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他克林诱导电鳐电器官中自发高量子含量事件释放增加。

Tacrine-induced increase in the release of spontaneous high quantal content events in Torpedo electric organ.

作者信息

Cantí C, Martí E, Marsal J, Solsona C

机构信息

Departament de Biologia Cel.lular i Anatomia Patológica, Facultat de Medicina, Hospital de Bellvitge, Universitat de Barcelona, Spain.

出版信息

Br J Pharmacol. 1994 May;112(1):19-22. doi: 10.1111/j.1476-5381.1994.tb13022.x.

Abstract
  1. The anticholinesterases, tacrine (100 microM) and physostigmine (60 microM) had different effects on the amplitude distribution and kinetics of miniature endplate currents (m.e.p.cs) recorded extracellularly from the electric organ of Torpedo marmorata. 2. Tacrine increased the ratio of giant miniatures (larger than 4 mV of amplitude) to more than 20% of recorded spontaneous events. In the presence of physostigmine such events represented only 4%. 3. Both tacrine and physostigmine increased the rise time and the decay phase of normal-sized m.e.p.cs when compared to control conditions. Both effects were significantly greater for tacrine. 4. We have tested the specificity of the tacrine effect on ectoenzyme activities associated with plasma membranes of these pure cholinergic nerve endings. Tacrine does not act unspecifically on every ectoenzyme, because it is not able to block the ectoapyrase activity even at a concentration 100 fold greater than that required to inhibit 94% of AChE. 5. We conclude that the differential effects of tacrine and physostigmine can be explained in terms of undetermined presynaptic actions of tacrine, while comparable effects of the two compounds can be explained through a shared anticholinesterase activity.
摘要
  1. 抗胆碱酯酶药物他克林(100微摩尔)和毒扁豆碱(60微摩尔),对从斑纹电鳐电器官细胞外记录的微小终板电流(m.e.p.cs)的幅度分布和动力学有不同影响。2. 他克林使巨型微小终板电流(幅度大于4毫伏)在记录的自发事件中的比例增加到20%以上。在毒扁豆碱存在的情况下,此类事件仅占4%。3. 与对照条件相比,他克林和毒扁豆碱均增加了正常大小的m.e.p.cs的上升时间和衰减阶段。他克林的这两种作用均明显更强。4. 我们测试了他克林对这些纯胆碱能神经末梢质膜相关外切酶活性影响的特异性。他克林并非对每种外切酶都有非特异性作用,因为即使在比抑制94%的乙酰胆碱酯酶所需浓度高100倍的情况下,它也无法阻断外切ATP酶活性。5. 我们得出结论,他克林和毒扁豆碱的不同作用可以用他克林未确定的突触前作用来解释,而这两种化合物的类似作用可以通过共同的抗胆碱酯酶活性来解释。

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Quantal release of neurotransmitter and long-term potentiation.
Cell. 1993 Jan;72 Suppl:55-63. doi: 10.1016/s0092-8674(05)80028-5.
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