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首页> 外文期刊>Pfluegers Archiv: European Journal of Physiology >Effects of sphingosine 1-phosphate on pacemaker activity in rabbit sino-atrial node cells.
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Effects of sphingosine 1-phosphate on pacemaker activity in rabbit sino-atrial node cells.

机译:1-磷酸鞘氨醇对兔窦房结细胞起搏器活性的影响。

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摘要

The effects of sphingosine 1-phosphate (S-1-P) on pacemaker activity and underlying membrane currents were studied in isolated rabbit sino-atrial (SA) node cells. S-1-P (0.1 microM) reversibly increased the cycle length of spontaneous pacemaker activity from 560 to 1434 ms, and hyperpolarized the maximal diastolic potential (MDP) from -67 to -70 mV. In voltage-clamp experiments, S-1-P (1 microM) activated a pertussis toxin-sensitive, inwardly-rectifying, time-independent K+ current (I(K,ACh)) that had a reversal potential of -88 mV (K+ equilibrium potential -86 mV). S-1-P (1 microM) had no measurable effect on the L-type Ca2+ current (I(Ca,L)) or the hyperpolarization-activated inward current (I(f)) under basal conditions. In the presence of the beta-adrenergic agonist, isoproterenol (ISO, 0.1 microM), S-1-P (1 microM) reversed the ISO-induced increase in pacing rate, hyperpolarized the MDP and decreased the ISO-induced enhancement of both I(Ca,L) (from 171 to 118% of control) and I(f) (from 211 to 135% of control). These results demonstrate that under basal conditions S-1-P can significantly slow spontaneous pacing in rabbit SA node cells mainly due to activation of a background, inwardly-rectifying K+ current. In the presence of ISO, S-1-P also slows the spontaneous pacing rate due to activation of the same K+ current, as well as inhibition of I(Ca,L) and I(f).
机译:在分离的兔窦房(SA)节点细胞中研究了1-磷酸鞘氨醇(S-1-P)对起搏器活性和潜在膜电流的影响。 S-1-P(0.1 microM)可逆地将自发性起搏器活动的周期长度从560毫秒增加到1434毫秒,并将最大舒张电位(MDP)从-67极化到-70毫伏。在电压钳实验中,S-1-P(1 microM)激活了百日咳毒素敏感,向内整流,时间独立的K +电流(I(K,ACh)),其反向电位为-88 mV(K +平衡电位-86 mV)。在基础条件下,S-1-P(1 microM)对L型Ca2 +电流(I(Ca,L))或超极化激活的内向电流(I(f))没有可测量的影响。在β-肾上腺素能激动剂异丙肾上腺素(ISO,0.1 microM),S-1-P(1 microM)逆转ISO引起的起搏率增加,MDP超极化并降低ISO引起的I增强(Ca,L)(从对照的171%至118%)和I(f)(从对照的211%至135%)。这些结果表明,在基础条件下,S-1-P可以显着减缓兔SA结节细胞的自发起搏,这主要是由于激活了背景,向内整流的K +电流。在存在ISO的情况下,S-1-P也会由于激活相同的K +电流以及抑制I(Ca,L)和I(f)而减慢自发起搏速度。

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