Hedlund B, Arhem P, Lorentz M, Sydbom A
Acta Physiol Scand. 1986 May;127(1):127-32. doi: 10.1111/j.1748-1716.1986.tb07884.x.
Membrane effects of scopolamine on N1E-115 neuroblastoma cells were studied using intracellular recording techniques. Scopolamine in concentrations of 50 nM-1 microM induced a depolarization together with a decreased cell input resistance. This response had a reversal potential at +10 to +20 mV in a medium with normal sodium concentration (146.5 mM), and a reversal potential around -10 mV when the sodium concentration in the medium was lowered to 80 mM. The scopolamine-induced depolarization could not be blocked by carbachol (100 microM), and had a reversal potential at +10 to +20 mV. The simplest explanation of the results obtained is that scopolamine increases the membrane permeability for sodium and potassium, in a manner which is not related to muscarinic cholinergic receptors.
利用细胞内记录技术研究了东莨菪碱对N1E-115神经母细胞瘤细胞的膜效应。浓度为50 nM - 1 μM的东莨菪碱可引起去极化,并伴有细胞输入电阻降低。在正常钠浓度(146.5 mM)的培养基中,该反应的反转电位为 +10至 +20 mV,而当培养基中的钠浓度降至80 mM时,反转电位约为 -10 mV。东莨菪碱诱导的去极化不能被卡巴胆碱(100 μM)阻断,其反转电位为 +10至 +20 mV。对所得结果最简单的解释是,东莨菪碱以与毒蕈碱胆碱能受体无关的方式增加了膜对钠和钾的通透性。