Literature DB >> 9023777

Pacemaker activity in a sensory ending with multiple encoding sites: the cat muscle spindle primary ending.

R W Banks1, M Hulliger, K A Scheepstra, E Otten.   

Abstract

1. A combined physiological, histological and computer modelling study was carried out on muscle spindles of the cat tenuissimus muscle to examine whether there was any correlation between the functional interaction of putative encoding sites, operated separately by static and dynamic fusimotor neurones, and the topological structure of the preterminal branches of the primary sensory ending. 2. Spindles, whose I a responses to stretch and separate and combined static and dynamic fusimotor stimulation were recorded in physiological experiments, were located in situ. Subsequently the ramifications of the sensory ending were reconstructed histologically, and the topology of the branch tree was used in computer simulations of I a responses to examine the effect of the electronic separation of encoding sites on the static-dynamic interaction pattern. 3. Interactions between separate static and dynamic inputs, manifest in responses to combineed stimulation, were quantified by a coefficient of interaction (Ci) which, by definition, was 1 for strictly linear summation of separate inputs and zero for maximum occlusion between inputs. 4. For the majority of spindles static-dynamic interactions were characterized by pronounced occlusion (C1 < 0.35). In these spindles putative encoding sites (the peripheral heminodes of the branches supplying the intrafusal fibres activated by individual fusimotor efferents) were separated by a minimum conduction path of between three and ten myelinated segments (2-9 nodes of Ranvier). In contrast, significant summation (C1, approximately 0.7) was found in only one spindle. In this case putative encoding sites were separated by a single node. 5. Occlusion was not due to encoder saturation and it could not be accounted for by any other known physiological mechanisms (intrafusal fatigue or unloading). It is therefore attributed to competitive pacemaker interaction between encoding sites which are largely selectively operated by static and dynamic fusimotor efferents. 6. Model simulations of real preterminal-branch tree structures confirmed that short conduction paths between encoding sites were associated with manifest summation, whereas longer minimum conduction paths favoured pronounced occlusion. 7. In the extreme, occlusion could be so pronounced as to give rise to negative values of C1 during critical segments of response cycles. This was associated with lower discharge rates during combined static and dynamic stimulation than the higher of the individual stimulation effects. This phenomenon is referred to as hyperocclusion. Computer simulations demonstrated that hyperocclusion could be accounted for by a slow ionic adaptation process. e.g. by a very slowly activating K+ conductance.

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Year:  1997        PMID: 9023777      PMCID: PMC1159243          DOI: 10.1113/jphysiol.1997.sp021850

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  29 in total

1.  FURTHER STUDIES OF STATIC AND DYNAMIC FUSIMOTOR FIBRES.

Authors:  A CROWE; P B MATTHEWS
Journal:  J Physiol       Date:  1964-10       Impact factor: 5.182

2.  Effects of combining static and dynamic fusimotor stimulation on the response of the muscle spindle primary ending to sinusoidal stretching.

Authors:  M Hulliger; P B Matthews; J Noth
Journal:  J Physiol       Date:  1977-06       Impact factor: 5.182

3.  Factors affecting modulation in post-stimulus histograms on static fusimotor stimulation.

Authors:  F Emonet-Dénand; M Hulliger; P B Matthews; J Petit
Journal:  Brain Res       Date:  1977-09-23       Impact factor: 3.252

4.  On the subdivision of static and dynamic fusimotor actions on the primary ending of the cat muscle spindle.

Authors:  F Emonet-Dénand; Y Laporte; P B Matthews; J Petit
Journal:  J Physiol       Date:  1977-07       Impact factor: 5.182

5.  Static and dynamic fusimotor interaction and the possibility of multiple pace-makers operating in the cat muscle spindle.

Authors:  M Hulliger; J Noth
Journal:  Brain Res       Date:  1979-09-07       Impact factor: 3.252

6.  Position and velocity sensitivity of muscle spindles in the cat. IV. Interaction between two fusimotor fibres converging on the same spindle ending.

