Balance of tumor necrosis factor alpha and interleukin-10 in a buccal infection in a streptozotocin-induced diabetic rat model

被引:8
作者
Furudoi, S
Yoshii, T
Komori, T
机构
[1] Kobe Univ, Grad Sch Med, Dept Oral & Maxillofacial Surg, Chuo Ku, Kobe, Hyogo 6500017, Japan
[2] Hyogo Prefectural Staff Hlth Ctr, Dept Dent & Oral Surg, Kobe, Hyogo 6508567, Japan
关键词
buccal abscess; diabetic rat model; streptozotocin; tumor necrosis factor alpha (TNF-alpha); interleukin-10 (IL-10);
D O I
10.1016/j.cyto.2003.08.011
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
This study evaluates the local levels of proinflammatory cytokine, tumor necrosis factor alpha (TNF-alpha), and anti-inflammatory cytokine, interleukin-10 (IL-10), in an experimental buccal abscess of a diabetic rat model. We prepared a buccal cavity induced by injection of carrageenin in a diabetic rat (blood glucose, 460.6 +/- 54.7 mg/dl, mean +/- SE) induced by streptozotocin (STZ). The buccal abscess was formed by the direct inoculation of Streptococcus pyogenes S-8 (2 X 10(7) cfu) into the buccal cavity at day 5 after carrageenin injection. Cytokine levels in the exudate of the buccal abscess were measured by enzyme-linked imummosorbent assay for 48 h after infection. Bacterial counts, weighing of exudate, and histological analysis were also performed. The mean TNF-alpha levels in the buccal abscess exudate of the diabetic group, which were generally higher than those of the control group, tended to increase over time until 48 h after infection, while the TNF-alpha levels in the control group peaked at 24 h after infection and then decreased. The IL-10 levels in the diabetic group remained almost unchanged until 48 h after infection, while the IL-10 levels in the control group were significantly higher than in the diabetic group at 12-24 h after infection. The mean ratio of TNF-alpha to IL-10 levels was 1.17-1.67 in the diabetic group, which was higher than the 0.26-0.69 of the control group. The bacterial counts in the buccal abscess and the weight of exudate were significantly higher in the diabetic group compared to the control group at 36-48 h. Histological findings showed that inflammatory cell infiltration was remarkable in the diabetic group compared to that of the control group. These results suggest that the elevated proinflammatory TNF-alpha levels and decreased anti-inflammatory IL-10 levels, which are produced at local infection sites, may at least in part be related to the severity of inflammation in this rat model with diabetes induced by STZ. (C) 2003 Elsevier Ltd. All rights reserved.
引用
收藏
页码:143 / 149
页数:7
相关论文
共 38 条
[1]  
Aggarwal BB, 1996, EUR CYTOKINE NETW, V7, P93
[2]   Relative production of tumour necrosis factor a and interleukin 10 in adult respiratory distress syndrome [J].
Armstrong, L ;
Millar, AB .
THORAX, 1997, 52 (05) :442-446
[3]   IMPAIRED LEUKOCYTE FUNCTION IN PATIENTS WITH POORLY CONTROLLED DIABETES [J].
BAGDADE, JD ;
ROOT, RK ;
BULGER, RJ .
DIABETES, 1974, 23 (01) :9-15
[4]   Sir Isaac Newton, sepsis, SIRS, and CARS [J].
Bone, RC .
CRITICAL CARE MEDICINE, 1996, 24 (07) :1125-1128
[5]   INFLAMMATORY CYTOKINES IN CYSTIC-FIBROSIS LUNGS [J].
BONFIELD, TL ;
PANUSKA, JR ;
KONSTAN, MW ;
HILLIARD, KA ;
HILLIARD, JB ;
GHNAIM, H ;
BERGER, M .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 1995, 152 (06) :2111-2118
[6]   IN-VIVO REGULATION OF REPLICATIVE LEGIONELLA-PNEUMOPHILA LUNG INFECTION BY ENDOGENOUS TUMOR-NECROSIS-FACTOR-ALPHA AND NITRIC-OXIDE [J].
BRIELAND, JK ;
REMICK, DG ;
FREEMAN, PT ;
HURLEY, MC ;
FANTONE, JC ;
ENGLEBERG, NC .
INFECTION AND IMMUNITY, 1995, 63 (09) :3253-3258
[7]  
Brouckaert P, 1996, CURR TOP MICROBIOL, V216, P167
[8]   THE DISCOVERY AND DEVELOPMENT OF THE BB RAT COLONY - AN ANIMAL-MODEL OF SPONTANEOUS DIABETES-MELLITUS [J].
CHAPPEL, CI ;
CHAPPEL, WR .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1983, 32 (07) :8-10
[9]   CACHECTIN TUMOR NECROSIS FACTOR STIMULATES COLLAGENASE AND PROSTAGLANDIN-E2 PRODUCTION BY HUMAN SYNOVIAL-CELLS AND DERMAL FIBROBLASTS [J].
DAYER, JM ;
BEUTLER, B ;
CERAMI, A .
JOURNAL OF EXPERIMENTAL MEDICINE, 1985, 162 (06) :2163-2168
[10]   THE BIOLOGY OF INTERLEUKIN-1 AND COMPARISON TO TUMOR NECROSIS FACTOR [J].
DINARELLO, CA .
IMMUNOLOGY LETTERS, 1987, 16 (3-4) :227-331