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本文引用的文献

1
Membrane mechanism associated with muscarinic receptor activation in single cells freshly dispersed from the rat anococcygeus muscle.从大鼠肛门尾骨肌新鲜分离的单细胞中与毒蕈碱受体激活相关的膜机制。
Br J Pharmacol. 1987 Oct;92(2):371-9. doi: 10.1111/j.1476-5381.1987.tb11333.x.
2
A calcium-dependent rather than a G-protein mechanism is involved in the inward current evoked by muscarinic receptor stimulation in dialysed single smooth muscle cells of small intestine.在小肠透析的单个平滑肌细胞中,毒蕈碱受体刺激诱发的内向电流涉及一种钙依赖性机制,而非G蛋白机制。
Br J Pharmacol. 1988 Oct;95(2):325-7. doi: 10.1111/j.1476-5381.1988.tb11649.x.
3
Are junction potentials essential? Dual mechanism of smooth muscle cell activation by transmitter released from autonomic nerves.结电位是必不可少的吗?自主神经释放的递质激活平滑肌细胞的双重机制。
Q J Exp Physiol. 1986 Jan;71(1):1-28. doi: 10.1113/expphysiol.1986.sp002960.
4
ATP-activated channels gate calcium entry in single smooth muscle cells dissociated from rabbit ear artery.ATP激活的通道控制着从兔耳动脉分离出的单个平滑肌细胞中的钙内流。
J Physiol. 1989 Dec;419:689-701. doi: 10.1113/jphysiol.1989.sp017893.
5
Membrane ionic mechanisms activated by noradrenaline in cells isolated from the rabbit portal vein.去甲肾上腺素激活兔门静脉分离细胞中的膜离子机制。
J Physiol. 1988 Oct;404:557-73. doi: 10.1113/jphysiol.1988.sp017306.
6
Muscarinic activation of ionic currents measured by a new whole-cell recording method.通过一种新的全细胞记录方法测量的毒蕈碱对离子电流的激活作用。
J Gen Physiol. 1988 Aug;92(2):145-59. doi: 10.1085/jgp.92.2.145.
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Acetylcholine activates single sodium channels in smooth muscle cells.乙酰胆碱激活平滑肌细胞中的单个钠通道。
Pflugers Arch. 1987 Sep;410(1-2):69-74. doi: 10.1007/BF00581898.
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Action of noradrenaline on single smooth muscle cells freshly dispersed from the rat anococcygeus muscle.去甲肾上腺素对从大鼠肛门尾骨肌新鲜分离的单个平滑肌细胞的作用。
J Physiol. 1987 Aug;389:513-25. doi: 10.1113/jphysiol.1987.sp016669.
9
Acetylcholine activates an inward current in single mammalian smooth muscle cells.乙酰胆碱可激活单个哺乳动物平滑肌细胞中的内向电流。
Nature. 1985;316(6026):345-7. doi: 10.1038/316345a0.
10
Effect of membrane potential on acetylcholine-induced inward current in guinea-pig ileum.膜电位对豚鼠回肠中乙酰胆碱诱导的内向电流的影响。
J Physiol. 1990 May;424:57-71. doi: 10.1113/jphysiol.1990.sp018055.

用制霉菌素全细胞法在兔门静脉细胞中记录的去甲肾上腺素诱发的阳离子电导。

Noradrenaline-evoked cation conductance recorded with the nystatin whole-cell method in rabbit portal vein cells.

作者信息

Wang Q, Large W A

机构信息

Department of Pharmacology, St. George's Hospital Medical School, London.

出版信息

J Physiol. 1991 Apr;435:21-39. doi: 10.1113/jphysiol.1991.sp018496.

