Exposure of pregnant mice to chromium picolinate results in skeletal defects in their offspring

被引:52
作者
Bailey, M. M.
Boohaker, J. G.
Sawyer, R. D.
Behling, J. E.
Rasco, J. F.
Jernigan, J. J.
Hood, R. D.
Vincent, J. B.
机构
[1] RD Hood & Associates Toxicol Consultants, Tuscaloosa, AL 35487 USA
[2] Stillman Coll, Dept Biol, Tuscaloosa, AL USA
[3] Univ Alabama, Dept Biol Sci, Tuscaloosa, AL USA
[4] Univ Alabama, Dept Chem, Tuscaloosa, AL 35487 USA
关键词
chromium picolinate; chromium; developmental toxicity; skeletal defects; mice;
D O I
10.1002/bdrb.20081
中图分类号
R73 [肿瘤学];
学科分类号
100214 [肿瘤学];
摘要
BACKGROUND: Chromium(III) picolinate, [Cr(pic)(3)], is a widely marketed dietary supplement. However, Cr(pic)(3) has been associated with oxidative damage to DNA in rats and mutations and DNA fragmentation in cell cultures. In isolated case reports, Cr(pic)(3) supplementation has been said to cause adverse effects, such as anemia, renal failure, liver dysfunction, and neuronal impairment. To date, no studies have been published regarding the safety of chromium picolinate supplementation to a developing fetus, although Cr(pic())3 has been recommended for pregnant women who are diagnosed with gestational diabetes. METHODS: From gestation days (GD) 6-17, pregnant CD-I mice were fed diets containing either 200 mg/kg Cr(pic)(3), 200 mg/kg CrCl3, 174 mg/kg picolinic acid, or the diet only to determine if Cr(pic)(3), CrCl3, or picolinic acid could cause developmental toxicity Dams were sacrificed on GD 17, and their litters were examined for adverse effects. RESULTS: The incidence of bifurcated cervical arches was significantly increased in fetuses from the Cr(pic)(3) group as compared to the diet-only group. Fetuses in the picolinic acid-treated group had an incidence double that of the control group; however, this increase was not statistically significant. Fetuses in the CrCl3 group did not differ from the controls in any variable examined. No maternal toxicity was observed in any of the treatment groups. CONCLUSIONS: High maternal oral exposures to chromium picolinate can cause morphological defects in developing offspring of mice.
引用
收藏
页码:244 / 249
页数:6
相关论文
共 47 条
[1]
THE EFFECTS OF CHROMIUM SUPPLEMENTATION ON SERUM GLUCOSE AND LIPIDS IN PATIENTS WITH AND WITHOUT NON-INSULIN-DEPENDENT DIABETES [J].
ABRAHAM, AS ;
BROOKS, BA ;
EYLATH, U .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1992, 41 (07) :768-771
[3]
SUPPLEMENTAL-CHROMIUM EFFECTS ON GLUCOSE, INSULIN, GLUCAGON, AND URINARY CHROMIUM LOSSES IN SUBJECTS CONSUMING CONTROLLED LOW-CHROMIUM DIETS [J].
ANDERSON, RA ;
POLANSKY, MM ;
BRYDEN, NA ;
CANARY, JJ .
AMERICAN JOURNAL OF CLINICAL NUTRITION, 1991, 54 (05) :909-916
[4]
ANDERSON RA, 1995, NUTRITION, V11, P83
[5]
CHROMIUM SUPPLEMENTATION OF HUMAN-SUBJECTS - EFFECTS ON GLUCOSE, INSULIN, AND LIPID VARIABLES [J].
ANDERSON, RA ;
POLANSKY, MM ;
BRYDEN, NA ;
ROGINSKI, EE ;
MERTZ, W ;
GLINSMANN, W .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1983, 32 (09) :894-899
[6]
[Anonymous], 1989, INT J BIOSOC MED RES
[7]
Cytotoxicity and oxidative mechanisms of different forms of chromium [J].
Bagchi, D ;
Stohs, SJ ;
Downs, BW ;
Bagchi, M ;
Preuss, HG .
TOXICOLOGY, 2002, 180 (01) :5-22
[8]
Bahadori B, 1997, ACTA MED AUST, V24, P185
[9]
Comparison of anaerobic components of the Wingate and Critical Power tests in males and females [J].
Bulbulian, R ;
Jeong, JW ;
Murphy, M .
MEDICINE AND SCIENCE IN SPORTS AND EXERCISE, 1996, 28 (10) :1336-1341
[10]
A re-investigation the electronic spectra of chromium(III) picolinate complexes and high yield synthesis and characterization of Cr2(μ-OH)2(pic)4•5H2O (Hpic=picolinic acid) [J].
Chakov, NE ;
Collins, RA ;
Vincent, JB .
POLYHEDRON, 1999, 18 (22) :2891-2897