Dopamine-derived salsolinol derivatives as endogenous monoamine oxidase inhibitors: Occurrence, metabolism and function in human brains

被引:95
作者
Naoi, M
Maruyama, W
Nagy, GM
机构
[1] Inst Appl Biochem, Dept Brain Sci, Gifu 5050116, Japan
[2] Natl Inst Longev Sci, Dept Basic Gerontol, Aichi 4748522, Japan
[3] Semmelweis Univ, Dept Human Morphol & Dev Biol, Neuroendocrine Res Lab, H-1085 Budapest, Hungary
基金
日本学术振兴会;
关键词
salsolinol; monoamine oxidase inhibitor; Parkinson's disease; neurotoxin; prolactin;
D O I
10.1016/S0161-813X(03)00099-8
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Salsolinol, 1-methyl-6,7-dihydroxy-1,2,3,4-tetrahydroisoquinoline, is an endogenous catechol isoquinoline detected in humans by M. Sandler In human brain, a series of catechol isoquinolines were identified as the condensation products of dopamine or other monoamines with aldehydes or keto-acids. Recently selective occurrence of the (R)enantiomers of salsolinol derivatives was confirmed in human brain, and they are synthesized by enzymes in situ, but not by the nonenzymatic Pictet-Spengler reaction. A (R)salsolinol synthase catalyzes the enantio-specific synthesis of (R)salsolinol front dopamine and acetaldehyde, and (R)salsolinol N-methyltransferase synthesizes N-methyl(R)salsolinol, which is further oxidized into 1,2-dimethyl-6,7-dihydroxyisoquinolinium ion by non-enzymatic and enzymatic oxidation. The stepwise reactions, N-methylation and oxidation, induce the specified distribution of the N-methylated and oxidized derivatives in the human nigro-striatum, suggesting that these derivatives may be involved in the function of dopamine neurons under physiological and pathological conditions. As shown by in vivo and in vitro experiments, salsolinol derivatives affect the levels of monoamine neurotransmitters though the inhibition of enzymes related in the metabolism of catechol- and indoleamines. In addition, the selective neurotoxicity of N-methyl(R)salsolinol to dopamine neurons was confirmed by preparation of an animal model of Parkinson's disease in rats. The involvement of N-methyl(R)salsolinol in the pathogenesis of Parkinson's disease was further indicated by the increase in the N-methyl(R)salsolinol levels in the cerebrospinal fluid and that in the activity of its synthesizing enzyme, a neural (R)salsolinol N-methyltransferase, in the lymphocytes prepared from parkinsonian patients. N-Methyl(R)salsolinol induces apoptosis in dopamine neurons, which is mediated by death signal transduction in mitochondria. In addition, salsolinol was found to function as a signal transmitter for the prolactin release in the neuro-intermediate lobe of the brain. These results are discussed in relation to role of dopamine-derived endogenous salsolinol derivatives as the regulators of neurotransmission, dopaminergic neurotoxins and neuro-hormonal transmitters in the human brain. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:193 / 204
页数:12
相关论文
共 62 条
[1]   Mitochondrial permeability transition mediates apoptosis induced by N-methyl(R)salsolinol, an endogenous neurotoxin, and is inhibited by Bcl-2 and rasagiline, N-propargyl-1(R)-aminoindan [J].
Akao, Y ;
Maruyama, W ;
Shimizu, S ;
Yi, H ;
Nakagawa, Y ;
Shamoto-Nagai, M ;
Youdim, MBH ;
Tsujimoto, Y ;
Naoi, M .
JOURNAL OF NEUROCHEMISTRY, 2002, 82 (04) :913-923
[2]   Apoptosis induced by an endogenous neurotoxin, N-methyl(R)salsolinol, is mediated by activation of caspase 3 [J].
Akao, Y ;
Nakagawa, Y ;
Maruyama, W ;
Takahashi, T ;
Naoi, M .
NEUROSCIENCE LETTERS, 1999, 267 (03) :153-156
[3]  
BAUM SS, 1994, J CHROMATOGR B, V660, P235
[4]   INHIBITION OF MONOAMINE OXIDASE-A AND MONOAMINE OXIDASE-B BY SIMPLE ISOQUINOLINE ALKALOIDS - RACEMIC AND OPTICALLY-ACTIVE 1,2,3,4-TETRAHYDRO-ISOQUINOLINE, 3,4-DIHYDRO-ISOQUINOLINE, AND FULLY AROMATIC ISOQUINOLINE [J].
BEMBENEK, ME ;
ABELL, CW ;
CHRISEY, LA ;
ROZWADOWSKA, MD ;
GESSNER, W ;
BROSSI, A .
JOURNAL OF MEDICINAL CHEMISTRY, 1990, 33 (01) :147-152
[5]   RATIO OF THE R-ENANTIOMER AND S-ENANTIOMER OF SALSOLINOL IN FOOD AND HUMAN-URINE [J].
BENEDETTI, MS ;
BELLOTTI, V ;
PIANEZZOLA, E ;
MORO, E ;
CARMINATI, P ;
DOSTERT, P .
JOURNAL OF NEURAL TRANSMISSION, 1989, 77 (01) :47-53
[6]   IDENTIFICATION OF CATECHOLAMINE-DERIVED ALKALOIDS IN MAMMALS BY GAS-CHROMATOGRAPHY AND MASS-SPECTROMETRY [J].
CASHAW, JL ;
MCMURTREY, KD ;
BROWN, H ;
DAVIS, VE .
JOURNAL OF CHROMATOGRAPHY, 1974, 99 (NOV6) :567-573
[7]   INHIBITION OF CATECHOL-O-METHYLTRANSFERASE BY 6,7-DIHYDROXY-3,4-DIHYDROISOQUINOLINES RELATED TO DOPAMINE - DEMONSTRATION USING LIQUID-CHROMATOGRAPHY AND A NOVEL SUBSTRATE FOR O-METHYLATION [J].
CHENG, BY ;
ORIGITANO, TC ;
COLLINS, MA .
JOURNAL OF NEUROCHEMISTRY, 1987, 48 (03) :779-786
[8]   ALKALOIDS FROM CATECHOLAMINES IN ADRENAL TISSUE - POSSIBLE ROLE IN ALCOHOLISM [J].
COHEN, G ;
COLLINS, M .
SCIENCE, 1970, 167 (3926) :1749-&
[9]   DOPAMINE-DERIVED TETRAHYDROISOQUINOLINE ALKALOIDS - INHIBITORS OF NEUROAMINE METABOLISM [J].
COLLINS, AC ;
CASHAW, JL ;
DAVIS, VE .
BIOCHEMICAL PHARMACOLOGY, 1973, 22 (18) :2337-2348
[10]  
Collins M A, 1980, Adv Exp Med Biol, V126, P87