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 inJapanese Journal of Pharmacology Vol. 89; no. 3; pp. 235 - 241
Main Authors Ozaki, Yukio, Kunimatsu, Kazushi, Hara, Yoshitaka, Kato, Ihachi, Aoki, Yosuke, Yamamoto, Kenji, Kato, Yuzo
Format Journal Article
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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.
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
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10.1002/art.1780260809
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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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References 16 Ozaki Y, Kunimatsu K, Tajiri K, Hara Y, Kato Y, Aoki Y and Kato I: Role of medullasin in nifedipine-induced gingival overgrowth in rats. Archs Oral Biol 43, 801 – 810 (1998)
7 Tipton DA, Fry HR and Dabbous MK: Altered collagen metabolism in nifedipine-induced gingival overgrowth. J Periodont Res 29, 401 – 409 (1994)
14 Kunimatsu K, Ozaki Y, Hara Y, Aoki Y, Yamamoto K and Kato I: Immunohistochemical study of cathepsin G and medullasin in inflamed gingival tissues from periodontal patients. J Periodont Res 32, 264 – 270 (1997)
13 Kunimatsu K, Mine N, Kato I, Hase T, Aoki Y and Yamamoto K: Possible functions of human neutrophil serine proteinases, medullasin and cathepsin G, in periodontal tissue breakdown. J Periodont Res 28, 547 – 549 (1993)
23 Saito K, Mori S, Iwakura M and Sakamoto S: Immuohistochemical localization of transforming growth factor β and heparan sulphate glycosaminoglycan in gingival hyperplasia induced by nifedipine and phenytoin. J Periodont Res 31, 545 – 555 (1996)
24 Heijl L and Sundin Y: Nitrendipine-induced gingival overgrowth in dogs. J Periodontol 60, 104 – 112 (1989)
8 Aoki Y: Crystallization and characterization of a new protease in mitochondria of bone marrow cells. J Biol Chem 253, 2026 – 2032 (1978)
5 Nishikawa S, Nagata T, Morisaki I, Oka T and Ishida H: Pathogenesis of drug-induced gingival overgrowth. A review of studies in the rat model. J Periodontol 67, 463 – 471 (1996)
15 Kunimatsu K, Ozaki Y, Aoki Y and Kato I: Possible roles of medullasin in nifedipine-induced human gingival overgrowth. Archs Oral Biol 41, 111 – 115 (1996)
11 Aoki Y and Machinami R: Medullasin in inflammation (part II). Asian Med J 26, 15 – 37 (1983)
19 Hassell TM: Evidence for production of an inactive collagenase by fibroblasts from phenytoin-enlarged human gingivae. J Oral Pathol 11, 310 – 317 (1982)
3 Brown RS, Beaver WT and Bottomley WK: On the mechanism of drug-induced gingival hyperplasia. J Oral Pathol Med 20, 201 – 209 (1991)
22 Pagliarini A, Stabellini G, Carinci F, Calura G, Tognon M and Evangelisti R: Heterogeneity of fibroblasts derived from human free and attached gingiva. Glycosaminoglycan synthesis and effects of phenytoin (PHT) treatment. J Oral Pathol Med 24, 72 – 77 (1995)
1 Kimball OP: The treatment of epilepsy with sodium diphenyl hydantoinate. J Am Med Assoc 112, 1244 – 1245 (1939)
6 Fujii A, Matsumoto H, Nakao S, Teshigawara H and Akimoto Y: Effect of calcium-channel blockers on cell proliferation, DNA synthesis and collagen synthesis of cultured gingival fibroblasts derived from human nifedipine responders and non-responders. Archs Oral Biol 39, 99 – 104 (1994)
12 Kunimatsu K, Ichimaru E, Kato I, Kato Y, Sonoda Y, Aoki Y and Yamamoto K: Granulocyte medullasin levels in gingival crevicular fluid from chronic adult periodontitis patients and experimental gingivitis subjects. J Periodont Res 25, 352 – 357 (1990)
17 Morisaki I, Kato K, Loyola-Rodriguez JP, Nagata T and Ishida H: Nifedipine-induced gingival overgrowth in the presence or absence of gingival inflammation in rats. J Periodont Res 28, 396 – 403 (1993)
21 Lucas RM, Howell LP and Wall BA: Nifedipine-induced gingival hyperplasia. A histochemical and ultrastructural study. J Periodontol 56, 211 – 215 (1985)
9 Okano K, Aoki Y, Sakurai T, Kajitani M, Kanai S, Shimazu T, Shimizu H and Naruto M: Molecular cloning of complementary DNA for human medullasin: an inflammatory serine proteinase in bone marrow cells. J Biochem 102, 13 – 16 (1987)
