Influence of subcutaneous administration of recombinant TNF-α on ligature-induced periodontitis in rats

被引:43
作者
Gaspersic, R
Stiblar-Martincic, D
Osredkar, J
Skaleric, U
机构
[1] Univ Ljubljana, Fac Med, Dept Oral Med & Periodontol, Ljubljana 1000, Slovenia
[2] Univ Ljubljana, Fac Med, Inst Histol & Embryol, Ljubljana 1000, Slovenia
[3] Ctr Clin, Clin Inst Clin Chem & Biochem, Ljubljana, Slovenia
关键词
rats; tumor necrosis factor alpha; ligature; periodontitis;
D O I
10.1034/j.1600-0765.2003.01395.x
中图分类号
R78 [口腔科学];
学科分类号
1003 ;
摘要
Proinflammatory cytokine tumor necrosis factor alpha (TNF-alpha) was found in inflamed periodontal tissues and many studies pointed to its significant role in development of periodontal disease. In this study, the influence of subcutaneously administered recombinant human TNF-alpha (rhTNF-alpha) on inflammatory reaction and periodontal breakdown in rats was analyzed during experimental periodontitis. induced by placing silk ligatures around the maxillary right second molar tooth. The rats were divided into two groups with five annuals in each: the first group was infused subcutaneously with rhTNF-alpha via osmotic pumps for 2 weeks and the second group was infused with phosphate-buffered saline (PBS) in the same manner. Inflammatory reaction and periodontal breakdown was evaluated morphometrically on hematoxylin and eosin stained sections. Serum ionized calcium and inorganic phosphates were monitored colorimetrically. Serum calcium and phosphate levels were similar in rats receiving rhTNF-alpha and PBS. Ligation resulted in accelerated periodontal breakdown, while subcutaneous rhTNFalpha-administration by itself had no significant effect. Combined effect of subcutaneous rhTNF-alpha administration and ligation resulted in a significantly greater inflammatory reaction and periodontal breakdown then either treatment alone. We concluded that the subcutaneous administration of rhTNF-alpha accelerates the progression of experimental periodontitis in rats.
引用
收藏
页码:198 / 203
页数:6
相关论文
共 30 条
[1]  
ASSUMA R, 1998, J IMMUNOL, V319, P516
[2]   STIMULATION OF BONE-RESORPTION AND INHIBITION OF BONE-FORMATION INVITRO BY HUMAN-TUMOR NECROSIS FACTORS [J].
BERTOLINI, DR ;
NEDWIN, GE ;
BRINGMAN, TS ;
SMITH, DD ;
MUNDY, GR .
NATURE, 1986, 319 (6053) :516-518
[3]  
BRAHN E, 1992, LYMPHOKINE CYTOK RES, V11, P253
[4]   Effects of chlorpromazine on alveolar bone loss in experimental periodontal disease in rats [J].
de Lima, V ;
Bezerra, MM ;
Alencar, VBD ;
Vidal, FDP ;
da Rocha, FAC ;
Brito, GAD ;
Ribeiro, RD .
EUROPEAN JOURNAL OF ORAL SCIENCES, 2000, 108 (02) :123-129
[5]   Proinflammatory cytokines [J].
Dinarello, CA .
CHEST, 2000, 118 (02) :503-508
[6]   Cytokine activation of the HPA axis [J].
Dunn, AJ .
NEUROIMMUNOMODULATION: PERSPECTIVES AT THE NEW MILLENNIUM, 2000, 917 :608-617
[7]   HOST RESPONSES IN PERIODONTAL-DISEASES - CURRENT CONCEPTS [J].
GENCO, RJ .
JOURNAL OF PERIODONTOLOGY, 1992, 63 (04) :338-355
[8]   TUMORS PRODUCING HUMAN-TUMOR NECROSIS FACTOR INDUCE HYPERCALCEMIA AND OSTEOCLASTIC BONE-RESORPTION IN NUDE-MICE [J].
JOHNSON, RA ;
BOYCE, BF ;
MUNDY, GR ;
ROODMAN, GD .
ENDOCRINOLOGY, 1989, 124 (03) :1424-1427
[9]   IN-VIVO ADMINISTRATION OF IL-1-BETA ACCELERATES SILK LIGATURE-INDUCED ALVEOLAR BONE-RESORPTION IN RATS [J].
KOIDE, M ;
SUDA, S ;
SAITOH, S ;
OFUJI, Y ;
SUZUKI, T ;
YOSHIE, H ;
TAKAI, M ;
ONO, Y ;
TANIGUCHI, Y ;
HARA, K .
JOURNAL OF ORAL PATHOLOGY & MEDICINE, 1995, 24 (09) :420-434
[10]  
LE JM, 1987, LAB INVEST, V56, P234