Effect of Manganese Deficiency on Insulin Secretion and Carbohydrate Homeostasis in Rats

The effects of manganese (Mn) deficiency on carbohydrate metabolism in the Sprague-Dawley rat were investigated. Oral glucose tolerance tests were performed on offspring from Mn-sufficient female rats fed 45 µg Mn per gram diet (C-C), offspring from Mn-deficient female rats fed 1 µg Mn per gram diet...

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Veröffentlicht in:The Journal of nutrition 1984-08, Vol.114 (8), p.1438-1446
Hauptverfasser: Baly, Deborah L., Curry, Donald L., Keen, Carl L., Hurley, Lucille S.
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Sprache:eng
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Zusammenfassung:The effects of manganese (Mn) deficiency on carbohydrate metabolism in the Sprague-Dawley rat were investigated. Oral glucose tolerance tests were performed on offspring from Mn-sufficient female rats fed 45 µg Mn per gram diet (C-C), offspring from Mn-deficient female rats fed 1 µg Mn per gram diet (D1-D1) and rats not exposed to Mn deficiency in utero but fed D1 diet from weaning to maturity (D1). Mn-deficient rats, D1 and D1-D1, had significantly lower concentrations of Mn in liver, kidney, heart and pancreas than controls. D1-D1 rats responded with a diabetic type of glucose tolerance curve when given oral glucose. Insulin levels of D1-D1 rats were not commensurate with their high glucose levels. Measurements made by using an isolated perfused-pancreas preparation indicate that insulin output due to release of stored hormone was 76% of control levels in D1-D1 rats. This suggests either lower insulin stores or impaired release of insulin in D1-D1 rats. Second phase insulin release was also significantly lower in D1-D1 rats than in controls. Pancreatic insulin content was 63% of control levels in D1-D1 rats, further supporting the idea of lower insulin stores in Mn-deficient rats. No differences in plasma glucose levels were observed between D1 rats and controls after an oral-glucose load. These findings indicate that dietary Mn deficiency can result in impaired insulin secretion producing impaired carbohydrate metabolism; however, the timing of the deficiency may be a critical factor in the expression of this abnormality.
ISSN:0022-3166
1541-6100
DOI:10.1093/jn/114.8.1438