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蛋白激酶C激活导致大鼠迷走神经无髓鞘纤维去极化。

Depolarization of nonmyelinated fibers of the rat vagus nerve produced by activation of protein kinase C.

作者信息

Rang H P, Ritchie J M

机构信息

Sandoz Institute for Medical Research, London, England.

出版信息

J Neurosci. 1988 Jul;8(7):2606-17. doi: 10.1523/JNEUROSCI.08-07-02606.1988.

Abstract

The effect of activation of protein kinase C by phorbol esters has been studied on the nonmyelinated (C) fibers of the rat vagus nerve. Grease-gap recording at room temperature was used to monitor changes in the resting and action potentials. Effects of phorbol esters on the rate of efflux of 86Rb and 14C-guanidinium were also measured. The active isomer beta-phorbol 12,13-dibutyrate (PDBu), applied for 10 min at concentrations of 10 nM to 3 microM, caused a slowly developing depolarization, which persisted after the drug was washed out. The action potential was concomitantly reduced. These effects did not occur with the inactive isomer alpha-phorbol 12,13-didecanoate. The PDBu-induced depolarization was reduced by about 75% if Na+ was replaced by the impermeant cation N-methyl-(+)-glucamine (NMG); the residual effect was almost abolished if the nerves were presoaked in a solution containing gluconate in place of Cl-. It was concluded that increases in conductance mainly to Na+ and Cl- were responsible for the depolarization. The response was unaffected by tetrodotoxin or calcium-channel blockers. Omission of Ca2+, surprisingly, enhanced the PDBu-induced depolarization 3-5-fold; furthermore, addition of 2 mM Ca2+ following a PDBu-induced depolarization recorded in Ca2+-free solution caused a pronounced repolarization. This effect of Ca2+ occurred also with Sr2+ and Ba2+, but not with other divalent cations or with La3+. Divalent cations known to block Ca channels inhibited the repolarizing action of Ca2+. These results suggested that Ca2+ acts intracellularly, either to block Na channels opened by PDBu or to activate protein phosphatases. The PDBu-induced response in Ca2+-free solution was increased 2-fold by a reduction in pH from 7.4 to 6.5. Under normal conditions the nerve was reversibly depolarized by this pH change; after PDBu this pH sensitivity was enhanced, and depolarization occurred at a less acidic pH. PDBu caused a 3-4-fold increase in the rate of efflux of 86Rb (a marker for K+ ions) and of 14C-guanidinium (a marker for Na+ ions) from preloaded nerves. These effects, in contrast to the depolarization, were transient.(ABSTRACT TRUNCATED AT 400 WORDS)

摘要

已对佛波酯激活蛋白激酶C对大鼠迷走神经无髓鞘(C)纤维的作用进行了研究。在室温下采用油脂间隙记录法监测静息电位和动作电位的变化。还测定了佛波酯对86Rb和14C-胍流出速率的影响。活性异构体β-佛波醇12,13-二丁酸酯(PDBu)以10 nM至3 μM的浓度作用10分钟,引起缓慢发展的去极化,药物洗脱后该去极化仍持续存在。动作电位随之降低。非活性异构体α-佛波醇12,13-二癸酸酯未出现这些效应。如果用不透性阳离子N-甲基-(+)-葡糖胺(NMG)取代Na+,PDBu诱导的去极化降低约75%;如果将神经预先浸泡在含葡萄糖酸盐而非Cl-的溶液中,残余效应几乎消除。得出的结论是,主要对Na+和Cl-的电导增加是去极化的原因。该反应不受河豚毒素或钙通道阻滞剂的影响。令人惊讶的是,去除Ca2+可使PDBu诱导的去极化增强3至5倍;此外,在无Ca2+溶液中记录到PDBu诱导的去极化后加入2 mM Ca2+会引起明显的复极化。Ca2+的这种作用在Sr2+和Ba2+存在时也会出现,但在其他二价阳离子或La3+存在时不会出现。已知能阻断钙通道的二价阳离子会抑制Ca2+的复极化作用。这些结果表明,Ca2+在细胞内起作用,要么阻断由PDBu打开的Na通道,要么激活蛋白磷酸酶。将pH从7.4降至6.5可使无Ca2+溶液中PDBu诱导的反应增加2倍。在正常情况下,神经会因这种pH变化而可逆地去极化;在PDBu作用后,这种pH敏感性增强,在酸性较低的pH时就会发生去极化。PDBu使预加载神经中86Rb(K+离子标志物)和14C-胍(Na+离子标志物)的流出速率增加3至4倍。与去极化相反,这些效应是短暂的。(摘要截取自400字)

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