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Updated: Jul 11, 2026

Fat Preference: A Novel Model of Eating Behavior in Rats
Published on: June 27, 2014
A high fat, high sugar diet exacerbates persistent post-surgical pain and modifies the brain-microbiota-gut axis in
Sabrina Salberg1, Matthew Macowan2, Angela Doshen3
1Department of Neuroscience, Monash University, Melbourne, VIC, Australia; Gastroenterology, Immunology, Neuroscience (GIN) Discovery Program, Australia.
Insights
A high-fat, high-sugar diet worsens persistent post-surgical pain (PPSP) and alters brain structure in adolescent rats. Diet and surgery interact to change the brain microbiome, impacting brain-gut axis function.
Area of Science:
- Neuroscience
- Microbiology
- Gastroenterology
Background:
- Persistent post-surgical pain (PPSP) affects many patients.
- Chronic pain and diet significantly alter the gut microbiome.
- The gut microbiome influences brain development and function.
Purpose of the Study:
- To investigate how a high-fat, high-sugar (HFHS) diet affects PPSP development, brain structure/function, and the microbiome.
- To identify correlations between the microbiome and brain changes in PPSP models.
- To understand the role of the brain-microbiota-gut axis in PPSP.
Main Methods:
- Rats were fed control or HFHS diets and underwent sham or surgical procedures.
- Mechanical nociceptive sensitivity was assessed using the von Frey task.
- In-vivo MRI examined brain volume and diffusivity, followed by 16S rRNA sequencing of fecal samples.
Main Results:
- HFHS diet exacerbated PPSP in adolescent rats.
- HFHS diet reduced brain volume and increased white/grey matter density.
- Diet and surgery interacted to alter brain diffusivity, correlating with microbiome changes.
Conclusions:
- Premorbid dietary factors influence PPSP development.
- The gut microbiome is linked to PPSP-induced brain alterations.
- Findings advance understanding of the brain-microbiota-gut axis in pain.
Abstract:
Persistent post-surgical pain (PPSP) occurs in a proportion of patients following surgical interventions. Research suggests that specific microbiome components are important for brain development and function, with recent studies demonstrating that chronic pain results in changes to the microbiome. Consumption of a high fat, high sugar (HFHS) diet can drastically alter composition of the microbiome and is a modifiable risk factor for many neuroinflammatory conditions. Therefore, we investigated how daily consumption of a HFHS diet modified the development of PPSP, brain structure and function, and the microbiome. In addition, we identified significant correlations between the microbiome and brain in animals with PPSP. Male and female rats were maintained on a control or HFHS diet. Animals were further allocated to a sham or surgery on postnatal day (p) p35. The von Frey task measured mechanical nociceptive sensitivity at a chronic timepoint (p65-67). Between p68-72 rats underwent in-vivo MRI to examine brain volume and diffusivity. At p73 fecal samples were used for downstream 16 s rRNA sequencing. Spearman correlation analyses were performed between individual microbial abundance and MRI diffusivity to determine if specific bacterial species were associated with PPSP-induced brain changes. We found that consumption of a HFHS diet exacerbated PPSP in adolescents. The HFHS diet reduced overall brain volume and increased white and grey matter density. The HFHS diet interacted with the surgical intervention to modify diffusivity in numerous brain regions which were associated with specific changes to the microbiome. These findings demonstrate that premorbid characteristics can influence the development of PPSP and advance our understanding of the contribution that the microbiome has on function of the brain-microbiota-gut axis.
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