Souhrada M, Souhrada J F
Respir Physiol. 1981 Jun;44(3):311-23. doi: 10.1016/0034-5687(81)90026-8.
We tested the hypothesis that temperature may directly influence the resting membrane potential (Em), (Na+ + K+)-ATPase activity, and the contractile response to histamine of bovine and guinea pig airway smooth muscle. To determine the resting membrane potential of airway smooth muscle, glass microelectrodes filled with 3M KCl were used. As a measure of (Na+ + K+)-ATPase activity, potassium-induced relaxation was used employing the method of Webb and Bohr (1978). The resting membrane potential and ATPase activity of airway smooth muscle was assessed 60 minutes after incubation in a normal oxygenated physiological salt solution (pH = 7.38 +/- 0.02) at each of the following temperatures: 21 degrees, 29 degrees, 37 degrees and 40 degrees C. The effect of ouabain (10(-5) M) and histamine (10(-3) M) on resting membrane potential of airway smooth muscle cells was also determined at each of these temperatures. It was found that: (1) resting membrane potential of airway smooth muscle cells from both bovine and guinea pigs, was directly proportional to the temperature; (2) the administration of ouabain reduced the dependency of resting membrane potential on the temperature of the experimental medium; (3) at lower temperatures (21 degrees C and 29 degrees C), histamine-induced a statistically significant (P less than 0.01) depolarization, and the contractile response of airway smooth muscle was also significantly (P less than 0.01) potentiated; (4) a decrease in the temperature (29 degrees C) significantly (P less than 0.001) decreased (Na+ + K+)-ATPase activity of airway smooth muscle as measured by potassium-induced relaxation. It is concluded that a change in temperature has a direct influence on airway smooth muscle cells, affecting resting membrane potential, (Na+ + K+)-ATPase activity of airway smooth muscle cells, and the contractile response of these cells to histamine.
温度可能直接影响牛和豚鼠气道平滑肌的静息膜电位(Em)、(钠 + 钾)-ATP 酶活性以及对组胺的收缩反应。为了测定气道平滑肌的静息膜电位,使用了填充有 3M KCl 的玻璃微电极。作为(钠 + 钾)-ATP 酶活性的一种度量,采用了 Webb 和 Bohr(1978 年)的方法,通过钾诱导的舒张来进行测定。在以下每个温度下:21 摄氏度、29 摄氏度、37 摄氏度和 40 摄氏度,将气道平滑肌在正常含氧生理盐溶液(pH = 7.38 ± 0.02)中孵育 60 分钟后,评估其静息膜电位和 ATP 酶活性。还在这些温度下分别测定了哇巴因(10⁻⁵ M)和组胺(10⁻³ M)对气道平滑肌细胞静息膜电位的影响。结果发现:(1)牛和豚鼠气道平滑肌细胞的静息膜电位与温度成正比;(2)使用哇巴因降低了静息膜电位对实验介质温度的依赖性;(3)在较低温度(21 摄氏度和 29 摄氏度)下,组胺引起了具有统计学意义(P < 0.01)的去极化,并且气道平滑肌的收缩反应也显著(P < 0.01)增强;(4)温度降低(29 摄氏度)显著(P < 0.001)降低了通过钾诱导舒张测定的气道平滑肌(钠 + 钾)-ATP 酶活性。结论是温度变化对气道平滑肌细胞有直接影响,影响气道平滑肌细胞的静息膜电位、(钠 + 钾)-ATP 酶活性以及这些细胞对组胺的收缩反应。