β-carotene breakdown products may impair mitochondrial functions -: potential side effects of high-dose β-carotene supplementation

被引:100
作者
Siems, W [1 ]
Wiswedel, I
Salerno, C
Crifò, C
Augustin, W
Schild, L
Langhans, CD
Sommerburg, O
机构
[1] Loges Sch Phys Med & Rehabil, D-38667 Bad Harzburg, Germany
[2] Univ Magdeburg, Inst Biochem & Clin Pathobiochem, Inst Biochem Pathobiochem, D-39120 Magdeburg, Germany
[3] Univ Roma La Sapienza, Biochim Clin Lab, I-00185 Rome, Italy
[4] Univ Roma La Sapienza, Dept Biochem Sci, I-00185 Rome, Italy
[5] Univ Heidelberg, Dept Paediat, D-69120 Heidelberg, Germany
[6] Univ Ulm, Dept Paediat, D-89077 Ulm, Germany
关键词
beta-carotene; carotenoid; carotenoid breakdown products; oxidative stress; respiration; mitochondria; antioxidant; aldehydes; malondialdehyde (MDA); free radicals; neutrophils; lung;
D O I
10.1016/j.jnutbio.2005.01.009
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
beta-Carotene (BC) and other carotenoids are mainly considered as belonging to the group of micronutrients. As they are contained in fruit and vegetables and thus part of human diet, a regular low-dose intake from natural sources is normally assured. In the last decade high-dose supplementation with synthetic carotenoids has been used successfully in the treatment of diseases believed to be associated with oxidative stress. However, in a few clinical studies harmfull effects have been observed as well, e.g., a higher incidence of lung cancer after BC was given in high doses to smokers. Our studies aim at shedding light on the causal mechanisms of the known side effects that we have investigated. Possibilities of preventing them are discussed. Obviously, on certain conditions of high-dose carotenoid supplementation, both the antioxidant and prooxidant reactions may arise. Carotenoid breakdown products (CBP) including very reactive aldehydes and epoxides are formed during oxidative attack in the course of antioxidative action. Carotenoid breakdown products inhibit state 3 respiration of isolated rat liver mitochondria at concentrations between 0.5 and 20 mu M. In vivo stimulated neutrophils might represent an important source for the generation of CBP, and the lung might be a critical organ in CBP formation. The inhibition of mitochondrial state 3 respiration by CBP is accompanied by a reduced content of protein sulfbydryl groups, decreasing glutathione levels and redox state, and also elevated accumulation of malondialdehyde. Changes in mitochondrial membrane potential favour functional deterioration of the adenine nucleotide translocator (ANT). The findings reflect a basic mechanism of the side effects of BC supplementation in circumstances of severe oxidative stress induced by CBP representing a class of lipid oxidation products. We are striving for safe conditions of carotenoid supplementation in order to protect patients in need of this kind of medical treatment from possible side effects, such as unwanted prooxidative reactions. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:385 / 397
页数:13
相关论文
共 134 条
[1]   Molecular control of neutrophil apoptosis [J].
Akgul, C ;
Moulding, DA ;
Edwards, SW .
FEBS LETTERS, 2001, 487 (03) :318-322
[2]   alpha-tocopherol and beta-carotene supplements and lung cancer incidence in the Alpha-Tocopherol, Beta-Carotene Cancer Prevention Study: Effects of base-line characteristics and study compliance [J].
Albanes, D ;
Heinonen, OP ;
Taylor, PR ;
Virtamo, J ;
Edwards, BK ;
Rautalahti, M ;
Hartman, AM ;
Palmgren, J ;
Freedman, LS ;
Haapakoski, J ;
Barrett, MJ ;
Pietinen, P ;
Malila, N ;
Tala, E ;
Liippo, K ;
Salomaa, ER ;
Tangrea, JA ;
Teppo, L ;
Askin, FB ;
Taskinen, E ;
Erozan, Y ;
Greenwald, P ;
Huttunen, JK .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1996, 88 (21) :1560-1570
[3]   Signal processing times in neutrophil activation: dependence on ligand concentration and the relative phase of metabolic oscillations [J].
Albrecht, E ;
Kindzelskii, AL ;
Petty, HR .
BIOPHYSICAL CHEMISTRY, 2003, 106 (03) :211-219
[4]   BIOLOGICAL REACTIVITY OF HYPOCHLOROUS ACID - IMPLICATIONS FOR MICROBICIDAL MECHANISMS OF LEUKOCYTE MYELOPEROXIDASE [J].
ALBRICH, JM ;
MCCARTHY, CA ;
HURST, JK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1981, 78 (01) :210-214
[5]   Inflammation and structural changes in the airways of patients with atopic and nonatopic asthma [J].
Amin, K ;
Lúdvíksdóttir, D ;
Janson, C ;
Nettelbladt, O ;
Björnsson, E ;
Roomans, GM ;
Boman, G ;
Sevéus, L ;
Venge, P .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2000, 162 (06) :2295-2301
[6]   Relationship between inflammatory cells and structural changes in the lungs of asymptomatic and never smokers:: a biopsy study [J].
Amin, K ;
Ekberg-Jansson, A ;
Löfdahl, CG ;
Venge, P .
THORAX, 2003, 58 (02) :135-142
[7]   Inflammation and structural changes in the airways of patients with primary Sjogren's syndrome [J].
Amin, K ;
Lúdvíksdóttir, D ;
Janson, C ;
Nettelbladt, O ;
Gudbjörnsson, B ;
Valtysdóttir, S ;
Björnsson, E ;
Roomans, GM ;
Boman, G ;
Sevéus, L ;
Venge, P .
RESPIRATORY MEDICINE, 2001, 95 (11) :904-910
[8]   Oxidative and nitrosative events in asthma [J].
Andreadis, AA ;
Hazen, SL ;
Comhair, SAA ;
Erzurum, SC .
FREE RADICAL BIOLOGY AND MEDICINE, 2003, 35 (03) :213-225
[9]  
BADWEY JA, 1989, J BIOL CHEM, V264, P14947
[10]   Vitamin A deficiency causes oxidative damage to liver mitochondria in rats [J].
Barber, T ;
Borrás, E ;
Torres, L ;
García, C ;
Cabezuelo, F ;
Lloret, A ;
Pallardó, FV ;
Viña, JR .
FREE RADICAL BIOLOGY AND MEDICINE, 2000, 29 (01) :1-7