth. Thirty-two, 20-day-old male Fischer 344 rats were fed a diet containing phenytoin and sacrificed at 1 , 2, 4 and 8 weeks. Control rats (n = 40) were fed the same diet, but without the drug and killed at the same weeks as experimental rats (n = 32) and 0 week (n = 8). The mandible specimens were resected and sectioned bucco-lingually between the first and second molars. A marked inflammatory-cell infiltration and elongated rete pegs were seen in the phenytoin-treated group. The extent of the overgrowth assessed by computer image analysis and the density of medullasin-positive cells by immunohistochemistry in the approximal gingiva showed a significant increase in the phenytoin-treated group compared to the control group. A marked infiltration of the positive cells in experimental rats was observed as early as 2 weeks when gingival overgrowth was not fully established. Medullasin-positive cells were mostly neutrophils and partly macrophage-1ike cells. These findings suggest that medullasin may be involved in mainly host defense and secondarily collagen metabolism in the phenytoin-induced rat model of gingival overgrowth. |
Author | Hara, Yoshitaka Yamamoto, Kenji Aoki, Yosuke Kato, Yuzo Kato, Ihachi Ozaki, Yukio Kunimatsu, Kazushi |
Author_xml | – sequence: 1 givenname: Yukio surname: Ozaki fullname: Ozaki, Yukio organization: Departments of Periodontology and Nagasaki University School of Dentistry, 1-7-1 Sakamoto, Nagasaki 852-8588, Japan – sequence: 2 givenname: Kazushi surname: Kunimatsu fullname: Kunimatsu, Kazushi email: kakuma@net.nagasaki-u.ac.jp organization: Departments of Periodontology and Nagasaki University School of Dentistry, 1-7-1 Sakamoto, Nagasaki 852-8588, Japan – sequence: 3 givenname: Yoshitaka surname: Hara fullname: Hara, Yoshitaka organization: Departments of Periodontology and Nagasaki University School of Dentistry, 1-7-1 Sakamoto, Nagasaki 852-8588, Japan – sequence: 4 givenname: Ihachi surname: Kato fullname: Kato, Ihachi organization: Departments of Periodontology and Nagasaki University School of Dentistry, 1-7-1 Sakamoto, Nagasaki 852-8588, Japan – sequence: 5 givenname: Yosuke surname: Aoki fullname: Aoki, Yosuke organization: Department of Food and Health Sciences, Jissen Women’s University Faculty of Life Sciences, 4-1-1 Osakaue, Hino 191-8510, Japan – sequence: 6 givenname: Kenji surname: Yamamoto fullname: Yamamoto, Kenji organization: Department of Pharmacology, Kyushu University Graduate School of Dental Sciences, 3-1-1 Maidashi, Higashi-ku, Fukuoka 812-8582, Japan – sequence: 7 givenname: Yuzo surname: Kato fullname: Kato, Yuzo organization: Departments of Pharmacology, Nagasaki University School of Dentistry, 1-7-1 Sakamoto, Nagasaki 852-8588, Japan |
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Cites_doi | 10.1111/j.1600-051X.1996.tb02072.x 10.1177/10454411910020010201 10.1177/10454411970080020801 10.1902/jop.1989.60.2.104 10.1002/art.1780260809 10.1111/jre.1993.28.6.396 10.1111/j.1600-0765.1996.tb00519.x 10.1111/j.1600-0765.1997.tb00533.x 10.1111/j.1600-0714.1982.tb00171.x 10.1016/0003-9969(90)90099-V 10.1111/j.1600-0765.1993.tb02122.x 10.1111/j.1600-051X.1994.tb00314.x 10.1111/j.1600-0714.1995.tb01142.x 10.1016/S0003-9969(98)00063-6 10.1016/0003-9969(94)90103-1 10.1016/S0021-9258(19)62350-1 10.1016/0003-9969(95)00108-5 10.1001/jama.1939.02800130028009 10.1902/jop.1996.67.5.463 10.1111/j.1600-0765.1994.tb01241.x 10.1902/jop.1994.65.7.641 10.1902/jop.1985.56.4.211 10.1111/j.1600-0714.1991.tb00419.x 10.1093/oxfordjournals.jbchem.a122024 10.1111/j.1600-0765.1990.tb00927.x 10.1111/j.1600-0714.1990.tb00868.x |
