Flonta M L, Nistor M, Frangopol P T
University of Bucharest, Faculty of Biology, Biophysical Laboratory, Romania.
Arch Int Physiol Biochim Biophys. 1991 Aug;99(4):335-7. doi: 10.3109/13813459109146946.
Procaine has different effects on various ionic conductive pathways through the frog skin. We investigated the season and temperature dependence of the stimulation by mucosal procaine, of the Na-conductive pathway. For this stimulation, we found higher half-maximal saturation constants (KNa) in winter animals (6.38 +/- 0.8 mmol/l), than in summer ones (4.03 +/- 0.7 mmol/l). Summer frogs kept for 2 weeks at 4 degrees C, reacted like winter frogs (6.24 +/- 0.8 mmol/l). However, the maximal sodium currents (INa max) did not depend on temperature adaptation. Procaine-induced increased of KNa is associated with an increase of INa. The effects of procaine associated with BIG (benzoylimidazole-2-guanidine) were non-additive, while with vasopressin they were additive. A biphasic, dose-dependent response was recorded after procaine application to the inner surface. Vasopressin counteracted the serosal procaine-induced inhibition of the Na-transport.
普鲁卡因对蛙皮的各种离子传导途径有不同影响。我们研究了黏膜普鲁卡因对钠传导途径刺激的季节和温度依赖性。对于这种刺激,我们发现冬季动物(6.38±0.8 mmol/L)的半数最大饱和常数(KNa)高于夏季动物(4.03±0.7 mmol/L)。在4℃下饲养2周的夏季青蛙,其反应与冬季青蛙相似(6.24±0.8 mmol/L)。然而,最大钠电流(INa max)并不依赖于温度适应。普鲁卡因诱导的KNa增加与INa增加相关。与BIG(苯甲酰咪唑-2-胍)相关的普鲁卡因效应是非相加性的,而与血管加压素相关的效应是相加性的。将普鲁卡因应用于内表面后记录到双相、剂量依赖性反应。血管加压素抵消了浆膜普鲁卡因诱导的钠转运抑制。