Effects of polychlorinated biphenyls on dopamine release from PC12 cells

被引:28
作者
Angus, WGR
Contreras, ML
机构
[1] MICHIGAN STATE UNIV, INST ENVIRONM TOXICOL, DEPT PHARMACOL & TOXICOL, E LANSING, MI 48824 USA
[2] MICHIGAN STATE UNIV, PROGRAM NEUROSCI, E LANSING, MI 48824 USA
关键词
aroclor; polychlorinated biphenyl; neurotoxicity; dopamine; PC12;
D O I
10.1016/S0378-4274(96)03810-6
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
In PC12 cells, Aroclor 1254 produced a concentration-dependent decrease in basal and K+-evoked dopamine (DA) release, and cellular DA levels. Aroclor 1254 did not alter the fraction of cellular DA released, suggesting that the decreased release of DA was solely due to decreased cellular levels of DA, and not to decreased packaging of DA or inhibition of neurotransmitter release. The coplanar congener 3,3',4,4',5-pentachlorobiphenyl decreased cellular DA levels and release of DA at levels that produced cytotoxicity. Absent of any apparent cytotoxicity, the ortho-substituted PCB congeners 2,2',5,5'-tetrachlorobiphenyl, 2,2',3,3',4,4'-hexachlorobiphenyl, 2,3',4,4',5-pentachlorobiphenyl, and 2,2',4,4',5,5'-hexachlorobiphenyl were effective in decreasing the amount of DA released from PC12 cells. These results suggest that or tho-chlorinated PCBs can cause decreased K+-evoked DA release through non-Ah receptor-mediated mechanisms. Furthermore, the PCB-mediated decrease in DA release was not due to impairment of DA packaging or release, but only due to decreased cellular DA levels.
引用
收藏
页码:191 / 199
页数:9
相关论文
共 35 条
[1]   3,4,3',4'-TETRACHLOROBIPHENYL GIVEN TO MICE PRENATALLY PRODUCES LONG-TERM DECREASES IN STRIATAL DOPAMINE AND RECEPTOR-BINDING SITES IN THE CAUDATE-NUCLEUS [J].
AGRAWAL, AK ;
TILSON, HA ;
BONDY, SC .
TOXICOLOGY LETTERS, 1981, 7 (06) :417-424
[2]  
ANGUS WGR, 1994, NEUROTOXICOLOGY, V15, P809
[3]   RELEASE OF NEWLY SYNTHESIZED DOPAMINE FROM DOPAMINE-CONTAINING TERMINALS IN STRIATUM OF RAT [J].
BESSON, MJ ;
CHERAMY, A ;
FELTZ, P ;
GLOWINSKI, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1969, 62 (03) :741-+
[4]   TRANSPORT AND CELLULAR UPTAKE OF POLYCHLORINATED-BIPHENYLS (PCBS) .2. ASSOCIATION OF INDIVIDUAL PCB ISOMERS AND CONGENERS WITH PLASMA-LIPOPROTEINS AND PROTEINS IN THE PIGEON [J].
BORLAKOGLU, JT ;
WELCH, VA ;
WILKINS, JPG ;
DILS, RR .
BIOCHEMICAL PHARMACOLOGY, 1990, 40 (02) :265-272
[5]   CORRELATION OF PCB BODY BURDEN WITH BEHAVIORAL-TOXICOLOGY IN MONKEYS [J].
BOWMAN, RE ;
HEIRONIMUS, MP ;
ALLEN, JR .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 1978, 9 (01) :49-56
[6]   COGNITIVE-DEVELOPMENT OF YU-CHENG (OIL DISEASE) CHILDREN PRENATALLY EXPOSED TO HEAT-DEGRADED PCBS [J].
CHEN, YCJ ;
GUO, YL ;
HSU, CC ;
ROGAN, WJ .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1992, 268 (22) :3213-3218
[7]  
Chou S M, 1979, Ann N Y Acad Sci, V320, P373, DOI 10.1111/j.1749-6632.1979.tb56619.x
[8]  
GEWIRTZ GP, 1970, J PHARMACOL EXP THER, V175, P514
[9]   EFFECTS OF PERINATAL POLYCHLORINATED-BIPHENYLS AND DICHLORODIPHENYL DICHLOROETHENE ON LATER DEVELOPMENT [J].
GLADEN, BC ;
ROGAN, WJ .
JOURNAL OF PEDIATRICS, 1991, 119 (01) :58-63
[10]  
Hansen L.G., 1987, Environmental Toxin Series, V1, P15