Bose R, Bose D
Am J Physiol. 1977 Jul;233(1):C8-13. doi: 10.1152/ajpcell.1977.233.1.C8.
Multiunit canine tracheal smooth muscle responded to carbachol with graded depolarization and tonic contraction. The same concentration of carbachol, after metabolic depletion by substrate removal, produced rhythmic contractions and action potentials. Similar mechanical effects were also observed with acetylcholine or histamine. These effects were reversed by reintroducing glucose or beta-hydroxybutyrate, but not by 3-O-methylglucose, which is not metabolized; hence, the structural requirements for glucose, per se, or any osmotic effect were ruled out. Sensitivity to extracellular Ca2+ was increased. A Ca2+-influx blocker, D-600, in low concentration (2 X 10(-8) M) abolished the rhythmic contractions without affecting the tonic contraction. Progressive metabolic depletion in presence of carbachol led to fluctuations in membrane potential with a crest of depolarization and appearance of action potentials, each of which resulted in a small contraction. Many of the small contractions partially fused to form the major rhythmic contractions which appeared at a frequency of one per minute. Rhythmicity could not be produced by increasing extracellular K+ concentration (20-120 mM) in presence of atropine (13(-7) M), but instead a tonic contraction occurred. These results suggest changes in excitation-contraction coupling mechanism with agonists like acetylcholine, carbachol, or histamine during substrate deprivation.
多单位犬气管平滑肌对卡巴胆碱产生分级去极化和强直性收缩反应。在通过去除底物使代谢耗尽后,相同浓度的卡巴胆碱产生了节律性收缩和动作电位。乙酰胆碱或组胺也观察到类似的机械效应。重新引入葡萄糖或β-羟基丁酸可逆转这些效应,但不能被不代谢的3-O-甲基葡萄糖逆转;因此,排除了葡萄糖本身的结构要求或任何渗透效应。对细胞外Ca2+的敏感性增加。低浓度(2×10(-8)M)的Ca2+内流阻滞剂D-600消除了节律性收缩,而不影响强直性收缩。在卡巴胆碱存在下进行性代谢耗尽导致膜电位波动,出现去极化峰和动作电位,每个动作电位都导致一个小的收缩。许多小的收缩部分融合形成主要的节律性收缩,频率为每分钟一次。在阿托品(13(-7)M)存在下增加细胞外K+浓度(20-120mM)不能产生节律性,而是发生强直性收缩。这些结果表明在底物剥夺期间,与乙酰胆碱、卡巴胆碱或组胺等激动剂的兴奋-收缩偶联机制发生了变化。