Exercise Modulates High-fat Diet Induced Alterations in Lipid Profiles, Neuropeptides, and Hippocampal Function in Rats


Yilmaz Tasci S., KAYABEKİR M., Gundogdu G., TERİM KAPAKİN K. A., DEMİRKAYA MİLOĞLU F., BAYRAM C., ...Daha Fazla

Bratislava Medical Journal, 2026 (SCI-Expanded, Scopus) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Basım Tarihi: 2026
  • Doi Numarası: 10.1007/s44411-026-00594-2
  • Dergi Adı: Bratislava Medical Journal
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Anahtar Kelimeler: Cognitive function, Exercise, Ghrelin, Gut–brain peptides, High-fat diet, Hippocampal degeneration, Learning, Lipid profiles, Obestatin, Orexins
  • Atatürk Üniversitesi Adresli: Evet

Özet

Aim: This study aimed to assess the modulatory effects of exercise on long-term high-fat diet (HFD)-induced variations in lipid parameters, cognitive performance, gut–brain peptides, and hippocampal histopathology in rats. Materials and Methods: Male Wistar albino rats were randomly divided into four experimental groups (n = 10 each): Sedentary-(SED), Exercise-(EX), High-Fat Diet-(HFD), and High-Fat-Diet + Exercise (HFD + EX). Exercise protocol was applied from the 4th weeks of experiment. The Morris Water Maze-(MWM) test was performed at the 4th, 8th, and 12th weeks of experiment to assess spatial learning. Serum levels of lipid profiles (triglyceride-(TG), total cholesterol-(TC), High Density Lipoprotein-(HDL), Low Density Lipoprotein-(LDL)) ghrelin, obestatin, and orexin A/B were measured. Hippocampal tissues were evaluated by hematoxylin–eosin and toluidine blue staining. Group comparisons were evaluated using both parametric (One-Way ANOVA) and non-parametric (Kruskal–Wallis H) statistical tests. Results: Through 6th week of the experiment, both HFD and HFD + EX groups showed lower body weight (p < 0.05). and at 7th week of experiment, only the HFD + EX group remained lighter (p < 0.05). TG, TC and LDL levels were increased in HFD (218.56 ± 57.43, 68.78 ± 12.43, 23.22 ± 4.60 mg/dL) and HFD + EX (159.22 ± 55.15, 70.78 ± 8.07, 26.9 ± 5.16 mg/dL) groups (p < 0.05). Ghrelin was highest in the HFD + EX group (5.58 ± 1.00 ng/mL, p < 0.05), and obestatin levels were decreased in HFD (7.08 ± 0.85 ng/mL) and HFD + EX (7.11 ± 0.45 ng/mL) groups (p < 0.001). Orexin A decreased in the HFD group (2713.38 ± 380.61 pg/mL, p < 0.05), and orexin B was highest in the EX group (7.23 ± 2.21 pg/mL, p < 0.01). MWM test revealed major increase in latency time in the HFD (59 s) group at 12th week of experiment (p < 0.001). Histopathological analysis showed significant hippocampal degeneration, necrosis, and gliosis in HFD and HFD + EX groups (p < 0.001). Conclusion: This study offers a comprehensive evaluation of long-term HFD exposure and exercise by jointly assessing metabolic outcomes, cognition, gut–brain peptides, and hippocampal histopathology—an approach seldom combined in a single design. The findings show that exercise offers limited neuroprotective and metabolic benefits but does not fully prevent HFD-induced hippocampal damage, highlighting a novel multidimensional perspective and pointing to the need for additional protective strategies.