Effect of Food Azo Dye Tartrazine on Learning and Memory Functions in Mice and Rats, and the Possible Mechanisms Involved

被引:111
作者
Gao, Yonglin [1 ]
Li, Chunmei [2 ]
Shen, Jingyu [1 ]
Yin, Huaxian [1 ]
An, Xiulin [1 ]
Jin, Haizhu [1 ]
机构
[1] Yantai Univ, Sci & Technol Coll Chem & Biol, Yantai 264005, Peoples R China
[2] Yantai Univ, Sch Pharm, Yantai 264005, Peoples R China
关键词
learning and memory; oxidative stress; pathological lesion; tartrazine; CHRONIC TOXICITY CARCINOGENICITY; YELLOW NO-5 TARTRAZINE; BEHAVIOR; FD; STRESS; ADSORPTION; DEFICITS; MODELS; MAZE; TIME;
D O I
10.1111/j.1750-3841.2011.02267.x
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Tartrazine is an artificial azo dye commonly used in human food and pharmaceutical products. The present study was conducted to evaluate the toxic effect of tartrazine on the learning and memory functions in mice and rats. Animals were administered different doses of tartrazine for a period of 30 d and were evaluated by open-field test, step-through test, and Morris water maze test, respectively. Furthermore, the biomarkers of the oxidative stress and pathohistology were also measured to explore the possible mechanisms involved. The results indicated that tartrazine extract significantly enhanced active behavioral response to the open field, increased the escape latency in Morris water maze test and decreased the retention latency in step-through tests. The decline in the activities of catalase, glutathione peroxidase (GSH-Px), and superoxide dismutase (SOD) as well as a rise in the level of malonaldehyde (MDA) were observed in the brain of tartrazine-treated rats, and these changes were associated with the brain from oxidative damage. The dose levels of tartrazine in the present study produced a few adverse effects in learning and memory functions in animals. The mechanisms might be attributed to promoting lipid peroxidation products and reactive oxygen species, inhibiting endogenous antioxidant defense enzymes and the brain tissue damage.
引用
收藏
页码:T125 / T129
页数:5
相关论文
共 33 条
[1]   Effect of food azo dyes tartrazine and carmoisine on biochemical parameters related to renal, hepatic function and oxidative stress biomarkers in young male rats [J].
Amin, K. A. ;
Hameid, H. Abdel, II ;
Abd Elsttar, A. H. .
FOOD AND CHEMICAL TOXICOLOGY, 2010, 48 (10) :2994-2999
[2]   CHRONIC TOXICITY CARCINOGENICITY STUDIES OF FD-AND-C YELLOW NO-5 (TARTRAZINE) IN RATS [J].
BORZELLECA, JF ;
HALLAGAN, JB .
FOOD AND CHEMICAL TOXICOLOGY, 1988, 26 (03) :179-187
[3]   A CHRONIC TOXICITY CARCINOGENICITY STUDY OF FD-AND-C YELLOW NO-5 (TARTRAZINE) IN MICE [J].
BORZELLECA, JF ;
HALLAGAN, JB .
FOOD AND CHEMICAL TOXICOLOGY, 1988, 26 (03) :189-194
[4]   Tamoxifen and toremifene impair retrieval, but not acquisition, of spatial information processing in mice [J].
Chen, D ;
Wu, CF ;
Shi, B ;
Xu, YM .
PHARMACOLOGY BIOCHEMISTRY AND BEHAVIOR, 2002, 72 (1-2) :417-421
[5]   The Involvement of Retinoic Acid Receptor-α in Corticotropin-Releasing Hormone Gene Expression and Affective Disorders [J].
Chen, Xiao-Ning ;
Meng, Qing-Yuan ;
Bao, Ai-Min ;
Swaab, Dick F. ;
Wang, Guang-Hui ;
Zhou, Jiang-Ning .
BIOLOGICAL PSYCHIATRY, 2009, 66 (09) :832-839
[6]   CHRONIC RAT + DOG TOXICITY STUDIES ON TARTRAZINE [J].
DAVIS, KJ ;
FITZHUGH, OG ;
NELSON, AA .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1964, 6 (05) :621-&
[7]   Pharmacological and genetic inhibition of NADPH oxidase does not reduce brain damage in different models of perinatal brain injury in newborn mice [J].
Doverhag, Christina ;
Keller, Matthias ;
Karlsson, Anna ;
Hedtjarn, Maj ;
Nilsson, Ulf ;
Kapeller, Edith ;
Sarkozy, Gergely ;
Klimaschewski, Lars ;
Humpel, Christian ;
Hagberg, Henrik ;
Simbruner, Georg ;
Gressens, Pierre ;
Savman, Karin .
NEUROBIOLOGY OF DISEASE, 2008, 31 (01) :133-144
[8]   Effects on anxiety and memory of systemic and intra-amygdala injection of 5-HT3 receptor antagonist BRL 46470A [J].
Gargiulo, PA ;
Viana, MB ;
Graeff, FG ;
Silva, MAD ;
Tomaz, C .
NEUROPSYCHOBIOLOGY, 1996, 33 (04) :189-195
[9]   Chronic mild unpredictable stress after noradrenergic denervation:: attenuation of behavioural and biochemical effects of DSP-4 treatment [J].
Harro, J ;
Häidkind, R ;
Harro, M ;
Modiri, AR ;
Gillberg, PG ;
Pähkla, R ;
Matto, V ;
Oreland, L .
EUROPEAN NEUROPSYCHOPHARMACOLOGY, 1999, 10 (01) :5-16
[10]   Pentylenetetrazol-induced recurrent seizures in rat pups: Time course on spatial learning and long-term effects [J].
Huang, LT ;
Yang, SN ;
Liou, CW ;
Hung, PL ;
Lai, MC ;
Wang, CL ;
Wang, TJ .
EPILEPSIA, 2002, 43 (06) :567-573