1975
DOI: 10.1113/jphysiol.1975.sp011150
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Cinematographic analysis of contractile events produced in intrafusal muscle fibres by stimulation of static and dynamic fusimotor axons.

Abstract: SUMMARY1. Muscle spindles with an intact blood supply and uninterrupted connexions with ventral and dorsal spinal roots (Bessou & Pages, 1967 have been prepared in cat's tenuissimus muscles with the aim of cinephotographically recording intrafusal movements induced by the stimulation ofsingle static or dynamic y axons; the time course ofthese movements and the morphological kind of activated intrafusal muscle fibres have been established.2. Displacements of spindle guiding marks in the equatorial region elicit… Show more

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Cited by 86 publications
(27 citation statements)
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References 19 publications
(32 reference statements)
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“…This effect, observed in extrafusal fibers, is believed to result from the influence of myofilament lattice spacing on cross-bridge kinetics (Brown et al 1999). Under most physiological conditions the sarcomere length of the intrafusal fiber's polar region tends to follow that of extrafusal fibers (extrafusal sarcomere: Scott et al 1996;intrafusal sarcomere: Barker 1974;Bessou et al 1975;Boyd 1976;Poppele and Quick 1981), so the extrafusal fiber measurements were used to estimate the length (R) of the polar region of intrafusal fibers for this effect (assuming that length changes in sensory region are minor comparing to those in the polar region; see Implementation of the spindle model and parameter determination).…”
Section: The Intrafusal Fiber Modelmentioning
confidence: 99%
“…This effect, observed in extrafusal fibers, is believed to result from the influence of myofilament lattice spacing on cross-bridge kinetics (Brown et al 1999). Under most physiological conditions the sarcomere length of the intrafusal fiber's polar region tends to follow that of extrafusal fibers (extrafusal sarcomere: Scott et al 1996;intrafusal sarcomere: Barker 1974;Bessou et al 1975;Boyd 1976;Poppele and Quick 1981), so the extrafusal fiber measurements were used to estimate the length (R) of the polar region of intrafusal fibers for this effect (assuming that length changes in sensory region are minor comparing to those in the polar region; see Implementation of the spindle model and parameter determination).…”
Section: The Intrafusal Fiber Modelmentioning
confidence: 99%
“…This is probably due to the fact that, at that low frequency, the sustained contraction of bag2 fibres is already a large fraction of the maximal contraction observed at 60-70 stimuli/s. This is not so for chain fibres which, at this frequency, give unfused oscillations and whose maximal contraction is obtained only for much higher frequencies (Bessou & Pages, 1975;Boyd, 1976). That difference was already evoked to explain that the ratio of the increase in firing frequency of primary and secondary endings lying in the same spindle elicited by stimulation at 30 stimuli/s to that observed at 100 stimuli/s was greater when bag2 fibres were involved (Celichowski, Emonet-Denand, Gladden, Laporte & Petit, 1993).…”
Section: Preparationmentioning
confidence: 84%
“…At 30 stimuli/s, the contraction of bag2 fibres is nearly fused (Bessou & Pages, 1975) and can be expected to elicit a sustained and regular increase in the discharge frequency of primary endings. On the other hand, the contraction of chain fibres presents large oscillations (Bessou & Pages, 1975;Boyd, 1976) capable of eliciting either a 1: 1 driven response or an increase in the frequency of discharge of the primary endings with large variations in instantaneous frequency.…”
Section: Preparationmentioning
confidence: 99%
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“…A bag fiber is subjected to traction at its distal terminal, and the tapering pole leading up to it slips freely through the capsule collar and then places stress on the sensory ending adherent to its surface. The annulospiral wrappings of the Ia afferent are principally affected (Bessou and Pages, 1975;Boyd and Ward, 1975). Most chain fibers do not emerge from the capsule and are pulled on through attachments to the fusiform capsule and its inner continuation around the axial bundle (Bridgman et al, 1969;Sahgal et al, 1987), that is, they lengthen secondary to deformation of the capsule.…”
Section: Representation By Capsular and Extracapsular Componentsmentioning
confidence: 99%