2. Pechova A, Pavlata L. Chromium as an essential nutrient: a review. Vet Med (Praha) 2007; 52:1
3. Dowling HJ, Offenbacher EG, Pi-Sunyer FX. Absorption of inorganic, trivalent chromium from the vascularly perfused rat small intestine. J Nutr 1989; 119:1138–45.
https://doi.org/10.1093/jn/119.8.1138
4. Qiao W, Peng Z, Wang Z, Wei J, Zhou A. Chromium improves glucose uptake and metabolism through upregulating the mRNA levels of IR, GLUT4, GS, and UCP3 in skeletal muscle cells. Biol Trace Elem Res 2009; 131:133–42.
https://doi.org/10.1007/s12011-009-8357-2
5. Lien TF, Wu CP, Wang BJ, et al. Effect of supplemental levels of chromium picolinate on the growth performance, serum traits, carcass characteristics and lipid metabolism of growing-finishing pigs. Anim Sci 2001; 72:289–96.
https://doi.org/10.1017/S1357729800055788
6. US Food and Drug Administration. CFR-code of federal regulations title 21 Part 556 tolerances for residues of new animal drugs in food. Rockville, MD, USA: US Food and Drug Administration; 2017.
7. Spears JW. Chromium supplementation in cattle diets. In : Florida Rumint Nutrion Symphosium; Gainesville, FL, USA. 2010. p. 143–55.
9. Anderson RA, Polansky MM, Bryden NA, Canary JJ. Supplemental-chromium effects on glucose, insulin, glucagon, and urinary chromium losses in subjects consuming controlled low-chromium diets. Am J Clin Nutr 1991; 54:909–16.
https://doi.org/10.1093/ajcn/54.5.909
14. Mooney K, Cromwell G. Effects of dietary chromium picolinate supplementation on growth, carcass characteristics, and accretion rates of carcass tissues in growing-finishing swine. J Anim Sci 1995; 73:3351–7.
https://doi.org/10.2527/1995.73113351x
18. Janovick-Guretzky N, Dann H, Carlson D, Murphy M, Loor J, Drackley J. Housekeeping gene expression in bovine liver is affected by physiological state, feed intake, and dietary treatment. J Dairy Sci 2007; 90:2246–52.
https://doi.org/10.3168/jds.2006-640
19. Spears JW, Whisnant CS, Huntington GB, et al. Chromium propionate enhances insulin sensitivity in growing cattle. J Dairy Sci 2012; 95:2037–45.
https://doi.org/10.3168/jds.2011-4845
21. Bernhard BC, Burdick NC, Rounds W, et al. Chromium supplementation alters the performance and health of feedlot cattle during the receiving period and enhances their metabolic response to a lipopolysaccharide challenge. J Anim Sci 2012; 90:3879–88.
https://doi.org/10.2527/jas.2011-4981
22. Anderson RA, Bryden NA, Evock-Clover CM, Steele NC. Beneficial effects of chromium on glucose and lipid variables in control and somatotropin-treated pigs are associated with increased tissue chromium and altered tissue copper, iron, and zinc. J Anim Sci 1997; 75:657–61.
https://doi.org/10.2527/1997.753657x
23. Kanai F, Ito K, Todaka M, et al. Insulin-stimulated GLUT4 translocation is relevant to the phosphorylation of IRS-1 and the activity of PI3 kinase. Biochem Biophys Res Commun 1993; 195:762–8.
https://doi.org/10.1006/bbrc.1993.2111
24. Chen G, Liu P, Pattar GR, et al. Chromium activates glucose transporter 4 trafficking and enhances insulin-stimulated glucose transport in 3T3-L1 adipocytes via a cholesterol-dependent mechanism. Mol Endocrinol 2006; 20:857–70.
https://doi.org/10.1210/me.2005-0255
26. Moonsie-Shageer S, Mowat D. Effect of level of supplemental chromium on performance, serum constituents, and immune status of stressed feeder calves. J Anim Sci 1993; 71:232–8.
https://doi.org/10.2527/1993.711232x
31. Smith S, Lin K, Wilson J, Lunt D, Cross H. Starvation depresses acylglycerol biosynthesis in bovine subcutaneous but not intramuscular adipose tissue homogenates. Comp Biochem Physiol B Biochem Mol Biol 1998; 120:165–74.
https://doi.org/10.1016/S0305-0491(98)10005-6
34. Park H, Kaushik VK, Constant S, et al. Coordinate regulation of malonyl-CoA decarboxylase, sn-glycerol-3-phosphate acyltransferase, and acetyl-CoA carboxylase by AMP-activated protein kinase in rat tissues in response to exercise. J Biol Chem 2002; 277:32571–7.
https://doi.org/10.1074/jbc.M201692200
35. Kelly M, Keller C, Avilucea PR, et al. AMPK activity is diminished in tissues of IL-6 knockout mice: the effect of exercise. Biochem Biophys Res Commun 2004; 320:449–54.
https://doi.org/10.1016/j.bbrc.2004.05.188
37. Sakoda H, Ogihara T, Anai M, et al. Activation of AMPK is essential for AICAR-induced glucose uptake by skeletal muscle but not adipocytes. Am J Physiol Endocrinol Metab 2002; 282:E1239–E44.
https://doi.org/10.1152/ajpendo.00455.2001
38. Salt IP, Connell JM, Gould GW. 5-aminoimidazole-4-carboxamide ribonucleoside (AICAR) inhibits insulin-stimulated glucose transport in 3T3-L1 adipocytes. Diabetes 2000; 49:1649–56.
https://doi.org/10.2337/diabetes.49.10.1649
40. Hawley SA, Davison M, Woods A, et al. Characterization of the AMP-activated protein kinase kinase from rat liver and identification of threonine 172 as the major site at which it phosphorylates AMP-activated protein kinase. J Biol Chem 1996; 271:27879–87.
https://doi.org/10.1074/jbc.271.44.27879