The endogenous amine 1-methyl-1,2,3,4-tetrahydroisoquinoline prevents the inhibition of complex I of the respiratory chain produced by MPP+

被引:28
作者
Parrado, J [1 ]
Absi, E [1 ]
Ayala, A [1 ]
Castaño, A [1 ]
Cano, J [1 ]
Machado, A [1 ]
机构
[1] Univ Sevilla, Fac Farm, Dept Bioquim Bromatol & Toxicol, E-41012 Seville, Spain
关键词
1-methyl-1,2,3,4-tetrahydroisoquinoline; MPP+; Parkinson's disease; mitochondria; complex I; dopaminergic neurotoxin; neuroprotection;
D O I
10.1046/j.1471-4159.2000.0750065.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The endogenous monoamine 1-methyl-1,2,3,4-tetrahydroisoquinoline has been shown to prevent the neurotoxic effect of MPP+ and other endogenous neurotoxins, which produce a parkinsonian-like syndrome in humans. We have tested its potential protective effect in vivo by measuring the protection of 1-methyl-1,2,3,4-tetrahydroisoquinoline in the neurotoxicity elicited by MPP+ in rat striatum by tyrosine hydroxylase immunocytochemistry. Because we know that cellular damage caused by MPP+ is primarily the result of mitochondrial respiratory inhibition at the complex I lever, we have extended the study further to understand this protective mechanism. We found that the inhibitory effect on the mitochondrial respiration rate induced by MPP+ in isolated rat liver mitochondria and striatal synaptosomes was prevented by addition of 1-methyl-1,2,3,4-tetrahydroisoquinoline. This compound has no antioxidant capacity; therefore, this property is not involved in its protective effect. Thus, we postulate that the preventive effect that 1-methyl-1,2,3,4-tetrahydroisoquinoline has on mitochondrial inhibition for MPP+ could be due to a "shielding effect," protecting the energetic machinery, thus preventing energetic failure. These results suggest that this endogenous amine may protect against the effect of several parkinsonism-inducing compounds that are associated with progressive impairment of the mitochondrial function.
引用
收藏
页码:65 / 71
页数:7
相关论文
共 38 条
[1]   MITOCHONDRIAL RESPIRATORY INHIBITION BY N-METHYLATED BETA-CARBOLINE DERIVATIVES STRUCTURALLY RESEMBLING N-METHYL-4-PHENYLPYRIDINE [J].
ALBORES, R ;
NEAFSEY, EJ ;
DRUCKER, G ;
FIELDS, JZ ;
COLLINS, MA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (23) :9368-9372
[2]  
AYALA A, 1994, BRAIN RES, V638, P332
[3]   Implication of dopamine transporter system on 1-methyl-4-phenylpyridinium and rotenone effect in striatal synaptosomes [J].
Bougria, M ;
Vitorica, J ;
Cano, J ;
Machado, A .
EUROPEAN JOURNAL OF PHARMACOLOGY-MOLECULAR PHARMACOLOGY SECTION, 1995, 291 (03) :407-415
[4]   IRREVERSIBLE INHIBITION OF MITOCHONDRIAL COMPLEX-I BY 1-METHYL-4-PHENYLPYRIDINIUM - EVIDENCE FOR FREE-RADICAL INVOLVEMENT [J].
CLEETER, MWJ ;
COOPER, JM ;
SCHAPIRA, AHV .
JOURNAL OF NEUROCHEMISTRY, 1992, 58 (02) :786-789
[5]   BETA-CARBOLINE ANALOGS OF N-METHYL-4-PHENYL-1,2,5,6-TETRA-HYDROPYRIDINE (MPTP) - ENDOGENOUS FACTORS UNDERLYING IDIOPATHIC PARKINSONISM [J].
COLLINS, MA ;
NEAFSEY, EJ .
NEUROSCIENCE LETTERS, 1985, 55 (02) :179-184
[6]   CHRONIC PARKINSONISM SECONDARY TO INTRAVENOUS-INJECTION OF MEPERIDINE ANALOGS [J].
DAVIS, GC ;
WILLIAMS, AC ;
MARKEY, SP ;
EBERT, MH ;
CAINE, ED ;
REICHERT, CM ;
KOPIN, IJ .
PSYCHIATRY RESEARCH, 1979, 1 (03) :249-254
[7]  
GLAZER AN, 1990, METHOD ENZYMOL, V186, P161
[8]   PARKINSONISM-INDUCING NEUROTOXIN, N-METHYL-4-PHENYL-1,2,3,6-TETRAHYDROPYRIDINE - UPTAKE OF THE METABOLITE N-METHYL-4-PHENYLPYRIDINE BY DOPAMINE NEURONS EXPLAINS SELECTIVE TOXICITY [J].
JAVITCH, JA ;
DAMATO, RJ ;
STRITTMATTER, SM ;
SNYDER, SH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (07) :2173-2177
[9]  
Kawai H, 1998, J NEUROCHEM, V70, P745
[10]   TETRAHYDROISOQUINOLINE AND 1-METHYL-TETRAHYDROISOQUINOLINE AS NOVEL ENDOGENOUS AMINES IN RAT-BRAIN [J].
KOHNO, M ;
OHTA, S ;
HIROBE, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1986, 140 (01) :448-454