Department of Physiology, Monash University, Clayton, Victoria 3800, Australia.
Department of Perinatal Medicine Pregnancy Research Centre, Royal Women's Hospital, Parkville, Victoria 3052, Australia.
Nat Commun. 2014 Jun 17;5:4108. doi: 10.1038/ncomms5108.
Human ether-a-go-go-related gene (hERG) potassium channels determine cardiac action potential and contraction duration. Human uterine contractions are underpinned by an action potential that also possesses an initial spike followed by prolonged depolarization. Here we show that hERG channel proteins (α-conducting and β-inhibitory subunits) and hERG currents exist in isolated patch-clamped human myometrial cells. We show that hERG channel activity suppresses contraction amplitude and duration before labour, thereby facilitating quiescence. During established labour, expression of β-inhibitory protein is markedly enhanced, resulting in reduced hERG activity that is associated with an increased duration of uterine action potentials and contractions. Thus, changes in hERG channel activity contribute to electrophysiological mechanisms that produce contractions during labour. We also demonstrate that this system fails in women with elevated BMI, who have enhanced hERG activity as a result of low β-inhibitory protein expression, which likely contributes to the weak contractions and poor labour outcomes observed in many obese women necessitating caesarean delivery.
人 ether-a-go-go 相关基因 (hERG) 钾通道决定心脏动作电位和收缩持续时间。人类子宫收缩是由动作电位支撑的,该动作电位也具有初始尖峰,随后是长时间去极化。在这里,我们表明 hERG 通道蛋白(α 传导和β抑制亚基)和 hERG 电流存在于分离的夹闭的人子宫平滑肌细胞中。我们表明,hERG 通道活性在分娩前抑制收缩幅度和持续时间,从而促进静止。在已建立的分娩过程中,β抑制蛋白的表达显著增强,导致 hERG 活性降低,与子宫动作电位和收缩持续时间增加相关。因此,hERG 通道活性的变化有助于产生分娩时收缩的电生理机制。我们还证明,该系统在 BMI 升高的女性中失效,由于低β抑制蛋白表达导致 hERG 活性增强,这可能导致许多肥胖女性的宫缩无力和分娩结局不佳,需要剖腹产。