Division of Human Sciences, Faculty of Engineering, Section for Health-Related Physical Education, Osaka Institute of Technology, Osaka, Japan.
Graduate Course in Applied Chemistry, Environmental and Biomedical Engineering, Osaka Institute of Technology, Osaka, Japan.
Physiol Rep. 2021 May;9(9):e14856. doi: 10.14814/phy2.14856.
Functional interaction between the selective water channel AQP4 and several ion channels, such as TRPV4, NKCC1, and Na /K -ATPase, closely participate to regulate osmotic homeostasis. In the skeletal muscles, the decrease in APQ4 expression due to denervation was followed by the restoration of AQP4 expression during reinnervation. These findings raised the possibility that innervation status is an essential factor to regulate AQP4 expression in the skeletal muscles. This study investigated this hypothesis using disuse muscle atrophy model with innervation. Adult female Fischer 344 rats (8 weeks of age) were randomly assigned to either control (C) or cast immobilization (IM) groups (n = 6 per group). Two weeks after cast immobilization, the tibialis anterior muscles of each group were removed and the expression levels of some target proteins were quantified by western blot analysis. The expression level of AQP4 significantly decreased at 2 weeks post-immobilization (p < 0.05). Moreover, the expression levels of TRPV4, NKCC1, and Na /K -ATPase significantly decreased at 2 weeks post-immobilization (p < 0.05). This study suggested that innervation status is not always a key regulatory factor to maintain the expression of AQP4 in the skeletal muscles. Moreover, the transport of water and ions by AQP4 may be changed during immobilization-induced muscle atrophy.
水通道蛋白 AQP4 与几种离子通道(如 TRPV4、NKCC1 和 Na+/K+-ATPase)的功能相互作用,密切参与调节渗透平衡。在骨骼肌中,去神经支配导致 AQP4 表达减少,随后在神经再支配期间恢复 AQP4 表达。这些发现提出了这样一种可能性,即神经支配状态是调节骨骼肌中 AQP4 表达的一个重要因素。本研究使用具有神经支配的失用性肌肉萎缩模型来研究这一假说。成年雌性 Fischer 344 大鼠(8 周龄)被随机分为对照组(C)或石膏固定组(IM)(每组 n=6)。石膏固定 2 周后,从每组中取出比目鱼肌,并通过 Western blot 分析定量测定一些靶蛋白的表达水平。AQP4 的表达水平在固定后 2 周时显著降低(p<0.05)。此外,TRPV4、NKCC1 和 Na+/K+-ATPase 的表达水平在固定后 2 周时显著降低(p<0.05)。本研究表明,神经支配状态并不总是维持骨骼肌中 AQP4 表达的关键调节因素。此外,AQP4 介导的水和离子转运可能在固定诱导的肌肉萎缩过程中发生变化。