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从豚鼠膀胱分离出的单细胞中ATP诱导的去极化和电流的特性。

The properties of the ATP-induced depolarization and current in single cells isolated from the guinea-pig urinary bladder.

作者信息

Inoue R, Brading A F

机构信息

University Department of Pharmacology, Oxford.

出版信息

Br J Pharmacol. 1990 Jul;100(3):619-25. doi: 10.1111/j.1476-5381.1990.tb15856.x.

DOI:10.1111/j.1476-5381.1990.tb15856.x
PMID:1697199
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1917811/
Abstract
  1. The actions of exogenously applied ATP were investigated with the whole-cell patch clamp method in single cells isolated from guinea-pig urinary bladder with a modified concentration jump technique. 2. Rapid application of ATP (threshold ca. 100 nM) depolarized the cell membrane with superimposition of action potentials which was followed by transient hyperpolarization. In the presence of D600, the amplitude of the ATP-induced depolarization was a function of the ATP concentration (EC50: 0.5-1 microM). 3. ATP activated a dose-dependent inward current with a short latency (18 ms with 10 microM ATP; measured as the time between the start of application and 10% of the peak). The relationship of the peak current versus ATP concentration was well fitted by a Michaelis-Menten equation with a Hill coefficient (n) of 1.7 and a dissociation constant (Kd) of 2.3 microM. The current desensitized rapidly and the time course of desensitization was a function of the ATP concentration and could be fitted by two exponentials. 4. The reversal potential of the ATP-activated current was near 0 mV. Replacement of extracellular Na by other monovalent or divalent cations indicated that the current flows through nonselective cation channels. 5. alpha,beta-Methylene ATP also produced a dose-dependent inward current but was less potent than ATP (n: 1.6, Kd: 10.4 microM). alpha,beta-Methylene ATP blocked the response to ATP by desensitization of the receptor. 6. alpha,beta-Methylene ATP was 50-100 times more potent than ATP at eliciting a contractile response of strips of detrusor smooth muscle. 7. The relevance of the above results to the possible role of ATP as the fast excitatory transmitter is discussed.
摘要
  1. 采用改良的浓度阶跃技术,运用全细胞膜片钳方法,在从豚鼠膀胱分离出的单细胞中研究了外源性应用ATP的作用。2. 快速施加ATP(阈值约为100 nM)使细胞膜去极化,并叠加动作电位,随后出现短暂的超极化。在存在D600的情况下,ATP诱导的去极化幅度是ATP浓度的函数(半数有效浓度:0.5 - 1 microM)。3. ATP激活了一种剂量依赖性内向电流,潜伏期短(10 microM ATP时为18 ms;测量为施加开始至峰值的10%之间的时间)。峰值电流与ATP浓度的关系通过米氏方程拟合良好,希尔系数(n)为1.7,解离常数(Kd)为2.3 microM。电流迅速脱敏,脱敏的时间进程是ATP浓度的函数,可由两个指数拟合。4. ATP激活电流的反转电位接近0 mV。用其他单价或二价阳离子替代细胞外Na表明,电流通过非选择性阳离子通道流动。5. α,β-亚甲基ATP也产生剂量依赖性内向电流,但效力低于ATP(n:1.6,Kd:10.4 microM)。α,β-亚甲基ATP通过使受体脱敏来阻断对ATP的反应。6. 在引发逼尿肌平滑肌条收缩反应方面,α,β-亚甲基ATP的效力比ATP强50 - 100倍。7. 讨论了上述结果与ATP作为快速兴奋性递质可能作用的相关性。

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