Conduction Velocity Groups Research Articles

On Parallel Streams through the Mouse Dorsal Lateral Geniculate Nucleus.

The mouse visual system is an emerging model for the study of cortical and thalamic circuit function. To maximize the usefulness of this model system, it is important to analyze the similarities and differences between the organization of all levels of the murid visual system with other, better studied systems (e.g., non-human primates and the domestic cat). While the understanding of mouse retina and cortex has expanded rapidly, less is known about mouse dorsal lateral geniculate nucleus (dLGN). Here, we study whether parallel processing streams exist in mouse dLGN. We use a battery of stimuli that have been previously shown to successfully distinguish parallel streams in other species: electrical stimulation of the optic chiasm, contrast-reversing stationary gratings at varying spatial phase, drifting sinusoidal gratings, dense noise for receptive field reconstruction, and frozen contrast-modulating noise. As in the optic nerves of domestic cats and non-human primates, we find evidence for multiple conduction velocity groups after optic chiasm stimulation. As in so-called “visual mammals”, we find a subpopulation of mouse dLGN cells showing non-linear spatial summation. However, differences in stimulus selectivity and sensitivity do not provide sufficient basis for identification of clearly distinct classes of relay cells. Nevertheless, consistent with presumptively homologous status of dLGNs of all mammals, there are substantial similarities between response properties of mouse dLGN neurons and those of cats and primates.

The Effect of Tramadol on the Rat Sciatic Nerve Conduction: A Numerical Analysis and Conduction Velocity Distribution Study

The aim of this study was to document the effect of tramadol as an opioid on individual fibers of rat sciatic nerve. To accomplish this objective, compound action potentials (CAPs) were recorded from isolated nerves treated with tramadol from five different concentration levels. Then recorded CAPs and the control group were analyzed by numerical methods namely Conduction Velocity Distribution (CVD) and Fast Fourier Transform (FFT). The results show that the area under CAP and the time derivative of CAP curves decreases, and the excitability of the nerve trunk falls as well (rheobase and chronaxie increases) with increasing tramadol concentration. CVD deduced by model study was divided into subgroups as SLOW (8-26 m/s), MODERATE (26-44 m/s), MEDIUM (44-60 m/s) and FAST (60-78 m/s). The decrement in percentage relative contribution of these conduction velocity groups starts with a concentration of 0.25 mM tramadol, especially in the subgroup named FAST. The power spectrum shifts from higher frequency region to lower frequency region as the tramadol concentration increases. These findings show that fast conducting fibers are more susceptible to tramadol than medium and moderate groups and tramadol possibly acts on channel activity rather than passive properties (such as space and time constant) of nerve fibers.

Subclinical Neuropathy Among Diabetes Control and Complications Trial Participants Without Diagnosable Neuropathy at Trial Completion

We sought to evaluate the prevalence of subclinical neuropathy in intensive and conventional treatment groups at completion of the Diabetes Control and Complications Trial (DCCT). We assessed neuropathy using nerve conduction results obtained at DCCT completion after stratifying the DCCT cohort to exclude subjects with progressively less severe degrees of diagnosable neuropathy. We began with those who had confirmed clinical neuropathy (the primary DCCT end point) and eventually excluded all subjects with any clinical or electrodiagnostic evidence of neuropathy. After excluding subjects with confirmed clinical neuropathy at DCCT completion, 8 of 10 nerve conduction measures (including all lower-extremity measures) were significantly improved in the intensive treatment group (O'Brien rank-sum test across all nerve conduction measures, P < 0.0001). Conduction velocity group differences were substantial, and the peroneal conduction velocity averaged 3.1 m/s faster in the intensive compared with the conventional treatment group (45.1 vs. 42.0 m/s, P < 0.0001). Numerous significant differences in median and peroneal motor conduction velocities favoring the intensive treatment group persisted, regardless of the exclusion criteria applied. Intensive and conventional treatment group subjects without diagnosable neuropathy at DCCT completion had significant differences in electrophysiologic measurements favoring the intensive treatment group. Differences in subsequent incident neuropathy between the original treatment groups may reflect, in part, their levels of subclinical neuropathy at DCCT completion, rather than persistent metabolic effects.

