Induction of nephrotoxic serum nephritis in inbred mice and suppressive effect of colchicine on the development of this nephritis

被引:16
作者
Chen, SM
Mukoyama, T
Sato, N
Yamagata, SI
Arai, Y
Satoh, N
Ueda, S
机构
[1] Chiba Univ, Grad Sch Pharmaceut Sci, Dept Drug Informat & Commun, Inage Ku, Chiba 2638522, Japan
[2] Showa Univ, Sch Med, Dept Pharmacol, Shinagawa Ku, Tokyo 1428555, Japan
关键词
nephrotoxic serum nephritis (NTS nephritis); polymorphonuclear leucocytes (PMN); colchicine; anti-glomerular basement membrane antibody (anti-GBM antibody); mouse;
D O I
10.1006/phrs.2002.0948
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Accelerated nephrotoxic serum (NTS) nephritis is successfully produced in C57BL/6 mice, using anti-murine glomerular basement membrane (GBM) rabbit antiserum. Anti-murine GBM rabbits antiserum was obtained by immunization of New Zealand white rabbit with trypsinized GBM antigen from normal C57BL/6 mice. Preimmunization with normal rabbit IgG and injection with 150 mul of NTS induced typical NTS nephritis with cellular proliferation in glomeruli, occlusion of glomerular loops, crescents, tubulointerstitial changes and hyperazotemia within 14 days. Polymorphonuclear leucocytes (PMN) have an important role in induction and development of NTS nephritis. Furthermore, clinically used colchicine is thought to suppress functions of PMN. Therefore, the therapeutic effect of colchicine on NTS nephritis was examined The histological score (HS) of the group treated with 60 mug kg(-1) of colchicine (2.8 +/- 0.5) was significantly lower than that of positive control group (4.03 +/- 0.3). The direct immunofluorescent microscopic study revealed that there is no quantitative difference in the deposition of rabbit IgG, mouse IgG and C3 in GBM between these two groups. Urinary protein excretion and hyperazotemia were significantly suppressed by treatment with 60 mug kg(-1) of colchicine. A NTS nephritis model was established, it was found that colchicine may have a suppressive effect on the development of glomerular nephritis. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:319 / 324
页数:6
相关论文
共 35 条
[1]   LIPOXIN-A4 ANTAGONIZES CELLULAR AND INVIVO ACTIONS OF LEUKOTRIENE-D4 IN RAT GLOMERULAR MESANGIAL CELLS - EVIDENCE FOR COMPETITION AT A COMMON RECEPTOR [J].
BADR, KF ;
DEBOER, DK ;
SCHWARTZBERG, M ;
SERHAN, CN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (09) :3438-3442
[2]  
BADR KF, 1992, KIDNEY INT, V42, pS101
[3]   PRESERVATION OF THE GLOMERULAR CAPILLARY ULTRAFILTRATION COEFFICIENT DURING RAT NEPHROTOXIC SERUM NEPHRITIS BY A SPECIFIC LEUKOTRIENE D4 RECEPTOR ANTAGONIST [J].
BADR, KF ;
SCHREINER, GF ;
WASSERMAN, M ;
ICHIKAWA, I .
JOURNAL OF CLINICAL INVESTIGATION, 1988, 81 (06) :1702-1709
[4]   CHEMOATTRACTANTS PROVOKE MONOCYTE ADHESION TO HUMAN MESANGIAL CELLS AND MESANGIAL CELL INJURY [J].
BRADY, HR ;
DENTON, MD ;
JIMENEZ, W ;
TAKATA, S ;
PALLISER, D ;
BRENNER, BM .
KIDNEY INTERNATIONAL, 1992, 42 (02) :480-487
[6]   ANTIMYELOPEROXIDASE ANTIBODIES STIMULATE NEUTROPHILS TO DAMAGE HUMAN ENDOTHELIAL-CELLS [J].
EWERT, BH ;
JENNETTE, JC ;
FALK, RJ .
KIDNEY INTERNATIONAL, 1992, 41 (02) :375-383
[7]  
FRUHMAN GJ, 1960, P SOC EXP BIOL MED, V104, P284
[8]  
FUJIMOTO T, 1964, ACTA PATHOL JAPON, V14, P275
[9]  
Fujinaka H, 1997, J IMMUNOL, V158, P4978
[10]  
FUJITA Y, 1983, BUNSEKI KAGAKU, V32, pE379