Paraquat: A useful tool for the in vivo study of mechanisms of neuronal cell death

被引:63
作者
Corasaniti, MT
Strongoli, MC
Rotiroti, D
Bagetta, G
Nistico, G
机构
[1] Univ Catanzaro, Fac Pharm, Chair Pharmacol, I-88100 Catanzaro, Italy
[2] CNR, IBAF Inst, I-88100 Catanzaro, Italy
[3] Univ Calabria, Dept Pharmacobiol, I-87036 Cosenza, Italy
[4] Univ Roma Tor Vergata, Dept Biol, Chair Pharmacol, I-00133 Rome, Italy
来源
PHARMACOLOGY & TOXICOLOGY | 1998年 / 83卷 / 01期
关键词
D O I
10.1111/j.1600-0773.1998.tb01434.x
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The present article reviews the results of experimental studies on paraquat neurotoxicity, started by our group several years ago - when clinical and experimental reports had increased the interest for the possibility that environmental chemicals, including paraquat, may be related to the development of Parkinson's disease -, and which are still continuing since paraquat appears to be a promising tool to study the mechanisms of neuronal cell death in vivo. Our observations have demonstrated that paraquat causes evident neurotoxic effects after intracerebroventricular or intracerebral injection in experimental animals; however, it seems that the herbicide does not exibit a selective neurotoxicity towards the dopaminergic nigro-striatal system since potent behavioural and electrocortical changes are induced by paraquat after injection in brain areas other than the substantia nigra and caudate nucleus. By studying the mechanisms through which paraquat induces neurotoxic effects in vivo, it was shown that either free radical production and activation of cholinergic and glutamatergic transmission may be regarded as related events which play a crucial role in paraquat-induced neurotoxicity. In addition, it was observed that in rats paraquat penetrates the blood-brain barrier following systemic administration to give rise to a differential brain regional distribution; the latter observation rises some concern over the hazard of paraquat as a potential environmental neurotoxin. Indeed, paraquat, administered systemically in rats produces behavioural excitation and brain damage. The brain damage appears to be selective for the pyriform cortex and this does not seem to be strictly related to the high concentrations reached by the herbicide in this area but to the higher vulnerability of this cortical area to the enhanced cholinergic transmission. The recent observation that paraquat, injected into the rat hippocampus, induces the expression of apoptotic neuronal cell death, appears of valuable interest also with a view to paraquat as an useful experimental model in the development of neuroprotective drugs able to block the molecular events which, once activated, are responsible for the induction of neuronal cell death.
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页码:1 / 7
页数:7
相关论文
共 53 条
[1]   NEURODEGENERATION PRODUCED BY INTRAHIPPOCAMPAL INJECTION OF PARAQUAT IS REDUCED BY SYSTEMIC ADMINISTRATION OF THE 21-AMINOSTEROID U74389F IN RATS [J].
BAGETTA, G ;
IANNONE, M ;
VECCHIO, I ;
RISPOLI, V ;
ROTIROTI, D ;
NISTICO, G .
FREE RADICAL RESEARCH, 1994, 21 (02) :85-93
[2]   PRODUCTION OF LIMBIC MOTOR SEIZURES AND BRAIN-DAMAGE BY SYSTEMIC AND INTRACEREBRAL INJECTIONS OF PARAQUAT IN RATS [J].
BAGETTA, G ;
CORASANITI, MT ;
IANNONE, M ;
NISTICO, G ;
STEPHENSON, JD .
PHARMACOLOGY & TOXICOLOGY, 1992, 71 (06) :443-448
[3]  
BAGETTA G, 1993, PHARM COMMUN, V3, P357
[4]   ETIOLOGY OF PARKINSONS-DISEASE - A RESEARCH STRATEGY [J].
BARBEAU, A .
CANADIAN JOURNAL OF NEUROLOGICAL SCIENCES, 1984, 11 (01) :24-28
[5]   COMPARATIVE BEHAVIORAL, BIOCHEMICAL AND PIGMENTARY EFFECTS OF MPTP, MPP+ AND PARAQUAT IN RANA-PIPIENS [J].
BARBEAU, A ;
DALLAIRE, L ;
BUU, NT ;
POIRIER, J ;
RUCINSKA, E .
LIFE SCIENCES, 1985, 37 (16) :1529-1538
[6]   NITRIC-OXIDE AS A MEDIATOR OF OXIDANT LUNG INJURY DUE TO PARAQUAT [J].
BERISHA, HI ;
PAKBAZ, H ;
ABSOOD, A ;
SAID, SI .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (16) :7445-7449
[7]   ACCIDENTAL POISONING BY PARAQUAT - REPORT OF 2 CASES IN MAN [J].
BULLIVANT, CM .
BMJ-BRITISH MEDICAL JOURNAL, 1966, 1 (5498) :1272-+
[8]   A PRIMATE MODEL OF PARKINSONISM - SELECTIVE DESTRUCTION OF DOPAMINERGIC-NEURONS IN THE PARS COMPACTA OF THE SUBSTANTIA NIGRA BY N-METHYL-4-PHENYL-1,2,3,6-TETRAHYDROPYRIDINE [J].
BURNS, RS ;
CHIUEH, CC ;
MARKEY, SP ;
EBERT, MH ;
JACOBOWITZ, DM ;
KOPIN, IJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1983, 80 (14) :4546-4550
[9]   PARAQUAT - MODEL FOR OXIDANT-INITIATED TOXICITY [J].
BUS, JS ;
GIBSON, JE .
ENVIRONMENTAL HEALTH PERSPECTIVES, 1984, 55 (APR) :37-46
[10]   SELECTIVE VULNERABILITY OF HIPPOCAMPAL CA3 NEURONS AFTER MICROINFUSION OF PARAQUAT INTO THE RAT SUBSTANTIA-NIGRA OR INTO THE VENTRAL TEGMENTAL AREA [J].
CALO, M ;
IANNONE, M ;
PASSAFARO, M ;
NISTICO, G .
JOURNAL OF COMPARATIVE PATHOLOGY, 1990, 103 (01) :73-78