Morphine Directly Inhibits Nociceptors in Inflamed Skin

Peripherally delivered opiates attenuate mechanical and thermal hyperalgesia in experimental models of inflammation, suggesting that activation of peripheral opioid receptors decreases the excitability of nociceptors in inflamed tissues. The current study examines the effects of peripheral morphine sulfate on response properties of sensory neurons in healthy and inflamed skin. Afferent units (185) were isolated from tibial nerve of rats using an in vitro glabrous skin-nerve teased-fiber preparation. Of these, 107 units were from normal healthy skin, and 78 were from inflamed skin 18 h after intraplantar injection of complete Freund's adjuvant. As a population, C-fiber units innervating inflamed skin exhibited properties characteristic of sensitization when compared with units innervating healthy control skin. Mechanical thresholds were lowered, responses to noxious mechanical and thermal stimuli were elevated, a greater proportion of units was spontaneously active, and the average rate of spontaneous discharge was higher. Response properties in other conduction velocity groups remained unchanged. Fifty-eight percent of C and C/Adelta nociceptors innervating inflamed skin were opiate-sensitive, and their excitability was attenuated by direct application of morphine to their receptive fields. All morphine-sensitive units were nociceptors from inflamed skin with conduction velocities <1.3 m/s. Morphine effects were concentration-dependent and naloxone-sensitive, indicating that the effects were receptor-mediated. These findings provide direct evidence that morphine acts through peripheral opioid receptors to inhibit the activity of cutaneous nociceptors under conditions of inflammation.

DEEP PERONEAL MOTOR NERVE CONDUCTION VELOCITY DISTRIBUTION AND CORRELATION BETWEEN NERVE CONDUCTION GROUPS AND THE NUMBER OF INNERVATED MUSCLE FIBERS

In this study, the distribution of peroneal-nerve conduction velocity was studied in 17 normal subjects, using the collision method. Paired supramaximal stimuli with predetermined interstimulus intervals (ISI) were applied at distal and proximal points of peroneal nerve and the resultant compound muscle action potentials (CMAPs) were recorded. The change in CMAP amplitudes and areas with ISI were deduced, and the relative number of fibers corresponding to each conduction velocity group (CVG) were computed. Conduction velocities of the peroneal motor nerve innervating the Extensor Digitorum Brevis (EDB) muscle were found to be in the range of 28-52 m/s and CVG innervating the greatest number appears to be in 40-48 m/s range, which consists of 70% of all fibers. These results show that, compared with the median motor nerve, deep peroneal motor nerve that innervates the EDB muscle consist of slow fibers.

CORRELATION OF MOTOR NERVE CONDUCTION VELOCITY AND NUMBER OF INNERVATED MUSCLE FIBERS

Distal and proximal motor (M) responses were recorded from the "Abductor Pollicis Brevis" (APB) muscle by using the collision method; median motor nerve was stimulated at distal (elbow) and proximal (wrist) regions in a concurrent manner. The delay between two stimuli (ISI: Inter-stimulus Interval), beginning at 9 ms, was decreased by 0.1 ms steps, until the proximal potential completely disappeared. Areas of M responses recorded for each ISI were calculated. Because the area difference between two subsequent ISIs is proportional to the number of muscle fibers innervated by the conduction velocity group at that interval, the relative numbers of muscle fibers for each velocity group were calculated. The results show that the motor nerve conduction velocities belonging to the innervating APB muscle vary between 38 m/s and 57 m/s; the conduction velocity of the group innervating the greatest number of muscle nerves was found to be 55-57 m/s, which comprised 10% of all fibers

Phenotype and Function of Somatic Primary Afferent Nociceptive Neurones with C-, Aδ- or Aα/β-Fibres.

Nociceptive dorsal root ganglion (DRG) neurones have fibres that conduct in the C, Aδ and Aα/β conduction velocity range. The properties of nociceptive compared with non-nociceptive somatic afferent dorsal root ganglion neurones appear to fall into two patterns, A and B. Pattern A properties of nociceptive neurones, the more common type, include longer action potential duration and slower maximum rate of fibre firing, as well as a greater expression of substance P and calcitonin gene-related peptide immunoreactivity. The values of pattern A properties appear to be graded according to the conduction velocity group (C, Aδ or Aα/β) of the fibres. The most pronounced forms of A-type properties are expressed by nociceptive neurones with C-fibres, and these become less pronounced in nociceptive neurones with Aδ-fibres and least pronounced in those with Aα/β fibres (C > Aδ > Aα/β). Some of these properties are also expressed in a less extreme but similarly graded manner through C, Aδ and Aα/β groups of non-nociceptive low threshold mechanoreceptive (LTM) neurone. The less common pattern B properties of nociceptive neurones have similar values in C-, Aδ- and Aα/β-fibre nociceptive neurones but these clearly differ from LTM units with C-, Aδ- and Aα/β-fibre conduction velocities. These features of nociceptive neurones include consistently larger action potential overshoots and longer after-hyperpolarisation durations in nociceptive than in LTM neurones.

