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PubMed2001

Effect of chromium picolinate and chromium propionate on glucose and insulin kinetics of growing barrows and on growth and carcass traits of growing-finishing barrows.

Two experiments were conducted to determine the effects of dietary Cr tripicolinate (CrPic) or Cr propionate (CrProp) on growth, carcass traits, plasma metabolites, glucose tolerance, and insulin sensitivity in pigs. In Exp. 1, 36 barrows (12 per treatment; initial and final BW were 20 and 38 kg) were allotted to the following treatments: 1) corn-soybean meal basal diet (control), 2) as 1 + 200 ppb Cr as CrPic, or 3) as 1 + 200 ppb Cr as CrProp. Growth performance data were collected for 28 d, and then 23 pigs (seven, eight, and eight pigs for treatments 1, 2, and 3, respectively) were fitted with jugular catheters and a glucose tolerance test (500 mg glucose/kg BW) and an insulin challenge test (0.1 IU of porcine insulin/kg BW) were conducted. Both CrPic and CrProp decreased (P < 0.05) ADG and ADFI but did not affect gain:feed (P > 0.10). Fasting plasma glucose, total cholesterol, urea N, insulin, and high-density lipoprotein cholesterol:total cholesterol concentrations were not affected (P > 0.10) by either Cr source. Pigs fed CrPic had lower (P < 0.02) fasting plasma NEFA concentrations than control pigs, but plasma NEFA concentrations of pigs fed CrProp were not affected (P > 0.10). During the glucose tolerance test, glucose and insulin kinetics were not affected by treatment (P > 0.10). During the insulin challenge test, glucose clearance was increased (P < 0.01) in pigs fed CrProp but not affected (P > 0.10) in pigs fed CrPic. Glucose half-life was decreased (P < 0.03) in pigs fed CrPic or CrProp, but insulin kinetics were not affected (P > 0.10). In Exp. 2, 48 barrows (four replicates of four pigs per replicate; initial and final BW were 23 and 115 kg) were allotted to the same dietary treatments in a growing-finishing study. Average daily gain, ADFI, and gain:feed were not affected (P > 0.10) by treatments. Carcass length tended (P = 0.10) to be greater in pigs fed CrPic than in pigs fed CrProp, but other carcass measurements were not affected (P > 0.10). Glucose kinetics from the insulin challenge test indicate that both CrPic and CrProp increase insulin sensitivity and that both Cr sources are bioavailable.

Animals↗
PubMed1985

Long-term corrosion studies in vitro of gold, cobalt-chromium, and nickel-chromium alloys in contact.

Specimens of various types of dental casting alloys were stored in phosphate-buffered 0.9% NaCl solution for 35 weeks. Every 7 weeks the solutions were changed and analyzed with regard to elements released from the alloys. The release of Cu from type III gold alloy increased in contact with gold alloys for metallo-ceramic use in a 1:2 area relation. However, when the area relation was reversed, no difference in the amounts of elements released was observed. Crevice corrosion was initiated with one of the Co-Cr alloys in contact with type III gold alloy. The crevice corrosion increased the amounts of Co and Cr released into the solutions. The release of Ni and Cr from the Ni-Cr alloys was prominent. These alloys were very susceptible to crevice corrosion. With one of the Ni-Cr alloys the release of elements increased in contact with type III gold alloy.

Chemical Phenomena↗
PubMed1987

Serum and urine chromium as indices of chromium status in tannery workers.

Serum and urinary Cr levels of a selected group of men exposed to CrIII in four Southern Ontario tanneries were compared with those of men not exposed to Cr. Fasted blood samples were obtained from 72 tannery workers (TW; mean age +/- SD = 36 +/- 12 years) and from 52 controls (CS; mean age +/- SD = 41 +/- 13 years). Serum Cr levels as determined by graphite furnace atomic absorption spectrophotometry were significantly higher (P = 0.0001) for TW (median 0.49 ng/ml, range 0.37-0.81) than for CS (median 0.15 ng/ml, range 0.12-0.20). Urine samples were collected from 49 TW and 43 CS on a Friday pm and from 42 TW on a Monday am. Urinary creatine (Cre) was determined by the Jaffe reaction. For Friday samples, the median urinary Cr/Cre ratio was significantly higher (P = 0.0001) for TW (median 0.83 ng/mg, range 0.48-1.82) than for CS (median 0.18 ng/mg, range 0.13-0.26). For TW, Cr/Cre was correlated with serum Cr (r = 0.72, P = 0.0001). Neither urinary Cr/Cre nor serum Cr was correlated with length of employment in the tanning industry. There were significant differences in serum Cr levels and urinary Cr/Cre ratios among TW employed in different areas of the tanneries. For TW, the median urinary Cr/Cre ratio for Monday morning samples was significantly lower than for Friday afternoon samples (P = 0.03). These data indicate that CrIII is absorbed and that serum and urine Cr in tannery workers may be indices of Cr exposure and status.

Adult↗
PubMed1975

[Influence of chromium as a trace element on the hormonal regulation in the rat. 2. Physiological function of chromium in carbohydrate metabolism].

Young growing rats were fed additional doses of Cr-III-acetate to a balanced basic diet. The investigations of Cr metabolism indicated: 1. Rats supplied with sufficient Cr as well as those on Cr-poor diet showed the same level of blood glucose. With the Cr-poor group however a significantly smaller glycogen depot in the liver was obtained. 2. After a starving period the hypoglycaemic status of Cr-supplied rats was significantly lower than that of the Cr-depleted controls. 3. Adequate charge of adrenalin to hypoglycaemic rats showed a rise of blood glucose to the same physiological level with both Cr-supplied groups and control groups. Adding adrenalin the level of blood glucose of Cr-supplied rats decreased significantly higher than that of the controls. 4. With rats, being made hypoglycaemic by a starving period and than fed higher doses of glucose up to a slight hyperglycaemia, supplementation of sulfonylurea decreased the level of blood glucose more with the Cr-supplied groups than with the control groups. The experiments proved that adequate feeding of Cr to rats led to a higher level of bound insulin in the blood. The depot of insulin is easier mobilizable. It may be assumed that Cr acts as a insulin activator. However it seems more likely to consider other effects of Cr probably as activator to the permeability of cell membranes which as well may explain the higher glycogen depot of Cr supplied animals.

Animals↗