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肝脏 PHD2/HIF-1α 轴参与运动后全身能量稳态。

Hepatic PHD2/HIF-1α axis is involved in postexercise systemic energy homeostasis.

机构信息

School of Kinesiology, Shanghai University of Sport, Shanghai, China.

Department of Cell Biology, Second Military Medical University, Shanghai, China.

出版信息

FASEB J. 2018 Sep;32(9):4670-4680. doi: 10.1096/fj.201701139R. Epub 2018 Mar 30.

Abstract

Exercise plays an important role in the prevention and treatment of chronic liver disease and associated metabolic disorders. A single bout of exercise induces tissue blood flow redistribution, which decreases splanchnic circulation and leads to physiologic hypoxia in the gastrointestinal system and liver. The transcription factor, hypoxia inducible factor-1α (HIF-1α), and its regulator, prolylhydroxylase 2 (PHD2), play pivotal roles in the response to oxygen flux by regulating downstream gene expression levels in the liver. We hypothesized that exercise increases the HIF-1α levels in the liver, and that the hepatic PHD2/HIF-1α axis is involved in postexercise restoration of systemic energy homeostasis. Through constant O consumption, CO production, food and water intake, and physical activity detection with metabolic chambers, we observed that one 30-min session of swimming exercise enhances systemic energy metabolism in mice. By using the noninvasive bioluminescence imaging ROSA26 oxygen-dependent domain Luc mouse model, we reveal that exercise increases in vivo HIFα levels in the liver. Intraperitoneal injections of the PHD inhibitor, dimethyloxalylglycine, mimicked exercise-induced HIFα increase, whereas the HIF-1α inhibitor, PX-478, blocked this effect. We next constructed liver-specific knockout (LKO) mouse models with albumin- Cre-mediated, hepatocyte-specific Hif1a and Phd2 deletion. Compared with their controls, Hif1a-LKO and Phd2-LKO mice exhibited distinct patterns of hepatic metabolism-related gene expression profiles. Moreover, Hif1a-LKO mice failed to restore systemic energy homeostasis after exercise. In conclusion, the current study demonstrates that a single bout of exercise disrupts systemic energy homeostasis, increasing the HIF-1α levels in the liver. These findings also provide evidence that the hepatic PHD2/HIF-1α axis is involved in postexercise systemic metabolic homeostasis.-Luo, B., Xiang, D., Wu, D., Liu, C., Fang, Y., Chen, P., Hu, Y.-P. Hepatic PHD2/HIF-1α axis is involved in postexercise systemic energy homeostasis.

摘要

运动在慢性肝病和相关代谢紊乱的预防和治疗中起着重要作用。单次运动诱导组织血流重新分布,减少内脏循环,导致胃肠道系统和肝脏发生生理性缺氧。转录因子缺氧诱导因子-1α(HIF-1α)及其调节剂脯氨酰羟化酶 2(PHD2)在通过调节肝脏下游基因表达水平来响应氧通量方面发挥着关键作用。我们假设运动增加肝脏中的 HIF-1α 水平,并且肝 PHD2/HIF-1α 轴参与运动后全身能量稳态的恢复。通过代谢室检测恒定的 O 消耗、CO 生成、食物和水摄入以及体力活动,我们观察到单次 30 分钟游泳运动增强了小鼠的全身能量代谢。通过使用非侵入性生物发光成像 ROSA26 氧依赖性结构域 Luc 小鼠模型,我们揭示运动增加了肝脏中的 HIFα 水平。腹腔内注射 PHD 抑制剂二甲氧酰基甘氨酸模拟运动诱导的 HIFα 增加,而 HIF-1α 抑制剂 PX-478 则阻断了这种作用。我们接下来构建了白蛋白 Cre 介导的、肝细胞特异性 Hif1a 和 Phd2 缺失的肝特异性敲除(LKO)小鼠模型。与对照相比,Hif1a-LKO 和 Phd2-LKO 小鼠表现出明显的肝脏代谢相关基因表达谱模式。此外,Hif1a-LKO 小鼠在运动后无法恢复全身能量稳态。总之,本研究表明单次运动扰乱了全身能量稳态,增加了肝脏中的 HIF-1α 水平。这些发现还提供了证据表明肝 PHD2/HIF-1α 轴参与运动后全身代谢稳态。

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