Differences in the size of the somatic action potential overshoot between nociceptive and non-nociceptive dorsal root ganglion neurones in the guinea-pig

Intracellular action potentials evoked by dorsal root stimulation were intracellularly recorded from L6 and S1 dorsal root ganglion neurones in deeply anaesthetised guinea-pigs in vivo. Units were classed as C, Aδ or Aα/β units and as nociceptive, low-threshold mechanoreceptive or unresponsive. Units with membrane potentials of at least −40 mV and action potentials with an amplitude of >20 mV were included.Nociceptive neurones had significantly larger somatic action potential overshoots than low-threshold mechanoreceptors in C, Aδ and Aα/β units. A higher proportion of low-threshold mechanoreceptors than of nociceptors had action potentials that failed to overshoot in all conduction velocity groups. 60% of muscle spindle afferents failed to overshoot. The size of the overshoot was correlated positively with log10 action potential duration, log10 action potential rise time, log10 afterhyperpolarisation duration, action potential amplitude and membrane potential and negatively (weakly) with log10 conduction velocity.We conclude that nociceptive neurones are more likely to have somatic action potential overshoots than low-threshold mechanoreceptors in any conduction velocity group. This effect was not due to electrode properties or conduction failure at site(s) of failure of action potential regeneration. Differences in overshoot may affect the influence of neuronal firing on cellular processes. If an overshooting action potential is used as a selection criterion, a bias towards nociceptive neurones is likely to occur. An overshooting action potential coupled with a long afterhyperpolarisation or broad action potential may help in identifying sensory neurones as nociceptive.

Conduction velocity groups in the retino-tectal and retino-thalamic visual pathways of the pigeon (Columbia livia).

The anatomical characteristics of the avian visual system are well known. However, there are wide gaps in our knowledge with respect to the physiological characteristics of their visual system. For example, we lack both an operational identification of the different ganglion cell types present in the retinae of birds, and a description of their presumptive differential central projections. The results presented here address this latter point by classifying the conduction velocity groups of fibers present in the optic tract of the pigeon. We report the existence of at least 5 groups of axons in the optic tract of the pigeon, with conduction velocities of 22-18 m/s, 12-10 m/s, 8 m/s, 6 m/s and less than 2.5 m/s. All five groups project to the tectum but only the four fastest groups project to the dorsal thalamic complex. The homologies with the populations of retinal axons found in cats are discussed.

Diode laser irradiation selectively diminishes slow component of axonal volleys to dorsal roots from the saphenous nerve in the rat

Ga-Al-As laser irradiation (830 nm wavelength) inhibits the action potentials in the dorsal roots elicited from the saphenous nerve of the rat. Following laser irradiation to the saphenous nerve, the amplitude of slower conduction parts of action potentials (conduction velocity <12 m/s) were suppressed. This suppression was irradiation time dependent. After 3 min irradiation, slowest conduction velocity group (<1.3 m/s) were totally diminished and 1.3–12 m/s group were reduced to 12–67%. In contrast, faster component (>12 m/s) was unaffected by laser irradiation. These findings suggest that laser irradiation may selectively target fibers conducting at slow velocities which include afferent axons from nociceptors.

Soma neurofilament immunoreactivity is related to cell size and fibre conduction velocity in rat primary sensory neurons.

1. Intracellular recordings were made in dorsal root ganglia in vitro at 37 degrees C. The L4, L5 and L6 ganglia from 46- to 51-day-old female Wistar rats were used. In each neuron conduction velocity (CV) was measured and fluorescent dye was injected. Later the intensity of the immunoreactivity to RT97 (a monoclonal antibody to the phosphorylated 200 kDa neurofilament subunit) as well as the cell size (cross-sectional area at the nuclear level) were measured in the dye-injected neurons. RT97 was used to distinguish between the L (light, neurofilament-rich) and the SD (small dark, neurofilament-poor) neuronal somata. 2. Neurons were classified as C neurons (CV less than 1.3 m/s), C/A delta neurons (1.3-2 m/s), A delta neurons (2-12 m/s) or A alpha/beta neurons (greater than 12 m/s). 3. All A-fibre somata were RT97 positive (L) and all C-fibre somata were RT97 negative (SD), although in the C/A delta group both positive and negative neurons were seen. Thus, RT97-negative somata had C (unmyelinated) or C/A delta fibres, while RT97-positive somata had A (myelinated) or C/A delta fibres. 4. The size distributions of A neurons and C neurons were consistent with their classification as L- and SD-cell neurons respectively. The size distribution of A delta cells was skewed with a peak of small cells and a tail of medium-sized cells. 5. There was a loose positive correlation between cell size and fibre CV. 6. RT97 intensity was positively correlated with CV if all neurons were considered together, but no correlation was seen within the C, A delta or A alpha/beta CV groups. 7. RT97 intensity was positively correlated with cell size when all neurons were considered together. Although no correlation was seen within the C or the A delta CV groups, a clear positive correlation was seen for A alpha/beta neurons. 8. The relationship of RT97 intensity to cell size was not demonstrably altered by axotomy, time in vitro or the presence of intracellular dye in control experiments. 9. RT97-negative and -positive neurons could be seen in neonatal rat ganglia. Their size distributions resembled, respectively, the SD- and L-neuron populations at this age. RT97 immunoreactivity may therefore be a useful predictor of the cell type and myelinated state which a sensory cell is destined to reach in the adult rat.

