scholarly journals Some effects of Ca-free choline-Ringer solution on frog skeletal muscle

1963 ◽  
Vol 166 (1) ◽  
pp. 75-86 ◽  
Author(s):  
B. A. Curtis
Keyword(s):  
Skeletal Muscle ◽  
Ringer Solution ◽  
Frog Skeletal Muscle ◽  
Free Choline

The Threshold for Potassium-Induced Contractures of Frog Skeletal Muscle. Potentiation of Potassium-Induced Contractures by Preexposure to Subthreshold Potassium Concentrations

1972 ◽  
Vol 50 (1) ◽  
pp. 37-44 ◽  
Author(s):  
E. C. Vos ◽  
G. B. Frank
Keyword(s):  
Skeletal Muscle ◽  
Potassium Concentration ◽  
Ringer Solution ◽  
Frog Skeletal Muscle ◽  
Contractile Apparatus ◽  
Tension Development ◽  
Eventual Loss ◽  
Active Processes ◽  
Muscle Potentiation ◽  
Small Bundle

A brief exposure (about 10–30 s) of a frog's toe muscle or a small bundle of fibers from the semi-tendinosus muscle to just subthreshold potassium concentrations potentiated contractures subsequently produced by exposing the muscles to a potassium concentration slightly above the threshold. The contractures thus potentiated had greater maximum tensions, and greater rates of tension development and relaxation than control contractures elicited by the same final potassium concentration. The resistance to stretch (R.T.S.) in the first few seconds of the potentiated contractures was about twice that of control contractures. Maximum potentiation occurred with preexposures of about 30 s; longer preexposures led to a decrease of potentiation and eventually to a depression of the contracture. The potentiation was not immediately abolished when the muscle was reexposed to Ringer solution but persisted for 2 min or longer (the 'washout effect'). It was concluded that exposing a muscle to low subcontracture threshold concentrations of potassium for a few seconds primes the intracellular contractile apparatus, probably by causing an increased sarcoplasmic concentration of Ca2+ ions, resulting in a potentiation of subsequently induced submaximal potassium contractures. The increase in metabolism (or 'Solandt effect') seen under these conditions is temporally related to the decline and eventual loss of the potentiation and is probably a reflection of active processes involved in reducing the sarcoplasmic concentration of Ca2+ ions.

scholarly journals Simultaneous measurement of Ca2+ in muscle with Ca electrodes and aequorin. Diffusible cytoplasmic constituent reduces Ca(2+)-independent luminescence of aequorin.

1991 ◽  
Vol 98 (6) ◽  
pp. 1141-1160 ◽  
Author(s):  
L A Blatter ◽  
J R Blinks
Keyword(s):  
Skeletal Muscle ◽  
Simultaneous Measurement ◽  
Light Emission ◽  
Ringer Solution ◽  
Light Signal ◽  
Frog Skeletal Muscle ◽  
Stable Level ◽  
Total Absence ◽  
Normal Ringer

Estimates of cytoplasmic Ca2+ concentration ([Ca2+]i) were made essentially simultaneously in the same intact frog skeletal muscle fibers with aequorin and with Ca-selective microelectrodes. In healthy fibers under truly resting conditions [Ca2+]i was too low to be measured reliably with either technique. The calibration curves for both indicators were essentially flat in this range of [Ca2+], and the aequorin light signal was uniformly below the level to be expected in the total absence of Ca2+. When [Ca2+]i had been raised to a stable level below the threshold for contracture by increasing [K+]o to 12.5 mM, [Ca2+]i was 38 nM according to aequorin and 59 nM according to the Ca-selective microelectrodes. These values are not significantly different. Our estimates of [Ca2+]i are lower than most others obtained with microelectrodes, probably because the presence of aequorin in the cells allowed us to detect damaging microelectrode impalements that otherwise we would have had no reason to reject. The observation that the light emission from aequorin-injected fibers in normal Ringer solution was below the level expected from the Ca(2+)-independent luminescence of aequorin in vitro was investigated further, with the conclusion that the myoplasm contains a diffusible macromolecule (between 10 and 30 kD) that interacts with aequorin to reduce light emission in the absence of Ca2+.

Ultra-Rapid Freezing of Isolated Skeletal Muscle Fibers

1977 ◽  
Vol 35 ◽  
pp. 576-577
Author(s):  
Joachim R. Sommer ◽  
Nancy R. Wallace
Keyword(s):  
Skeletal Muscle ◽  
Sarcoplasmic Reticulum ◽  
Granular Material ◽  
Nuclear Envelope ◽  
Intracellular Calcium ◽  
Ruthenium Red ◽  
Threshold Concentration ◽  
Rapid Freezing ◽  
Frog Skeletal Muscle ◽  
Electrical Isolation

After Howell (1) had shown that ruthenium red treatment of fixed frog skeletal muscle caused collapse of the intermediate cisternae of the sarcoplasmic reticulum (SR), forming a pentalaminate structure by obi iterating the SR lumen, we demonstrated that the phenomenon involves the entire SR including the nuclear envelope and that it also occurs after treatment with other cations, including calcium (2,3,4).From these observations we have formulated a hypothesis which states that intracellular calcium taken up by the SR at the end of contraction causes the M rete to collapse at a certain threshold concentration as the first step in a subsequent centrifugal zippering of the free SR toward the junctional SR (JSR). This would cause a) bulk transport of SR contents, such as calcium and granular material (4) into the JSR and, b) electrical isolation of the free SR from the JSR.

Electron Probe Analysis of Muscle

1982 ◽  
Vol 40 ◽  
pp. 398-401
Author(s):  
A. V. Somlyo ◽  
H. Shuman ◽  
A. P. Somlyo
Keyword(s):  
Skeletal Muscle ◽  
Smooth Muscle ◽  
Sarcoplasmic Reticulum ◽  
Resting State ◽  
Binding Sites ◽  
Electron Probe ◽  
Frog Skeletal Muscle ◽  
Electron Probe Analysis ◽  
Probe Analysis

Electron probe analysis of frozen dried cryosections of frog skeletal muscle, rabbit vascular smooth muscle and of isolated, hyperpermeab1 e rabbit cardiac myocytes has been used to determine the composition of the cytoplasm and organelles in the resting state as well as during contraction. The concentration of elements within the organelles reflects the permeabilities of the organelle membranes to the cytoplasmic ions as well as binding sites. The measurements of [Ca] in the sarcoplasmic reticulum (SR) and mitochondria at rest and during contraction, have direct bearing on their role as release and/or storage sites for Ca in situ.

Different actions of aconitine and veratrum alkaloids on frog skeletal muscle

1990 ◽  
Vol 21 (6) ◽  
pp. 863-868 ◽  
Author(s):  
Péter P. Nánási ◽  
Tamás Kiss ◽  
Miklós Dankó ◽  
David A. Lathrop
Keyword(s):  
Skeletal Muscle ◽  
Frog Skeletal Muscle ◽  
Veratrum Alkaloids

scholarly journals Permeability of Frog Skeletal Muscle Cells to Choline

1961 ◽  
Vol 44 (6) ◽  
pp. 1159-1164 ◽  
Author(s):  
Eugene M. Renkin
Keyword(s):  
Skeletal Muscle ◽  
Muscle Cells ◽  
Skeletal Muscle Cells ◽  
Frog Skeletal Muscle

Using choline-methyl-C14 as a tracer, it has been shown that choline+ penetrates into the cells of resting frog skeletal muscle at a rate similar to that of Na+, and that it escapes from these cells much more slowly than does Na+. Some implications of these findings are discussed.

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