Mitochondria-associated membranes contribution to exercise-mediated alleviation of hepatic insulin resistance: Contrasting high-intensity interval training with moderate-intensity continuous training in a high-fat diet mouse model

IF 3 2区 医学 Q2 ENDOCRINOLOGY & METABOLISM Journal of Diabetes Pub Date : 2024-04-10 DOI:10.1111/1753-0407.13540
Xi Li, Jun Yang Yang, Wen Zhi Hu, YuXin Ruan, Hong Ying Chen, Qiang Zhang, Zhe Zhang, Zhe Shu Ding
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Abstract

Objective

Mitochondria-associated membranes (MAMs) serve pivotal functions in hepatic insulin resistance (IR). Our aim was to explore the potential role of MAMs in mitigating hepatic IR through exercise and to compare the effects of different intensities of exercise on hepatic MAMs formation in high-fat diet (HFD) mice.

Methods

Male C57BL/6J mice were fed an HFD and randomly assigned to undergo supervised high-intensity interval training (HIIT) or moderate-intensity continuous training (MICT). IR was evaluated using the serum triglyceride/high-density lipoprotein cholesterol ratio (TG/HDL-C), glucose tolerance test (GTT), and insulin tolerance test (ITT). Hepatic steatosis was observed using hematoxylin–eosin (H&E) and oil red O staining. The phosphatidylinositol 3-kinase/protein kinase B/glycogen synthase kinase 3 beta (PI3K-AKT-GSK3β) signaling pathway was assessed to determine hepatic IR. MAMs were evaluated through immunofluorescence (colocalization of voltage-dependent anion-selective channel 1 [VDAC1] and inositol 1,4,5-triphosphate receptor [IP3R]).

Results

After 8 weeks on an HFD, there was notable inhibition of the hepatic PI3K/Akt/GSK3β signaling pathway, accompanied by a marked reduction in hepatic IP3R-VDAC1 colocalization levels. Both 8-week HIIT and MICT significantly enhanced the hepatic PI3K/Akt/GSK3β signaling and colocalization levels of IP3R-VDAC1 in HFD mice, with MICT exhibiting a stronger effect on hepatic MAMs formation. Furthermore, the colocalization of hepatic IP3R-VDAC1 positively correlated with the expression levels of phosphorylation of protein kinase B (p-AKT) and phosphorylation of glycogen synthase kinase 3 beta (p-GSK3β), while displaying a negative correlation with serum triglyceride/high-density lipoprotein cholesterol levels.

Conclusion

The reduction in hepatic MAMs formation induced by HFD correlates with the development of hepatic IR. Both HIIT and MICT effectively bolster hepatic MAMs formation in HFD mice, with MICT demonstrating superior efficacy. Thus, MAMs might wield a pivotal role in exercise-induced alleviation of hepatic IR.

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线粒体相关膜对运动介导的肝脏胰岛素抵抗缓解的贡献在高脂饮食小鼠模型中对比高强度间歇训练和中等强度持续训练
目的 线粒体相关膜(MAMs)在肝脏胰岛素抵抗(IR)中发挥着关键作用。我们的目的是探索线粒体相关膜在通过运动减轻肝脏胰岛素抵抗中的潜在作用,并比较不同强度的运动对高脂饮食(HFD)小鼠肝脏线粒体相关膜形成的影响。 方法 雄性C57BL/6J小鼠以高脂肪饮食为饲料,并随机分配其接受有监督的高强度间歇训练(HIIT)或中等强度持续训练(MICT)。使用血清甘油三酯/高密度脂蛋白胆固醇比值(TG/HDL-C)、葡萄糖耐量试验(GTT)和胰岛素耐量试验(ITT)评估IR。使用苏木精-伊红(H&E)和油红 O 染色观察肝脏脂肪变性。评估磷脂酰肌醇3-激酶/蛋白激酶B/糖原合成酶激酶3β(PI3K-AKT-GSK3β)信号通路以确定肝脏IR。通过免疫荧光(电压依赖性阴离子选择性通道 1 [VDAC1] 和 1,4,5-三磷酸肌醇受体 [IP3R]的共定位)对 MAMs 进行评估。 结果 高脂饮食 8 周后,肝脏 PI3K/Akt/GSK3β 信号通路明显受到抑制,同时肝脏 IP3R-VDAC1 共定位水平明显下降。为期 8 周的 HIIT 和 MICT 均能显著增强高纤维脂肪肝小鼠肝脏 PI3K/Akt/GSK3β 信号传导和 IP3R-VDAC1 共定位水平,其中 MICT 对肝脏 MAMs 形成的影响更大。此外,肝脏 IP3R-VDAC1 的共定位与蛋白激酶 B 磷酸化(p-AKT)和糖原合酶激酶 3 beta 磷酸化(p-GSK3β)的表达水平呈正相关,而与血清甘油三酯/高密度脂蛋白胆固醇水平呈负相关。 结论 HFD 引起的肝脏 MAMs 形成减少与肝脏 IR 的发展相关。HIIT 和 MICT 都能有效促进 HFD 小鼠肝 MAMs 的形成,其中 MICT 的疗效更佳。因此,MAMs 可能在运动诱导的肝IR缓解过程中发挥关键作用。
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来源期刊
Journal of Diabetes
Journal of Diabetes ENDOCRINOLOGY & METABOLISM-
CiteScore
6.50
自引率
2.20%
发文量
94
审稿时长
>12 weeks
期刊介绍: Journal of Diabetes (JDB) devotes itself to diabetes research, therapeutics, and education. It aims to involve researchers and practitioners in a dialogue between East and West via all aspects of epidemiology, etiology, pathogenesis, management, complications and prevention of diabetes, including the molecular, biochemical, and physiological aspects of diabetes. The Editorial team is international with a unique mix of Asian and Western participation. The Editors welcome submissions in form of original research articles, images, novel case reports and correspondence, and will solicit reviews, point-counterpoint, commentaries, editorials, news highlights, and educational content.
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