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Diabetes Technology & Therapeutics
Effects of Chromium Picolinate on Food Intake and Satiety
To cite this article:
Stephen D. Anton, Christopher D. Morrison, William T. Cefalu, Corby K. Martin, Sandra Coulon, Paula Geiselman, Hongmei Han, Christy L. White, Donald A. Williamson.
Diabetes Technology & Therapeutics.
October 2008,
10(5): 405-412.
doi:10.1089/dia.2007.0292.
Published in Volume: 10 Issue 5: August 21, 2008
Stephen D. Anton, Ph.D.Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, Louisiana. Department of Aging and Geriatric Research, University of Florida, Gainesville, Florida. Christopher D. Morrison, Ph.D.Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, Louisiana. William T. Cefalu, M.D.Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, Louisiana. Corby K. Martin, Ph.D.Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, Louisiana. Sandra Coulon, B.A.Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, Louisiana. Paula Geiselman, Ph.D.Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, Louisiana. Department of Psychology, Louisiana State University, Baton Rouge, Louisiana. Hongmei Han, M.S.Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, Louisiana. Christy L. White, D.V.M.Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, Louisiana. Donald A. Williamson, Ph.D.Pennington Biomedical Research Center, Louisiana State University, Baton Rouge, Louisiana. Abstract Background: Chromium picolinate (CrPic) has been shown to attenuate weight gain, but the mechanism underlying this effect is unknown. Methods: We assessed the effect of CrPic in modulating food intake in healthy, overweight, adult women who reported craving carbohydrates (Study 1) and performed confirmatory studies in Sprague-Dawley rats (Study 2). Study 1 utilized a double-blind placebo-controlled design and randomly assigned 42 overweight adult women with carbohydrate cravings to receive 1,000 μg of chromium as CrPic or placebo for 8 weeks. Food intake at breakfast, lunch, and dinner was directly measured at baseline, week 1, and week 8. For Study 2, Sprague-Dawley rats were fasted for 24 h and subsequently injected intraperitoneally with 0, 1, 10, or 50 μg/kg CrPic. Subsequently, rats were implanted with an indwelling third ventricular cannula. Following recovery, 0, 0.4, 4, or 40 ng of CrPic was injected directly into the brain via the intracerebroventricular cannula, and spontaneous 24-h food intake was measured. Results: Study 1 demonstrated that CrPic, as compared to placebo, reduced food intake (P < 0.0001), hunger levels (P < 0.05), and fat cravings (P < 0.0001) and tended to decrease body weight (P = 0.08). In study 2, intraperitoneal administration resulted in a subtle decrease in food intake at only the highest dose (P = 0.03). However, when administered centrally, CrPic dose-dependently decreased food intake (P < 0.05).  This paper was cited by:The effects of whey protein and chromium picolinate supplementation on visceral fat and metabolic status in high-fat-fed rats Kazim Sahin, Vijaya Juturu, Mehmet Tuzcu, Nurhan Sahin, Gurkan Cikim, James R. Komorowski Mediterranean Journal of Nutrition and Metabolism. Jan 2010, Vol. 2, No. 3: 213-219 CrossRef Chromium III Histidinate Exposure Modulates Gene Expression in HaCaT Human Keratinocytes Exposed to Oxidative Stress Florence Hazane-Puch, Rachida Benaraba, Kita Valenti, Mireille Osman, François Laporte, Alain Favier, Richard A. Anderson, Anne-Marie Roussel, Isabelle Hininger-Favier Biological Trace Element Research. Dec 2009 CrossRef Current literature in diabetes Diabetes/Metabolism Research and Reviews. Apr 2009, Vol. 25, No. 3: i-viii CrossRef
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