Effects of benzene on splenic, thymic, and femoral lymphocytes in mice

被引:35
作者
Farris, GM [1 ]
Robinson, SN [1 ]
Wong, BA [1 ]
Wong, VA [1 ]
Hahn, WP [1 ]
Shah, R [1 ]
机构
[1] CHEM IND INST TOXICOL,RES TRIANGLE PK,NC 27709
关键词
immunotoxicity; benzene; mouse; inhalation; proliferation; apoptosis; lymphocytes;
D O I
10.1016/S0300-483X(96)03606-2
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Chronic exposure to high concentrations of benzene, primarily by inhalation, can affect the function of the human immune system. Limited data are available on the immunotoxic effects of low concentrations of benzene. This study evaluated the effects of 1, 5, 10, 100, and 200 ppm benzene on lymphocytes in mice exposed by inhalation for up to 8 weeks, Exposure to 100 or 200 ppm benzene induced rapid and persistent reductions in femoral B-, splenic T- and B-, and thymic T-lymphocytes. The percentage of femoral B-lymphocytes and thymic T-lymphocytes in apoptosis was increased 6- to 15-fold by 200 ppm benzene compared to controls. Replication of femoral B-lymphocytes was increased during the exposure period in the bone marrow as a compensation for the lymphocyte loss induced by 100 and 200 ppm benzene. Exposure of mice to 10 ppm benzene or less did not have a statistically significant effect on numbers or replication of the lymphocyte populations evaluated. A reduced number of splenic B-lymphocytes after 2 weeks of exposure to benzene appeared to be the most sensitive end point and time point for evaluating benzene cytotoxicity in this study. (C) 1997 Elsevier Science Ireland Ltd.
引用
收藏
页码:137 / 148
页数:12
相关论文
共 28 条
[1]   HEMATOTOXICITY AND CARCINOGENICITY OF BENZENE [J].
AKSOY, M .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1989, 82 :193-197
[2]   MALIGNANCIES DUE TO OCCUPATIONAL EXPOSURE TO BENZENE [J].
AKSOY, M .
AMERICAN JOURNAL OF INDUSTRIAL MEDICINE, 1985, 7 (5-6) :395-402
[3]   BENZENE AS A LEUKEMOGENIC AND CARCINOGENIC AGENT [J].
AKSOY, M .
AMERICAN JOURNAL OF INDUSTRIAL MEDICINE, 1985, 8 (01) :9-20
[5]   IDENTIFICATION OF DNA-REPLICATING LYMPHOCYTE SUBSETS USING A NEW METHOD TO LABEL THE BROMO-DEOXYURIDINE INCORPORATED INTO THE DNA [J].
CARAYON, P ;
BORD, A .
JOURNAL OF IMMUNOLOGICAL METHODS, 1992, 147 (02) :225-230
[6]   BIOLOGICAL BASIS OF CHEMICAL CARCINOGENESIS - INSIGHTS FROM BENZENE [J].
COX, LA .
RISK ANALYSIS, 1991, 11 (03) :453-464
[7]  
CRONKITE EP, 1986, BLOOD CELLS, V12, P129
[8]   IMMUNOHISTOCHEMICAL DETECTION OF PROLIFERATING CELLS INVIVO [J].
DEFAZIO, A ;
LEARY, JA ;
HEDLEY, DW ;
TATTERSALL, MHN .
JOURNAL OF HISTOCHEMISTRY & CYTOCHEMISTRY, 1987, 35 (05) :571-577
[9]   CARCINOGENICITY OF INHALED BENZENE IN CBA MICE [J].
FARRIS, GM ;
EVERITT, JI ;
IRONS, RD ;
POPP, JA .
FUNDAMENTAL AND APPLIED TOXICOLOGY, 1993, 20 (04) :503-507
[10]   Benzene-induced micronuclei in erythrocytes: An inhalation concentration-response study in B6C3F1 mice [J].
Farris, GM ;
Wong, VA ;
Wong, BA ;
Janszen, DB ;
Shah, RS .
MUTAGENESIS, 1996, 11 (05) :455-462