首页> 美国卫生研究院文献>The Journal of Physiology >Inhibitory effect of muscarinic receptor activation on Ca2+ channel current in smooth muscle cells of guinea-pig ileum.
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Inhibitory effect of muscarinic receptor activation on Ca2+ channel current in smooth muscle cells of guinea-pig ileum.

机译:毒蕈碱受体激活对豚鼠回肠平滑肌细胞Ca2 +通道电流的抑制作用。

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摘要

1. The effect of muscarinic receptor stimulation on voltage-gated calcium channel currents was examined in whole-cell voltage-clamped smooth muscle cells of the guinea-pig ileum. 2. In cells voltage clamped at -60 mV and in which calcium channel currents (ICa) were elicited repeatedly by depolarizing pulses (25 ms duration, 0.25 Hz frequency) to 0 mV, carbachol (CCh, 10 microM) induced an inward current (ICCh) and were suppressed ICa, in a biphasic manner; an initial transient component was followed by a more sustained one. 3. A calcium channel current (IBa), when Ba2+ was used as a charge carrier, was also suppressed by CCh in a biphasic manner, as with ICa. The sustained phase of the IBa suppression was significantly smaller than that of the ICa suppression, suggesting that Ca2+ entry exerts a potentiating effect on the current suppression. 4. CCh had little or no effect on calcium channel currents (ICa and IBa) in cells dialysed with a pipette solution containing EGTA (20 mM). 5. Inclusion of GDP-beta-S (1 mM) in the pipette solution abolished ICCh and the suppression of IBa. With GTP-gamma-S (10 microM) in the pipette, the sustained phase of the IBa suppression remained almost unchanged even after removal of CCh. 6. Pretreatment with 2 micrograms ml-1 pertussis toxin (PTX), which abolished ICCh, did not change noticeably the initial transient and sustained phases of IBa suppression. 7. Neomycin (100 microM) or heparin (5 mg ml-1) in the pipette each abolished the initial transient component of ICCh as well as the initial transient phase of IBa suppression. 8. The biphasic effect of CCh on IBa was observed in the presence of either staurosporine (1 microM) or 1-(5-isoquinolinesulphonyl)-2-methylpiperazine (100 microM). Phorbol 12-myristate 13-acetate and phorbol 12,13-dibutyrate (up to 10 microM) had no inhibitory effect on ICa and IBa. 9. The results suggest that stimulation of the muscarinic receptor causes a biphasic suppression of the voltage-gated calcium channel currents through a PTX-insensitive G protein in guinea-pig ileal smooth muscle cells. The initial transient phase may be brought about by the release of Ca2+ from internal storage sites, and the sustained phase by a Ca(2+)-dependent mechanism which is independent of the phosphatidylinositol pathway.
机译:1.在豚鼠回肠全细胞电压钳制的平滑肌细胞中检测了毒蕈碱受体刺激对电压门控钙通道电流的影响。 2.在电压固定在-60 mV的电池中,其中通过去极化脉冲(持续时间25 ms,频率0.25 Hz)重复激发钙通道电流(ICa)至0 mV,卡巴胆碱(CCh,10 microM)感应向内电流( ICCh)和被抑制的ICa,处于双相状态;最初的瞬态分量之后是持续的分量。 3.当将Ba2 +用作电荷载体时,钙离子通道电流(IBa)也像ICa一样被CCh以双相方式抑制。 IBa抑制的持续阶段显着小于ICa抑制的持续阶段,表明Ca2 +的进入对电流抑制产生了增强作用。 4. CCh对用含EGTA(20 mM)的移液器透析的细胞中的钙通道电流(ICa和IBa)几乎没有影响。 5.在移液器中加入GDP-β-S(1 mM)消除了ICCh和IBa的抑制。用移液管中的GTP-γ-S(10 microM),即使去除了CCh,IBa抑制的持续阶段也几乎保持不变。 6.取消了ICCh的2微克ml-1百日咳百日咳毒素(PTX)进行的预处理并未明显改变IBa抑制的初始瞬时和持续阶段。 7.移液器中的新霉素(100 microM)或肝素(5 mg ml-1)均消除了ICCh的初始瞬时组分以及IBa抑制的初始瞬时阶段。 8.在星形孢菌素(1 microM)或1-(5-异喹啉磺酰基)-2-甲基哌嗪(100 microM)存在下,观察到CCh对IBa的双相作用。佛波醇12-肉豆蔻酸酯13-醋酸酯和佛波醇12,13-二丁酸酯(最高10 microM)对ICa和IBa没有抑制作用。 9.结果表明,对毒蕈碱受体的刺激通过豚鼠回肠平滑肌细胞中的PTX不敏感G蛋白引起电压门控钙通道电流的双相抑制。初始瞬态阶段可能是由内部存储位置释放的Ca2 +引起的,而持续阶段则是由独立于磷脂酰肌醇途径的Ca(2+)依赖性机制引起的。

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