20 Salo T, Oikarinen KS and Oikarinen AI: Effect of phenytoin and nifedipine on collagen gene expression in normal human gingival fibroblast. J Oral Pathol Med 19, 404 – 407 (1990)
25 Bullon P, Machuca G, Martinez-Sahuquillo A, Rios JV, Rojas J and Lacalle JR: Clinical assessment of gingival hyperplasia in patients treated with nifedipine. J Clin Periodontol 21, 256 – 259 (1994)
4 Seymour RA, Thomason JM and Ellis JS: The pathogenesis of drug-induced gingival overgrowth. J Clin Periodontol 23, 165 – 175 (1996)
18 Morisaki I, Mihara J, Kato K, Kitamura K, Adachi C, Sobue S and Hamada S: Phenytoin-induced gingival overgrowth in rats infected with streptococcus sobrinus 6715. Archs Oral Biol 35, 753 – 758 (1990)
27 Dennison DK, Vallone DR, Pinero GJ, Rittman B and Caffesse RG: Differential effect of TGF-β1 and PDGF on proliferation of periodontal ligament cells and gingival fibroblasts. J Periodontol 65, 641 – 648 (1994)
26 Havemose-Poulsen A and Holmstrup P: Factors affecting IL-1 mediated collagen metabolism by fibroblasts and the pathogenesis of periodontal disease. A review of the literature. Crit Rev Oral Biol Med 8, 217 – 236 (1997)
2 Hassell TM and Hefti AF: Drug-induced gingival overgrowth. Old problem, new problem. Crit Rev Oral Biol Med 2, 103 – 137 (1991)
10 Aoki Y and Machinami R: Role of medullasin in granulocytes in the development of inflammation. I. Phlogistic activity and the effect on functions of macrophages and granulocytes. Arthritis Rheum 26, 1002 – 1010 (1983)
Havemose-Poulsen (10.1254/jjp.89.235_bib26) 1997; 8
Hassell (10.1254/jjp.89.235_bib19) 1982; 11
Ozaki (10.1254/jjp.89.235_bib16) 1998; 43
Morisaki (10.1254/jjp.89.235_bib18) 1990; 35
Lucas (10.1254/jjp.89.235_bib21) 1985; 56
Pagliarini (10.1254/jjp.89.235_bib22) 1995; 24
Brown (10.1254/jjp.89.235_bib3) 1991; 20
Aoki (10.1254/jjp.89.235_bib10) 1983; 26
Nishikawa (10.1254/jjp.89.235_bib5) 1996; 67
Kunimatsu (10.1254/jjp.89.235_bib15) 1996; 41
Okano (10.1254/jjp.89.235_bib9) 1987; 102
Salo (10.1254/jjp.89.235_bib20) 1990; 19
Fujii (10.1254/jjp.89.235_bib6) 1994; 39
Bullon (10.1254/jjp.89.235_bib25) 1994; 21
Kunimatsu (10.1254/jjp.89.235_bib12) 1990; 25
Hassell (10.1254/jjp.89.235_bib2) 1991; 2
Seymour (10.1254/jjp.89.235_bib4) 1996; 23
Aoki (10.1254/jjp.89.235_bib8) 1978; 253
Tipton (10.1254/jjp.89.235_bib7) 1994; 29
Aoki (10.1254/jjp.89.235_bib11) 1983; 26
Kunimatsu (10.1254/jjp.89.235_bib13) 1993; 28
Kimball (10.1254/jjp.89.235_bib1) 1939; 112
Heijl (10.1254/jjp.89.235_bib24) 1989; 60
Saito (10.1254/jjp.89.235_bib23) 1996; 31
Dennison (10.1254/jjp.89.235_bib27) 1994; 65
Kunimatsu (10.1254/jjp.89.235_bib14) 1997; 32
Morisaki (10.1254/jjp.89.235_bib17) 1993; 28
References_xml – volume: 23
  start-page: 165
  year: 1996
  ident: 10.1254/jjp.89.235_bib4
  article-title: The pathogenesis of drug-induced gingival overgrowth
  publication-title: J Clin Periodontol
  doi: 10.1111/j.1600-051X.1996.tb02072.x
  contributor:
    fullname: Seymour
– volume: 2
  start-page: 103
  year: 1991
  ident: 10.1254/jjp.89.235_bib2
  article-title: Drug-induced gingival overgrowth. Old problem, new problem
  publication-title: Crit Rev Oral Biol Med
  doi: 10.1177/10454411910020010201
  contributor:
    fullname: Hassell
– volume: 8
  start-page: 217
  year: 1997
  ident: 10.1254/jjp.89.235_bib26
  article-title: Factors affecting IL-1 mediated collagen metabolism by fibroblasts and the patho-genesis of periodontal disease. 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. Glycosaminoglycan synthesis and effects of phenytoin (PHT) treatment
  publication-title: J Oral Pathol Med
  doi: 10.1111/j.1600-0714.1995.tb01142.x
  contributor:
    fullname: Pagliarini
– volume: 43
  start-page: 801
  year: 1998
  ident: 10.1254/jjp.89.235_bib16
  article-title: Role of medullasin in nifedipine-induced gingival overgrowth in rats
  publication-title: Archs Oral Biol
  doi: 10.1016/S0003-9969(98)00063-6
  contributor:
    fullname: Ozaki
– volume: 39
  start-page: 99
  year: 1994
  ident: 10.1254/jjp.89.235_bib6
  article-title: Effect of calcium-channel blockers on cell proliferation, DNA synthesis and collagen synthesis of cultured gingival fibro-blasts derived from human nifedipine responders and non-responders
