The Effect of Hypertonicity on the Time Course of the Active State in Single Skeletal Muscle Fibres of the Frog

1973 ◽  
Vol 88 (2) ◽  
pp. 149-159 ◽  
Author(s):  
K.-E. Andersson
1979 ◽  
Vol 181 (3) ◽  
pp. 545-557 ◽  
Author(s):  
P Darveniza ◽  
J A Morgan-Hughes ◽  
E J Thompson

1. Intact synaptic acetylcholine receptors on freshly isolated rat skeletal-muscle fibres were characterized by their interaction with di-iodinated 125I-labelled alpha-bungarotoxin, acetylcholine and other cholinergic ligands at room temperature (22 deggrees C). 2. The time course and concentration dependence of 125I-labelled alpha-bungarotoxin association conformed to a bimolecular mechanism. In time-course experiments with different concentrations of 125I-labelled alpha-bungarotoxin (1.4–200 nM) the bimolecular-association rate constant, k + 1, was (2.27 +/- 0.49) × 10(4)M-1.S-1 (mean +/- S.D., N = 10). In concentration-dependence experiments, k + 1 was 2.10 × 10(4)M-1.S-1 and 1.74 × 10(4) M-1.S-1 with 10 and 135 min incubations respectively. In association experiments the first-order rate constant was proportional to the 125I-labelled alpha-bungarotoxin concentration. 125I-Labelled alpha-bungarotoxin dissociation was first order with a dissociation constant, k-1, less than or equal to 3 × 10(-6)S(-1) (half-life greater than or equal to 60 h.) The results indicated a single class of high-affinity toxin-binding sites at the end-plate with an equilibrium dissociation constant, Kd, equal to or less than 100 pM. The number of toxin-binding sites was (3.62 +/- 0.46) × 10(7) (mean +/- S.D., n = 22) per rat end-plate. 3. The apparent inhibitor dissociation constants, Ki, for reversible cholinergic ligands were determined by studying their effect at equilibrium on the rate of 125I-labelled alpha-bungarotoxin binding. There was heterogeneity of binding sites for cholinergic ligands, which were independent and non-interacting with antagonists. In contrast agonist affinity decreased with increasing receptor occupancy. Cholinergic ligands in excess inhibited over 90% of 125I-labelled alpha-bungarotoxin binding. 4. Cholinergic ligand binding was accompanied by an increase in entropy, which was greater for the agonist carbachol (delta So = +0.46 kJ.mol-1.K-1) than the antagonist tubocurarine (delta So = +0.26 kJ.mol-1.K-1). 5. The entropy and affinity changes that accompanied agonist binding suggested that agonists induced significant conformational changes in intact acetylcholine receptors. 6. The affinity and specificity of 125I-labelled alpha-bungarotoxin and tubocurarine binding to synaptic acetylcholine receptors from slow and fast muscle fibres were the same. 7. The study of binding only requires milligram amounts of tissue and may have application to other neurobiological studies and to the study of human neuromuscular disorders.


1979 ◽  
Vol 57 (2) ◽  
pp. 221-223 ◽  
Author(s):  
K. Lundholm ◽  
T. Scherstén

Amino acids were incorporated into soluble proteins, myosin and myoglobin at constant rates for at least 4 h on incubation of isolated human skeletal muscle fibres. The time course of incorporation of leucine into proteins not attached to ribosomes was approximately constant, suggesting a continuous termination of proteins. A comparison between estimated pool size of ribosomes and incorporation rate of leucine into proteins indicated that initiation of peptides occurred even in the absence of insulin.


If a frog’s skeletal muscle is soaked in modified Ringer’s fluid, containing bromide, nitrate or iodide in place of chloride, the tension and duration of a twitch, and its heat production, are largely increased, in the order Br<NO 3 <I. In a tetanic contraction, however, the tension, the heat production and the velocity of shortening under any load are unaffected. The primary effect of these anions, acting on the excitable surface of the muscle fibres, is to increase the duration of the active state after a shock; the increased tension and heat in a twitch result from this. The rate at which the effect comes on after sudden immersion of a muscle in iodide-Ringer depends solely on the rate at which iodide diffuses into the interspaces between the fibres; the rate of penetration of iodide into the fibres is very slow. The effect is not due to any direct action of the anion on the contractile mechanism, for (1) it passes off rapidly, when a muscle after long soaking in iodide-Ringer is transferred to chloride-Ringer, although iodide remains inside for a long time, and (2) the tetanic contraction is unaffected. If the fundamental 'unit’ of contraction were a cycle of events triggered by excitation and then running its own course to completion, the duration of the active state would be an intrinsic property of the contractile mechanism and would not depend on something outside it. But if the active contractile state is set up and maintained in the interior by some influence transmitted from the excitable surface outside, its duration would depend on the time course of the responsible process at the surface. The facts ( a ) that the duration is greatly affected by the presence of, for example, iodide in the interspaces between the fibres, at a time when there is practically none of it inside the fibres, and ( b ) that the effect rapidly passes off as iodide is removed from the interspaces although a large amount of it may still be inside, is decisive evidence for the second view. These abnormal anions somehow affect the time course of the process, started by excitation, in the surface of the fibres from which the active contractile state is transmitted into and maintained in the interior. This exposes a new link in the chain of events connecting excitation with contraction.


1989 ◽  
Vol 504 (2) ◽  
pp. 306-310 ◽  
Author(s):  
Inger Nennesmo ◽  
Tomas Olsson ◽  
Åke Ljungdahl ◽  
Krister Kristensson ◽  
Peter H. Van der Meide

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