DOI:10.1113/jphysiol.1991.sp018496
PMID:1770436
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1181448/
Abstract
  1. Noradrenaline-evoked currents were studied with the perforated patch technique (nystatin in the patch pipette) in freshly dispersed rabbit portal vein cells. 2. With potassium-containing solutions noradrenaline produced an inward current at -50 mV and an outward current (IK(Ca] at 0 mV. In potassium-free conditions noradrenaline elicited two distinct membrane currents which could be differentiated according to their sensitivity to the presence of caffeine in the bathing solution. One current was blocked whereas the second response was unaffected by caffeine. 3. The reversal potential (Er = -2.0 mV) of the caffeine-sensitive current was altered when external chloride was replaced with more permeant anions but Er was not changed when external sodium was replaced by Tris. Therefore the caffeine-sensitive current appears to be a calcium-activated chloride current (ICl(Ca]. 4. Er (+6.0 mV) of the caffeine-insensitive current was not altered by anion substitution but was changed when external sodium was replaced by Tris and barium ions. Thus the caffeine-insensitive conductance is a non-selective cation current (Icat). 5. When external NaCl was replaced by BaCl2, Er was shifted to more positive potentials which suggests that the cation conductance is more permeable to barium than to sodium. Icat was not affected by 10(-6) M-nifedipine. 6. The steady-state current-voltage relationship was linear between -50 and +50 mV for ICl(Ca) but the cation conductance mechanism displayed pronounced inward rectification and little outward current flowed across the membrane at positive potentials. 7. Caffeine (which releases calcium from internal stores) and the calcium ionophore ionomycin, which are expected to increase intracellular calcium concentration, evoked ICl(Ca) but not Icat. Thus ICl(Ca) but not Icat can be activated directly by an increase in intracellular calcium concentration. 8. When calcium was removed from the bathing solution the amplitude of Icat was not altered at early times in Ca(2+)-free conditions but was abolished after 10 min. Icat was readily activated by noradrenaline in the presence of ionomycin, which inactivated ICl(Ca). A permissive role for calcium in the generation of Icat is suggested. 9. The times between the application of noradrenaline and the onset of the chloride and cationic conductances were similar (0.75 and 0.9 s respectively). In contrast the rise time (3.9 s) and half-decay time (11 s) of Icat were much longer than the corresponding values of ICl(Ca) (respectively 1.9 and 2 s). In high-barium solution noradrenaline sometimes evoked a response that lasted for up to 10 min.(ABSTRACT TRUNCATED AT 400 WORDS)
摘要
  1. 采用穿孔膜片钳技术(膜片电极内加入制霉菌素),在新鲜分离的兔门静脉细胞中研究去甲肾上腺素诱发的电流。2. 在含钾溶液中,去甲肾上腺素在-50 mV时产生内向电流,在0 mV时产生外向电流(IK(Ca))。在无钾条件下,去甲肾上腺素引发两种不同的膜电流,可根据它们对浴液中咖啡因存在的敏感性进行区分。一种电流被阻断,而第二种反应不受咖啡因影响。3. 当外部氯离子被更易通透的阴离子取代时,咖啡因敏感电流的反转电位(Er = -2.0 mV)发生改变,但当外部钠离子被 Tris 取代时,Er 不变。因此,咖啡因敏感电流似乎是一种钙激活氯电流(ICl(Ca))。4. 咖啡因不敏感电流的 Er(+6.0 mV)不受阴离子取代的影响,但当外部钠离子被 Tris 和钡离子取代时发生改变。因此,咖啡因不敏感电导是一种非选择性阳离子电流(Icat)。5. 当外部 NaCl 被 BaCl2 取代时,Er 向更正电位移动,这表明阳离子电导对钡的通透性比对钠更高。Icat 不受 10(-6) M硝苯地平的影响。6. ICl(Ca)在-50 至+50 mV之间的稳态电流-电压关系呈线性,但阳离子电导机制表现出明显的内向整流特性,在正电位时几乎没有外向电流通过膜。7. 咖啡因(从内部储存库释放钙)和钙离子载体离子霉素,预期会增加细胞内钙浓度,诱发 ICl(Ca)但不诱发 Icat。因此,ICl(Ca)而非 Icat 可直接由细胞内钙浓度的增加激活。8. 当从浴液中去除钙时,在无钙条件下早期 Icat 的幅度未改变,但 10 分钟后被消除。在离子霉素存在下,去甲肾上腺素很容易激活 Icat,而离子霉素使 ICl(Ca)失活。提示钙在 Icat 的产生中起允许作用。9. 去甲肾上腺素施加与氯和阳离子电导开始之间的时间相似(分别为 0.75 和 0.9 秒)。相比之下,Icat 的上升时间(3.9 秒)和半衰期(11 秒)比 ICl(Ca)的相应值长得多(分别为 1.9 和 2 秒)。在高钡溶液中,去甲肾上腺素有时会诱发持续长达 10 分钟的反应。(摘要截断于 400 字)