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A review of the literature publication-title: Crit Rev Oral Biol Med doi: 10.1177/10454411970080020801 contributor: fullname: Havemose-Poulsen – volume: 60 start-page: 104 year: 1989 ident: 10.1254/jjp.89.235_bib24 article-title: Nitrendipine-induced gingival overgrowth in dogs publication-title: J Periodontol doi: 10.1902/jop.1989.60.2.104 contributor: fullname: Heijl – volume: 26 start-page: 1002 year: 1983 ident: 10.1254/jjp.89.235_bib10 article-title: Role of medullasin in granulocytes in the development of inflammation. I. Phlogistic activity and the effect on functions of macrophages and granulocytes publication-title: Arthritis Rheum doi: 10.1002/art.1780260809 contributor: fullname: Aoki – volume: 28 start-page: 396 year: 1993 ident: 10.1254/jjp.89.235_bib17 article-title: Nifedipine-induced gingival overgrowth in the presence or absence of gingival inflammation in rats publication-title: J Periodont Res doi: 10.1111/jre.1993.28.6.396 contributor: fullname: Morisaki – volume: 31 start-page: 545 year: 1996 ident: 10.1254/jjp.89.235_bib23 article-title: Immuohisto-chemical localization of transforming growth factor β and heparan sulphate glycosaminoglycan in gingival hyperplasia induced by nifedipine and phenytoin publication-title: J Periodont Res doi: 10.1111/j.1600-0765.1996.tb00519.x contributor: fullname: Saito – volume: 32 start-page: 264 year: 1997 ident: 10.1254/jjp.89.235_bib14 article-title: Immunohistochemical study of cathepsin G and medullasin in inflamed gingival tissues from periodontal patients publication-title: J Periodont Res doi: 10.1111/j.1600-0765.1997.tb00533.x contributor: fullname: Kunimatsu – volume: 11 start-page: 310 year: 1982 ident: 10.1254/jjp.89.235_bib19 article-title: Evidence for production of an inactive collagenase by fibroblasts from phenytoin-enlarged human gingivae publication-title: J Oral Pathol doi: 10.1111/j.1600-0714.1982.tb00171.x contributor: fullname: Hassell – volume: 35 start-page: 753 year: 1990 ident: 10.1254/jjp.89.235_bib18 article-title: Phenytoin-induced gingival overgrowth in rats infected with streptococcus sobrinus 6715 publication-title: Archs Oral Biol doi: 10.1016/0003-9969(90)90099-V contributor: fullname: Morisaki – volume: 28 start-page: 547 year: 1993 ident: 10.1254/jjp.89.235_bib13 article-title: Possible functions of human neutrophil serine proteinases, medullasin and cathepsin G, in periodontal tissue breakdown publication-title: J Periodont Res doi: 10.1111/j.1600-0765.1993.tb02122.x contributor: fullname: Kunimatsu – volume: 21 start-page: 256 year: 1994 ident: 10.1254/jjp.89.235_bib25 article-title: Clinical assessment of gingival hyperplasia in patients treated with nifedipine publication-title: J Clin Periodontol doi: 10.1111/j.1600-051X.1994.tb00314.x contributor: fullname: Bullon – volume: 24 start-page: 72 year: 1995 ident: 10.1254/jjp.89.235_bib22 article-title: Heterogeneity of fibroblasts derived from human free and attached gingiva. 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SubjectTerms | Animals Gingiva - chemistry Gingiva - drug effects Gingiva - metabolism Gingival Hyperplasia - chemically induced Gingival Hyperplasia - metabolism Gingival overgrowth Granulocytes - chemistry Granulocytes - drug effects Granulocytes - metabolism Immunohistochemistry Male Medullasin Phenytoin Phenytoin - pharmacology Rats Rats, Inbred F344 Serine Endopeptidases - analysis Serine Endopeptidases - biosynthesis Serine proteinase |
Title | An Involvement of Granulocyte Medullasin in Phenytoin-Induced Gingival Overgrowth in Rats |
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