A thermally processed cafeteria diet reproducibly mimics early metabolic syndrome through obesity, insulin resistance, and inflammatory activation in Wistar rats
Year: 2026
Type: article
Abstract: The obesogenic nutrient composition and processing characteristics of ultra-processed foods may contribute to metabolic dysfunction. The present study evaluated a standardized cafeteria diet, alone or combined with low-dose streptozotocin (STZ), in male Wistar rats. Animals (n = 32) were allocated to Healthy Control, STZ (35 mg/kg), Cafeteria Diet (CAF), and CAF + STZ groups. The diet contained standard chow, condensed milk, refined sugar, hydrogenated fat, soybean oil, and chocolate-filled biscuits, homogenized and thermally processed at 180°C. After 102 days, anthropometric, metabolic, inflammatory, gene expression, microbiota, and histopathological parameters were assessed. CAF induced a marked obesogenic phenotype, with increased body weight (+172.3%) and abdominal circumference (+38.7%; P < 0.01). CAF showed hyperglycemia (median glucose, 403 mg/dl) and higher HOMA-IR than Healthy Control (P < 0.01); CAF + STZ also showed increased HOMA-IR (P < 0.05). CAF increased IL-1β and IL-6 (P < 0.05), triglycerides, adipocyte hypertrophy (P < 0.01), and adipose leptin expression (P < 0.05), while reducing muscle Slc2a4/GLUT4 expression (P < 0.01). Liver, kidney, and pancreatic histopathological scores did not differ significantly. Gut microbiota showed marked compositional imbalance and low taxonomic evenness, with Firmicutes (99.83%), Ligilactobacillus (99.36%), and Lactobacillaceae (99.52%) predominating, while Enterobacteriaceae represented 0.14%. Despite no reduction in Shannon or Simpson indices, extreme Ligilactobacillus dominance indicated a restricted and uneven community. Overall, the cafeteria diet reproduced obesity-associated metabolic dysfunction, characterized by hyperglycemia, insulin resistance, inflammation, adipocyte hypertrophy, altered glucose and leptin expression, and substantial microbiota restructuring.
Source: Bioscience Reports
DOI: 10.1042/bsr20260388
Authors: Susana Barbosa Ribeiro, Rômulo Camilo de Oliveira Melo, Lucas Vinicius Souza de Carvalho, Arnóbio Antônio da Silva Júnior, Raimundo Fernandes de Araújo Júnior, Amanda Silveira da Silva, Gabrielle Marques de Paiva, Vinicus Barreto Garcia, Ana Heloneida de Araújo Morais, Ana Júlia Felipe Camelo Aguiar, Caroline Addison Carvalho Xavier de Medeiros, Maiara de Morais, Bruna Rafaela Martins dos Santos, Rafael Lino Mokwa, Francisco Caninde de Souza Junior, Maíra Conceição Jerônimo de Souza Lima, Ciro Dantas Soares, Aurigena Antunes de Araújo
Language: English
Subfield: Endocrinology, Diabetes and Metabolism
Field: Medicine
Domain: Health Sciences
Open Access status: gold
Estimated APC paid: $1,960
OpenAlex ID: W7220408762
