Effectiveness of high-intensity interval training and high-protein diet on TNF-α protein level in colon tissue of obese male rats: The importance of diet modifying

نویسندگانMarziyeh Saghebjoo
نشریهObesity Medicine
شماره صفحات1-9
شماره سریال31
شماره مجلد2022
نوع مقالهFull Paper
تاریخ انتشار2022
نوع نشریهالکترونیکی
کشور محل چاپبلژیک
نمایه نشریهScopus
کلید واژه هاHigh, intensity interval training, protein diet, Interleukin, 37, Tumor necrosis factor, alpha, obesity, Bowel inflammation

چکیده مقاله

Purpose: High-fat diets (HFDs) are a risk factor for obesity, insulin resistance, non-alcoholic fatty liver disease, hypertension, inflammatory bowel disease, and atherosclerosis. The present study aimed to investigate the effect of high-intensity interval training (HIIT) and high-protein diet (HPD) on interleukin-37 (IL-37) and tumor necrosis factor-alpha (TNF-α) protein levels in the colon tissue of obese male rats fed a high-fat diet (HFD). Methods: Forty obese male Wistar rats were randomly assigned into six equal groups: 1) HIIT, 2) HPD, 3) HIIT+ HPD, 4) Obese control 1 with HFD (Ct1), and 5) obese control 2 with breaking a HFD at the start of the study (Ct2). Eight rats were given a standard diet in the normal control group (NCt). Rats were sacrificed 48 h after the last intervention session and colon tissue was removed. Results: The protein level of TNF-α was significantly lower in the HIIT, HPD, HIIT+ HPD, and Ct2 groups compared with the Ct1, with more lowering effects in the HPD and HIIT+ HPD and almost similar effects between the HIIT and Ct2 groups. No significant difference was observed in the IL- 37 protein level between experimental groups. Conclusion: These findings suggest that HIIT, HPD, and HIIT+HPD may reduce colon inflammation through lowering of TNF-α inflammatory marker in colon tissue of obese rats receiving HFD. Although, the HPD alone and along with HIIT represent a more reducing effect than HIIT alone. However, breaking the HFD and replacing it with the standard diet was similar to the HIIT for reducing TNF-α.

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