Krivoĭ I I, Kravtsova V V, Prokof'ev A V, Vashchinkina E V, Kubasov I V, Drabkina T M
Ross Fiziol Zh Im I M Sechenova. 2006 Dec;92(12):1463-73.
Effects of Na+,K(+)-ATPase inhibitor: marinobufagenin, on contractile and electric characteristics of isolated rat diaphragm were studied for the first time. Marinobufagenin induced dose-dependent (EC50 = 0.3 +/- 0.1 nM) increase in the contraction force (positive inotropic effect). At 1-2 nM, it slowed down the fatigue induced by continuous direct stimulation (2/s) of the muscle. Marinobufagenin at the same concentrations did not affect resting membrane potential or parameters of action potentials of muscle fibers, while at 10 and 20 nM it induced hyperpolarization by approximately 2 mV. Marinobufagenin blocked dose-dependently (IC50 = 2.9 +/- 2.0 nM) hyperpolarizing effect of acetylcholine (100 nM) mediated by increase in electrogenic contribution of alpha2 isoform of the Na+,K(+)-ATPase. This result suggests a capability of marinobufagenin to inhibit this isoform of the Na+,K(+)-ATPase. Possible mechanisms of marinobufagenin effects in skeletal muscle are discussed.
首次研究了Na +,K(+)-ATP酶抑制剂:海蟾蜍精对离体大鼠膈肌收缩和电特性的影响。海蟾蜍精诱导收缩力呈剂量依赖性增加(EC50 = 0.3±0.1 nM)(正性肌力作用)。在1-2 nM时,它减缓了肌肉连续直接刺激(2次/秒)引起的疲劳。相同浓度的海蟾蜍精不影响静息膜电位或肌纤维动作电位参数,而在10和20 nM时,它诱导超极化约2 mV。海蟾蜍精通过增加Na +,K(+)-ATP酶α2同工型的生电作用剂量依赖性地阻断(IC50 = 2.9±2.0 nM)乙酰胆碱(100 nM)的超极化作用。该结果表明海蟾蜍精具有抑制Na +,K(+)-ATP酶这种同工型的能力。讨论了海蟾蜍精在骨骼肌中作用的可能机制。