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R S Waters

Publications and source records attributed to R S Waters.

36 records · Page 2Linked to original sources
PubMed1990

Early development of SI cortical barrel subfield representation of forelimb in normal and deafferented neonatal rat as delineated by peroxidase conjugated lectin, peanut agglutinin (PNA).

Development of the barrel field representation of the forelimb in the primary somatosensory cortex (SI) was studied in normal and deafferented neonatal rat pups by means of the peroxidase conjugated lectin peanut agglutinin (PNA), which most likely binds to radial glial cells within barrel boundaries. 1. Alterations in lectin binding were seen in animals sacrificed on postnatal day 8 (PND-8) if deafferentation took place on PND-1 (day of birth) through PND-6. 2. Deafferentation on PND-5 or on PND-6 had the least effect on lectin binding. In these animals, lectin binding was reduced, although the prospective representation was intact. 3. Deafferentation on PND-2, 3, and 4 had the greatest effect on lectin binding. In these animals, lectin binding was reduced and the prospective cortical representation was disrupted. 4. Deafferentation on PND-1 resulted in reduced lectin binding, however the prospective cortical representation was only slightly impaired compared to that in animals deafferented on PND-2, 3, and 4. 5. These results suggest that SI barrel field boundaries are important to plasticity and that a sensitive period for predevelopment of the forelimb barrels consists of postnatal days 1 through 6. Furthermore, the formation of normal SI barrel field boundaries requires an ongoing interaction between incoming afferents and radial glial cells.

Afferent Pathways↗
PubMed1990

Absence of responses to microstimulation at the hand-face border in baboon primary motor cortex.

Intracortical microstimulation (ICMS) was used to map the primary motor cortex of four adult female baboons, anesthetized with a mixture of halothane and nitrous oxide and supplemented with sodium pentobarbital. The sequence of observed muscle contractions in response to ICMS provided evidence of an orderly mototopic representation of the tongue, face, hand, forearm and upper body. A zone of cortex unresponsive to microstimulation was consistently observed at the border between the face and hand representation of the mototopic map. This zone was observed in all four animals and was consistent over time. Repeated confirmations of the unresponsive nature of these regions were obtained both early and late in the same experiment. No motor-unit responses or muscle contractions were detected by electromyographic (EMG) recording during stimulation of the unresponsive zones. The absence of both visually observed and EMG-recorded contractions and the fact that muscle contractions could be elicited from adjacent regions of cortex with ICMS as low as 1-5 microA provide compelling evidence that the finding reflects a true physiological condition rather than an experimental artifact.

Animals↗
PubMed1990

Topographic organization of baboon primary motor cortex: face, hand, forelimb, and shoulder representation.

(1) The fine details of the motor organization of the forelimb, face, and tongue representation of the baboon (Papio h. anubis) primary motor cortex were studied in four adult animals, using intracortical microstimulation (ICMS). (2) A total of 293 electrode penetrations were made. ICMS was delivered to 10,052 sites, and of these, 6,186 sites were verified to have been located within the grey matter. Motor effects were evoked from 30% of these sites. (3) The baboon motor cortex is confined, in large part, to the cortical tissue lying along the anterior bank of the central sulcus. When the electrode penetrations were confined to the precentral gyrus, few sites were capable of evoking movement when stimulated by currents of 40 microA or less. (4) The details of the motor maps varied among the four animals; nonetheless, a general topographic organization existed, with the tongue musculature being represented most laterally, followed by a medial progression of the face, digits, wrist, forearm, and shoulder. Within the representation of a given body part, the muscles were organized as a mosaic, wherein the same muscle was multiply represented. (5) A zone of unresponsive cortex was observed to lie consistently between the face and forelimb representation in all four animals. Repeated electrode penetrations within the unresponsive zone failed to elicit muscle contractions even with stimulating currents as high as 80 microA. (6) Our results suggest that the baboon motor cortex is topographically organized; however, embedded within this overall pattern lies a fine-grained mosaic incorporating multiple representations of the same muscle.

