scholarly journals Effects of extracellular calcium and other divalent cations on mechanical response of frog skeletal muscle.

1988 ◽  
Vol 38 (6) ◽  
pp. 905-915
Author(s):  
Junna HATAE ◽  
Hiroshi KAWATA
1988 ◽  
Vol 66 (9) ◽  
pp. 1210-1213 ◽  
Author(s):  
G. B. Frank ◽  
L. Konya ◽  
T. Subrahmanyam Sudha

The effects of the organic calcium channel blocker nitrendipine was tested on electrically evoked twitches and on potassium depolarization-induced contractures of rat lumbricalis muscles. Nitrendipine (10−7 to 5 × 10−5 M) blocked only the potassium contractures. It was concluded that blocking calcium uptake through the slow voltage-senstitive calcium channels during potassium depolarization blocks the mechanical response of the muscle. Thus extracellular calcium ions are required for the excitation–contraction (E–C) coupling during depolarization contractures. On the other hand, electrically evoked twitches were not affected by nitrendipine; therefore, extracellular calcium ions entering via the slow voltage-sensitive channels are not required for E–C coupling during the twitch.


1977 ◽  
Vol 55 (5) ◽  
pp. 1122-1134 ◽  
Author(s):  
J. G. Foulks ◽  
Florence A. Perry ◽  
P. Tsang

The depressant effect of acidity on twitches and K contractures in frog skeletal muscle was greatly accentuated in the presence of organic anions, particularly anions such as butyrate, which also reduced these responses at neutral pH. Conversely, alkaline pH antagonized the depression of contractile responses by butyrate. Most of the effects of acid pH were rapid in onset and were accomplished without any change in membrane resting or action potentials, although depolarization developed in the presence of carboxylate anions when pH was reduced below 6.0. Simultaneous variation in pH and butyrate concentration showed that the undissociated acid exerted a prominent depressant effect only when its concentration reached 1–10 mM, and that the marked depressant action of butyrate at neutral pH was produced primarily by the dissociated anion. Similar experiments showed that the dissociated anion also was largely responsible for the enhanced depolarizing effect of acidity in media containing carboxylates. Acid-induced depolarization was not facilitated in media containing methane sulfonate, but in spite of its low pKa, this anion also increased the sensitivity of contractile responses to the depressant effects of acidity. Hence, the accentuation of the effects of organic anions by acid pH must be exerted on the sequence of membrane events which link excitation and contraction. The effect of acidity was greater when longer apolar hydrocarbon chains were attached to the anionic group for both the carboxylate and the sulfonate series of ions. These depressant effects may be produced by interference with the membrane-stabilizing actions of divalent cations, and may involve increased membrane fluidity.


1973 ◽  
Vol 51 (12) ◽  
pp. 966-975
Author(s):  
N. F. Clinch ◽  
V. Tennant

Isometric contractions of frog sartorii in response to paired stimuli (I ms apart) were compared with isometric twitches following single shocks in order to find the time of the first detectable mechanical response to the second shock (ts). For I > 25 ms at 0°, ts = 0.99 I + 13.3 ms; while for I < 25 ms, ts was found to be independent of I. Electrical recording from the muscle surface showed that for I < 25 ms, the second action potential fell within the relative refractory period of the first. The plateau region of the ts–I plot is consistent with the active state theory, but can also be interpreted as (a) a measurement artifact, or (b) revealing electrical properties of the membrane rather than a property of the contractile mechanism itself.


1985 ◽  
Vol 63 (6) ◽  
pp. 693-703
Author(s):  
James G. Foulks ◽  
Lillian Morishita

D2O and perchlorate manifest opposing effects on the contractile function of skeletal muscle (amplitude of twitches and maximum K contractures, potential dependence of contraction activation and inactivation), and when combined the influence of one may effectively antagonize that of the other. The ratio of perchlorate concentrations required to produce effects of equal intensity (e.g., twitch enhancement and restoration of maximum K contractures in media lacking divalent cations or containing a depressant concentration of a cationic amphipath) in H2O and D2O solutions was generally rather constant. These findings are compatible with the view that both agents can influence contractile function by virtue of their effects on solvent structure. In the absence of divalent cations, the effects of reduced temperature resemble those of D2O whereas the effects of increased temperature resemble those of the chaotropic anion. However, in other media, variation in temperature was found to result in additional nonsolvent effects so that low temperature could oppose rather than enhance the effects of D2O. These observations are discussed in terms of a model which postulates a role for solvent influences on the kinetics of two separate potential-dependent conformational transitions of membrane proteins which mediate the activation and inactivation of contraction in skeletal muscle.


