首页> 外文期刊>The Korean Journal of Physiology & Pharmacology >Transient Receptor Potential C4/5 Like Channel Is Involved in Stretch-Induced Spontaneous Uterine Contraction of Pregnant Rat
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Transient Receptor Potential C4/5 Like Channel Is Involved in Stretch-Induced Spontaneous Uterine Contraction of Pregnant Rat

机译:瞬时受体电位C4 / 5样通道参与妊娠大鼠牵拉诱发的自发性子宫收缩

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Spontaneous myometrial contraction (SMC) in pregnant uterus is greatly related with gestational age and growing in frequency and amplitude toward the end of gestation to initiate labor. But, an accurate mechanism has not been elucidated. In human and rat uterus, all TRPCs except TRPC2 are expressed in pregnant myometrium and among them, TRPC4 are predominant throughout gestation, suggesting a possible role in regulation of SMC. Therefore, we investigated whether the TRP channel may be involved SMC evoked by mechanical stretch in pregnant myometrial strips of rat using isometric tension measurement and patch-clamp technique. In the present results, hypoosmotic cell swelling activated a potent outward rectifying current in G protein-dependent manner in rat pregnant myocyte. The current was significantly potentiated by 1μM lanthanides (a potent TRPC4/5 stimulator) and suppressed by 10μM 2-APB (TRPC4-7 inhibitor). In addition, in isometric tension experiment, SMC which was evoked by passive stretch was greatly potentiated by lanthanide (1μM) and suppressed by 2-APB (10μM), suggesting a possible involvement of TRPC4/5 channel in regulation of SMC in pregnant myometrium. These results provide a possible cellular mechanism for regulation of SMC during pregnancy and provide basic information for developing a new agent for treatment of premature labor.
机译:妊娠子宫的自发性子宫肌层收缩(SMC)与胎龄和在妊娠末期开始分娩的频率和幅度的增加密切相关。但是,尚未阐明精确的机制。在人和大鼠子宫中,除TRPC2以外的所有TRPCs均在怀孕的子宫内膜中表达,其中TRPC4在整个妊娠过程中占主导地位,表明可能在调节SMC中发挥作用。因此,我们使用等轴测张力和膜片钳技术研究了在怀孕的子宫肌层条带中机械拉伸引起的TRPC通道是否可能参与了SMC。在目前的结果中,低渗细胞膨胀以依赖于G蛋白的方式激活了大鼠妊娠心肌细胞中的强力向外整流电流。 1μM镧系元素(一种有效的TRPC4 / 5刺激物)可显着增强电流,而10μM2-APB(TRPC4-7抑制剂)可抑制电流。此外,在等轴测张力实验中,被动拉伸诱发的SMC被镧系元素(1μM)大大增强,并被2-APB(10μM)抑制,这提示TRPC4 / 5通道可能参与了妊娠子宫肌层SMC的调节。这些结果为妊娠期间SMC的调控提供了可能的细胞机制,并为开发用于治疗早产的新药物提供了基本信息。

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