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Vestibular and proprioceptive modulation of postural synergies in normal subjects.

One way of investigating different muscle synergies underlying human balance control is to assume that only 1 or 2 centrally preprogrammed synergies are available to reestablish upright stance when it is perturbed. According to this hypothesis, the many, apparently different, synergies elicited by rotation or translation of a support-surface on which test subjects stand, in fact, result from a modulation of muscle responses induced by different amplitudes of afferent inputs. To test this hypothesis, we probed the balance control of 16 normal subjects with 5 combinations of rotation and translation of the support surface. Each combination yielded a constant angle (3 or 4 degrees) and angular velocity (18 and 36 degrees/s, respectively) over the first 120 ms of ankle dorsiflexion but resulted in differing velocities of upper leg, trunk, and head movements. These first 120 ms of link movements and the resulting muscle responses were analysed for amplitude and timing modulation using 3 techniques. First, velocities of initial link movements and areas of muscle EMG activity were examined separately for the minimum number of descriptors, which would optimally describe the linear variation of the interlink amplitude synergy with respect to the amount of support-surface rotation or translation employed to perturb balance. Initial trunk angular velocity, which was highly correlated with head linear acceleration (r = 0.9), provided the first best descriptor of initial link movements. Ankle angular velocity provided the second descriptor because it was not correlated with trunk angular velocity. The amplitude modulation synergy of EMG responses could be characterised by the modulation of tibialis anterior and paraspinal muscles between 160 and 240 ms and by that of soleus between 80 and 120 ms after stimulus onset. The linear combination of these best descriptors of link movements and that for EMG response amplitudes changed continuously in an identical manner with changes in the stimulus combination. Second, multivariate linear correlations between the amplitudes of initial link velocities and muscle EMG response areas best describing the response amplitude synergy were examined. Several significant correlations (r > 0.6) were obtained between leg and trunk muscle activity 120 ms after stimulus onset and trunk, or upper leg angular velocity, or head linear velocity, prior to 120 ms. Finally, crosscorrelations between muscle responses were examined for consistent interlink timing synergies between muscle responses.(ABSTRACT TRUNCATED AT 400 WORDS)

Afferent Pathways↗

Synaptic potentials in the central terminals of locust proprioceptive afferents generated by other afferents from the same sense organ.

Afferent neurons from a proprioceptor [the femoral chordotonal organ (FCO)] at the femoro-tibial joint of a locust hindleg carry patterns of spikes to the CNS in which information is coded about the positions and movements of the tibia. Intracellular recordings from the afferents of this organ as they enter the CNS reveal spikes and depolarizing post-synaptic potentials (PSPs) during voluntary or imposed movements of the joint. Some of these PSPs are generated as a result of spikes in other FCO afferents, and can be evoked experimentally by electrical stimulation of the nerve from the organ. One afferent does not appear to synapse directly on another, but instead activates reliable pathways involving other central neurons. Current clamping of individual afferents in isolated ganglia shows that the PSPs are increased in amplitude by hyperpolarizing currents injected into an afferent, and decreased by depolarizing ones. They reverse at about -68 mV (n = 5). At the normal resting potential of the afferents, -72 mV (+/- 0.42 SE, n = 57), the PSPs are therefore depolarizing, and are associated with an increased conductance of the membrane. The changes in membrane potential and conductances associated with the PSPs can be mimicked by pressure injection of GABA into the regions of neuropil that contain the terminals of the afferents. The potential evoked by GABA is associated with an increased conductance of the membrane and reverses at the same potential as the PSPs. GABA also reduces the PSPs evoked in the terminals, either by movements of the FCO or by electrical stimulation of its nerve. The PSPs and the effects of the GABA-evoked potentials are mimicked by the GABA agonist muscimol. The PSPs are blocked reversibly by picrotoxin. The PSPs and the GABA-evoked potentials both alter the excitability of an afferent terminal by reducing the ability of the membrane to support an action potential. It is suggested that the PSPs are depolarizing, inhibitory potentials generated in the terminals of the afferents by central neurons that release GABA, and that their role is to change the efficacy of the afferent spikes at their first output synapses in the CNS. These interactions could form a graded, gain control mechanism for synaptic transmission at the afferent output synapses that is directly dependent on the features of the mechanical movements of the joint.

Action Potentials↗

[The occlusal plane: an architectural myth or a proprioceptive myth?].

From two radiographic pictures of the head in profile, in meantime of few years, with the same person, the author proves that occlusal plane doesn't vary during growth in comparison with the pterygo-clivien compass (Stable zone leasing against pterygoïd process and superior clivus). The orientation of occlusal plane crossing by contact of the first molars and the middle of incisive intersection has an approximately analogous value. This value is equal to 110 degrees for the sample population, whatever the person's morphology and the lapsed time is. The occlusal plane moves parallel to himself and gets lower on a sagittal téléradiographic picture.

Adolescent↗

Disconnected mutants show disruption to the central projections of proprioceptive neurons in Drosophila melanogaster.

We used a P[GAL4] enhancer-trap line, C161, in conjunction with the UAS-lacZ reporter construct to visualize the central projections of a defined set of thoracic and abdominal sensory neurons in a disconnected (disco) mutant background. The results show defects in the organization of sensory axons in the larval and adult central nervous system. The defects are indicative of problems with axon growth and development and include (a) poor axon fasciculation, (b) aberrant axon growth, (c) excessive terminal branching, and (d) ectopic innervation. Sensory neuron identity appears to be normal. The defects are comparable to those previously described for larval photoreceptor and adult retinular cells in disco mutants and extend the known effects of this mutation. Reduced larval and adult viability are likely to result from locomotory defects related to the disruption of the sensory system.

Animals↗

Proprioceptive input to feeding motor programs in Aplysia.

Although central pattern generators (CPGs) can produce rhythmic activity in isolation, it is now generally accepted that under physiological conditions information from the external and internal environment is incorporated into CPG-induced motor programs. Experimentally advantageous invertebrate preparations may be particularly useful for studies that seek to characterize the cellular mechanisms that make this possible. In these experiments, we study sensorimotor integration in the feeding circuitry of the mollusc Aplysia. We show that a premotor neuron with plateau properties, B51, is important for generating the radula closing/retraction phase of ingestive motor programs. When B51 is depolarized in semi-intact preparations, radula closing/retractions are enhanced. When B51 is hyperpolarized, radula closing/retractions are reduced in size. In addition to being important as a premotor interneuron, B51 is also a sensory neuron that is activated when the feeding apparatus, the radula, rotates backward. The number of centripetal spikes in B51 is increased if the resistance to backward rotation is increased. Thus, B51 is a proprioceptor that is likely to be part of a feedback loop that insures that food will be moved into the buccal cavity when difficulty is encountered. Our data suggest, therefore, that Aplysia are able to adjust feeding motor programs to accommodate the specific qualities of the food ingested because at least one of the neurons that generates the basic ingestive motor program also serves as an on-line monitor of the success of radula movements.

Action Potentials↗