首页> 美国卫生研究院文献>The Journal of Physiology >The effect of noradrenaline on the ion permeability of isolated mammalian hepatocytes studied by intracellular recording.
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The effect of noradrenaline on the ion permeability of isolated mammalian hepatocytes studied by intracellular recording.

机译:通过细胞内记录研究了去甲肾上腺素对分离的哺乳动物肝细胞离子渗透性的影响。

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1. The influence of noradrenaline on the membrane potential and conductance of isolated guinea-pig and rabbit hepatocytes in short-term (2-8 h) tissue culture has been studied by intracellular recording. 2. Resting hepatocytes had linear current-voltage relationships, with input resistances of 166 and 216 M omega in guinea-pig and rabbit cells respectively. The recorded membrane potential was -18 mV in each species, though the true resting potential is likely to have been up to 10 mV greater. 3. The hepatocytes sometimes slowly hyperpolarized during intracellular recording, and this was associated with a fall in membrane resistance, and an increase followed by a decrease in membrane potential noise. These effects were abolished by quinine (200 microM) but not by apamin (50 nM), and are attributable to a K+ conductance activated by cell swelling. 4. Noradrenaline (2 microM, in the presence of propranolol at 1 microM) was applied to individual hepatocytes by pressure ejection (puffer pipette technique). After a short latency, the cells hyperpolarized by a mean of 18 mV in both guinea-pig and rabbit preparations. This was associated with a large rise in membrane conductance (50 nS in guinea-pig, 54 nS in rabbit cells). The reversal potential for this action was -38 mV. 5. The experiments were repeated in the presence of apamin (50 nM) to block the Ca2+-dependent K+ permeability which noradrenaline activates in these cells. Noradrenaline still caused some hyperpolarization and a substantial increase (approximately 40 nS) in conductance, with a reversal potential (Er) of -31 mV. This can be attributed to an increase in Cl- conductance. 6. In keeping with this interpretation, noradrenaline applied in the absence of Cl- (replaced by isethionate or gluconate) caused a much greater hyperpolarization (58 mV in guinea-pig, 40 mV in rabbit cells) associated with a smaller rise in conductance (approximately 12 nS). Er for this action was -95 mV (guinea-pig) and -68 mV rabbit), suggesting that the conductance increase was now mainly to K+. 7. The magnitudes of the conductance changes produced by noradrenaline under the various experimental conditions suggest that the increase in the conductance to Cl- (delta GCl) is 3-fold greater than that to K+ (delta GK). 8. The activation of delta GCl occurs either at the same time as delta GK, or (in ca. one cell in ten) a few seconds later.(ABSTRACT TRUNCATED AT 400 WORDS)
机译:1.通过细胞内记录研究了去甲肾上腺素对短期(2-8 h)组织培养中分离的豚鼠和兔肝细胞膜电位和电导的影响。 2.静止的肝细胞具有线性的电流-电压关系,豚鼠和兔细胞的输入电阻分别为166和216MΩ。每个物种记录的膜电位为-18 mV,尽管真实的静息电位可能高达10 mV。 3.在细胞内记录期间,肝细胞有时会缓慢超极化,这与膜抵抗力下降,膜电位噪声增加,膜阻力降低有关。奎宁(200 microM)消除了这些作用,而阿帕明(50 nM)消除了这些作用,并且归因于细胞膨胀激活的K +电导。 4.通过压力喷射(河豚移液器技术)将去甲肾上腺素(2μM,在普萘洛尔存在下为1μM)施用于单个肝细胞。短暂的潜伏期后,豚鼠和兔子制剂中的细胞均极化为18 mV。这与膜电导的大幅增加有关(豚鼠为50 nS,兔子细胞为54 nS)。此动作的反向电位为-38 mV。 5.在木瓜蛋白酶(50 nM)的存在下重复实验,以阻断去甲肾上腺素在这些细胞中激活的Ca2 +依赖性K +渗透性。去甲肾上腺素仍然引起一些超极化和电导的实质性增加(约40 nS),反向电势(Er)为-31 mV。这可以归因于Cl-电导的增加。 6.按照这种解释,去甲肾上腺素在不存在Cl-的情况下(被羟乙磺酸盐或葡萄糖酸盐替代)引起更大的超极化作用(豚鼠为58 mV,兔子细胞为40 mV),电导率上升幅度较小(大约12 ns)。此动作的Er为-95 mV(豚鼠)和-68 mV兔),这表明电导的增加主要集中在K +上。 7.去甲肾上腺素在各种实验条件下产生的电导变化幅度表明,对Cl-(δGCl)的电导增加比对K +(δGK)的电导增加3倍。 8. delta GCl的激活与delta GK同时发生,或者在几秒钟后(大约在十个单元中)发生。(抽象截断为400字)

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