Effects of treadmill exercise on PI3K/AKT/GSK-3β pathway and tau protein in high-fat diet-fed rats.

Jae-Hoon Jeong, Eun-Bum Kang
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引用次数: 20

Abstract

Purpose: This study aimed to clearly evaluate the effects of obesity on cerebral health. Thus, we induced obesity in rats using a long-term high-fat diet (HFD), then investigated its effects on insulin signaling and tau hyperphosphorylation. Additionally, we examined the effects of 8 weeks of treadmill exercise (TE) on insulin signaling and tau hyperphosphorylation.

Methods: Rats were separated into Normal Diet-Control, HFD-Control, and HFD-TE groups. TE loads were gradually increased. A passive avoidance test was used to evaluate cognitive function. Western blots were used to examine the abundance of the insulin receptor,phosphoinositide 3-kinase, protein kinase B, glycogen synthase kinase-3β, and tau proteins in the cerebral cortex; immunohistochemical analyses were used to examine the abundance of hyperphosphorylated tau in the cerebral cortex.

Results: TE in HFD-fed rats resulted in a significant lowering of bodyweight, abdominal visceral fat (AVF), the area under the glucose response curve, and the homeostatic model assessment-insulin resistance index, while it improved working memory. In addition, TE in HFD-fed rats decreased tau hyperphosphorylation and aggregation, while increasing insulin signaling-related protein activity.

Conclusion: After a 20-week HFD, the experimental animals exhibited increased weight, as well as impaired insulin resistance and blood glucose metabolism. HFD rats demonstrated abnormal insulin signaling and tau hyperphosphorylation in the cerebral cortex, as well as memory impairments that suggested reduced cerebral function. However, TE reduced AVF, improved insulin resistance in the peripheral tissues by increasing insulin sensitivity, and alleviated memory impairments by restoring insulin signaling and reducing tau hyperphosphorylation in the cerebral cortex.

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跑步机运动对高脂饮食大鼠PI3K/AKT/GSK-3β通路和tau蛋白的影响
目的:探讨肥胖对大脑健康的影响。因此,我们使用长期高脂肪饮食(HFD)诱导大鼠肥胖,然后研究其对胰岛素信号传导和tau蛋白过度磷酸化的影响。此外,我们研究了8周的跑步机运动(TE)对胰岛素信号传导和tau蛋白过度磷酸化的影响。方法:将大鼠分为正常饮食对照组、hfd对照组和HFD-TE组。TE负荷逐渐增加。采用被动回避测试评估认知功能。Western blots检测大鼠大脑皮层胰岛素受体、磷酸肌肽3激酶、蛋白激酶B、糖原合成酶激酶3β和tau蛋白的丰度;免疫组织化学分析用于检测大脑皮层中过度磷酸化的tau蛋白的丰度。结果:TE能显著降低hfd大鼠的体重、腹部内脏脂肪(AVF)、葡萄糖反应曲线下面积和稳态模型评估-胰岛素抵抗指数,改善工作记忆。此外,TE在hfd喂养的大鼠中降低了tau蛋白的过度磷酸化和聚集,同时增加了胰岛素信号相关蛋白的活性。结论:经过20周的HFD后,实验动物表现出体重增加,胰岛素抵抗和血糖代谢受损。HFD大鼠表现出异常的胰岛素信号和大脑皮层的tau蛋白过度磷酸化,以及表明大脑功能下降的记忆障碍。然而,TE降低了AVF,通过增加胰岛素敏感性改善了外周组织的胰岛素抵抗,并通过恢复胰岛素信号和减少大脑皮层的tau过度磷酸化来减轻记忆障碍。
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