Kasamaki Y, Guo A C, Shuba L M, Ogura T, McDonald T F
Department of Physiology and Biophysics, Dalhousie University, Halifax, Nova Scotia.
Can J Cardiol. 1998 Feb;14(2):285-94.
To identify factors involved in the modification of cardiac electromechanical activity caused by hyperosmotic solution.
Membrane potentials and contractions were recorded from isolated papillary muscles, and membrane ionic currents were measured in isolated ventricular myocytes by using the ruptured patch or perforated patch voltage clamp method.
Adult male guinea-pigs weighing 250 to 350 g were used. Normal Tyrode's solution for superfusing experimental preparations was replaced with hyperosmotic Tyrode's solution for observation periods of up to 10 mins. The hyperosmotic solution was normal Tyrode's solution supplemented with 50 or 150 mM sucrose (1.2 or 1.5 times normal osmolality). Sodium pump activity (hyperpolarization in muscles; outward current in myocytes) was activated by switching to pump-activating cation (cesium, potassium) solution from pump-inactivating potassium-free solution under conditions in which other ionic currents were suppressed.
Hyperosmotic solution lengthened action potentials and enhanced developed tension in papillary muscles. Superfusion of myocytes with hyperosmotic solution inhibited inward L-type calcium current (ICa,L) by approximately 30% and the outward delayed rectifier potassium current (Ik) by approximately 50%. Hyperosmotic treatment also partially inhibited sodium pump-generated hyperpolarizations in papillary muscles. However, sodium pump current in myocytes was relatively small under isosmotic conditions and, therefore, unlikely to be a major factor in action potential lengthening.
Inhibition of potassium current is a major factor in the lengthening of the action potential by hyperosmotic solution. It seems likely that the accompanying positive inotropy is due to an elevation of intracellular calcium caused by enhanced calcium influx related to action potential prolongation and sodium pump inhibition.
确定高渗溶液引起心脏机电活动改变所涉及的因素。
从分离的乳头肌记录膜电位和收缩情况,并使用破膜片或穿孔膜片电压钳法在分离的心室肌细胞中测量膜离子电流。
使用体重250至350克的成年雄性豚鼠。在长达10分钟的观察期内,将用于灌注实验制剂的正常台氏液替换为高渗台氏液。高渗溶液是在正常台氏液中添加50或150 mM蔗糖(分别为正常渗透压的1.2倍或1.5倍)。在其他离子电流被抑制的条件下,通过从无钾的泵失活溶液切换到泵激活阳离子(铯、钾)溶液来激活钠泵活性(肌肉中的超极化;心肌细胞中的外向电流)。
高渗溶液延长了乳头肌的动作电位并增强了其收缩张力。用高渗溶液灌注心肌细胞可使内向L型钙电流(ICa,L)抑制约30%,外向延迟整流钾电流(Ik)抑制约50%。高渗处理还部分抑制了乳头肌中钠泵产生的超极化。然而,在等渗条件下心肌细胞中的钠泵电流相对较小,因此不太可能是动作电位延长的主要因素。
钾电流的抑制是高渗溶液延长动作电位的主要因素。伴随的正性肌力作用似乎是由于动作电位延长和钠泵抑制导致钙内流增加,从而使细胞内钙升高所致。