Evaluation of the potential genotoxicity of chromium picolinate in mammalian cells in vivo and in vitro

被引:47
作者
Andersson, Maria A.
Grawe, Kierstin V. Petersson
Karlsson, Oskar M.
Abramsson-Zetterberg, Lilianne A. G.
Hellman, Bjorn E.
机构
[1] Uppsala Univ, Div Toxicol, Dept Pharmaceut Biosci, SE-75124 Uppsala, Sweden
[2] Natl Food Adm Toxicol Lab, Div Toxicol, Res & Dev Dept, SE-75126 Uppsala, Sweden
关键词
chromium picolinate; Comet assay; flow-cytometric micronucleus test; mouse hepatocytes; mouse bone marrow cells; mouse and human lymphocytes; mouse lymphoma cells;
D O I
10.1016/j.fct.2006.11.008
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Chromium picolinate (CrPic) is a synthetic nutritional supplement primarily used for weight loss and muscle building. Recent studies have indicated that CrPic might be genotoxic and these findings together with the wide-spread consumer use, have increased the concern about its safety. In the present study we investigated the potential genotoxicity of CrPic in mice given a single intraperitoneal injection (up to 3 mg/kg b.wt.) by evaluating the frequency of micronucleated polychromatic erythrocytes (fMNPCE) in peripheral blood, and DNA damage in lymphocytes and hepatocytes. The fMNPCE was evaluated after 42 h and DNA damage after 16 h. Using the Comet assay DNA damage was also monitored in extended-term cultures of human lymphocytes and in L5178Y mouse lymphoma cells that had been exposed for 3 h to 500 mu M CrPic under different exposure conditions. A slight, but significant CrPic-induced increase in DNA damage (P < 0.001) was observed in the human lymphocytes, but only when these cells were exposed in the absence of serum. In all other experiments CrPic was found to be without genotoxic effects, both in vivo and in vitro. Taken together, our results suggest that a high concentration of CrPic might be DNA damaging, but only under non-physiological conditions. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1097 / 1106
页数:10
相关论文
共 64 条
[1]   The time-course of micronucleated polychromatic erythrocytes in mouse bone marrow and peripheral blood [J].
AbramssonZetterberg, L ;
Zetterberg, G ;
Grawe, J .
MUTATION RESEARCH-FUNDAMENTAL AND MOLECULAR MECHANISMS OF MUTAGENESIS, 1996, 350 (02) :349-358
[2]   FLOW CYTOMETRIC ANALYSIS OF MICRONUCLEUS INDUCTION IN MICE BY INTERNAL EXPOSURE TO CS-137 AT VERY-LOW DOSE-RATES [J].
ABRAMSSONZETTERBERG, L ;
GRAWE, J ;
ZETTERBERG, G .
INTERNATIONAL JOURNAL OF RADIATION BIOLOGY, 1995, 67 (01) :29-36
[3]   Glucose and insulin responses to dietary chromium supplements: a meta-analysis [J].
Althuis, MD ;
Jordan, NE ;
Ludington, EA ;
Wittes, JT .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 2002, 76 (01) :148-155
[4]   THE EFFECT OF VARIOUS ANTIOXIDANTS AND OTHER MODIFYING AGENTS ON OXYGEN-RADICAL-GENERATED DNA-DAMAGE IN HUMAN-LYMPHOCYTES IN THE COMET ASSAY [J].
ANDERSON, D ;
YU, TW ;
PHILLIPS, BJ ;
SCHMEZER, P .
MUTATION RESEARCH, 1994, 307 (01) :261-271
[5]   Lack of toxicity of chromium chloride and chromium picolinate in rats [J].
Anderson, RA ;
Bryden, NA ;
Polansky, MM .
JOURNAL OF THE AMERICAN COLLEGE OF NUTRITION, 1997, 16 (03) :273-279
[6]   Elevated intakes of supplemental chromium improve glucose and insulin variables in individuals with type 2 diabetes [J].
Anderson, RA ;
Cheng, NZ ;
Bryden, NA ;
Polansky, MM ;
Cheng, NP ;
Chi, JM ;
Feng, JG .
DIABETES, 1997, 46 (11) :1786-1791
[7]   NUTRITIONAL ROLE OF CHROMIUM [J].
ANDERSON, RA .
SCIENCE OF THE TOTAL ENVIRONMENT, 1981, 17 (01) :13-29
[8]  
Anderson RA, 1996, J TRACE ELEM EXP MED, V9, P11, DOI 10.1002/(SICI)1520-670X(199607)9:1&lt
[9]  
11::AID-JTRA2&gt
[10]  
3.0.CO