Beckett Elizabeth A H, McCloskey Conor, O'Kane Neil, Sanders Kenton M, Koh Sang Don
Department of Physiology and Cell Biology, University of Nevada School of Medicine, MS 352, Reno, NV 89557, USA.
J Physiol. 2006 Jun 1;573(Pt 2):453-68. doi: 10.1113/jphysiol.2006.107375. Epub 2006 Mar 31.
Idiopathic constipation is higher in women of reproductive age than postmenopausal women or men, suggesting that female steroid hormones influence gastrointestinal motility. How female hormones affect motility is unclear. Colonic motility is regulated by ion channels in colonic myocytes. Voltage-dependent K(+) channels serve to set the excitability of colonic muscles. We investigated regulation of Kv 4.3 channel expression in response to acute or chronic changes in female hormones. Patch clamp experiments and quantitative PCR were used to compare outward currents and transcript expression in colonic myocytes from male, non-pregnant, pregnant and ovariectomized mice. Groups of ovariectomized mice received injections of oestrogen or progesterone to investigate the effects of hormone replacement. The capacitance of colonic myocytes from non-pregnant females was larger than in males. Net outward current density in male and ovariectomized mice was higher than in non-pregnant females and oestrogen-treated ovariectomized mice. Current densities in late pregnancy were lower than in female controls. Progesterone had no effect on outward currents. A-type currents were decreased in non-pregnant females compared with ovariectomized mice, and were further decreased by pregnancy or oestrogen replacement. Kv 4.3 transcripts did not differ significantly between groups; however, expression of the potassium channel interacting protein KChIP1 was elevated in ovariectomized mice compared with female controls and oestrogen-treated ovariectomized mice. Delayed rectifier currents were not affected by oestrogen. In the mouse colon, oestrogen suppresses A-type currents, which are important for regulating excitability. These observations suggest a possible link between female hormones and altered colonic motility associated with menses, pregnancy and menopause.
特发性便秘在育龄女性中比绝经后女性或男性更为常见,这表明女性甾体激素会影响胃肠动力。女性激素如何影响胃肠动力尚不清楚。结肠动力受结肠肌细胞中的离子通道调节。电压依赖性钾通道可调节结肠肌肉的兴奋性。我们研究了女性激素急性或慢性变化时Kv 4.3通道表达的调节情况。采用膜片钳实验和定量PCR比较雄性、未孕、怀孕和去卵巢小鼠结肠肌细胞的外向电流和转录本表达。给去卵巢小鼠注射雌激素或孕酮,以研究激素替代的作用。未孕雌性小鼠结肠肌细胞的电容大于雄性小鼠。雄性和去卵巢小鼠的净外向电流密度高于未孕雌性小鼠和雌激素处理的去卵巢小鼠。妊娠晚期的电流密度低于雌性对照。孕酮对外向电流无影响。与去卵巢小鼠相比,未孕雌性小鼠的A型电流降低,妊娠或雌激素替代会使其进一步降低。各组间Kv 4.3转录本无显著差异;然而,与雌性对照和雌激素处理的去卵巢小鼠相比,去卵巢小鼠中钾通道相互作用蛋白KChIP1的表达升高。延迟整流电流不受雌激素影响。在小鼠结肠中,雌激素抑制对调节兴奋性很重要的A型电流。这些观察结果表明,女性激素与月经、妊娠和绝经相关的结肠动力改变之间可能存在联系。