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钾通道阻滞对青蛙传入神经末梢和轴突的相对不应期有不同影响。

Potassium channel blockade differentially affects the relative refractory period of frog afferent terminals and axons.

作者信息

Tkacs N C, Wurster R D

机构信息

Department of Physiology, Loyola University Medical Center, Maywood, Illinois 60153.

出版信息

Cell Mol Neurobiol. 1990 Sep;10(3):405-21. doi: 10.1007/BF00711183.

Abstract
  1. The effects of potassium channel blockade on afferent axons and terminal regions in frog dorsal roots and spinal cords, respectively, were investigated in vitro. 2. A condition-test (C-T) protocol was used to assess the population relative refractory period. Characteristics of main axons were evaluated by stimulation at the proximal end of transected dorsal roots (DR). Characteristics of terminal regions were tested by stimulation at the base of the dorsal horn (DH). 3. DH recovery of excitability was delayed by low concentrations of 4-aminopyridine (4-AP) and tetraethylammonium (TEA) alone or combined. The same treatments did not affect recovery to DR stimulation. 4. DH recovery of excitability was not delayed by solutions suppressing terminal calcium influx. 5. We conclude that sensitivity of the relative refractory period to potassium channel blocking agents differs between main axons and axon terminal regions. This may indicate differences between axon terminals and main axons in the mechanism of action potential repolarization. 6. We hypothesize that rapid action potential repolarization by pharmacologically sensitive potassium channels in presynaptic terminal regions keeps terminal action potentials short. Terminal action potential brevity would limit calcium influx, thus preventing terminal calcium overload but contributing to transmission failures at spinal synapses.
摘要
  1. 分别在体外研究了钾通道阻断对青蛙背根和脊髓中传入轴突及终末区域的影响。2. 使用条件测试(C-T)方案评估群体相对不应期。通过刺激横断背根(DR)近端来评估主要轴突的特征。通过刺激背角(DH)基部来测试终末区域的特征。3. 单独或联合使用低浓度的4-氨基吡啶(4-AP)和四乙铵(TEA)会延迟DH兴奋性的恢复。相同处理对DR刺激后的恢复无影响。4. 抑制终末钙内流的溶液不会延迟DH兴奋性的恢复。5. 我们得出结论,相对不应期对钾通道阻断剂的敏感性在主要轴突和轴突终末区域之间存在差异。这可能表明轴突终末和主要轴突在动作电位复极化机制上存在差异。6. 我们假设,突触前终末区域中对药物敏感的钾通道使动作电位快速复极化,从而使终末动作电位保持短暂。终末动作电位短暂会限制钙内流,从而防止终末钙超载,但会导致脊髓突触传递失败。

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