scholarly journals Corticospinal and reciprocal inhibition actions on human soleus motoneuron activity during standing and walking

2015 ◽  
Vol 3 (2) ◽  
pp. e12276 ◽  
Author(s):  
Berthe Hanna-Boutros ◽  
Sina Sangari ◽  
Louis-Solal Giboin ◽  
Mohamed-Mounir El Mendili ◽  
Alexandra Lackmy-Vallée ◽  
...  
Keyword(s):  
Reciprocal Inhibition ◽  
Motoneuron Activity

Reciprocal Interactions in the Turtle Hindlimb Enlargement Contribute to Scratch Rhythmogenesis

1999 ◽  
Vol 81 (6) ◽  
pp. 2977-2987 ◽  
Author(s):  
Scott N. Currie ◽  
Gregory G. Gonsalves
Keyword(s):  
Power Spectra ◽  
Knee Extensor ◽  
Reciprocal Inhibition ◽  
Bilateral Stimulation ◽  
Motor Patterns ◽  
Reciprocal Interactions ◽  
Unilateral Stimulation ◽  
Before And After ◽  
Motoneuron Activity ◽  
Stimulation Of

Reciprocal interactions in the turtle hindlimb enlargement contribute to scratch rhythmogenesis. We examined interactions between the spinal networks that generate right and left rostral scratch motor patterns in turtle hindlimb motoneurons before and after transecting the spinal cord within the anterior hindlimb enlargement. Our results provide evidence that reciprocal inhibition between hip circuit modules can generate hip rhythmicity during the rostral scratch reflex. “Module” refers here to the group of coactive motoneurons and interneurons that controls either flexion or extension of the hip on one side and coordinates that activity with synergist and antagonist motor pools in the same limb and in the contralateral limb. The “bilateral shared core” hypothesis states that hip flexor and extensor (HF and HE) circuit modules interact via crossed and uncrossed spinal pathways: HF modules make reciprocal inhibitory connections with contralateral HF and ipsilateral HE modules and mutual excitatory connections with contralateral HE modules. It is currently unclear how much reciprocal inhibition between modules contributes to scratch rhythmogenesis. To address this issue, fictive scratch motor patterns were recorded bilaterally as electroneurograms from HF, HE, knee extensor (KE), and respiratory (d.D8) muscle nerves in immobilized animals. D 3 -end (low-spinal) preparations had intact spinal cords posterior to a complete D2–D3 transection. Unilateral stimulation of rostral scratch in D3-end turtles elicited rhythmic alternation between ipsilateral HF and HE bursts in most cycles; consecutive HF bursts were separated by complete silent (hf-off ) periods. D 3 –D 9 and D 3 –D 8 preparations received a second spinal transection at the caudal end of segment D9 or D8, respectively, within the anterior hindlimb enlargement. This second transection disconnected most HE circuitry (located mainly in segments D10–S2of the posterior enlargement) from the rostral scratch network and thereby reduced the HE-associated inhibition of HF circuitry. Unilateral stimulation of rostral scratch in most D3–D9 and D3-D8preparations evoked rhythmic or weakly modulated ipsilateral HF discharge without hf-off periods between bursts and without ipsilateral HE activity in the majority of cycles. In contrast, bilateral stimulation in D3–D9 and D3–D8 preparations reconstructed thehf-off periods, increased HF rhythmicity (assessed by fast Fourier transform power spectra and autocorrelation analyses), and reestablished weak HE-phase motoneuron activity. We suggest that bilateral stimulation produced these effects by simultaneously activating reciprocally inhibitory hip modules on opposite sides (right and left HF) and the same side (HF and residual ipsilateral HE circuitry). Our data support the hypothesis that reciprocal inhibition can contribute to spinal rhythmogenesis during the scratch reflex.

