New therapeutic possibility of blocking cytokine-induced neutrophil chemoattractant on transient ischemic brain damage in rats

被引:99
作者
Yamasaki, Y
Matsuo, Y
Zagorski, J
Matsuura, N
Onodera, H
Itoyama, Y
Kogure, K
机构
[1] SHIONOGI PHARMACEUT CO LTD,DEV RES CTR,OSAKA 561,JAPAN
[2] NIDR,NIH,IMMUNOL LAB,BETHESDA,MD 20892
[3] TOHOKU UNIV,SCH MED,DEPT NEUROL,SENDAI,MIYAGI 980,JAPAN
[4] KANTO NEUROSURG HOSP,INST NEUROPATHOL,KUMAGAYA,SAITAMA 366,JAPAN
关键词
cytokine-induced neutrophil chemoattractant; focal cerebral ischemia; ischemic neuronal damage; neutrophil; rat;
D O I
10.1016/S0006-8993(97)00251-5
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Earlier we indicated that neutrophilic invasion into cerebral parenchyma is an important step in rat cerebral ischemia-reperfusion injury and the production of chemotactic factors, cytokine-induced neutrophil chemoattractant (CINC) precede the neutrophilic invasion. The aim of the present study was to evaluate the role of CINC production and the therapeutic possibility of blocking CINC activity in the transient ischemic brain damage in rats. Focal transient ischemia was produced by intraluminal occlusion of the right middle cerebral artery for 60 min. An enzyme immunoassay was used to measure the brain concentration of CINC and myeloperoxidase activity in ischemic areas was measured as a marker of neutrophilic accumulation. An immunohistochemical staining technique was used to detect the immunopositive cells for anti-CINC antibody. Further, application of anti-CINC antibody or anti-neutrophil antibody to rats was used to evaluate the role of CINC production. In ischemic areas, CINC production was detected and peaked 12 h after reperfusion, which followed 60 min of ischemia. Intraperitoneal injection of anti-neutrophil antibody 24 h before and immediately after reperfusion significantly reduced the brain water content and partially reduced the CINC production in ischemic areas. Further, immunohistochemical staining showed that anti-CINC antibody was found on the endothelial surface of venules and on parts of neutrophils that had invaded the ischemic area 6 to 24 h after reperfusion. Also, treatment with anti-CINC antibody reduced ischemic edema formation 24 h after reperfusion and the size of infarction areas 7 days after reperfusion. It thus appears that CINC, mainly produced by endothelium activated by factors released from neutrophils, plays an important role in ischemic brain damage. Furthermore, the blocking of CINC activity with antibody suggests an immune-therapeutic approach to the treatment of stroke patients,
引用
收藏
页码:103 / 111
页数:9
相关论文
共 50 条
[1]   REPERFUSION INCREASES NEUTROPHILS AND LEUKOTRIENE-B4 RECEPTOR-BINDING IN RAT FOCAL ISCHEMIA [J].
BARONE, FC ;
SCHMIDT, DB ;
HILLEGASS, LM ;
PRICE, WJ ;
WHITE, RF ;
FEUERSTEIN, GZ ;
CLARK, RK ;
LEE, EV ;
GRISWOLD, DE ;
SARAU, HM .
STROKE, 1992, 23 (09) :1337-1347
[2]   POLYMORPHONUCLEAR LEUKOCYTE INFILTRATION INTO CEREBRAL FOCAL ISCHEMIC TISSUE - MYELOPEROXIDASE ACTIVITY ASSAY AND HISTOLOGIC VERIFICATION [J].
BARONE, FC ;
HILLEGASS, LM ;
PRICE, WJ ;
WHITE, RF ;
LEE, EV ;
FEUERSTEIN, GZ ;
SARAU, HM ;
CLARK, RK ;
GRISWOLD, DE .
JOURNAL OF NEUROSCIENCE RESEARCH, 1991, 29 (03) :336-345
[3]   MEASUREMENT OF CUTANEOUS INFLAMMATION - ESTIMATION OF NEUTROPHIL CONTENT WITH AN ENZYME MARKER [J].
BRADLEY, PP ;
PRIEBAT, DA ;
CHRISTENSEN, RD ;
ROTHSTEIN, G .
JOURNAL OF INVESTIGATIVE DERMATOLOGY, 1982, 78 (03) :206-209
[4]   POSTISCHEMIC ADMINISTRATION OF AN ANTI-MAC-1 ANTIBODY REDUCES ISCHEMIC CELL-DAMAGE AFTER TRANSIENT MIDDLE CEREBRAL-ARTERY OCCLUSION IN RATS [J].
CHOPP, M ;
ZHANG, RL ;
CHEN, H ;
LI, Y ;
JIANG, N ;
RUSCHE, JR .
STROKE, 1994, 25 (04) :869-875
[5]   LEUKOTRIENES PROMOTE PLASMA LEAKAGE AND LEUKOCYTE ADHESION IN POST-CAPILLARY VENULES - INVIVO EFFECTS WITH RELEVANCE TO THE ACUTE INFLAMMATORY RESPONSE [J].
DAHLEN, SE ;
BJORK, J ;
HEDQVIST, P ;
ARFORS, KE ;
HAMMARSTROM, S ;
LINDGREN, JA ;
SAMUELSSON, B .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (06) :3887-3891
[6]  
DEFORGE LE, 1933, J BIOL CHEM, V34, P25568
[7]   POLYMORPHONUCLEAR LEUKOCYTES OCCLUDE CAPILLARIES FOLLOWING MIDDLE CEREBRAL-ARTERY OCCLUSION AND REPERFUSION IN BABOONS [J].
DELZOPPO, GJ ;
SCHMIDSCHONBEIN, GW ;
MORI, E ;
COPELAND, BR ;
CHANG, CM .
STROKE, 1991, 22 (10) :1276-1283
[8]   RECOMBINANT EXPRESSION, BIOCHEMICAL-CHARACTERIZATION, AND BIOLOGICAL-ACTIVITIES OF THE HUMAN MGSA-GRO PROTEIN [J].
DERYNCK, R ;
BALENTIEN, E ;
HAN, JH ;
THOMAS, HG ;
WEN, DZ ;
SAMANTHA, AK ;
ZACHARIAE, CO ;
GRIFFIN, PR ;
BRACHMANN, R ;
WONG, WL ;
MATSUSHIMA, K ;
RICHMOND, A .
BIOCHEMISTRY, 1990, 29 (44) :10225-10233
[9]   ESSENTIAL ROLE OF SURFACE-BOUND CHEMO-ATTRACTANT IN LEUKOCYTE MIGRATION [J].
DIERICH, MP ;
WILHELMI, D ;
TILL, G .
NATURE, 1977, 270 (5635) :351-352
[10]   HISTOLOGIC ASSESSMENT OF NEURONS IN RAT MODELS OF CEREBRAL-ISCHEMIA [J].
EKE, A ;
CONGER, KA ;
ANDERSON, M ;
GARCIA, JH .
STROKE, 1990, 21 (02) :299-304