Animals↗
PubMed1989

Physiological properties and patterns of projection in the cortico-cortical connections from the second somatosensory cortex to the motor cortex, area 4 gamma, in the cat.

The physiological properties of neurons in the second somatosensory cortex (SII), and the pattern of projection of these neurons to area 4 gamma of the motor cortex in cat were studied by using single unit recording and collision techniques. Antidromically activated neurons were recorded along the anterior and posterior regions of the lateral bank of the anterior suprasylvian sulcus (ASSS) and from the middle part of the anterior ectosylvian gyrus (AESG) following weak intracortical microstimulation (ICMS) to area 4 gamma. Stimulation of the region around the activated neurons failed to produce muscle contraction or movement with currents of 30 microA or less. The majority of antidromically identified neurons received somatotopically organized afferent inputs from the skin on the contralateral side of the body. A small number of SII neurons received bilateral input. In 91% of the cases receptive field information was available for both the antidromically activated SII neuron and for neurons around the stimulating electrode in area 4 gamma. In 71% of these cases, both cortical sites were activated by sensory input from the same or adjacent peripheral area of the body. Neurons in the rostrocaudal region of the lateral bank of ASSS and the upper part of AESG (forelimb area) projected to the lateral cruciate gyrus of the motor cortex (forelimb area), while neurons in the ventrocaudal region of the medial part of AESG (hindlimb area) projected to the medial part of the postcruciate subregion of the motor cortex (hindlimb area). Antidromically activated SII neurons were typically found in layer III. These results suggest a topographically organized pattern of projection to the motor cortex from SII.

Animals↗
PubMed1989

Early development of the representation of the body surface in SI cortex barrel field in neonatal rats as demonstrated with peanut agglutinin binding: evidence for differential development within the rattunculus.

Physiological studies have demonstrated a highly organized somatotopic representation of the body surface in SI cortex of rat. This representation is correlated morphologically with the presence of barrel-shaped structures in layer IV. Conventional staining techniques reveal barrels in the latter part of the first postnatal week. Recently, the peroxidase conjugates of lectins, which recognize glycosylated molecules, have been used to study barrel field formation. Con A, for example, has been shown to bind primarily to prospective barrel sides and septa as early as postnatal day 3 (PND-3) in mouse. To date, investigations of SI cortex using the lectin (Arachis hypogaea) peanut agglutinin (PNA) have been confined to the study of the barrel field representation of the face and mystacial vibrissae in the mouse. In the present study we extend these findings to the development of the representation of the entire body surface called the rattunculus. Rats ranging from PND-1 (first 24 h after birth) to PND-12 were anesthetized with Nembutal and perfused with 4% paraformaldehyde and 2% glutaraldehyde in 0.2 M sodium cacodylate buffer. Brains were removed, flattened tangentially, and sectioned on a vibratome at 30-120 microns. Sections were blocked in TRIS-buffered saline (TBS) plus 2% bovine serum albumin and incubated in peanut lectin at 4 degrees C. Following incubation, sections were washed with TBS and processed using peroxidase histochemistry. Lectin binding in the prospective forelimb representation was apparent by PND-5 whereas lectin binding to the prospective face-mystacial vibrissae representation occurred before PND-4. These results suggest that body part representations show individual variations during early pattern formation.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMed1988

Mechanism of death in patients with the automatic implantable cardioverter defibrillator.

Fifty patients underwent primary implantation of an automatic implantable cardioverter defibrillator between August 1983 and April 1988 and were entered into a long-term surveillance program. There were a total of 14 deaths (28%) in the entire group occurring at a mean of 8.7 months postimplantation. Eleven deaths were cardiac and three were noncardiac (two pneumonia, one leukemia). The group of deceased patients were similar to the survivors in all respects except for a statistically lower ejection fraction (23% vs 32%) at the time of implantation. In addition, 13/14 (93%) of the deceased patients experienced at least one appropriate AICD discharge at a mean of 4.5 months post implantation. Recorded ECGs at the time of death revealed that most of the sudden deaths were due to electromechanical dissociation and not to AICD-treatable arrhythmias. These data suggest therefore that death in AICD patients is usually cardiac, due primarily to low ejection fraction and occurs in patients who have previously received AICD discharges.

