Glucocorticoids increase the accumulation of reactive oxygen species and enhance adriamycin-induced toxicity in neuronal culture

被引:175
作者
McIntosh, LJ
Sapolsky, RM
机构
[1] Department of Biological Sciences, Stanford University, Stanford
关键词
D O I
10.1006/exnr.1996.0154
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Glucocorticoids (GCs), the adrenal steroids secreted during stress, are known to affect diverse processes involving reactive oxygen species, from exacerbation of ischemic damage to alteration of antioxidant enzyme activities. To determine whether GCs have a direct effect on oxidative processes, we constructed a dose-response curve using adriamycin, an oxygen radical generator, in primary neuronal cultures. In cultures derived from the hippocampus, which has the greatest concentration of corticosteroid receptors in the brain, higher levels of GCs significantly increased adriamycin toxicity, while not being toxic themselves. In cortical cultures, which contain lesser amounts of corticosteroid receptors, GCs had no effect on the adriamycin dose-response. Surprisingly, when tested with dichlorofluorescein for levels of reactive oxygen species (ROS), GCs increased ROS by approximately 10% basally and at all adriamycin doses in both hippocampal and cortical cultures. Thus, greater generation of ROS does not account for the increased susceptibility of the hippocampus to oxidative damage. (C) 1996 Academic Press, Inc.
引用
收藏
页码:201 / 206
页数:6
相关论文
共 46 条
[31]  
SAPOLSKY RM, 1985, J NEUROSCI, V5, P1228
[32]  
SMITHSWINTOSKY V, 1996, IN PRESS J CEREBRAL
[33]   MITOCHONDRIAL OXIDATIVE DAMAGE, HYDROGEN-PEROXIDE RELEASE, AND AGING [J].
SOHAL, RS ;
DUBEY, A .
FREE RADICAL BIOLOGY AND MEDICINE, 1994, 16 (05) :621-626
[34]  
Spoerri P E, 1984, Monogr Dev Biol, V17, P210
[35]   HIPPOCAMPAL-FORMATION VOLUME, MEMORY DYSFUNCTION, AND CORTISOL-LEVELS IN PATIENTS WITH CUSHINGS-SYNDROME [J].
STARKMAN, MN ;
GEBARSKI, SS ;
BERENT, S ;
SCHTEINGART, DE .
BIOLOGICAL PSYCHIATRY, 1992, 32 (09) :756-765
[36]   CHEMICAL ADRENALECTOMY REDUCES HIPPOCAMPAL DAMAGE INDUCED BY KAINIC ACID [J].
STEIN, BA ;
SAPOLSKY, RM .
BRAIN RESEARCH, 1988, 473 (01) :175-180
[37]  
STEINBEHRENS B, 1994, J NEUROSCI, V14, P5373
[38]   GLUCOCORTICOIDS EXACERBATE KAINIC ACID-INDUCED EXTRACELLULAR ACCUMULATION OF EXCITATORY AMINO-ACIDS IN THE RAT HIPPOCAMPUS [J].
STEINBEHRENS, BA ;
ELLIOTT, EM ;
MILLER, CA ;
SCHILLING, JW ;
NEWCOMBE, R ;
SAPOLSKY, RM .
JOURNAL OF NEUROCHEMISTRY, 1992, 58 (05) :1730-1735
[39]   DEXAMETHASONE POTENTIATES NMDA RECEPTOR-MEDIATED NEURONAL INJURY IN THE POSTNATAL RAT [J].
SUPKO, DE ;
JOHNSTON, MV .
EUROPEAN JOURNAL OF PHARMACOLOGY-ENVIRONMENTAL TOXICOLOGY AND PHARMACOLOGY SECTION, 1994, 270 (01) :105-113
[40]   SIMILAR EFFECTS OF AGING AND CORTICOSTERONE TREATMENT ON MOUSE HIPPOCAMPAL FUNCTION [J].
TALMI, M ;
CARLIER, E ;
SOUMIREUMOURAT, B .
NEUROBIOLOGY OF AGING, 1993, 14 (03) :239-244