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KB-R7943 及肌浆网 Ca(2+)ATP 酶抑制剂对兔房室结细胞自发性活动的抑制作用。

Inhibition of spontaneous activity of rabbit atrioventricular node cells by KB-R7943 and inhibitors of sarcoplasmic reticulum Ca(2+) ATPase.

机构信息

School of Physiology and Pharmacology, Medical Sciences Building, University of Bristol, UK.

出版信息

Cell Calcium. 2011 Jan;49(1):56-65. doi: 10.1016/j.ceca.2010.11.008. Epub 2010 Dec 15.

DOI:10.1016/j.ceca.2010.11.008
PMID:21163524
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3048929/
Abstract

The atrioventricular node (AVN) can act as a subsidiary cardiac pacemaker if the sinoatrial node fails. In this study, we investigated the effects of the Na-Ca exchange (NCX) inhibitor KB-R7943, and inhibition of the sarcoplasmic reticulum calcium ATPase (SERCA), using thapsigargin or cyclopiazonic acid (CPA), on spontaneous action potentials (APs) and Ca(2+) transients from cells isolated from the rabbit AVN. Spontaneous Ca(2+) transients were monitored from undialysed AVN cells at 37°C using Fluo-4. In separate experiments, spontaneous APs and ionic currents were recorded using the whole-cell patch clamp technique. Rapid application of 5 μM KB-R7943 slowed or stopped spontaneous APs and Ca(2+) transients. However, in voltage clamp experiments in addition to blocking NCX current (I(NCX)) KB-R7943 partially inhibited L-type calcium current (I(Ca,L)). Rapid reduction of external [Na(+)] also abolished spontaneous activity. Inhibition of SERCA (using 2.5 μM thapsigargin or 30 μM CPA) also slowed or stopped spontaneous APs and Ca(2+) transients. Our findings are consistent with the hypothesis that sarcoplasmic reticulum (SR) Ca(2+) release influences spontaneous activity in AVN cells, and that this occurs via Ca(2+)-activated I(NCX); however, the inhibitory action of KB-R7943 on I(Ca,L) means that care is required in the interpretation of data obtained using this compound.

摘要

房室结 (AVN) 在窦房结失功时可作为辅助性心脏起搏器。在本研究中,我们研究了钠钙交换 (NCX) 抑制剂 KB-R7943 的作用,以及使用 thapsigargin 或环匹阿尼酸 (CPA) 抑制肌浆网钙 ATP 酶 (SERCA) 对兔 AVN 细胞分离的自发性动作电位 (AP) 和 Ca(2+) 瞬变的影响。使用 Fluo-4 在 37°C 下从未透析的 AVN 细胞中监测自发性 Ca(2+) 瞬变。在单独的实验中,使用全细胞膜片钳技术记录自发性 AP 和离子电流。快速应用 5 μM KB-R7943 会减缓或停止自发性 AP 和 Ca(2+) 瞬变。然而,在电压钳实验中,除了阻断 NCX 电流 (I(NCX)) 外,KB-R7943 还部分抑制 L 型钙电流 (I(Ca,L))。快速降低细胞外 [Na(+)] 也会消除自发性活动。SERCA 抑制(使用 2.5 μM thapsigargin 或 30 μM CPA)也会减缓或停止自发性 AP 和 Ca(2+) 瞬变。我们的发现与以下假说一致,即肌浆网 (SR) Ca(2+) 释放影响 AVN 细胞的自发性活动,并且这种作用是通过 Ca(2+)-激活的 I(NCX) 实现的;然而,KB-R7943 对 I(Ca,L) 的抑制作用意味着在使用该化合物获得的数据解释中需要谨慎。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4e3/3048929/704db4b752cc/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4e3/3048929/f8224f3e39f1/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4e3/3048929/0c31689e9eea/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4e3/3048929/3b090aeae982/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4e3/3048929/704db4b752cc/gr4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4e3/3048929/f8224f3e39f1/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4e3/3048929/0c31689e9eea/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4e3/3048929/3b090aeae982/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b4e3/3048929/704db4b752cc/gr4.jpg

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