Ward S M, Vogalis F, Blondfield D P, Ozaki H, Fusetani N, Uemura D, Publicover N G, Sanders K M
Department of Physiology, University of Nevada School of Medicine, Reno 89557.
Am J Physiol. 1991 Jul;261(1 Pt 1):C64-70. doi: 10.1152/ajpcell.1991.261.1.C64.
The effects of calyculin A, a phosphatase inhibitor isolated from the marine sponge Discodermia calyx, on the electrical activity of colonic and gastric muscles were studied. Calyculin A reduced the amplitude and duration of slow waves, primarily by inhibiting the plateau component. Okadaic acid, another phosphatase inhibitor, also reduced the amplitude and duration of gastric slow waves. The mechanism of action of calyculin A was investigated by studying its effects on inward currents of isolated gastric and colonic myocytes. Calyculin A reduced the amplitude of the peak and the sustained components of the inward current. Okadaic acid had similar effects. These data suggest that phosphorylation of Ca2+ channels of gastrointestinal smooth muscles may inhibit Ca2+ currents. This mechanism may provide an important means of regulating the currents responsible for excitation-contraction coupling in these muscles.
研究了从海洋海绵皮盘菌中分离出的磷酸酶抑制剂花萼海绵诱癌素A对结肠和胃肌肉电活动的影响。花萼海绵诱癌素A主要通过抑制平台成分来降低慢波的幅度和持续时间。另一种磷酸酶抑制剂冈田酸也降低了胃慢波的幅度和持续时间。通过研究花萼海绵诱癌素A对分离的胃和结肠肌细胞内向电流的影响,探讨了其作用机制。花萼海绵诱癌素A降低了内向电流的峰值幅度和持续成分。冈田酸也有类似作用。这些数据表明,胃肠道平滑肌Ca2+通道的磷酸化可能抑制Ca2+电流。这一机制可能为调节这些肌肉中负责兴奋-收缩偶联的电流提供重要手段。