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High selectivity of calcium channels in single dialysed heart cells of the guinea-pig.

机译:豚鼠的单个透析心脏细胞中钙通道的选择性高。

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摘要

Membrane currents and action potentials were recorded in single ventricular cells obtained from guinea-pig hearts by enzymatic dissociation. Ca2+ channel currents carried by Ba2+ or Ca2+ were recorded with a suction pipette (5-10 microns diameter) for voltage clamp and internal dialysis. Currents through Na+, K+ and non-selective monovalent cation channels were suppressed by suitable holding potentials and external and internal solutions. The dialysis method allowed exchange within minutes of alkali metal cations (e.g. Cs+) and small molecules (e.g. quaternary derivatives of lidocaine and verapamil). Nevertheless, Ca2+ channels remained functional for considerable periods, typically 20 min and sometimes more than 1 h. With Ba2+ outside and Cs+ inside, current flow through Ca2+ channels changed from inward to outward at strongly positive levels beyond a clear-cut reversal potential Erev. Several methods for defining Erev were in close agreement: (1) zero-crossing of leak-subtracted peak current, (2) inversion of time-dependent current changes during channel activation or inactivation, (3) inversion of drug-sensitive current as defined by channel blockers such as Cd2+ or D-600. Erev varied with external Ba2+ or internal Cs+. Erev increased by 29 mV per 10-fold increase in Ba2+. Interpreted with constant-field theory, Erev values correspond to PBa/PCs of approximately 1360. With 5 mM-Ca2+ outside and 151 mM-Cs+ inside, Ca2+ channel current reversed near + 75 mV, corresponding to PCa/PCs approximately 6000. Earlier measurements of Erev (Lee & Tsien, 1982) suggest that PCa/PK greater than 1000. At strongly positive membrane potentials where channel activation is maximal, the Ca2+ channel current-voltage relationship is strongly non-linear, with conductance increasing on either side of an inflexion point near Erev. Activation of inward or outward currents through Ca2+ channels follows a sigmoid time course, as expected if activation were a multi-step process.
机译:在通过酶解从豚鼠心脏获得的单个心室细胞中记录了膜电流和动作电位。用吸管(直径5-10微米)记录Ba2 +或Ca2 +携带的Ca2 +通道电流,以进行电压钳和内部透析。通过Na +,K +和非选择性单价阳离子通道的电流被合适的保持电位以及内部和内部溶液抑制。透析方法允许在几分钟之内交换碱金属阳离子(例如Cs +)和小分子(例如利多卡因和维拉帕米的季衍生物)。然而,Ca 2+通道在相当长的一段时间(通常为20分钟,有时超过1小时)内仍保持功能。在外部有Ba2 +且内部有Cs +的情况下,流经Ca2 +通道的电流以很强的正向电平从内向外变化,超过了明显的反转电位Erev。定义Erev的几种方法非常吻合:(1)减去泄漏的峰值电流的过零;(2)在通道激活或失活期间随时间变化的电流变化的反转;(3)所定义的药物敏感电流的反转通过通道阻止器(例如Cd2 +或D-600)。 Erev因外部Ba2 +或内部Cs +而异。每增加10倍Ba2 +,Erev就会增加29 mV。用恒定场理论解释,Erev值对应于大约1360的PBa / PCs。在外部5 mM-Ca2 +和内部151 mM-Cs +的情况下,Ca2 +通道电流反向+75 mV,对应于大约6000的PCa / PCs。 Erev(Lee&Tsien,1982)的研究表明,PCa / PK大于1000。在膜活化极强且通道激活最大的情况下,Ca2 +通道电流-电压关系呈非线性,电导率在任一侧增加。 Erev附近的拐点。如果激活是一个多步骤过程,则可以预期,通过Ca2 +通道的向内或向外电流的激活遵循S型时间过程。

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