Ia inhibitory interneurons and Renshaw cells as contributors to the spinal mechanisms of fictive locomotion

1987 ◽  
Vol 57 (1) ◽  
pp. 56-71 ◽  
Author(s):  
C. A. Pratt ◽  
L. M. Jordan
Keyword(s):  
Maximal Activity ◽  
Cell Types ◽  
Reciprocal Inhibition ◽  
Extension Phase ◽  
Inhibitory Interneurons ◽  
Fictive Locomotion ◽  
Renshaw Cells ◽  
Step Cycle ◽  
Extensor Motoneuron ◽  
Motoneuron Activity

The activity of selected single alpha-motoneurons, Renshaw cells (RCs), and Ia inhibitory interneurons (IaINs) during fictive locomotion was recorded via microelectrodes in decerebrate (precollicular-postmammillary) cats in which fictive locomotion was induced by stimulation of the mesencephalic locomotor region. The interrelationships in the timing and frequency of discharge among these three interconnected cell types were determined by comparing their averaged step cycle firing histograms, which were normalized in reference to motoneuron activity recorded in ventral root filaments. Previous findings that RCs are rhythmically active during locomotion and discharge in phase with the motoneurons from which they are excited were confirmed, and further details of the phase relationships between RC and alpha-motoneuron activity during fictive locomotion were obtained. Flexor and extensor RCs became active after the onset of flexor and extensor motoneuron activity, respectively. Maximal activity in extensor RCs occurred at the end of the extension phase coincidental with the onset of hyperpolarization and a decrease in activity in extensor motoneurons. Maximal flexor RC activity occurred during middle to late flexion and was temporally related to the onset of reduced flexor motoneuron activity. The IaINs recorded in the present experiments were rhythmically active during fictive locomotion, as previously reported. The quadriceps IaINs were mainly active during the extension phase of the step cycle, along with extensor RCs. Thus the known inhibition of quadriceps IaINs by RCs coupled to quadriceps and other extensor motoneurons is obviously not sufficient to interfere with the appropriate phasing of IaIN activity and reciprocal inhibition during fictive locomotion, as had been speculated. Most of the quadriceps IaINs analyzed exhibited a decrease in discharge frequency at the end of the extension phase of the step cycle, which was coincidental with increased rates of firing in extensor RCs. These data are consistent with the possibility that extensor RCs contribute to the reduction in quadriceps IaIN discharge at the end of the extension phase of the step cycle. The possibility that IaIN rhythmicity during fictive locomotion arises from periodic inhibition, possibly from Renshaw cells, was tested by stimulating the reciprocal inhibitory pathway throughout the fictive step cycle. The amplitude of Ia inhibitory postsynaptic potentials (IPSPs) varied significantly throughout the fictive step cycle in 14 of the 17 motoneurons tested, and, in 11 of these 14 motoneurons, the Ia IPSPs were maximal during the phase of the step cycle in which the motoneuron was most

Reciprocal inhibition of voltage-gated potassium currents (IK(V)) by activation of cannabinoid CB1and dopamine D1receptors in ON bipolar cells of goldfish retina

2005 ◽  
Vol 22 (1) ◽  
pp. 55-63 ◽  
Author(s):  
SHIH-FANG FAN ◽  
STEPHEN YAZULLA
Keyword(s):  
G Protein ◽  
Receptor Agonist ◽  
Lucifer Yellow ◽  
Reciprocal Inhibition ◽  
Receptor Activation ◽  
Light Signal ◽  
Bipolar Cells ◽  
Protein G ◽  
Calcium Dependent ◽  
Voltage Dependent