Adult↗
PubMed1985

Caudal cuneate nucleus projection to the direct thalamic relay to the motor cortex: an electrophysiological study.

We previously reported that injection of horseradish peroxidase (HRP) into a physiologically identified region of the thalamus between the ventrolateral nucleus and ventroposterolateral nucleus, VL-VPL, in cat results in labeled cell bodies in the caudal cuneate nucleus (CCN) of the dorsal column nuclei (DCN). We recognized, however, that the spread of HRP to localized regions of less than 1.0 mm distance from the injection site and subsequent uptake by neighboring fibers might have accounted for the resulting label in CCN. In the present study, therefore, we reexamined the DCN input to VL-VPL using a more sensitive physiological method. First, we used the microstimulation technique and corroborated the previous result. In 5 additional preparations, a modified collision procedure was used to ascertain that the same VL-VPL neuron which projects to the motor cortex also receives input from CCN. We report, for the first time, evidence of a lemniscal input to neurons in VL-VPL which are physiologically identified as projecting to the motor cortex.

Afferent Pathways↗
PubMed1985

Anatomical and physiological properties of the projection from the sensory cortex to the motor cortex in normal cats: the difference between corticocortical and thalamocortical projections.

Details of the distribution of terminal sites of the projection fibers from area 2 of the sensory cortex to the motor cortex were studied and compared with the distribution of terminals from the ventrolateral (VL) nucleus of the thalamus to the motor cortex. The results obtained were as follows: Intracortical microstimulation (ICMS) in area 2 produced measurable short-latency EPSPs only in neurons located in layers II and III of the motor cortex, whereas VL stimulation produced short-latency EPSPs in neurons throughout the depths of the motor cortex. The time from the beginning to the peak of the EPSPs was not significantly different for area 2- and VL-elicited EPSPs suggesting that there was no systematic difference between effective terminal sites for both inputs. However, there was a difference when a given neuron received both inputs suggesting that there was a segregation between the two inputs within a given cell. The majority of area 2-elicited EPSPs were smooth and monophasic, but some (40%) of them showed double peaks indicating that some neurons received mono- and disynaptic inputs from area 2. Intracellular injections of HRP suggested that neurons receiving input from area 2 were predominantly multipolar non-pyramidal neurons in layers II and III whereas neurons receiving thalamic input were pyramidal as well as non-pyramidal cells. Field potentials in the motor cortex evoked by area 2 stimulation did not change polarity in the depths of the cortex and therefore, differed from the VL-evoked potentials suggesting differences in the mechanisms of generating the electrical fields. It is concluded that association fibers effective for producing EPSPs terminate primarily on non-pyramidal cells in layer II and III whereas VL fibers terminate not only on pyramidal but also on non-pyramidal cells in layers III and V. This study provided a basis for examining the modifiability of association fibers after elimination of VL input to the motor cortex which is reported in the following paper.

Animals↗
PubMed1985

Motor effects produced by stimulation of secondary somatosensory (SII) cortex in the monkey.

Threshold for evoking movements by microstimulation of the second somatosensory area of the cynomolgus monkey's cortex to intracortical microstimulation was examined. Motor effects were obtained contralateral to the side of stimulation, in a region histologically verified to be in grey matter deep in the sylvian cortex, and which corresponds to the second somatosensory cortex. The thresholds were low but higher than for movements evoked by stimulation of the motor cortex. The results are explained in terms of increased specialization of the motor cortex for movements in the monkey compared with the cat.

Animals↗
PubMed1984

Caudal cuneate nucleus projection to the direct thalamic relay to motor cortex in cat: an electrophysiological and anatomical study.