  publication-title: Archs Oral Biol
  doi: 10.1016/0003-9969(94)90103-1
  contributor:
    fullname: Fujii
– volume: 253
  start-page: 2026
  year: 1978
  ident: 10.1254/jjp.89.235_bib8
  article-title: Crystallization and characterization of a new protease in mitochondria of bone marrow cells
  publication-title: J Biol Chem
  doi: 10.1016/S0021-9258(19)62350-1
  contributor:
    fullname: Aoki
– volume: 41
  start-page: 111
  year: 1996
  ident: 10.1254/jjp.89.235_bib15
  article-title: Possible roles of medullasin in nifedipine-induced human gingival overgrowth
  publication-title: Archs Oral Biol
  doi: 10.1016/0003-9969(95)00108-5
  contributor:
    fullname: Kunimatsu
– volume: 112
  start-page: 1244
  year: 1939
  ident: 10.1254/jjp.89.235_bib1
  article-title: The treatment of epilepsy with sodium diphenyl hydantoinate
  publication-title: J Am Med Assoc
  doi: 10.1001/jama.1939.02800130028009
  contributor:
    fullname: Kimball
– volume: 67
  start-page: 463
  year: 1996
  ident: 10.1254/jjp.89.235_bib5
  article-title: Patho-genesis of drug-induced gingival overgrowth. A review of studies in the rat model
  publication-title: J Periodontol
  doi: 10.1902/jop.1996.67.5.463
  contributor:
    fullname: Nishikawa
– volume: 29
  start-page: 401
  year: 1994
  ident: 10.1254/jjp.89.235_bib7
  article-title: Altered collagen metabolism in nifedipine-induced gingival overgrowth
  publication-title: J Periodont Res
  doi: 10.1111/j.1600-0765.1994.tb01241.x
  contributor:
    fullname: Tipton
– volume: 65
  start-page: 641
  year: 1994
  ident: 10.1254/jjp.89.235_bib27
  article-title: Differential effect of TGF-β 1 and PDGF on proliferation of periodontal ligament cells and gingival fibroblasts
  publication-title: J Peri-odontol
  doi: 10.1902/jop.1994.65.7.641
  contributor:
    fullname: Dennison
– volume: 56
  start-page: 211
  year: 1985
  ident: 10.1254/jjp.89.235_bib21
  article-title: Nifedipine-induced gingival hyperplasia. A histochemical and ultrastructural study
  publication-title: J Periodontol
  doi: 10.1902/jop.1985.56.4.211
  contributor:
    fullname: Lucas
– volume: 26
  start-page: 15
  year: 1983
  ident: 10.1254/jjp.89.235_bib11
  article-title: Medullasin in inflammation (part II)
  publication-title: Asian Med J
  contributor:
    fullname: Aoki
– volume: 20
  start-page: 201
  year: 1991
  ident: 10.1254/jjp.89.235_bib3
  article-title: On the mechanism of drug-induced gingival hyperplasia
  publication-title: J Oral Pathol Med
  doi: 10.1111/j.1600-0714.1991.tb00419.x
  contributor:
    fullname: Brown
– volume: 102
  start-page: 13
  year: 1987
  ident: 10.1254/jjp.89.235_bib9
  article-title: Molecular cloning of complementary DNA for human medullasin: an inflammatory serine proteinase in bone marrow cells
  publication-title: J Biochem
  doi: 10.1093/oxfordjournals.jbchem.a122024
  contributor:
    fullname: Okano
– volume: 25
  start-page: 352
  year: 1990
  ident: 10.1254/jjp.89.235_bib12
  article-title: Granulocyte medullasin levels in gingival crevicular fluid from chronic adult periodontitis patients and experimental gingivitis subjects
  publication-title: J Periodont Res
  doi: 10.1111/j.1600-0765.1990.tb00927.x
  contributor:
    fullname: Kunimatsu
– volume: 19
  start-page: 404
  year: 1990
  ident: 10.1254/jjp.89.235_bib20
  article-title: Effect of phenytoin and nifedipine on collagen gene expression in normal human gingival fibroblast
  publication-title: J Oral Pathol Med
  doi: 10.1111/j.1600-0714.1990.tb00868.x
  contributor:
    fullname: Salo
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Snippet To investigate the relationship between histological changes and distributions of medullasin, a neutrophil elastase-like serine proteinase, in...
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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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https://www.jstage.jst.go.jp/article/jjp/89/3/89_3_235/_article/-char/en
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https://www.ncbi.nlm.nih.gov/pubmed/12184728
Volume 89
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