Cannabinoid CB1receptor (viaGs) and dopamine D2receptor (viaGi/o) antagonistically modulate goldfish cone membrane currents. As ON bipolar cells have CB1and D1receptors, but not D2receptors, we focused on whether CB1receptor agonist and dopamine interact to modulate voltage-dependent outward membrane K+currentsIK(V)of the ON mixed rod/cone (Mb) bipolar cells. Whole-cell currents were recorded from Mb bipolar cells in goldfish retinal slices. Mb bipolar cells were identified by intracellular filling with Lucifer yellow. The bath solution was calcium-free and contained 1 mM cobalt to block indirect calcium-dependent effects. Dopamine (10 μM) consistently increasedIK(V)by a factor of 1.57 ± 0.12 (S.E.M.,n= 15). A CB receptor agonist, WIN 55212-2 (0.25–1 μM), had no effect, but 4 μM WIN 55212-2 suppressedIK(V)by 60%. IfIK(V)was first increased by 10 μM dopamine, application of WIN 55212-2 (0.25–1 μM) reversibly blocked the effect of dopamine even though these concentrations of WIN 55212-2 had no effect of their own. If WIN 55212-2 was applied first and dopamine (10 μM) was added to the WIN-containing solution, 0.1 μM WIN 55212-2 blocked the effect of dopamine. All effects of WIN 55212-2 were blocked by coapplication of SR 141716A (CB1antagonist) and pretreatment with pertussis toxin (blocker of Gi/o) indicating actionviaCB1receptor activation of G protein Gi/o. Coactivation of CB1and D1receptors on Mb bipolar cells produces reciprocal effects onIK(V). The CB1-evoked suppression ofIK(V)is mediated by G protein Gi/o, whereas the D1-evoked enhancement is mediated by G protein Gs. As dopamine is a retinal “light” signal, these data support our notion that endocannabinoids function as a “dark” signal, interacting with dopamine to set retinal sensitivity.

Organization of Binocular Pathways: Modeling and Data Related to Rivalry

1991 ◽  
Vol 3 (1) ◽  
pp. 44-53 ◽  
Author(s):  
Sidney R. Lehky ◽  
Randolph Blake
Keyword(s):  
Lateral Geniculate Nucleus ◽  
Binocular Rivalry ◽  
Striate Cortex ◽  
Reciprocal Inhibition ◽  
Lateral Geniculate ◽  
Layer 4 ◽  
Inhibitory Coupling ◽  
Binocular Matching

It is proposed that inputs to binocular cells are gated by reciprocal inhibition between neurons located either in the lateral geniculate nucleus or in layer 4 of striate cortex. The strength of inhibitory coupling in the gating circuitry is modulated by layer 6 neurons, which are the outputs of binocular matching circuitry. If binocular inputs are matched, the inhibition is modulated to be weak, leading to fused vision, whereas if the binocular inputs are unmatched, inhibition is modulated to be strong, leading to rivalrous oscillations. These proposals are buttressed by psychophysical experiments measuring the strength of adaptational aftereffects following exposure to an adapting stimulus visible only intermittently during binocular rivalry.

Background Synaptic Activity as a Switch Between Dynamical States in a Network

2003 ◽  
Vol 15 (7) ◽  
pp. 1439-1475 ◽  
Author(s):  
Emilio Salinas
Keyword(s):  
Random Network ◽  
Red Light ◽  
Theoretical Models ◽  
Reciprocal Inhibition ◽  
Synaptic Activity ◽  
Dynamic State ◽  
Motor Action ◽  
Sustained Activity ◽  
Uniform Background ◽  
Background Input

A bright red light may trigger a sudden motor action in a driver crossing an intersection: stepping at once on the brakes. The same red light, however, may be entirely inconsequential if it appears, say, inside a movie theater. Clearly, context determines whether a particular stimulus will trigger a motor response, but what is the neural correlate of this? How does the nervous system enable or disable whole networks so that they are responsive or not to a given sensory signal? Using theoretical models and computer simulations, I show that networks of neurons have a built-in capacity to switch between two types of dynamic state: one in which activity is low and approximately equal for all units, and another in which different activity distributions are possible and may even change dynamically. This property allows whole circuits to be turned on or off by weak, unstructured inputs. These results are illustrated using networks of integrate-and-fire neurons with diverse architectures. In agreement with the analytic calculations, a uniform background input may determine whether a random network has one or two stable firing levels; it may give rise to randomly alternating firing episodes in a circuit with reciprocal inhibition; and it may regulate the capacity of a center-surround circuit to produce either self-sustained activity or traveling waves. Thus, the functional properties of a network may be drastically modified by a simple, weak signal. This mechanism works as long as the network is able to exhibit stable firing states, or attractors.