The input to the border region between the ventrolateral nucleus (VL) and ventroposterolateral nucleus (VPL) of the thalamus, VL-VPL, was studied in cats using a combined electrophysiological and anatomical technique. Neurons within this border region receive somatic afferent input and project to a region of the motor cortex having similar receptive fields. In this study we asked the question whether neurons in the VL-VPL border receive input from the dorsal column nuclei (DCN). To answer this question we delivered intra-cortical microstimulation (ICMS) to the motor cortex while a second electrode inserted into the VL-VPL border, filled with a 20% solution of HRP dissolved in KCl, was used to record antidromically activated neurons. When an antidromically activated neuron was encountered and the neuron responded to natural peripheral stimulation, HRP was iontophoretically injected through the recording electrode. After a 48-72 h survival time, cats were sacrificed, and the brain tissue processed according to the method of Hardy and Heimer. Labeled cell bodies were found in the caudal cuneate nucleus (CCN) in all injected animals. These results suggested that neurons in CCN project to cells in VL-VPL which in turn project to the motor cortex.

Animals↗
PubMed1984

Corticocortical connections to the motor cortex from the posterior parietal lobe (areas 5a, 5b, 7) in the cat demonstrated by the retrograde axonal transport of horseradish peroxidase.

Neurons in the parietal region of the cerebral cortex, projecting to the ipsilateral distal forelimb area of the motor cortex (area 4 gamma) were identified in the cat brain using the horseradish peroxidase (HRP) retrograde tracing method. After making microinjections of HRP into the distal forelimb area of the motor cortex, clusters of HRP-labeled cell bodies were observed in different regions of the ipsilateral parietal cortex. In particular these clusters of labeled cells were found in areas 5a, 5b and 7. The area 5a cluster is formed from closely packed irregularly-shaped cells, the area 5b cluster is made up of dispersed medium-sized pyramidal cells, while area 7 contains a cluster of widely dispersed small pyramidal cells. Typically, labeled cell bodies were found in lamina III of cortex. Labeled cell bodies were neither observed in the contralateral cortex nor in the visual cortex (areas 17, 18 and 19). Since parietal cortex receives projections from primary somatosensory and visual cortex, the projections from parietal to motor cortex may well form the neural substrate for the processing of convergent sensory information used in voluntary movements.

Afferent Pathways↗
PubMed1983

Low threshold motor effects produced by stimulation of area preinsularis (2 pr.i) of the secondary sensory cortex in the cat; input-output relationship.

Intracortical microstimulation (ICMS) delivered to area 2 perinsularis (area 2 pr. i) of the second somatosensory cortex, SII, elicited contralateral distal limb movements with threshold currents as low as 2 microA. The effective sites for a particular movement were located in a small area within the depth of the cortex extending along the direction of the radial fibers. Neurons in an area for a particular movement generally received peripheral input from the skin overlying the muscle to which the area projected. ICMS in area 2 pr.i produced powerful monosynaptic as well as disynaptic activation of pyramidal tract neurons, suggesting that the effect was mediated by the pyramidal tract. Ablation of the motor cortex did not eliminate or otherwise reduce the low threshold responses from area 2 pr.i suggesting that the described effect is independent of the motor cortex.

Animals↗
PubMed1983

Movement of facial muscles following intra-cortical microstimulation (ICMS) along the lateral branch of the posterior bank of the ansate sulcus, areas 5a and 5b, in the cat.

The lateral branch of the posterior bank of the ansate sulcus within the parietal cortex, areas 5a and 5b, was mapped using intracortical microstimulation (ICMS). Motor effective sites for contraction of facial muscles were identified using ICMS currents of less than 30 microA. Of the 177 effective sites, 78% were activated with threshold currents of less than 20 microA, and of these, 33% responded to stimulus strengths of less than 10 microA. Since neurons in this portion of the ansate region send projections to the face region of motor cortex, area 4 gamma, the possibility existed that the motor effects might be mediated through area 4 gamma. To examine this possibility we ablated both the anterior sigmoid gyrus (ASG) and the second somatosensory cortex, SII, including area 2pri, a region shown to contain a low threshold motor component, and report that the motor effect recorded from the ansate region is independent of both the ASG and area 2pri.

