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Elimination of the transient outward current and action potential prolongation in mouse atrial myocytes expressing a dominant negative Kv4 α subunit

机译:消除表达显性负Kv4α亚基的小鼠心房肌细胞的瞬时外向电流和动作电位延长

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class="enumerated" style="list-style-type:decimal">Analyses of whole-cell voltage-clamp recordings from isolated adult (C57BL6) mouse atrial myocytes reveal the presence of two prominent Ca2+-independent depolarization-activated K+ currents: a rapidly activating and inactivating, transient outward K+ current, Ito,f; and a non-inactivating, steady-state, K+ current, Iss.The properties of Ito,f and Iss in adult mouse atrial myocytes are similar to those of the analogous currents recently described in detail in adult mouse ventricular cells. A slowly inactivating K+ current, which is similar to IK,slow in ventricular cells, is detected in ≈40 % of adult mouse atrial myocytes, and when expressed, the density of this current component is substantially lower than the density of Ito,f or Iss.The similarity between atrial and ventricular Ito,f and the finding that both the Kv4 subfamily α subunits, Kv4.2 and Kv4.3, are expressed in wild-type mouse atria prompted us to determine if atrial Ito,f is affected in transgenic mice expressing a mutant Kv4.2 α subunit, Kv4.2W362F, that functions as a dominant negative.Similar to findings in ventricular cells, electrophysiological recordings reveal that Ito,f is selectively eliminated in atrial myocytes isolated from transgenic mice expressing Kv4.2W362F, thereby demonstrating directly that Kv4 subfamily members also underlie mouse atrial Ito,f.Neither the steady-state, non-inactivating K+ current Iss, nor the inwardly rectifying K+ current IK1, in atrial myocytes is affected by the expression of Kv4.2W362F.In contrast to previous findings in Kv4.2W362F-expressing mouse ventricular myocytes, there is no evidence that electrical remodelling occurs in atrial cells when Ito,f is functionally eliminated.The elimination of Ito,f is accompanied by marked increases in atrial action potential durations, although no electrocardiographic abnormalities attributable to, or suggestive of, altered atrial functioning are evident in Kv4.2W362F-expressing animals.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 对分离的成年(C57BL6)小鼠心房肌细胞进行全细胞电压钳记录的分析表明,存在两个突出的独立于Ca 2 + 的去极化激活的K + 电流:快速激活和灭活的瞬态向外K + 电流Ito,f;以及非灭活的稳态K + 电流Iss。 成年小鼠心房肌细胞Ito,f和Iss的性质与类似的最近在成年小鼠心室细胞中详细描述了电流。在约40%的成年小鼠心房肌细胞中检测到缓慢失活的K + 电流,类似于IK,在心室细胞中缓慢,并且在表达时,该电流成分的密度大大降低 心房和心室Ito,f之间的相似性以及发现Kv4亚家族α亚基Kv4.2和Kv4.3都在野生动物中表达的发现,类型的小鼠心房促使我们确定表达突变的Kv4.2α亚基Kv4.2W362F的转基因小鼠是否会影响心房Ito,f。 与心室细胞的发现相似,电生理记录表明,从表达Kv4.2W362F的转基因小鼠中分离出的心房肌细胞中Ito,f被选择性消除,从而直接证明Kv4亚家族成员也位于小鼠心房Ito,f的基础上。 这两个稳态都没有,非灭活的K + 当前Iss或向内整流的K + 当前的IK1,在心房肌细胞中受Kv4.2W362F表达的影响。 与先前在表达Kv4.2W362F的小鼠心室肌细胞中的发现相反,没有证据表明心房中发生电重构 消除Ito,f伴随着心房动作电位持续时间的显着增加,尽管没有明显的心电图异常归因于或暗示心房功能改变。表达Kv4.2W362F的动物。

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