PHASE DEPENDENT TRANSITION BETWEEN MULTISTABLE STATES IN A NEURAL NETWORK WITH RECIPROCAL INHIBITION

2004 ◽  
Vol 14 (05) ◽  
pp. 1559-1575 ◽  
Author(s):  
KATSUMI TATENO ◽  
HIDEYUKI TOMONARI ◽  
HATSUO HAYASHI ◽  
SATORU ISHIZUKA
Keyword(s):  
Neural Network ◽  
Network Model ◽  
Neural Network Model ◽  
Synaptic Input ◽  
Reciprocal Inhibition ◽  
Conduction Delay ◽  
Inhibitory Connection ◽  
Pacemaker Neurons ◽  
Excitatory Synaptic Input ◽  
Multistable State

We studied multistable oscillatory states of a small neural network model and switching of an oscillatory mode. In the present neural network model, two pacemaker neurons are reciprocally inhibited with conduction delay; one pacemaker neuron inhibits the other via an inhibitory nonpacemaker interneuron, and vice versa. The small network model shows bifurcations from quasi-periodic oscillation to chaos via period 3 with increase in the synaptic weight of the reciprocal inhibition. The route to chaos in the network model is different from that in the single pacemaker neuron. The network model exhibits several multistable states. In a regime of a weak inhibitory connection, in-phase beat, out-of-phase beat (period 3), and chaotic oscillation coexist at the multistable state. We can switch an oscillatory mode by an excitatory synaptic input to one of the pacemaker neurons through an afferent path. In a strong inhibitory connection regime, in-phase beat and out-of-phase beat (period 4) coexist at the multistable state. An excitatory synaptic input through the afferent path leads to the transition from the in-phase beat to the out-of-phase beat. The transition from the out-of-phase beat to the in-phase beat is induced by an inhibitory synaptic input via interneurons. A conduction delay, furthermore, causes the spontaneous transition from the in-phase beat to the out-of-phase beat. These transitions can be explained by phase response curves.

Activity and motor unit size in partially denervated rat medial gastrocnemius

1994 ◽  
Vol 76 (6) ◽  
pp. 2663-2671 ◽  
Author(s):  
L. J. Einsiedel ◽  
A. R. Luff
Keyword(s):  
Motor Unit ◽  
Gastrocnemius Muscle ◽  
Motor Units ◽  
Ventral Root ◽  
Treadmill Walking ◽  
Medial Gastrocnemius ◽  
Unit Size ◽  
Partial Denervation ◽  
Motoneuron Activity ◽  
Medial Gastrocnemius Muscle

The aim of the study was to determine whether increased motoneuron activity induced by treadmill walking would alter the extent of motoneuron sprouting in the partially denervated rat medial gastrocnemius muscle. An extensive partial denervation was effected by unilateral section of the L5 ventral root, and it is very likely that all units remaining in the medial gastrocnemius were used in treadmill walking. Rats were trained for 1.5 h/day and after 14 days were walking at least 1 km/day. Motor unit characteristics were determined 24 days after the partial denervation and were compared with units from partially denervated control (PDC) animals and with units from normal (control) animals. In PDC rats, force developed by slow, fast fatigue-resistant, and fast intermediate-fatigable motor units increased substantially compared with control animals; that of fast-fatigable units did not increase. In partially denervated exercised animals, force developed by slow and fast-fatigue-resistant units showed no further increase, but fast-intermediate- and fast-fatigable units showed significant increases compared with those in PDC animals. The changes in force were closely paralleled by changes in innervation ratios. We concluded that neuronal activity is an important factor in determining the rate of motoneuron sprouting.

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