Primary afferent depolarization of trigeminal fibres induced by stimulation of brain stem and peripheral nerves

1967 ◽  
Vol 23 (5) ◽  
pp. 398-400 ◽  
Author(s):  
F. Baldissera ◽  
G. Broggi ◽  
M. Mancia
Keyword(s):  
Brain Stem ◽  
Peripheral Nerves ◽  
Primary Afferent Depolarization ◽  
Primary Afferent ◽  
Stimulation Of

Excitability of primary afferents in feline spinal cord: taurine, homotaurine, and γ-aminobutyric acid compared

1982 ◽  
Vol 60 (6) ◽  
pp. 850-855 ◽  
Author(s):  
Radan Čapek ◽  
Barbara Esplin
Keyword(s):  
Primary Afferents ◽  
Aminobutyric Acid ◽  
Primary Afferent Depolarization ◽  
Conditioning Stimulation ◽  
Primary Afferent ◽  
Antagonistic Muscle ◽  
Consistent Change ◽  
Muscle Nerve ◽  
Gaba Synthesis ◽  
Stimulation Of

Effects of taurine and homotaurine (3-aminopropancsuIfonic acid), on excitability of primary afferents were compared with effects of γ-aminobutyric acid (GABA) in spinal unanaesthesized cats. Homotaurine and GABA, administered intravenously or topically, produced a marked increase in afferent excitability. Homotaurine was about 10 times more potent than GABA. Taurine (up to 2 mmol/kg i.v., or 10 mM topically) did not produce a consistent change in afferent excitability. The effect of homotaurine was antagonized by bicuculline or picrotoxin in doses which suppressed the primary afferent depolarization, as indicated by an increase of afferent excitability, evoked by conditioning stimulation of an antagonistic muscle nerve. Semicarbazidc, an inhibitor of GABA synthesis, did not attenuate the homotaurine-induced excitability changes of afferents while suppressing entirely the primary afferent depolarization. These findings suggest that homotaurine exerts a direct GABA-like action on feline primary afferents.

Neuronal responses in rostral trigeminal brain-stem nuclei of macaque monkeys after chronic trigeminal tractotomy

1986 ◽  
Vol 65 (4) ◽  
pp. 508-516 ◽  
Author(s):  
Ronald F. Young ◽  
Kent M. Perryman
Keyword(s):  
Electrical Stimulation ◽  
Brain Stem ◽  
Dental Pulp ◽  
Afferent Input ◽  
Tooth Pulp ◽  
Facial Skin ◽  
Trigeminal Nucleus ◽  
Primary Afferent ◽  
Stimulation Of ◽  
Relay Neurons

✓ Unilateral trigeminal tractotomy was carried out at the level of the obex, just rostral to the subnucleus caudalis, in five young adult Macaca fascicularis monkeys. The animals had been trained previously to perform a behavioral shock avoidance task in response to electrical stimulation of dental pulp and facial skin. Tractotomy produced an elevation in the stimulus strength which elicited escape behavior when facial skin was stimulated but not when the tooth pulp was stimulated. Unit activity, evoked by electrical stimulation of the tooth pulp and facial skin as well as innocuous and noxious mechanical stimulation of orofacial regions, was recorded from neurons in the trigeminal main sensory nucleus and the subnuclei oralis and interpolaris of the spinal nucleus 8 to 12 weeks after tractotomy. Primary afferent input to these nuclei is unaffected by the tractotomy which is located more caudally. The tractotomy interrupts primary afferent input into the trigeminal nucleus caudalis and also intranuclear connections between caudalis and the more rostral nuclei. Forty-one units contralateral and 47 ipsilateral to the tractotomy were studied. Thirty-six of the units responded only to low-threshold mechanical or electrical stimulation of orofacial zones, 46 were responsive to innocuous mechanical and electrical stimulation of orofacial zones and also to electrical stimulation of the dental pulp. Six units responded only to dental pulp stimulation. No statistically significant differences between the populations of neurons ipsilateral and contralateral to the tractotomies were found relating to the size or location of the peripheral receptive fields, latencies, thresholds, mean firing densities, or responsiveness to the various forms of stimulation. The behavioral results suggest that trigeminal relay neurons rostral to the obex are able to signal dental pain sensation, and the physiological studies confirm that the firing of such neurons is unaffected by tractotomy. The physiological studies demonstrate that the firing patterns of relay neurons activated by natural and electrical cutaneous facial stimuli and which are located in trigeminal brain-stem nuclei rostral to the obex are also not affected by tractotomy. The cutaneous facial analgesia observed after tractotomy thus appears to be due to deafferentation of relay neurons in trigeminal nucleus caudalis rather than to alterations in coding patterns in rostrally located trigeminal neurons due to interruption of the intratrigeminal pathway between the caudal and rostral nuclear groups.

