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Dietary resistant starch prevents urinary excretion of vitamin D metabolites and maintains circulating 25-hydroxycholecalciferol concentrations in Zucker diabetic fatty rats.
Koh, Gar Yee; Whitley, Elizabeth M; Mancosky, Kirsten; Loo, Yi Ting; Grapentine, Kelly; Bowers, Emily; Schalinske, Kevin L; Rowling, Matthew J.
Afiliación
  • Koh GY; Department of Food Science and Human Nutrition, Interdepartmental Graduate Program in Nutritional Sciences, and.
  • Whitley EM; Department of Veterinary Pathology, College of Veterinary Medicine, Iowa State University, Ames, IA.
  • Mancosky K; Department of Food Science and Human Nutrition.
  • Loo YT; Department of Food Science and Human Nutrition.
  • Grapentine K; Department of Food Science and Human Nutrition.
  • Bowers E; Department of Food Science and Human Nutrition.
  • Schalinske KL; Department of Food Science and Human Nutrition, Interdepartmental Graduate Program in Nutritional Sciences, and.
  • Rowling MJ; Department of Food Science and Human Nutrition, Interdepartmental Graduate Program in Nutritional Sciences, and mrowling@iastate.edu.
J Nutr ; 144(11): 1667-73, 2014 Nov.
Article en En | MEDLINE | ID: mdl-25165393
ABSTRACT

BACKGROUND:

Type 2 diabetes (T2D) is the leading cause of nephropathy in the United States. Renal complications of T2D include proteinuria and suboptimal serum 25-hydroxycholecalciferol (25D) concentrations. 25D is the major circulating form of vitamin D and renal reabsorption of the 25D-vitamin D-binding protein (DBP) complex via megalin-mediated endocytosis is believed to determine whether 25D can be activated to 1,25-dihydroxycholecalciferol (1,25D) or returned to circulation. We previously demonstrated that excessive urinary excretion of 25D-DBP and albuminuria occurred in rats with type 1 diabetes (T1D) and T2D. Moreover, feeding rats with T1D high-amylose maize partially resistant to digestion [resistant starch (RS)] prevented excretion of 25D-DBP without significantly affecting hyperglycemia.

OBJECTIVE:

We used Zucker diabetic fatty (ZDF) rats, a model of obesity-related T2D, to determine whether feeding RS could similarly prevent loss of vitamin D and maintain serum 25D concentrations.

METHODS:

Lean control Zucker rats (n = 8) were fed a standard semi-purified diet (AIN-93G) and ZDF rats were fed either the AIN-93G diet (n = 8) or the AIN-93G diet in which cornstarch was replaced with RS (550 g/kg diet; 35% resistant to digestion) (n = 8) for 6 wk.

RESULTS:

RS attenuated hyperglycemia by 41% (P < 0.01) and prevented urinary DBP excretion and albuminuria, which were elevated 3.0- (P < 0.01) and 3.6-fold (P < 0.01), respectively, in control diet-fed ZDF rats. Additionally, urinary excretion of 25D (P = 0.01) and 1,25D (P = 0.03) was higher (89% and 97%, respectively), whereas serum 25D concentrations were 31% lower (P < 0.001) in ZDF rats fed the control diet compared with RS-fed ZDF rats. Histopathologic scoring of the kidney revealed that RS attenuated diabetes-mediated damage by 21% (P = 0.12) despite an ∼50% decrease in megalin protein abundance.

CONCLUSIONS:

Taken together, these data provide evidence that suggests vitamin D balance can be maintained by dietary RS through nephroprotective actions in T2D, which are independent of vitamin D supplementation and renal expression of megalin.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Vitamina D / Calcifediol / Alimentación Animal Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: J Nutr Año: 2014 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Vitamina D / Calcifediol / Alimentación Animal Tipo de estudio: Prognostic_studies Límite: Animals Idioma: En Revista: J Nutr Año: 2014 Tipo del documento: Article
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