Thirty days of combined consumption of a high-fat diet and fructose-rich beverages promotes insulin resistance and modulates inflammatory response and histomorphometry parameters of liver, pancreas, and adipose tissue in Wistar rats

•Consumption of a high-fat diet and fructose-rich beverages promotes insulin resistance.•Consumption of a high-fat diet and fructose-rich beverages increases inflammatory response.•Consumption of a high-fat diet and fructose-rich beverages modulates the morphology tissues.•Short-term consumption is...

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Veröffentlicht in:Nutrition (Burbank, Los Angeles County, Calif.) Los Angeles County, Calif.), 2021-11, Vol.91-92, p.111403-111403, Article 111403
Hauptverfasser: Melo, Bruno Pereira, Zacarias, Aline Cruz, Oliveira, Joyce Camilla C., de Souza, Letícia Maria Cordeiro, Sabino, Josiana, Ferreira, Adaliene Versiani Matos, Tonoli, Cajsa, dos Santos, Mara Lívia, de Avelar, Gleide Fernandes, Meeusen, Romain, Heyman, Elsa, Soares, Danusa Dias
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Sprache:eng
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Zusammenfassung:•Consumption of a high-fat diet and fructose-rich beverages promotes insulin resistance.•Consumption of a high-fat diet and fructose-rich beverages increases inflammatory response.•Consumption of a high-fat diet and fructose-rich beverages modulates the morphology tissues.•Short-term consumption is sufficient for development of insulin resistance. The aim of this study was to verify the effects of consumption of a high-fat diet (HFD) combined with fructose-rich beverages (FRT) in promoting metabolic and physiologic changes associated with insulin resistance. Thirty-two male Wistar rats (250 ± 10 g) were randomly allocated into four groups (n = 8) that received either a standard diet (CON), HFD, FRT, or HFD + FRT for 30 d. Insulin sensitivity and glucose tolerance were evaluated using the insulin tolerance test (ITT) and oral glucose tolerance test (OGTT). Serum samples were used to analyze the metabolic parameters and hormone levels. Interleukin (IL)-6, IL-10, IL-1β, and tumor necrosis factor-α assays were performed in the liver, pancreas, gastrocnemius muscle, and epididymal adipose tissue by enzyme-linked immunosorbent assay. Histologic and morphometric analyses were performed on the liver, pancreas, and adipose tissues. Consumption of HFD + FRT promoted a significant increase (P < 0.05) in body weight, index adiposity, and in the area under the curve of ITT (P < 0.001) and OGTT (P < 0.001) when compared with the CON group. Consumption of FRT alone increased fasting glucose (P = 0.015), insulin (P = 0.035), and homeostasis model assessment index (P = 0.018), and these changes were of greater magnitude when FRT was combined with HFD. Moreover, the rats fed an HFD + FRT demonstrated a significant increase in lipid droplets in the liver (P < 0.001), an increase in adipocyte area, and an increase in inflammatory cytokines in the liver, pancreas, skeletal muscle, and adipose tissue. Consumption of an HFD + FRT promotes insulin resistance, increases inflammatory cytokines, and modulates histomorphometric parameters of the liver, pancreas, and adipose tissue, typical of insulin resistance in humans.
ISSN:0899-9007
1873-1244
DOI:10.1016/j.nut.2021.111403