Electrochemical investigation into the redox activity of Fe(II)/Fe(III) in the presence of nicotine and possible relations to neurodegenerative diseases

被引:47
作者
Bridge, MH
Williams, E
Lyons, MEG
Tipton, KF
Linert, W
机构
[1] Vienna Tech Univ, Inst Appl Synth Chem, A-1060 Vienna, Austria
[2] Trinity Coll Dublin, Dept Chem, Dublin 2, Ireland
[3] Trinity Coll Dublin, Dept Biochem, Dublin 2, Ireland
来源
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE | 2004年 / 1690卷 / 01期
关键词
nicotine; parkinsonism; electrochemical rate constant; cyclic voltammetry; formation constant;
D O I
10.1016/j.bbadis.2004.05.007
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 biological relevance of Fe(II)/Fe(III) is becoming evermore apparent, especially in relation to its potential role in the progression of neurodegenerative diseases such as Parkinson's and Alzheimer's disease. The reported relationship between smoking and a reduced incidence of neurodegenerative disorders prompted this work. In order to investigate whether nicotine can interact with iron, we have studied the electrochemical behaviour of a Fe(II)/Fe(III) redox couple in the presence of nicotine. Solubility issues and lack of available nonreacting salts of nicotine necessitated studies being conducted at low pH values. Cyclic voltammetry experiments revealed a definite alteration in the electrochemical behaviour of the Fe(II)/Fe(III) redox couple suggesting the capability of nicotine to complex with free iron and, hence, reduce its reactivity. This is evident from a slower rate of heterogeneous electron transfer, k(s), and a shift from reversible to quasi-reversible behaviour, as characterised from the diffusion coefficient (D), the full width half maximum (FWHM), DeltaE(p) and E-f. Additional complexation titrations, pH ranging from 1 to 7, confirm a weak complexation reaction occurring between Fe(III) and nicotine. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:77 / 84
页数:8
相关论文
共 33 条
[1]  
Bard A. L., 2001, ELECTROCHEMICAL METH, p[11, 540]
[2]   Formation of the oxidative damage marker 8-hydroxy-2′-deoxyguanosine from the nucleoside 2′-deoxyguanosine:: parameter studies and evidence of Fe(II) binding [J].
Colwell, BA ;
Morris, DL .
JOURNAL OF INORGANIC BIOCHEMISTRY, 2003, 94 (1-2) :100-105
[3]   Nicotine protects rat brain mitochondria against experimental injuries [J].
Cormier, A ;
Morin, C ;
Zini, R ;
Tillement, JP ;
Lagrue, G .
NEUROPHARMACOLOGY, 2003, 44 (05) :642-652
[4]  
Crichton RR, 1991, INORGANIC BIOCH IRON
[5]   Cathodic reduction of 2-nitronaphthothiophen-4,9-quinone: evidence of catalysis by proton donors and its simulation [J].
de Abreu, FC ;
Tonholo, J ;
Bottecchia, OL ;
Zani, CL ;
Goulart, MOF .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1999, 462 (02) :195-201
[6]  
DEXTER DT, 1992, ANN NEUROL, V32, P94
[7]  
DOLL R, 2000, BRIT MED J, V320, P53
[8]   ELECTROCHEMICAL OXIDATION OF SOME THERAPEUTIC 3-HYDROXYPYRIDIN-4-ONE IRON CHELATORS [J].
ELJAMMAL, A ;
TEMPLETON, DM .
ELECTROCHIMICA ACTA, 1993, 38 (15) :2223-2230
[9]   Iron-hydroxypyridone redox chemistry: Kinetic and thermodynamic limitations to Fenton activity [J].
ElJammal, A ;
Templeton, DM .
INORGANICA CHIMICA ACTA, 1996, 245 (02) :199-207
[10]  
F Allen J Bard L.R., 2001, Electrochemical Methods: Fundamentals and Applications