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Peer-reviewedCC BYBioscience reports

A thermally processed cafeteria diet reproducibly mimics early metabolic syndrome through obesity, insulin resistance, and inflammatory activation in Wistar rats.

6 more authors
14 affiliations
  1. 1Postgraduate Program in Pharmaceutical Science, Department of Pharmaceutical Science, Federal University of Rio Grande Norte, Natal, Brazil.
  2. 2Postgraduate Program in Oral Science, Department of Dentistry, Federal University of Rio Grande Norte, Natal, Brazil.
  3. 3Department of Pharmaceutical Science, Federal University of Rio Grande Norte, Natal, Brazil.
  4. 4Postgraduate Program in Pharmaceutical Science, Postgraduate Program in Health Sciences, Department of Pharmaceutical Science, Federal University of Rio Grande Norte, Natal, Brazil.
  5. 5Postgraduate Program in Health Sciences, Postgraduate Program in Functional and Structural Biology UFRN, Department of Morphology, Federal University of Rio Grande Norte, Natal, Brazil.
  6. 6Faculty of Health Sciences (FCS), Federal University of Rondonópolis (UFR), Rondonópolis, Brazil.
  7. 7Postgraduate Program in Biochemistry and Biology, Postgraduate Program in Nutrition, Department of Nutrition, Federal University of Rio Grande Norte, Natal, Brazil.
  8. 8Postgraduate Program in Biochemistry and Molecular Biology, Department of Biochemistry, Federal University of Rio Grande Norte, Natal, Brazil.
  9. 9Department of Biophysical and Pharmacology, Federal University of Rio Grande Norte, Natal, Brazil.
  10. 10Departament of Patology, Federal University of Rio Grande Norte, Natal, Brazil.
  11. 11Graduate Program in Health Science and Technology, Department of Dentistry, State University of Paraíba, Campina Grande, Paraíba, Brazil.
  12. 12Department of Biophysical and Pharmacology, Federal University of Rio Grande Norte, Anclivepa Natal Faculty, Natal, Rio Grande do Norte, Brazil.
  13. 13Graduate Program in Oral Pathology, Faculty of Dentistry of Piracicaba, University of Campinas (UNICAMP), Piracicaba, São Paulo, Brazil; Postgraduate Program in Oral Sciences, Department of Dentistry, Federal University of Rio Grande do Norte, Natal, Rio Grande do Norte, Brazil.
  14. 14Postgraduate Program in Oral Sciences, Postgraduate Program in Pharmaceutical Sciences Department of Biophysical and Pharmacology, Federal University of Rio Grande Norte, Natal, Brazil.

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.

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BibTeX
@article{ribeiro2026thermally,
  title = {{A thermally processed cafeteria diet reproducibly mimics early metabolic syndrome through obesity, insulin resistance, and inflammatory activation in Wistar rats.}},
  author = {Susana Barbosa Ribeiro and Rômulo Camilo de Oliveira Melo and Lucas Vinicius Souza de Carvalho and Arnóbio Antônio da Silva Júnior and Raimundo Fernandes de Araújo Júnior and Amanda Silveira da Silva and Gabrielle Marques de Paiva and Vinicus Barreto Garcia and Ana Heloneida de Araújo Morais and Ana Júlia Felipe Camelo Aguiar and Caroline Addison Carvalho Xavier de Medeiros and Maiara de Morais and Bruna Rafaela Martins Dos Santos and Rafael Lino Mokwa and Francisco Caninde de Souza Junior and Maíra Conceição Jerônimo de Souza Lima and Ciro Dantas Soares and Aurigena Antunes de Araújo},
  journal = {Bioscience reports},
  year = {2026},
  month = oct,
  doi = {10.1042/bsr20260388},
  url = {https://europepmc.org/article/MED/42831297},
  note = {CC BY},
}
RIS
TY  - JOUR
TI  - A thermally processed cafeteria diet reproducibly mimics early metabolic syndrome through obesity, insulin resistance, and inflammatory activation in Wistar rats.
AU  - Susana Barbosa Ribeiro
AU  - Rômulo Camilo de Oliveira Melo
AU  - Lucas Vinicius Souza de Carvalho
AU  - Arnóbio Antônio da Silva Júnior
AU  - Raimundo Fernandes de Araújo Júnior
AU  - Amanda Silveira da Silva
AU  - Gabrielle Marques de Paiva
AU  - Vinicus Barreto Garcia
AU  - Ana Heloneida de Araújo Morais
AU  - Ana Júlia Felipe Camelo Aguiar
AU  - Caroline Addison Carvalho Xavier de Medeiros
AU  - Maiara de Morais
AU  - Bruna Rafaela Martins Dos Santos
AU  - Rafael Lino Mokwa
AU  - Francisco Caninde de Souza Junior
AU  - Maíra Conceição Jerônimo de Souza Lima
AU  - Ciro Dantas Soares
AU  - Aurigena Antunes de Araújo
PY  - 2026
DA  - 2026/10/30
JO  - Bioscience reports
DO  - 10.1042/bsr20260388
UR  - https://europepmc.org/article/MED/42831297
AB  - 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.
SN  - 0144-8463
SN  - 1573-4935
ER  -