Authors:  G Lennerstrand
Journal:  Acta Physiol Scand       Date:  1968-11

7.  Afferent fibers with multiple encoding sites.

Authors:  J P Eagles; R L Purple
Journal:  Brain Res       Date:  1974-09-06       Impact factor: 3.252

8.  Anatomical evidence for multiple sources of action potentials in the afferent fibers of muscle spindles.

Authors:  D C Quick; W R Kennedy; R E Poppele
Journal:  Neuroscience       Date:  1980       Impact factor: 3.590

9.  Interaction of impulse activities originating from individual Golgi tendon organs innervated by branches of a single axon.

Authors:  Y Fukami
Journal:  J Physiol       Date:  1980-01       Impact factor: 5.182

10.  Dimensions of myelinated nerve fibers near the motor and sensory terminals in cat tenuissimus muscles.

Authors:  D C Quick; W R Kennedy; L Donaldson
Journal:  Neuroscience       Date:  1979       Impact factor: 3.590

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  18 in total

1.  Patterns of fusimotor activity during locomotion in the decerebrate cat deduced from recordings from hindlimb muscle spindles.

Authors:  A Taylor; R Durbaba; P H Ellaway; S Rawlinson
Journal:  J Physiol       Date:  2000-02-01       Impact factor: 5.182

2.  A novel path to chronic proprioceptive disability with oxaliplatin: Distortion of sensory encoding.

Authors:  Jacob A Vincent; Krystyna B Wieczerzak; Hanna M Gabriel; Paul Nardelli; Mark M Rich; Timothy C Cope
Journal:  Neurobiol Dis       Date:  2016-07-07       Impact factor: 5.996

3.  Model-based prediction of fusimotor activity and its effect on muscle spindle activity during voluntary wrist movements.

Authors:  Bernard Grandjean; Marc A Maier
Journal:  J Comput Neurosci       Date:  2013-12-01       Impact factor: 1.621

4.  A comparative analysis of the encapsulated end-organs of mammalian skeletal muscles and of their sensory nerve endings.

Authors:  R W Banks; M Hulliger; H H Saed; M J Stacey
Journal:  J Anat       Date:  2009-06       Impact factor: 2.610

5.  Correlated histological and physiological observations on a case of common sensory output and motor input of the bag1 fibre and a chain fibre in a cat tenuissimus spindle.

Authors:  R W Banks; M Hulliger; K A Scheepstra
Journal:  J Anat       Date:  1998-10       Impact factor: 2.610

6.  Distribution of TTX-sensitive voltage-gated sodium channels in primary sensory endings of mammalian muscle spindles.

Authors:  Dario I Carrasco; Jacob A Vincent; Timothy C Cope
Journal:  J Neurophysiol       Date:  2017-01-25       Impact factor: 2.714

7.  Changes in muscle spindle firing in response to length changes of neighboring muscles.

Authors:  Hiltsje A Smilde; Jake A Vincent; Guus C Baan; Paul Nardelli; Johannes C Lodder; Huibert D Mansvelder; Tim C Cope; Huub Maas
Journal:  J Neurophysiol       Date:  2016-04-13       Impact factor: 2.714

8.  Elastic tissue forces mask muscle fiber forces underlying muscle spindle Ia afferent firing rates in stretch of relaxed rat muscle.

Authors:  Kyle P Blum; Paul Nardelli; Timothy C Cope; Lena H Ting
Journal:  J Exp Biol       Date:  2019-08-02       Impact factor: 3.312

9.  Models of ensemble firing of muscle spindle afferents recorded during normal locomotion in cats.

Authors:  A Prochazka; M Gorassini
Journal:  J Physiol       Date:  1998-02-15       Impact factor: 5.182

Review 10.  The innervation of the muscle spindle: a personal history.

Authors:  Robert W Banks
Journal:  J Anat       Date:  2015-06-19       Impact factor: 2.610

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