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普萘洛尔和局部麻醉药对河蜗神经元钙电流抑制作用的进一步分析。

Further analysis of inhibitory effects of propranolol and local anaesthetics on the calcium current in Helix neurones.

作者信息

Akaike N, Ito H, Nishi K, Oyama Y

出版信息

Br J Pharmacol. 1982 May;76(1):37-43. doi: 10.1111/j.1476-5381.1982.tb09188.x.

Abstract

1 The effects of propranolol and local anaesthetics on Ca2+ current (Ica), individually separated from other ionic currents, in Helix neurones were studied under voltage clamp, using a suction pipette technique. 2 Increases in external Ca2+ concentrations overcame the inhibitory action of propranolol on Ica. Double reciprocal plots for peak Ica versus external Ca2+ concentrations in the presence or absence of propranolol did not intersect at the ordinate. 3 Internal application of propranolol (10-4M) inhibited Ica to about 40-60% of the control in a time-dependent manner. 4 Lignocaine and procaine at concentrations of 10-3-10-2 M inhibited Ica without shifting the threshold in the I-V relationships. Internal application of lignocaine (10-3-10-2M) also inhibited Ica: the ratio of depression of the Ica was almost equivalent to that of the agent applied externally. 5 The results provide evidence that propranolol inhibits Ica in the noncompetitive manner with Ca2+ at the cell membrane, and suggest that the agents may occupy the receptor site in the Ca2+-channel somewhere between the outer surface and inner phase of the membrane.

摘要
  1. 在电压钳制下,采用吸移管技术,研究了普萘洛尔和局麻药对分离于其他离子电流的河蚌神经元Ca2+电流(Ica)的影响。2. 细胞外Ca2+浓度升高可克服普萘洛尔对Ica的抑制作用。有无普萘洛尔时,Ica峰值与细胞外Ca2+浓度的双倒数作图在纵坐标上不相交。3. 胞内施加普萘洛尔(10-4M)以时间依赖方式将Ica抑制至对照的约40%-60%。4. 浓度为10-3-10-2M的利多卡因和普鲁卡因抑制Ica,且不改变I-V关系中的阈值。胞内施加利多卡因(10-3-10-2M)也抑制Ica:Ica的抑制率几乎与胞外施加该药物时相当。5. 结果表明普萘洛尔在细胞膜上以与Ca2+非竞争性方式抑制Ica,提示这些药物可能占据了膜外表面和内相之间Ca2+通道中的受体位点。

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