Diabetes induced immunological and biochemical changes in human colostrum

Autor(es)

Morceli, G. ^[1] ; Franca, E. L. ^[2] ; Magalhaes, V. B. ^[1] ; Damasceno, D. C. ^[1] ; Calderon, I. M. P. ^[1] ; Honorio-Franca, A. C. ^[2]

Afiliação do(s) autor(es)

^[1] Sao Paulo State Univ Unesp, Grad Program Gynecol, Obstet & Mastol Botucatu Med Sch, Sao Paulo - Brazil

^[2] UFMT, Inst Ciencias Biol & Saude, Pontal Araguaia MT, Pontal Araguaia, Mato Grosso - Brazil

• Tipo de documento: Artigo Científico
• Fonte: ACTA PAEDIATRICA; v. 100, n. 4, p. 550-556, APR 2011.
• Citações Web of Science: 31

Resumo

Aim: This article describes the changes and relationships between biochemical and immunological parameters in the colostrum and serum of diabetic women. Methods: Colostrum and blood samples were collected from 30 diabetic and 15 normoglycaemic women. Glucose, total protein, antibody, complement proteins (C3 and C4), fat and calorie content, amylase, lipase and superoxide dismutase (SOD) were determined. Results: Glucose was higher in both the colostrum and serum of diabetic mothers compared to that of their normoglycaemic counterparts. In both groups, total protein was higher in colostrum than in serum. IgA and IgG were lower in the colostrum of hyperglycaemic mothers, whereas IgM did not vary between the groups. Colostral C3 protein was significantly lower in diabetic mothers, but colostral C4 protein was similar between normoglycaemic and hyperglycaemic mothers. Fat content was lower in the colostrum of the diabetic mothers, although calorie content did not vary between the groups. Amylase was lower in colostrum than in serum in both groups. Lipase was higher in the colostrum and serum of diabetic mothers. Colostral SOD was similar between the groups. Conclusions: Our results support the hypothesis that the colostrum of diabetic mothers suffers biochemical and immunological alterations that affect the levels of its components. (AU)

• Processo FAPESP: 09/01188-8 - Atividade funcional de fagócitos do leite de mães hiperglicêmicas leve e diabéticas e sua regulação neuroimunoendocrinológica.
• Beneficiário: Glilciane Morceli
• Modalidade de apoio: Bolsas no Brasil - Doutorado