EFFECTS OF SUBACUTE TOLUENE EXPOSURE ON NEURONAL AND GLIAL MARKER PROTEINS IN RAT-BRAIN

被引:20
作者
HUANG, J [1 ]
KATO, K [1 ]
SHIBATA, E [1 ]
HISANAGA, N [1 ]
ONO, Y [1 ]
TAKEUCHI, Y [1 ]
机构
[1] AICHI PREFECTURAL COLONY, INST DEV RES, DEPT BIOCHEM, KASUGAI, AICHI 48003, JAPAN
关键词
Creatine kinase-B; Subacute inhalation; Toluene; α-Enolase; β-S100; protein; γ-Enolase;
D O I
10.1016/0300-483X(90)90013-7
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The behavior of marker proteins of neurons (γ-enolase) and glial cells (α-enolase, β-S100 protein and creatine kinase-B) was investigated quantitatively by using enzyme immunoassay systems in toluene-exposed rat brains. Three groups of animals were exposed to toluene vapor at 300 ppm, 1000 ppm, and 3000 ppm, respectively, 8 h/day, 6 days/week, for 2 weeks. After subacute repeated solvent exposure, both neuron-specific γ-enolase and glial marker proteins displayed an overall concentration-dependent increase tendency in separate brain regions. In cerebrum, only the 3000 ppm group showed a significant increase in α-enolase by 27% and creatine kinase-B (CK-B) by 26%. α-Enolase and γ-enolase exhibited a pronounced elevation in cerebellum relative to other brain regions, while β-S100 protein appeared to be the most markedly altered marker in brainstem. The development of gliosis, which is a frequent phenomenon following CNS damage, is presumed to be responsible for the elevation of glial marker content. Energy metabolism disruption in brain tissues may also bring about the compensatory oversynthesis of glycolytic enzymes such as γ-enolase, α-enolase and CK-B. The dose-dependent alteration patterns following toluene exposure suggest the feasibility of using these brain specific markers to evaluate solvent-induced CNS effects. © 1990.
引用
收藏
页码:109 / 117
页数:9
相关论文
共 31 条
[11]  
HUANG J, 1989, IN PRESS 12TH P AS C
[12]   SENSITIVE ENZYME-IMMUNOASSAY FOR S-100 PROTEIN - DETERMINATION IN HUMAN CEREBROSPINAL-FLUID [J].
KATO, K ;
NAKAJIMA, T ;
ISHIGURO, Y ;
TENHOSHIMARU, M .
BIOMEDICAL RESEARCH-TOKYO, 1982, 3 (01) :24-28
[13]   HIGHLY SENSITIVE IMMUNOASSAYS FOR 3 FORMS OF RAT-BRAIN ENOLASE [J].
KATO, K ;
SUZUKI, F ;
UMEDA, Y .
JOURNAL OF NEUROCHEMISTRY, 1981, 36 (03) :793-797
[14]  
KATO K, 1986, J NEUROCHEM, V46, P1783
[15]   PERMANENT ENCEPHALOPATHY FROM TOLUENE INHALATION [J].
KNOX, JW ;
NELSON, JR .
NEW ENGLAND JOURNAL OF MEDICINE, 1966, 275 (26) :1494-&
[16]   BRAIN LIPID CHANGES IN RATS EXPOSED TO XYLENE AND TOLUENE [J].
KYRKLUND, T ;
KJELLSTRAND, P ;
HAGLID, K .
TOXICOLOGY, 1987, 45 (02) :123-133
[17]   MULTIFOCAL CENTRAL NERVOUS-SYSTEM DAMAGE CAUSED BY TOLUENE ABUSE [J].
LAZAR, RB ;
HO, SU ;
MELEN, O ;
DAGHESTANI, AN .
NEUROLOGY, 1983, 33 (10) :1337-1340
[18]   S-100 ANTIGEN IN CEREBROSPINAL-FLUID AS A POSSIBLE INDEX OF CELL INJURY IN THE NERVOUS-SYSTEM [J].
MICHETTI, F ;
MASSARO, A ;
RUSSO, G ;
RIGON, G .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1980, 44 (2-3) :259-263
[20]  
ROSENGREN LE, 1989, BRIT J IND MED, V46, P316