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TM/MC  TM/MC
                                          PHARMACOLOGICAL ACTIVITIES - TOXICOLOGY - DRUG INTERACTIONS





            Chromium (Polynicotinate)


            Chromium is an essential dietary trace mineral involved in carbohydrate and lipid metabolism.
            Chromium is required for cellular uptake of glucose, and chromium deficiency causes insulin
            resistance.  Chromium  supplementation  may  improve  insulin  sensitivity  and  has  been  used
            as adjunct treatment of diabetes mellitus in humans. Chromium supplementation in diabetic
            dogs at a level of 2.5-7.5 µg/kg for several months was found to be safe (Schachter et al.,
            2001). Chromium has also been shown to be involved in protein synthesis, and nucleic acid
            metabolism (NRC, 2006). Signs of chromium deficiency in humans and several animal species
            have been found to include impaired glucose tolerance, elevated plasma insulin, hyperglycemia,
            impaired growth, elevated plasma triglycerides, neuropathy, encephalopathy, corneal lesions
            and decreased fertility and sperm count.



                TOXICOLOGY  Toxicity for chromium polynicotinate has not been documented in dogs and cats when administered orally in
                    therapeutic doses. Hexavalent chromium or chromium (Cr ) is a recognized carcinogen. In contrast, there is little
                                                                     +6
                    evidence that trivalent chromium (Cr ) is toxic to humans (FNB & IOB, 2001b). Intravenous LD  for nicotinic
                                                   +3
                                                                                                      50
                    acid bound chromium complexes is approximately 1 g/kg of body weight in rats (EFSA, 2008).


                           DRUG     Validated  interactions  studies  do  not  exist  for  chromium  preparations.  Clinical
                  INTERACTIONS      interactions  with  other  drugs  have  not  been  reported.  However,  large  doses  of  calcium
                                    carbonate  or  magnesium  hydroxide-containing  antacids  decreased  chromium  absorption
                                    in rats. In contrast, aspirin and indomethacin both increased chromium absorption in rats
                                    (Shils et al., 2006).





































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