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单侧等长收缩诱导雄性小鼠非收缩肌肉中的REDD1表达,并抑制胰岛素刺激的mTORC1和蛋白质合成。

Unilateral isometric contraction induces REDD1 and suppresses insulin-stimulated mTORC1 and protein synthesis in non-contracted muscle of male mice.

作者信息

Amar Munkhtuul Munkh, Murakami Taro

机构信息

Department of Nutrition, Shigakkan University, Obu, Aichi, Japan.

出版信息

Physiol Rep. 2025 Sep;13(18):e70574. doi: 10.14814/phy2.70574.

Abstract

Skeletal muscle hypertrophy is promoted by mechanical loading and is associated with activation of mTORC1 signaling. While REDD1, a stress-responsive inhibitor of mTORC1, is typically downregulated in contracting muscle, we previously reported that unilateral isometric contraction increases REDD1 expression in the contralateral non-contracted muscle. The functional significance of this response remains unclear. This study tested whether REDD1 induction in non-contracted muscle attenuates anabolic signaling under insulin-stimulated conditions. Male C57BL/6J mice underwent unilateral isometric contraction of the right gastrocnemius via percutaneous electrical stimulation. Insulin was administered systemically to stimulate mTORC1 signaling and protein synthesis. Western blotting was used to assess REDD1 protein levels and phosphorylation of mTORC1 downstream targets and Akt. REDD1 protein was significantly elevated in non-contracted muscle following contraction. This was accompanied by reduced insulin-stimulated phosphorylation of S6K1 and 4E-BP1, as well as decreased puromycin incorporation, indicating suppressed protein synthesis. Insulin-stimulated Akt phosphorylation was unchanged, suggesting that the suppression occurred downstream or independently of Akt. These findings demonstrate that isometric contraction can impair insulin-stimulated mTORC1 signaling and protein synthesis in non-contracted muscle in male mice, potentially via REDD1 induction.

摘要

机械负荷可促进骨骼肌肥大,且与mTORC1信号通路的激活相关。虽然应激反应性mTORC1抑制剂REDD1在收缩的肌肉中通常会下调,但我们之前报道过,单侧等长收缩会增加对侧未收缩肌肉中REDD1的表达。这种反应的功能意义仍不清楚。本研究测试了未收缩肌肉中REDD1的诱导是否会在胰岛素刺激条件下减弱合成代谢信号。雄性C57BL/6J小鼠通过经皮电刺激对右侧腓肠肌进行单侧等长收缩。全身给予胰岛素以刺激mTORC1信号通路和蛋白质合成。采用蛋白质免疫印迹法评估REDD1蛋白水平以及mTORC1下游靶点和Akt的磷酸化情况。收缩后,未收缩肌肉中的REDD1蛋白显著升高。这伴随着胰岛素刺激的S6K1和4E-BP1磷酸化减少,以及嘌呤霉素掺入减少,表明蛋白质合成受到抑制。胰岛素刺激的Akt磷酸化未发生变化,表明这种抑制发生在Akt的下游或独立于Akt。这些发现表明,等长收缩可能通过诱导REDD1损害雄性小鼠未收缩肌肉中胰岛素刺激的mTORC1信号通路和蛋白质合成。

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