Conduction velocity is related to morphological cell type in rat dorsal root ganglion neurones.

Combining intracellular recording and dye-injection techniques permitted direct correlation of neuronal soma size with peripheral nerve conduction velocity in individual neurones of the L4 dorsal root ganglion (d.r.g.) of the anaesthetized 5-8-week-old rat. The conduction velocities fell into two main groups; those greater than 14 m/s (A alpha and beta fibres) and those less than 8 m/s (A delta and C fibres). Fibres with conduction velocities in the A delta range (2.2-8 m/s) in the sciatic nerve between the sciatic notch and the neuronal soma in the d.r.g. often conducted more slowly, that is in the C-fibre range (less than 1.4 m/s), in the periphery from the tibial nerve to the sciatic notch. For the fast-conducting myelinated afferents, there was a loose positive correlation between cell size and the conduction velocity of the peripheral axon, whereas a clearer positive correlation existed between neuronal cell size and axonal conduction velocity both for A delta- and for C-fibre afferents. The relationship of the cell cross-sectional area (measured at the nucleolar level), to the cell volume for each neuronal soma was similar for the different conduction velocity groups. The somata of the fast-conducting myelinated A alpha and A beta fibres had a similar mean and range of cross-sectional areas to those of the large light cell population. The somata with A delta and C fibres were of a more uniform size and were restricted to the smaller cells within the ganglia. The mean and range of cross-sectional areas of the C cells was similar to those of the small dark cell population. A delta somata had a larger mean and range of cell sizes than those of the small dark cell population. The relationships of peripheral axon type to the morphological cell types are discussed.

Conduction of velocity groups in the optic nerve of the North American opossum (Didelphis virginiana): retinal origins and central projections.

The axonal conduction velocity groups in the optic nerve of the North American opossum were analyzed electrophysiologically and related to soma size groups of ganglion cells in terms of their retinal origin and laterality of projection. On the basis of analysis of field potentials and single unit responses recorded at the optic disc, three velocity groups were identified (d1, d2, and d3) and estimated to have average conduction velocities of 12, 8, and 5 meters/second. From recordings of the field potential around the perimeter of the optic disc, it was found that the d1 group was equally represented at all points around the disc, whereas the d2 group was largest in amplitude in superior temporal regions. Electrical stimulation of the optic tracts indicated that axons in the d1 group project either ipsilaterally or contralaterally, whereas the d2 group projects predominantly ipsilaterally, and the d3 group projects predominantly contralaterally. In order to relate these physiological data directly to soma size groups, horseradish peroxidase (HRP) was injected into one optic tract, and subsequently the retinae were processed for peroxidase reaction product in the ganglion cells. Labeled cells were seen in contralateral nasal, contralateral temporal, and ipsilateral temporal retina. Cells in all size classes were labeled in contralateral nasal retina. In contralateral temporal retina, labeled cells were either 10-17 micrometers diameter (small and medium) or 23-27 micrometer diameter (large), whereas in ipsilateral temporal retina, most labeled cells (94%) were 15-30 micrometer diameter (medium and large). The correspondence between these conduction velocity groups and the soma size groups described in the preceding paper (Rapaport et al., "81) is discussed.

The conduction velocity and central projections of retinofugal fibers in the rabbit

In anesthetized and paralyzed rabbits, action potentials were elicited antidromically following electrical stimulation of optic tract terminals at the geniculate level (LGN). The conduction velocity spectrum extended from 7 m.s −1 to 34 m.s −1. The distribution of conduction velocities indicated four major modes at 10, 18, 22 and 26 m.s −1. Antidromic compound action potentials exhibited good correlation between the conduction latency and the major modes of the distribution histogram. These results suggest that the rabbit optic tract is composed of four classes of fibers varying in their conduction velocities. The central projections of retinofugal axons were studied with electrical stimulations of the Superior Colliculus (CS) and the LGN while recording from the same optic tract fiber. Antidromic spikes could be elicited from all conduction velocity groups and 71% of axons responded to both sites of stimulation. This finding indicates that most retinofugal fibers branch to and innervate both CS and LGN. Further, there is a tendency for fast-conducting axons to have their receptive field located eccentrically relative to the optic axis of the eye.

