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Role of calcium stores and membrane voltage in the generation of slow wave action potentials in guinea-pig gastric pylorus

机译:钙储存和膜电压在豚鼠胃幽门慢波动作电位产生中的作用

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class="enumerated" style="list-style-type:decimal">Intracellular recordings made in single bundle strips of a visceral smooth muscle revealed rhythmic spontaneous membrane depolarizations termed slow waves (SWs). These exhibited ‘pacemaker’ and ‘regenerative’ components composed of summations of more elementary events termed spontaneous transient depolarizations (STDs).STDs and SWs persisted in the presence of tetrodotoxin, nifedipine and ryanodine, and upon brief exposure to Ca2+-free Cd2+-containing solutions; they were enhanced by ACh and blocked by BAPTA AM, cyclopiazonic acid and caffeine. SWs were also inhibited in heparin-loaded strips.SWs were observed over a wide range of membrane potentials (e.g. −80 to −45 mV) with increased frequencies at more depolarized potentials.Regular spontaneous SW activity in this preparation began after 1–3 h superfusion of the tissue with physiological saline following the dissection procedure. Membrane depolarization applied before the onset of this activity induced bursts of STD-like events (termed the ‘initial’ response) which, when larger than threshold levels initiated regenerative responses. The combined initial-regenerative waveform was termed the SW-like action potential.Voltage-induced responses exhibited large variable latencies (typical range 0.3–4 s), refractory periods of ≈11 s and a pharmacology that was indistinguishable from those of STDs and spontaneous SWs.The data indicate that SWs arise through more elementary inositol 1,4,5-trisphosphate (IP3) receptor-induced Ca2+ release events which rhythmically synchronize to trigger regenerative Ca2+ release and induce inward current across the plasmalemma. The finding that action potentials, which were indistinguishable from SWs, could be evoked by depolarization suggests that membrane potential modulates IP3 production. Voltage feedback on intracellular IP3-sensitive Ca2+ release is likely to have a major influence on the generation and propagation of SWs.
机译:class =“ enumerated” style =“ list-style-type:decimal”> <!-list-behavior =枚举前缀-word = mark-type = decimal max-label-size = 0-> 在内脏平滑肌的单束条带中进行的细胞内记录显示,节奏性自发性膜去极化称为慢波(SW)。这些表现出“起搏器”和“再生”成分,这些成分由更多的基本事件的总和构成,称为自发性瞬时去极化(STD)。 STD和SW在存在河豚毒素,硝苯地平和利诺丹碱的情况下以及在短暂暴露下均持续存在。到不含Ca 2 + 的Cd 2 + 溶液;它们被ACh增强,并被BAPTA AM,环吡嗪酸和咖啡因阻断。在载有肝素的条带中,SW也受到抑制。 在宽范围的膜电位(例如-80至-45 mV)上观察到的SWs随去极化电位的增加而增加。
  • 解剖过程中,在组织中加入生理盐水1–3 h后,该制剂中的常规自发性SW活性开始。在此活动开始之前应用膜去极化会诱发性病样事件的爆发(称为“初始”反应),当大于阈值水平时会引发再生反应。合并的初始再生波形称为SW样动作电位。 电压诱导的反应表现出较大的潜伏期(典型范围为0.3–4 s),不应期为≈11s,药理学为 数据表明,SW通过更多的基本肌醇1,4,5-三磷酸(IP3)受体诱导的Ca 2 + 释放而产生。节律性同步事件触发再生的Ca 2 + 释放并诱导跨质膜的内向电流。可以通过去极化诱发与SW难以区分的动作电位的发现表明膜电位调节IP3的产生。细胞内对IP3敏感的Ca 2 + 释放的电压反馈可能对SW的产生和传播产生重大影响。
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