Animals↗
PubMed1982

Pattern of projection and physiological properties of cortico-cortical connections from the posterior bank of the ansate sulcus to the motor cortex, area 4 gamma, in the cat.

The physiological properties of neurons lying along the posterior bank of the ansate sulcus and the projection of these neurons to area 4 gamma of the motor cortex of the cat were studied and the following results were obtained: (1) Short latency antidromic responses were recorded from neurons along the medial-lateral bank of the posterior ansate sulcus following intracortical microstimulation (ICMS) delivered to motor cortex, area 4 gamma. (2) The posterior ansate region projects topographically to the motor cortex. Neurons in the most medial part of the ansate region project to the medial part of 4 gamma, while neurons in the central and lateral parts of the ansate region project to the more lateral parts of area 4 gamma. (3) In 33 cases, receptive field information was available for both the antidromically activated ansate neuron and from neurons around the stimulating site in 4 gamma. In 58% of the cases, both cortical sites received afferent input from within the same part of the periphery. (4) Afferent input to the motor cortex was examined following combined ablations of the primary somatosensory cortex (SI) and third somatosensory cortex (SIII) including all of area 5. We conclude that the integrity of these cortical regions is not necessary for afferent input to reach the motor cortex.

Afferent Pathways↗
PubMed1982

Physiological properties and pattern of projection of cortico-cortical connections from the anterior bank of the ansate sulcus to the motor cortex, area 4 gamma, in the cat.

The physiological properties of neurons in the postsigmoid gyrus lying along the anterior bank of the ansate sulcus and the pattern of projection of these neurons to the motor cortex, area 4 gamma, were investigated in the cat and the following results were obtained. (1) Neurons lying along the anterior bank of the ansate sulcus receive somatotopically organized afferent input from the skin and deep structures on the contralateral side of the body. (2) Short latency antidromic responses were recorded from all regions along the bank of the sulcus following intra-cortical microstimulation (ICMS) of area 4 gamma. (3) The projection of neurons to area 4 gamma was topographically organized. Neurons in the lateral portions projected to more lateral parts of 4 gamma, whereas neurons in the medial region of the postsigmoid gyrus sent axons to the more medial regions of the motor cortex. (4) In 50 cases, receptive fields were recorded from both the antidromically identified postsigmoid gyrus neuron and from neurons around the activation site in area 4 gamma. In 62% of these instances, both cortical sites received afferent input from within the same part of the periphery.

Animals↗
PubMed1982

Physiological properties of neurons projecting from area 3a to area 4 gamma of feline cerebral cortex.

1. The corticocortical projection from area 3a to area 4 gamma was restudied using tranquilized cats. 2. Intracortical microstimulation (ICMS) of a given locus in area 3a produced effects on neurons in area 4 gamma that were located in a small area extending along the direction of the radial fibers constituting a columnar shape. 3. Cortical neurons in area 3a that projected to a particular neuron in area 4 gamma were located in a region that extended along the direction of the radial fibers and constituted a columnar shape. 4. Two-thirds of the projection neurons in area 3a had different receptive fields from those of neurons in the projected area in 4 gamma, thus suggesting that the 3a neurons are not simply transferring peripheral information to the 4 gamma neurons. 5. ICMS delivered to area 3a rarely excited 4 gamma neurons but rather facilitated their evoked discharges. 6. It is suggested that the activity of corticocortical projection from area 3a to 4 gamma can influence the activity of 4 gamma neurons only when combined with other inputs to the motor cortex.

Animals↗
PubMedDate not supplied

Ulnar nerve innervation of paw and SI cortex of cat: substrate for reorganization.

We studied the distribution of the peripheral nerves innervating the distal forepaw by recording receptive fields from fascicles of the ulnar, radial, and median nerves and compared this result with the peripheral nerve representation in primary somatosensory (SI) cortex of cat. Our findings suggest that SI cortex receives input, in large part, from multiple peripheral nerves even when those nerves do not show a strong overlapping pattern in the periphery. This overlap pattern observed in SI cortex may be responsible, in part, for the immediate reorganization which is known to follow peripheral nerve deafferentation.

Animals↗