1981
DOI: 10.1113/jphysiol.1981.sp013931
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Evolving views on the internal operation and functional role of the muscle spindle.

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Cited by 189 publications
(86 citation statements)
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References 66 publications
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“…We would argue against this however, in that the parallelism between aand y-motoneurone firing is not at all constant and the term 'co-activation' though not usually clearly defined, implies a rather rigid linkage between the two systems. It has been shown repeatedly that there is in fact considerable opportunity for independence of action (see especially Matthews, 1972 (chapter 9);1981).…”
Section: Discussionmentioning
confidence: 99%
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“…We would argue against this however, in that the parallelism between aand y-motoneurone firing is not at all constant and the term 'co-activation' though not usually clearly defined, implies a rather rigid linkage between the two systems. It has been shown repeatedly that there is in fact considerable opportunity for independence of action (see especially Matthews, 1972 (chapter 9);1981).…”
Section: Discussionmentioning
confidence: 99%
“…This leaves open the question of whether there may be some degree of separate control available over the bag2 and the chain fibres. Thus the interpretation offered for fusimotor action in reflex jaw movements is that the dynamic system provides 'parameter' control as visualized by Matthews (1981), while the static system generally provides a pattern of the intended movement, described as a 'temporal template'. This would mean that the static firing profile would generally resemble that of a activity, but the very different reflex connectivity of the two systems will cause frequent departures from a firm a-y co-activation (see also Appelberg et al 1983).…”
Section: Discussionmentioning
confidence: 99%
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“…Neurons were considered to respond to activated muscle proprioceptors when they (1) were sensitive to sinusoidal muscle stretching (Lundberg and Winsbury, 1960;Bianconi and van der Meulen, 1963;Brown et al, 1967;Matthews and Stein, 1969;Stuart et al, 1970;Mackie et al, 1998), showing a tight phase locking at the tested frequencies of 130 -135 Hz (Mackie et al, 1998); (2) produced spike bursting during stretching, a rapid drop in discharge on completion of the dynamic phase of stretching, and then a relatively slow drop during the holding phase (Matthews, 1933;Harvey and Matthews, 1961;Matthews, 1981;Edin and Vallbo, 1990); and (3) showed silenced firing during muscle shortening (stretch release) (Matthews, 1981;Edin and Vallbo, 1990;Grill and Hallet, 1995). It became clear during the first successful experiments in three distinct animals that cells responding in a 1:1 fashion to 130 -135 Hz muscular sinusoidal vibration also responded to manual muscle stretch (by flexing or extending the appropriated articulation), showing bursting discharges during the dynamic phase of stretching followed by a fall in discharge rate during holding and silenced firing during shortening.…”
Section: Methodsmentioning
confidence: 99%
“…Alternatively, GDNF may regulate the physiological function of developing or adult MNs Martin-Caraballo and Dryer, 2002). Finally, MN-specific Ret KOs should provide a unique tool to study the function of ␥-MNs, which modulate muscle spindle sensitivity to stretch and firing rate (Matthews, 1981) and therefore regulate proprioceptive function during a variety of behavioral tasks such as locomotion (Murphy and Martin, 1993).…”
Section: Fusimotor Mns Depend On Gdnf Only During the Period Of Develmentioning
confidence: 99%