The role of K+ channels in the force recovery elicited by Na+‐K+ pump stimulation in Ba2+‐paralysed rat skeletal muscle
T Clausen, K Overgaard - The Journal of Physiology, 2000 - Wiley Online Library
T Clausen, K Overgaard
The Journal of Physiology, 2000•Wiley Online Library1 The present experiments were performed to assess the role of K+ channels in hormonal
stimulation of the Na+‐K+ pump and to determine the contribution of Na+‐K+ pumps to the
recovery of excitability and contractility in depolarized skeletal muscle. 2 In soleus muscle,
Ba2+ (0.02 and 1 mm) was found to inhibit 42K+ efflux and 42K+ influx. Both in the absence
and the presence of Ba2+ (1 mm), salbutamol and calcitonin gene‐related peptide (CGRP)
induced a marked decrease in intracellular Na+ and stimulation of 42K+ uptake. 3 In soleus …
stimulation of the Na+‐K+ pump and to determine the contribution of Na+‐K+ pumps to the
recovery of excitability and contractility in depolarized skeletal muscle. 2 In soleus muscle,
Ba2+ (0.02 and 1 mm) was found to inhibit 42K+ efflux and 42K+ influx. Both in the absence
and the presence of Ba2+ (1 mm), salbutamol and calcitonin gene‐related peptide (CGRP)
induced a marked decrease in intracellular Na+ and stimulation of 42K+ uptake. 3 In soleus …
- 1The present experiments were performed to assess the role of K+ channels in hormonal stimulation of the Na+‐K+ pump and to determine the contribution of Na+‐K+ pumps to the recovery of excitability and contractility in depolarized skeletal muscle.
- 2In soleus muscle, Ba2+ (0.02 and 1 mm) was found to inhibit 42K+ efflux and 42K+ influx. Both in the absence and the presence of Ba2+ (1 mm), salbutamol and calcitonin gene‐related peptide (CGRP) induced a marked decrease in intracellular Na+ and stimulation of 42K+ uptake.
- 3In soleus muscles Ba2+ (0.1 and 1.0 mm) decreased twitch and tetanic force. Subsequent stimulation of the Na+‐K+ pumps by salbutamol, CGRP or repeated electrical stimulation produced a highly significant restoration of force development, which was suppressed by ouabain, but not by glibenclamide. Also, in extensor digitorum longus muscles Ba2+ (0.1 mm) produced a considerable force decline, which was partly restored by salbutamol and CGRP.
- 4The area of compound action potentials (M‐waves) elicited by indirect stimulation was decreased by Ba2+ (0.1 mm). This was associated with a concomitant decrease in tetanic force and depolarization. Salbutamol, CGRP or repeated electrical stimulation all elicited marked recovery of M‐wave area, force and membrane potential. All recordings showed close correlations between these three parameters.
- 5The data add further support to the concept that due to its electrogenic nature and large transport capacity, the Na+‐K+ pump is a rapid and efficient mechanism for the maintenance of excitability in skeletal muscle, acting independently of Ba2+‐ or ATP‐sensitive K+ channel function.
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