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环磷酸腺苷(cAMP)对兔窦房结单个超极化激活通道(I(f))的调节作用

Modulation of single hyperpolarization-activated channels (i(f)) by cAMP in the rabbit sino-atrial node.

作者信息

DiFrancesco D, Mangoni M

机构信息

Università di Milano, Dipartimento di Fisiologia e Biochimica Generali, Elettrofisiologia, Italy.

出版信息

J Physiol. 1994 Feb 1;474(3):473-82. doi: 10.1113/jphysiol.1994.sp020038.

Abstract
  1. The hyperpolarization-activated 'pacemaker' current (i(f)) was recorded in inside-out patches excised from rabbit sino-atrial (SA) node cell membranes. 2. Single-channel activity could be resolved in patches containing only a few channels; the voltage dependence of single-channel size and single-channel conductance (0.97 pS) were similar to those measured previously in cell-attached conditions. 3. Perfusion of the intracellular side of the patch membrane with 10 microM cAMP facilitated the opening of single i(f) channels on hyperpolarization. The cAMP-induced i(f) current activation occurred without modification of the single-channel conductance. 4. Modification by cAMP of the probability of channel opening was investigated with respect to the latency to first opening during hyperpolarization and in patches containing a large number of channels (macro-patches). First-latency histograms showed that cAMP shifts the probability curve of first openings to shorter times, in agreement with a cAMP-induced facilitation of channel opening. In macro-patches, measurement of the voltage dependence of the open probability by a slow voltage ramp protocol showed that cAMP shifts the probability curve to more positive voltages without modifying its shape. 5. In cell-free macro-patches the normalized open probability curve in control solutions was centred around -121.9 mV, a voltage some 30 mV more negative than in cell-attached macro-patches. Negative shifting of the curve after patch excision could only partly be explained by the removal of intracellular cAMP, and progressed with time during the ramp protocol, suggesting the presence of a run-down process independent from cAMP.
摘要
  1. 从兔窦房(SA)结细胞膜上切下的内向外膜片中记录到超极化激活的“起搏”电流(i(f))。2. 在仅含有少数通道的膜片中可分辨出单通道活性;单通道大小和单通道电导(0.97 pS)的电压依赖性与先前在细胞贴附条件下测得的相似。3. 用10 microM cAMP灌注膜片的细胞内侧,可促进超极化时单个i(f)通道的开放。cAMP诱导的i(f)电流激活发生时,单通道电导未发生改变。4. 针对超极化期间首次开放的延迟以及含有大量通道的膜片(大膜片),研究了cAMP对通道开放概率的影响。首次延迟直方图显示,cAMP将首次开放的概率曲线移至更短时间,这与cAMP诱导的通道开放促进作用一致。在大膜片中,通过缓慢电压斜坡协议测量开放概率的电压依赖性表明,cAMP将概率曲线移至更正的电压,而不改变其形状。5. 在无细胞大膜片中,对照溶液中的归一化开放概率曲线以-121.9 mV为中心,该电压比细胞贴附大膜片中的电压约负30 mV。膜片切除后曲线的负向移动只能部分由细胞内cAMP的去除来解释,并且在斜坡协议期间随时间进展,表明存在独立于cAMP的衰减过程。

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