Primary afferent depolarization of muscle afferents elicited by stimulation of joint afferents in cats with intact neuraxis and during reversible spinalization

1993 ◽  
Vol 70 (5) ◽  
pp. 1899-1910 ◽  
Author(s):  
J. Quevedo ◽  
J. R. Eguibar ◽  
I. Jimenez ◽  
R. F. Schmidt ◽  
P. Rudomin
Keyword(s):  
Spinal Cord ◽  
Knee Joint ◽  
High Threshold ◽  
Primary Afferent Depolarization ◽  
Delayed Response ◽  
Primary Afferent ◽  
Myelinated Fibers ◽  
Group I ◽  
Posterior Knee ◽  
Stimulation Of

1. In the anesthetized and artificially ventilated cat, stimulation of the posterior articular nerve (PAN) with low strengths (1.2-1.4 x T) produced a small negative response (N1) in the cord dorsum of the lumbosacral spinal cord with a mean onset latency of 5.2 ms. Stronger stimuli (> 1.4 x T) produced two additional components (N2 and N3) with longer latencies (mean latencies 7.5 and 15.7 ms, respectively), usually followed by a slow positivity lasting 100-150 ms. With stimulus strengths above 10 x T there was in some experiments a delayed response (N4; mean latency 32 ms). 2. Activation of posterior knee joint nerve with single pulses and intensities producing N1 responses only, usually produced no dorsal root potentials (DRPs), or these were rather small. Stimulation with strengths producing N2 and N3 responses produced distinct DRPs. Trains of pulses were clearly more effective than single pulses in producing DRPs, even in the low-intensity range. 3. Cooling the thoracic spinal cord to block impulse conduction, increased the DRPs and the N3 responses produced by PAN stimulation without significantly affecting the N2 responses. Reversible spinalization also increased the DRPs produced by stimulation of cutaneous nerves. In contrast, the DRPs produced by stimulation of group I afferents from flexors were reduced. 4. Conditioning electrical stimulation of intermediate and high-threshold myelinated fibers in the PAN depressed the DRPs produced by stimulation of group I muscle and of cutaneous nerves. 5. Analysis of the intraspinal threshold changes of single Ia and Ib fibers has provided evidence that stimulation of intermediate and high threshold myelinated fibers in the posterior knee joint nerve inhibits the primary afferent depolarization (PAD) of Ia fibers, and may either produce PAD or inhibit the PAD in Ib fibers, in the same manner as stimulation of cutaneous nerves. In 7/16 group I fibers the inhibition of the PAD was increased during reversible spinalization. 6. The results obtained suggest that intermediate and high-threshold myelinated fibers in the PAN have the same actions on Ia and Ib fibers as intermediate and high-threshold cutaneous afferents and may therefore be considered as belonging to the same functional system. They further indicate that in anesthetized preparations the pathways mediating the PAD of group I fibers, as well as the pathways mediating the inhibition of the PAD, may be subjected to a descending control that is removed by spinalization.