A correlation of receptive field properties with conduction velocity of cells in the rat's retino-geniculo-cortical pathway

1. The receptive field properties and responses to electrical stimulation of 126 P-cells recorded from the dorsal lateral geniculate nucleus (LGNd) were studied in the hooded rat. 2. Eighty-five cells had a concentric (Kuffler, 1953) receptive field organisation (46 off-centre on-surround; 39 on-centre off-surround). Of the remaining cells 29 had co-extensive on/off excitatory discharge regions, nine had on-centres with suppressive surrounds and two cells gave on-responses but had no suppressive surround. One cell was identified as suppressed-by-contrast. 3. On the basis of the battery of tests developed for the identification of cell types in the cat's retina and LGNd, 35 of the cells with a Kuffler-type receptive field organisation were identified as Y-like. The majority of the remaining cells, both concentric and others, reminded us of the different subclasses of W-cells of the cat. Nine concentric cells in most of the tests exhibited X-like properties. 4. All of the Y-like cells were driven by relatively fast conducting retinal ganglion cell axons, comprising the t1 conduction velocity group. The majority of the remaining cells were driven by slower axons comprising t2 or t3 conduction velocity groups. 5. Thus, in the rat, as in other mammalian species studied so far, there is a correlation between the conduction velocity groups in the retino-geniculo-cortical pathway and the functional groups based on the cells' receptive field properties. There seem to be functional equivalents of the cat's Y- and W-cell classes but evidence for a distinct X-like class of cells is lacking.

A Rose by Any Other Name...

Rowe and Stone dispose of descriptive terminologies for retinal units as 'essentialist' and argue for a 'neutral' multifactorial system redefined from previous W, X. Y nomenclatures. It is argued here that descriptive terminology need not be either essentialist or undesirable and that the W, X, Y terminology is too confused with false associations to be satisfactory. The synthetic power of the W, X, Y nomenclature was lost with the discovery of concentric W cell receptive fields, the projection of the W cells to the LGN and the suggestion of overlap between X and W conduction velocity groups. It was made methodologically unsound by its employment for the naming of Nissl stained soma classes before the identity of individual somas with the physiological entities can be demonstrated. Although now redefined, the identity of symbols in the several vintages of the W, X, Y system leads to inevitable confusion. The current tripartite division of a multidimensional quality space without cluster analysis is not neutral because it emphasises conduction velocity but represses the diversity of W receptive fields. The concise, apt and memorable descriptive receptive field terminologies are more desirable in that they are operationally based and approximate the unit's transfer function--the parameter most significant to the central nervous system in its information processing task; thus they are more suited for cross species comparison because of a probably bountiful source of functional hypotheses. The lack of taxonomic neutrality in the W, X, Y system has recently been emphasised by its failure to adequately classify rabbit retinal receptive field categories.

Conduction velocity groups in the cat's optic nerve classified according to their retinal origin.

By recording antidromic field potentials and unit responses generated in the retina by stimulation of the optic tract and optic disc, evidence was obtained which suggests the presence of four major conduction velocity groups in the cat's optic nerve. The axons from all peripheral retina appear to fall into two groups, fast and slow, which correspond to the two major velocity groups described by earlier workers. Evidence is presented that the axons which arise from the area centralis form two distinctly slower conduction velocity groups. For each conduction velocity group, and for 60 single units, conduction velocity was estimated for both the intraretinal (unmyelinated) and extraretinal (myelinated) segments of the axons. All axons encountered accelerated markedly on leaving the retina. An anatomical basis for the classification of conduction velocity groups is presented in an accompanying paper.

Optic nerve axon diameters measured in the cat retina: Some functional considerations

Because of the arrangement of axon bundles in the fibre layer of the cat's retina, it is possible to obtain electronmicroscopic sections of axon bundles which contain exclusively either axons arising from the area centralis, or axons arising from peripheral retina. From electronmicrographs of such sections we have constructed axon diameter spectra for central and peripheral axon samples. The centrally originating axons are markedly smaller than peripheral axons, in good agreement with their slower conduction velocity (described in an accompanying paper). The diameter spectra of both peripheral and area centralis axon samples are unimodal, in contrast to the two conduction velocity groups known to exist within each axon population. Alternative explanations of this discrepancy between diameter and conduction velocity spectra are discussed.