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挥发性麻醉剂对大鼠小脑颗粒细胞单个钾通道的激活作用。

Activation of single potassium channels in rat cerebellar granule cells by volatile anesthetics.

作者信息

Winegar B D, Yost C S

机构信息

Department of Anesthesia, University of California, San Francisco 94143-0648, USA.

出版信息

Toxicol Lett. 1998 Nov 23;100-101:287-91. doi: 10.1016/s0378-4274(98)00197-0.

Abstract
  1. We recently reported that volatile anesthetics activate a potassium channel (S channel) in neurons of the marine mollusk, Aplysia (Winegar et al., 1996. Anesthesiology 85(4) 889-900). 2. These studies were extended to investigate volatile anesthetic actions on potassium channels in rat cerebellar granule cells. 3. Noninactivating potassium channels were observed across a wide range of potentials. 4. Channel activity increased during volatile anesthetic perfusion while the i-V relations were unchanged and remained weakly inward-rectifying with a conductance at negative potentials of approximately 30 pS. 5. Frequent opening of inward rectifiers by volatile anesthetics may stabilize the resting potential near E(K) to resist depolarizing stimuli.
摘要
  1. 我们最近报道,挥发性麻醉剂可激活海洋软体动物海兔神经元中的一种钾通道(S通道)(Winegar等人,1996年。《麻醉学》85(4) 889 - 900)。2. 这些研究得以扩展,以探究挥发性麻醉剂对大鼠小脑颗粒细胞中钾通道的作用。3. 在很宽的电位范围内都观察到了非失活钾通道。4. 在挥发性麻醉剂灌注期间,通道活性增加,而电流-电压关系未变,且在负电位时仍保持弱内向整流,电导约为30 pS。5. 挥发性麻醉剂频繁开启内向整流器可能会使静息电位稳定在E(K)附近,以抵抗去极化刺激。

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