Effect of a highly purified phospholipase C on some electrophysiological properties of the frog muscle fibre membrane

Life Sciences ◽  
1973 ◽  
Vol 13 (2) ◽  
pp. 171-176 ◽  
Author(s):  
J Boethius

In the frog muscle, ext. long. dig. IV, there are two or three spindle systems. Each consists of a bundle of intrafusal muscle fibres with two, three or four discrete encapsulated sensory regions distributed in mechanical series along it. A sensory region is usually comprised of the coiled branches of one afferent axon. These embrace the intrafusal fibres and ultimately form long fine varicose endings on or near them. The intrafusal striations appear to be lost for a short distance within the sensory region, and in this region the intrafusal fibre nuclei crowd together. The ‘small’ extrafusal efferents break up into trusses of fine unmyelinated axons and terminate as ‘grape’ end-plates, several of which can occur on the same muscle fibre. This is the ‘tonic’ system. The ‘large’ extrafusal efferents terminate as ‘Endbiischel’ end-plates on muscle fibres not supplied by grape endings. This is the ‘twitch’ system. Both ‘grape' and ‘twitch’ end-plates occur on the intrafusal bundle (probably on separate fibres) between the sensory regions. They are supplied by branches of ‘small’ or ‘large’ axons respectively, which also innervate extrafusal fibres. Thus like the extrafusals the intrafusal bundle is composed of ‘tonic’ and ‘twitch’ muscle fibres. This situation contrasts with that of the mammal, where extrafusals are exclusively ‘twitch’ fibres and intrafusals ‘tonic’.


1982 ◽  
Vol 98 (1) ◽  
pp. 39-47
Author(s):  
P. J. Stephens ◽  
H. L. Atwood

1. Effects of temperature on the muscle fibre membrane and synapses of stretcher muscle preparations made from autotomized limbs of the Pacific shore crab (Pachygrapsus crassipes) were investigated. 2. Acclimation of the crabs to different temperatures modified properties of both muscle fibre membrane and synapses. 3. Increased temperature produced an increase in membrane potential of the muscle fibres. A semi-log plot of these data revealed two linear phases of the membrane potential-temperature relationship, with a change in slope near the acclimation temperature. 4. Maximum values for excitatory junction potential (EJP) amplitude and time constant of EJP decay, and minimum values for facilitation were obtained at temperatures close to the acclimation temperature. It is suggested that the decline in EJP amplitude and time constant of decay produced by deviations in temperature from the acclimation temperature is compensated for by an increase in the amount of facilitation. In this way, maximum tension can be produced by the stretcher muscle in a range of at least 8 degrees C around the acclimation temperature.


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