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POTENTIAL, IMPEDANCE, AND RECTIFICATION IN MEMBRANES.膜的电位、阻抗和整流。
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The effect of sodium ions on the electrical activity of giant axon of the squid.钠离子对鱿鱼巨大轴突电活动的影响。
J Physiol. 1949 Mar 1;108(1):37-77. doi: 10.1113/jphysiol.1949.sp004310.
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The dual effect of membrane potential on sodium conductance in the giant axon of Loligo.枪乌贼巨大轴突中膜电位对钠电导的双重作用。
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Spike potentials recorded from the insect photoreceptor.从昆虫光感受器记录到的锋电位。
J Gen Physiol. 1962 Mar;45(4):663-80. doi: 10.1085/jgp.45.4.663.
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Graded and all-or-none electrogenesis in arthropod muscle. II. The effects of alkali-earth and onium ions on lobster muscle fibers.节肢动物肌肉中的分级和全或无电发生。II. 碱土金属离子和鎓离子对龙虾肌肉纤维的影响。
J Gen Physiol. 1961 May;44(5):997-1027. doi: 10.1085/jgp.44.5.997.
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The ionic requirements for the production of action potentials in crustacean muscle fibres.甲壳类动物肌肉纤维中动作电位产生的离子需求。
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7
Surface density of calcium ions and calcium spikes in the barnacle muscle fiber membrane.藤壶肌纤维膜中钙离子的表面密度和钙尖峰
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Differences in Na and Ca spikes as examined by application of tetrodotoxin, procaine, and manganese ions.通过应用河豚毒素、普鲁卡因和锰离子检测钠峰和钙峰的差异。
J Gen Physiol. 1966 Mar;49(4):793-806. doi: 10.1085/jgp.49.4.793.
9
Image formation by a concave reflector in the eye of the scallop, Pecten maximus.扇贝(大扇贝)眼中凹面反射镜的成像。
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10
Slow and spike potentials recorded from retinula cells of the honeybee drone in response to light.从蜜蜂雄蜂小眼细胞记录到的对光反应的慢电位和锋电位。
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钙和钾通透性变化对扇贝超极化光感受器关闭反应的作用。

Contribution of calcium and potassium permeability changes to the off response of scallop hyperpolarizing photoreceptors.

作者信息

Cornwall M C, Gorman A L

出版信息

J Physiol. 1979 Jun;291:207-232. doi: 10.1113/jphysiol.1979.sp012808.

DOI:10.1113/jphysiol.1979.sp012808
PMID:480206
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1280896/
Abstract
  1. The membrane response of the distal photoreceptors in the retina of the scallop Pectin irradians to the termination of a bright white light (off response) is shown to be composed of the decay of the hyperpolarizing receptor potential and an action potential with slow kinetics. 2. The action potential can be produced in darkness in the absence of external Na+ ions by membrane depolarization. 3. The action potential is maintained by replacement of external Ca2+ with Sr2+ or Ba2+, but not by Mg2+. In normal external Ca2+ (9mM), the action potential is abolished by the addition of the Ca2+ inhibitors, La3+, Co2+, and Mn2+ or the organic Ca2+ antagonist D-600. 4. Elevated external Ca2+ concentrations increase the rate of rise and peak amplitude of the action potential as well as the rate of repolarization and after hyperpolarization, but decrease the duration. 5. The rate of rise and peak amplitude of the action potential are increased by the K+ antagonists tetraethylammonium (TEA) 4-amino-phyridine (4-AP), Ba2+ and procaine. The antagonists have different effects on subsequent phases of the response, however. External TEA and Ba2+ increase the duration, but decrease the rate of repolarization and abolish the after hyperpolarization, whereas external 4-AP and procaine increase the rate of repolarization, decrease the duration and increase the after hyperpolarization. 6. The ratio of the Ca2+ to K+ permeability (P Ca/P K) estimated from the constant field equation at the peak of the action potential in different external Ca2+ concentrations is close to 1. 7. The maximum rate of rise and the peak amplitude of the action potential are increased by membrane hyperpolarization and decreased by membrane depolarization. They are decreased by background light intensity relative to their value in the dark. 8. In normal ASW the action potential can be identified during the off response as a small overshoot of membrane potential relative to its value in the dark. 9. The rate of repolarization of the off response in normal ASW is reduced by agents or conditions which inhibit or reduce Ca2+ permeability changes, e.g. external Co2+ and La2+ or zero external Ca2+. 10. Our results suggest that a voltage-dependent increase in membrane permeability to Ca2+ and to K+ ions modifies the repolarizing phase of the receptor potential.
摘要
  1. 已证明,扇贝辐射海扇视网膜中远端光感受器对明亮白光终止(关闭反应)的膜反应由超极化感受器电位的衰减和具有缓慢动力学的动作电位组成。2. 在黑暗中,在没有外部钠离子的情况下,通过膜去极化可产生动作电位。3. 用锶离子或钡离子替代外部钙离子可维持动作电位,但镁离子不能。在正常外部钙离子浓度(9毫摩尔)下,添加钙离子抑制剂镧离子、钴离子和锰离子或有机钙离子拮抗剂D - 600可消除动作电位。4. 外部钙离子浓度升高会增加动作电位的上升速率和峰值幅度以及复极化速率和超极化后电位,但会缩短动作电位持续时间。5. 钾离子拮抗剂四乙铵(TEA)、4 - 氨基吡啶(4 - AP)、钡离子和普鲁卡因会增加动作电位的上升速率和峰值幅度。然而,这些拮抗剂对反应的后续阶段有不同影响。外部TEA和钡离子会增加动作电位持续时间,但会降低复极化速率并消除超极化后电位,而外部4 - AP和普鲁卡因会增加复极化速率,缩短动作电位持续时间并增加超极化后电位。6. 根据恒定场方程在不同外部钙离子浓度下动作电位峰值处估算的钙离子与钾离子通透性之比(P Ca/P K)接近1。7. 膜超极化会增加动作电位的最大上升速率和峰值幅度,膜去极化则会降低它们。相对于黑暗中的值,背景光强度会降低它们。8. 在正常人工海水(ASW)中,动作电位在关闭反应期间可被识别为相对于黑暗中膜电位的一个小的超调。9. 在正常ASW中,关闭反应的复极化速率会被抑制或降低钙离子通透性变化的试剂或条件所降低,例如外部钴离子和镧离子或零外部钙离子。1​​0. 我们的结果表明,膜对钙离子和钾离子通透性的电压依赖性增加会改变感受器电位的复极化阶段。