Somatosensory responses in the cat motor cortex. I. Identification and course of an afferent pathway

1991 ◽  
Vol 66 (6) ◽  
pp. 2041-2058 ◽  
Author(s):  
Y. Padel ◽  
J. L. Relova
Keyword(s):  
Spinal Cord ◽  
Motor Cortex ◽  
Brain Stem ◽  
Medial Lemniscus ◽  
Primary Afferent ◽  
Sensory Regulation ◽  
Afferent Fibers ◽  
Dorsal Columns ◽  
Primary Afferent Fibers ◽  
Stimulation Of

1. The main aim of the present series of experiments was to demonstrate with electrophysiological methods that the spinothalamocortical system may send somesthetic information to the pyramidal and corticospinal tract cells in the motor cortex of the cat. 2. Experiments were carried out on acutely prepared cats anesthetized with alpha-chloralose. Extra- and intracellular recordings were made from the cells located in the pericruciate motor cortex (the lateral portion of area 4 gamma). They were identified by their antidromic responses to pyramidal stimulation and/or stimulation of the dorsolateral funiculus of the spinal cord. The animals were subjected to a set of nervous tissue lesions to prevent any transit of extereoceptive information to the motor cortex via the cerebellum and the somatosensory cortex. A lesion of the dorsal part of the spinal cord was also made, leaving intact only the afferent inflow ascending in the spinal ventral half, i.e., the spinothalamic system. 3. In this cat preparation it was observed that both electrical and natural stimulation of the limbs still efficiently activated the motor cortical efferent cells. 4. The pathway was mapped by applying microstimulation along its whole course in the spinal cord and brain stem. Stimulation of the primary afferent fibers running in the dorsal columns caudally to the spinal cord lesion produced activation and/or inhibition of the cortical cells. The existence of these responses may be attributable to the existence of collaterals from primary afferent fibers located in the dorsal columns, which activate the spinothalamic tract cells either mono- or polysynaptically. In the brain stem the fibers join the medial lemniscus. 5. In view of the short latency of the responses (mean latency 10.5 ms from the spinal cord) it is suggested that this component of the spinothalamic system may play an important role in the sensory regulation of ongoing movements.

Excitability changes of terminal arborizations of single Ia and Ib afferent fibers produced by muscle and cutaneous conditioning volleys

1976 ◽  
Vol 39 (6) ◽  
pp. 1150-1159 ◽  
Author(s):  
W. D. Willis ◽  
R. Nunez ◽  
P. Rudomin
Keyword(s):  
Dorsal Root ◽  
Primary Afferent Depolarization ◽  
Motor Nucleus ◽  
Sodium Pentobarbital ◽  
Primary Afferent ◽  
Population Responses ◽  
Afferent Fibers ◽  
Conduction Velocities ◽  
The Central Nervous System ◽  
Stimulation Of

1. In cats anesthetized with sodium pentobarbital, recordings were made from dorsal root ganglion (DRG) cells having a peripheral process in the gastrocnemius-soleus (GS) nerve. The GS nerve was left in continuity with the muscle to allow identification of group Ia and Ib fibers by responses of the receptors to muscle stretch and contraction. The central processes of the DRG cells were activated antidromically by stimulation within the spinal cord so that changes in the excitability of the fibers could be examined following conditioning volleys in muscle and cutaneous nerves. 2. Recordings were made from 44 DRG cells. Of these, 15 were group Ia and 9 group Ib afferents of the GS nerve. 3. Of 15 Ia fibers, 12 were activated antidromically by stimulation in the motor nucleus, but no Ib fibers were discharged by such stimulation. Ib fibers could be antidromically activated by stimulation in the intermediate nucleus. 4. The central processes of the Ia DRG cells had slower conduction velocities than did the peripheral processes. 5. The thresholds to electrical stimulation of the peripheral processes of Ia and Ib fibers of the GS nerve showed considerable overlap. 6. All of the Ia DRG cells tested showed an increased excitability following conditioning volleys in the biceps-semitendinosus (BST) nerve. The increase in excitability was produced by the largest fibers of the BST nerve. 7. Stimulation of the sural (SU) or superficial peroneal (SP) cutaneous nerves also increased the excitability of some Ia fibers. However, other Ia fibers were unaffected, and in two cases the excitability was reduced. 8. The excitability of group Ib fibers was increased by conditioning volleys in the BST, SU, or SP nerves. 9. It is concluded that cutaneous volleys produce a mixture of primary afferent depolarization and primary afferent hyperpolarization in Ia fibers of anesthetized cats. Such converse actions probably cancel in excitability tests using population responses. 10. The excitability of single Ia fibers is not stationary in excitability presumably reflect slow alterations within the central nervous system, perhaps related to spontaneous alterations in the level of tonically maintained primary afferent depolarization.

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