4.7 Article

Perilla Seed Oil Alleviates Gut Dysbiosis, Intestinal Inflammation and Metabolic Disturbance in Obese-Insulin-Resistant Rats

期刊

NUTRIENTS
卷 13, 期 9, 页码 -

出版社

MDPI
DOI: 10.3390/nu13093141

关键词

gut microbiota; omega-3 fatty acids; inflammation; insulin resistance; systemic inflammation

资金

  1. Thailand Research Fund [MRG6280240]
  2. Office of the Higher Education Commission [MRG6280240]
  3. Thailand Science Research and Innovation Fund [FF64-UoE034]
  4. University of Phayao [FF64-UoE034]
  5. National Research Council of Thailand
  6. National Research Council of Thailand (NRCT)
  7. NSTDA Research Chair Grant from the National Science and Technology Development Agency Thailand
  8. Chiang Mai University Excellence Center Award

向作者/读者索取更多资源

The study found that PSO and metformin can effectively improve gut dysbiosis, inflammation, and metabolic disturbance in HFD-fed rats, with metformin showing greater benefits.
Background: High-fat diet (HFD) consumption induced gut dysbiosis, inflammation, obese-insulin resistance. Perilla seed oil (PSO) is a rich source of omega-3 polyunsaturated fatty acids with health promotional effects. However, the effects of PSO on gut microbiota/inflammation and metabolic disturbance in HFD-induced obesity have not been investigated. Therefore, we aimed to compare the effects of different doses of PSO and metformin on gut microbiota/inflammation, and metabolic parameters in HFD-fed rats. Methods: Thirty-six male Wistar rats were fed either a normal diet or an HFD for 24 weeks. At week 13, HFD-fed rats received either 50, 100, and 500 mg/kg/day of PSO or 300 mg/kg/day metformin for 12 weeks. After 24 weeks, the metabolic parameters, gut microbiota, gut barrier, inflammation, and oxidative stress were determined. Results: HFD-fed rats showed gut dysbiosis, gut barrier disruption with inflammation, increased oxidative stress, metabolic endotoxemia, and insulin resistance. Treatment with PSO and metformin not only effectively attenuated gut dysbiosis, but also improved gut barrier integrity and decreased gut inflammation. PSO also decreased oxidative stress, metabolic endotoxemia, and insulin resistance in HFD-fed rats. Metformin had greater benefits than PSO. Conclusion: PSO and metformin had the beneficial effect on attenuating gut inflammation and metabolic disturbance in obese-insulin resistance.

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