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Gut microbiota promoting propionic acid production accompanies caloric restriction-induced intentional weight loss in cats.
Rowe, J C; Winston, J A; Parker, V J; McCool, K E; Suchodolski, J S; Lopes, R; Steiner, J M; Gilor, C; Rudinsky, A J.
Afiliación
  • Rowe JC; Department of Veterinary Clinical Sciences, The Ohio State University College of Veterinary Medicine, Columbus, OH, USA.
  • Winston JA; Comparative Hepatobiliary Intestinal Research Program (CHIRP), The Ohio State University College of Veterinary Medicine, Columbus, OH, USA.
  • Parker VJ; Department of Veterinary Clinical Sciences, The Ohio State University College of Veterinary Medicine, Columbus, OH, USA. winston.210@osu.edu.
  • McCool KE; Comparative Hepatobiliary Intestinal Research Program (CHIRP), The Ohio State University College of Veterinary Medicine, Columbus, OH, USA. winston.210@osu.edu.
  • Suchodolski JS; Department of Veterinary Clinical Sciences, The Ohio State University College of Veterinary Medicine, Columbus, OH, USA.
  • Lopes R; Comparative Hepatobiliary Intestinal Research Program (CHIRP), The Ohio State University College of Veterinary Medicine, Columbus, OH, USA.
  • Steiner JM; Department of Clinical Sciences, North Carolina State University College of Veterinary Medicine, Raleigh, NC, USA.
  • Gilor C; Gastrointestinal Laboratory, Department of Small Animal Clinical Sciences, Texas A&M University College of Veterinary Medicine, College Station, TX, USA.
  • Rudinsky AJ; Gastrointestinal Laboratory, Department of Small Animal Clinical Sciences, Texas A&M University College of Veterinary Medicine, College Station, TX, USA.
Sci Rep ; 14(1): 11901, 2024 05 24.
Article en En | MEDLINE | ID: mdl-38789518
ABSTRACT
Rodent models and human clinical studies have shown gut microbiota-derived short-chain fatty acids (SCFAs) play roles in obesity and insulin resistance. These roles have been minimally explored in cats, where in the USA an estimated 60% of cats are overweight or obese. Overweight/obese research cats (n = 7) were transitioned from a maintenance diet to a reduced calorie diet fed ad libitum for 7 days, then calories were restricted to achieve 1-2% weight loss per week for an additional 77 days. Cats then received their original maintenance diet again for 14 days. Significant intentional weight loss was noted after calorie restriction (adjusted p < 0.0001). 16S rRNA gene amplicon sequencing and targeted SCFA metabolomics were performed on fecal samples. Fecal microbial community structure significantly differed between the four study phases (PERMANOVA p = 0.011). Fecal propionic acid was significantly higher during caloric restriction-induced weight loss (adjusted p < 0.05). Repeated measures correlation revealed the relative abundances of Prevotella 9 copri (correlation coefficient = 0.532, 95% CI (0.275, 0.717), p = 0.0002) significantly correlated with propionic acid composition. Like humans, obese cats experienced an altered microbial community structure and function, favoring propionic acid production, during caloric restriction-induced weight loss.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Propionatos / Pérdida de Peso / Restricción Calórica / Heces / Microbioma Gastrointestinal / Obesidad Idioma: En Revista: Sci Rep Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Propionatos / Pérdida de Peso / Restricción Calórica / Heces / Microbioma Gastrointestinal / Obesidad Idioma: En Revista: Sci Rep Año: 2024 Tipo del documento: Article