Alizade Safoura, Gaeini Abbas Ali, Faramarzi Mohammad
Department of Exercise Physiology, Faculty of Sport Sciences, University of Isfahan, Isfahan, Iran.
Department of Exercise Physiology, Faculty of Sport Sciences, University of Tehran, Tehran, Iran.
J Aging Res. 2025 Aug 4;2025:9916781. doi: 10.1155/jare/9916781. eCollection 2025.
Diabetes mellitus is linked to progressive cognitive decline and motor impairments, especially among the aging population, highlighting the importance of early detection through reliable neuronal biomarkers. Proteins such as neurofilament light chain (NFL), neurogranin (Ng), and visinin-like protein 1 (VILIP-1) have emerged as indicators of neurodegeneration and associated behavioral changes. This study examined the effects of combined endurance and resistance exercise, along with ursolic acid (UA) supplementation, on hippocampal neuronal biomarkers and exploratory-locomotor behavior in aged diabetic rats. In this experiment, 21-month-old male Wistar rats were assigned to seven groups. Diabetes was induced using a single intraperitoneal dose of streptozotocin (STZ) (30 mg/kg) in combination with a high-fat diet (55% fat, 31% carbohydrate, and 14% protein). Interventions included endurance training (60%-75% vVO), resistance training (60% MVCC), and daily oral UA administration (250 mg/kg) over eight weeks. Neuronal biomarkers (NFL, Ng, and VILIP-1) were measured in hippocampal tissue via western blot, and exploratory and locomotor behavior was assessed using the open-field test. The results showed that UA supplementation combined with resistance training significantly reduced the levels of neuronal biomarkers NFL ( < 0.001), Ng ( < 0.01), and VILIP-1 ( < 0.001) in diabetic rats compared to untreated diabetic controls. The study demonstrated that diabetes leads to a marked elevation in NFL, Ng, and VILIP-1 protein levels, while a combined intervention of exercise and UA mitigated neurodegenerative changes and improved exploratory-locomotor outcomes.
糖尿病与进行性认知衰退和运动障碍有关,尤其是在老年人群中,这凸显了通过可靠的神经元生物标志物进行早期检测的重要性。神经丝轻链(NFL)、神经颗粒蛋白(Ng)和视锥蛋白样蛋白1(VILIP-1)等蛋白质已成为神经退行性变及相关行为变化的指标。本研究考察了耐力和抗阻运动联合熊果酸(UA)补充对老年糖尿病大鼠海马神经元生物标志物及探索性-运动行为的影响。在本实验中,将21月龄雄性Wistar大鼠分为七组。采用腹腔注射单次剂量链脲佐菌素(STZ)(30 mg/kg)并结合高脂饮食(55%脂肪、31%碳水化合物和14%蛋白质)诱导糖尿病。干预措施包括八周的耐力训练(60%-75% vVO)、抗阻训练(60% MVCC)以及每日口服UA(250 mg/kg)。通过蛋白质免疫印迹法测定海马组织中的神经元生物标志物(NFL、Ng和VILIP-1),并使用旷场试验评估探索性和运动行为。结果显示,与未治疗的糖尿病对照组相比,补充UA联合抗阻训练可显著降低糖尿病大鼠神经元生物标志物NFL(<0.001)、Ng(<0.01)和VILIP-1(<0.001)的水平。该研究表明,糖尿病导致NFL、Ng和VILIP-1蛋白水平显著升高,而运动和UA的联合干预可减轻神经退行性变化并改善探索性-运动结果。