CYANIDE-INDUCED ALTERATION OF THE ADENYLATE ENERGY POOL IN A RAT NEUROSECRETORY CELL-LINE

被引:21
作者
MADUH, EU [1 ]
BOROWITZ, JL [1 ]
ISOM, GE [1 ]
机构
[1] PURDUE UNIV,SCH PHARM & PHARMACAL SCI,DEPT PHARMACOL & TOXICOL,W LAFAYETTE,IN 47907
关键词
CYANIDE; HISTOTOXIC HYPOXIA; NEUROTOXICITY;
D O I
10.1002/jat.2550110205
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
Cultures of a rat PC12 pheochromocytoma neurosecretory cell line were used to determine the responsiveness of oxidative energy status of isolated neuronal cells to cyanide exposure. Intracellular levels of ATP and its immediate metabolites, ADP and AMP, were measured in monolayer cultures of PC12 cells incubated for 0-30 min with KCN (10 mM). Over the period 2.5-30 min, cyanide treatment decreased ATP levels by 32-51% but ADP and AMP levels were not altered significantly. Additionally, ATP/ADP and ATP/AMP ratios were significantly reduced in KCN-intoxicated cells. These alterations in energy status may explain the prompt ablation of ion homeostasis reported previously in this model upon exposure to KCN. The energy-depleting actions of cyanide were not modified by pretreatment of cells with diltiazem, a calcium channel antagonist demonstrated to possess cytoprotective activity against histotoxic hypoxia induced by cyanide. Since PC12 cells rapidly respond to cyanide, with predictable depletions of the cell adenylate energy pool, this cell line can serve as a suitable in vitro model for studies of neurotoxicity involving ischemic/hypoxic conditions.
引用
收藏
页码:97 / 101
页数:5
相关论文
共 28 条
[11]  
ISOM GE, 1990, TOXICOLOGIST, V10, P111
[12]   EFFECT OF PENTOBARBITAL ON CYANIDE-INDUCED TREMORS IN MICE AND CALCIUM ACCUMULATION IN PC12 CELLS [J].
JOHNSON, JD ;
CONROY, WG ;
ISOM, GE .
BIOCHEMICAL PHARMACOLOGY, 1987, 36 (10) :1747-1749
[13]   CYANIDE-INDUCED NEUROTOXICITY - ROLE OF NEURONAL CALCIUM [J].
JOHNSON, JD ;
MEISENHEIMER, TL ;
ISOM, GE .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1986, 84 (03) :464-469
[14]   ALTERATION OF CYTOSOLIC CALCIUM LEVELS IN PC12 CELLS BY POTASSIUM CYANIDE [J].
JOHNSON, JD ;
CONROY, WG ;
ISOM, GE .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1987, 88 (02) :217-224
[15]   RAPID EFFECTS OF VERATRIDINE, TETRODOTOXIN, GRAMICIDIN-D, VALINOMYCIN AND NACN ON NA+, K+ AND ATP CONTENTS OF SYNAPTOSOMES [J].
LI, PP ;
WHITE, TD .
JOURNAL OF NEUROCHEMISTRY, 1977, 28 (05) :967-975
[16]   CYANIDE-INDUCED NEUROTOXICITY - CALCIUM MEDIATION OF MORPHOLOGICAL-CHANGES IN NEURONAL CELLS [J].
MADUH, EU ;
TUREK, JJ ;
BOROWITZ, JL ;
REBAR, A ;
ISOM, GE .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1990, 103 (02) :214-221
[17]   CYANIDE-INDUCED NEUROTOXICITY - MECHANISMS OF ATTENUATION BY CHLORPROMAZINE [J].
MADUH, EU ;
JOHNSON, JD ;
ARDELT, BK ;
BOROWITZ, JL ;
ISOM, GE .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1988, 96 (01) :60-67
[18]  
MADUH EU, IN PRESS TOXICOL APP
[19]   ETHANOL REGULATES CALCIUM CHANNELS IN CLONAL NEURAL CELLS [J].
MESSING, RO ;
CARPENTER, CL ;
DIAMOND, I ;
GREENBERG, DA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (16) :6213-6215
[20]   CYTOSOLIC-FREE CA-2+ AND CELL KILLING IN HEPATOMA 1C1C7 CELLS EXPOSED TO CHEMICAL ANOXIA [J].
NICOTERA, P ;
THOR, H ;
ORRENIUS, S .
FASEB JOURNAL, 1989, 3 (01) :59-64