1977 ◽  
Vol 55 (1) ◽  
pp. 21-33 ◽  
Author(s):  
J. F. Manery ◽  
E. E. Dryden ◽  
J. S. Still ◽  
G. Madapallimattam

Using small, intact frog muscles, the basic properties of Na+ and K+ transport were shown to resemble those of the (Na+ + K+) Mg2+ATPase (EC 3.6.1.3) isolated from skeletal muscle, (a) External K+ is essential for Na+ exit and K+ entry after the muscles are Na+-loaded and K+-depleted; (b) the ouabain concentration causing maximum inhibition of recovery is the same for transport as for the inhibition of the isolated enzyme. Ouabain causes a decrease in the sorbitol space and causes muscle fibre swelling. Absence of Ca2+ and Mg2+ inhibits recovery of normal Na+ and K+ concentrations and increases the sorbitol space. Insulin stimulates K+ uptake and Na+ loss in intact muscles but has no effect on the isolated sarcolemmal (Na+ + K+) Mg2+ATPase. Absence of divalent cations, addition of external ATP and of insulin enhance the ouabain inhibition of recovery.Bound ouabain was measured using [3H]ouabain and [14C]sorbitol (to measure the extracellular space). The process of binding was slowly reversible and was saturable within a range of ouabain concentrations from 1.48 × 10−7 to 5.96 × 10−7 M. From the nonexchangeable ouabain bound, the density of glycoside receptors was estimated to be 650 molecules per square micrometre of membrane surface. The absence of divalent cations, addition of external ATP and of insulin significantly enhanced the amount of ouabain bound. Substitution of Na+ and K+ by choline greatly reduced the bound ouabain.


1977 ◽  
Vol 55 (3) ◽  
pp. 700-708 ◽  
Author(s):  
J. G. Foulks ◽  
Florence A. Perry

When substituted for external chloride, organic anions differed markedly from one another in the extent to which they produced hyperexcitability and in the direction and intensity of their effects on twitch tension in frog skeletal muscle. All of the anions studied reduced the threshold [K]0 for K contractures and most enhanced twitch tension. Among carboxylate anions, increasing the size of the attached apolar hydrocarbon chain led to decreased hyperexcitability and to reduction in the amplitude of twitches and maximum K-contractures, butyrate being the most effective depressant of these responses. Sulfonate anions produced much less conspicuous changes in contractile performance. With γ-hydroxybutyrate, the introduction of a polar group on the hydrocarbon terminus resulted in twitch enhancement and partial restoration of maximum K-contracture tension. The depressant effect of butyrate on K contractures was partially overcome by a fivefold increase in the external concentration of calcium but twitches were unaffected. Perchlorate (12 mM) effectively antagonized the depressant actions of butyrate on twitches as well as K contractures. Most of the effects of these anions were prompt in onset. Impairment of contractile performance by butyrate was not accompanied by appreciable changes in membrane resting or action potentials or in the relation between [K]0 and membrane potential, and took place in spite of reduction in K-contracture threshold. Such effects must result from alteration in excitation–contraction coupling, possibly by interference with the binding of divalent cations to the membrane surface.


1973 ◽  
Vol 51 (5) ◽  
pp. 335-343 ◽  
Author(s):  
J. G. Foulks ◽  
J. A. D. Miller ◽  
Florence A. Perry

A number of agents were tested for their ability to restore potassium (K) contractures in calcium-free media. Effective agents included caffeine, chloroform, more polar permeant anions (e.g. nitrate and perchlorate) in place of external chloride, as well as divalent cations, e.g. Mg2+. The presence of sufficient EGTA to preclude significant increases in [Ca]0 did not affect the extent of K contracture restoration produced by these agents. The loss of K contracture capacity in calcium-free media, and its restoration by effective agents, appear to be related to the disproportionate effect of these procedures on the relation between log [K]0 and the potential-dependent processes which regulate contractile function.


1981 ◽  
Vol 240 (5) ◽  
pp. C193-C200 ◽  
Author(s):  
J. N. Howell ◽  
K. W. Snowdowne

Extracellular [Ca2+] in the range of 5-20 mM produces a concentration-dependent reversible reduction in tetanus tension in single frog skeletal muscle fibers. Both peak tension and ability to sustain tension during tetanus is reduced. The effect is unrelated to osmotic effects and independent of stimulation frequency in the range 100-200 Hz. The effect occurs both at 8 and 24 degrees C. Tetanus tension is most strongly inhibited by elevated extracellular [Ca2+] at short muscle lengths, but the effect can be seen at all lengths. Microelectrode recordings during tetanus indicate that action potentials remain undiminished in amplitude and duration throughout the tetanus. The evidence suggests that the inhibition results from a failure of action potentials propagation within the transverse tubular system.


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