Lee H K, Leikauf G D, Sperelakis N
Department of Physiology and Biophysics, University of Cincinnati College of Medicine, Ohio 45267.
J Appl Physiol (1985). 1990 Jan;68(1):417-20. doi: 10.1152/jappl.1990.68.1.417.
The effects of endothelin (ET) on transmembrane potential and isometric force were studied in ferret bronchial and tracheal smooth muscles. At rest, the muscle cells were electrically and mechanically quiescent. The mean resting potential for the bronchial cells was -70 +/- 1 mV (n = 25 cells/8 ferrets), and that of the tracheal cells was -60 +/- 1 mV (n = 7 cells/2 ferrets). ET depolarized and contracted both types of muscle cells in a concentration-dependent manner. At 1 nM ET, the bronchial muscle cells were significantly depolarized with concomitant force generation. In contrast, greater than 30 nM ET was required for the tracheal muscle cells to respond. The bronchial cells were further depolarized by 10 and 100 nM ET with electrical slow-wave activity present. The calcium channel antagonist verapamil substantially inhibited the contractions produced by 100 nM ET and abolished the slow-wave activity without affecting the base-line depolarization. Pretreatment of the bronchial muscle with 30 microM indomethacin did not affect the ET-induced contraction. These results suggest that ET modulates airway smooth muscle tone by direct activation and/or depolarization-induced activation of sarcolemmal calcium channels.
研究了内皮素(ET)对雪貂支气管和气管平滑肌跨膜电位及等长收缩力的影响。静息时,肌细胞在电和机械方面均处于静止状态。支气管细胞的平均静息电位为-70±1 mV(n = 25个细胞/8只雪貂),气管细胞的平均静息电位为-60±1 mV(n = 7个细胞/2只雪貂)。ET以浓度依赖的方式使两种类型的肌细胞去极化并收缩。在1 nM ET作用下,支气管肌细胞显著去极化并伴有收缩力产生。相比之下,气管肌细胞需要大于30 nM ET才能产生反应。10和100 nM ET使支气管细胞进一步去极化,并伴有电慢波活动。钙通道拮抗剂维拉帕米显著抑制100 nM ET引起的收缩,并消除慢波活动,但不影响基线去极化。用30 μM吲哚美辛预处理支气管肌肉不影响ET诱导的收缩。这些结果表明,ET通过直接激活和/或去极化诱导的肌膜钙通道激活来调节气道平滑肌张力。