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PubMed1989

Spatial spread of in-field afferent inhibition in the cat's spinocervical tract.

1. Extracellular microelectrode recordings were made from twenty-three spinocervical tract (SCT) cells in the lumbar spinal cord of cats anaesthetized with chloralose and paralysed with gallamine triethiodide. Excitation and inhibition of the cells were elicited by applying small brief (4 mN, 60 ms) localized jets of air to the clipped hair in and around the receptive fields. 2. Receptive field extents ranged from 40 to 180 mm. Excitation occurred in the period 30-130 ms after the start of the stimulus, and in-field afferent inhibition from 130 ms up to 700 ms or more. The inhibition was manifest as a reduction in background discharge and as a reduction in responsiveness to a test stimulus which followed a conditioning stimulus. 3. When the conditioning stimulus was spatially separated from the test stimulus, the degrees of in-field afferent inhibition depended on the spatial separation, even when both were within the excitatory receptive field. The spatial spread of in-field afferent inhibition was limited to 100 mm or less. 4. In two units only, afferent inhibition was produced from a narrow strip just outside the excitatory receptive field. In the other units, it could only be produced from within the excitatory receptive field. 5. The results suggest that the inhibitory input to SCT cells is organized in subdomains no more than 100 mm across, which may correspond to the receptive fields of interneurones between the primary afferent fibres and the SCT cells.

Afferent Pathways↗
PubMed1989

Receptive fields and in-field afferent inhibition of neurones in the cat's lateral cervical nucleus.

1. Extracellular microelectrode recordings were made from projection neurones of the lateral cervical nucleus (LCN) in cats anaesthetized with chloralose and paralysed with gallamine triethiodide. 2. The receptive fields of eight-five units were analysed. Most units had excitatory receptive fields similar in size and shape to those of spinocervical tract (SCT) cells. A few (14%) had either very large fields or 'stocking-like' fields. The majority of the LCN neurones (fifty-five, 65%) were excited by hair movement and, in addition, by noxious mechanical stimulation within the skin area responding to hair movement. Twenty-five units (29%) were excited by hair movement alone. For seven of these twenty-five neurones, noxious mechanical stimulation within the excitatory receptive field produced inhibition of the background discharge. One unit was excited by noxious mechanical stimulation and for the remaining four units no receptive field could be found. In six units inhibitory receptive fields outside the excitatory field were found. 3. Air-jet stimuli were used to define the excitatory profiles of the units' receptive fields to hair movement. In general, receptive fields had single regions of greatest sensitivity usually at or near the centre of the field, where that was oval in shape, with the sensitivity declining towards the field's circumference. In some units with very large fields that included parts of one or two limbs and the trunk there could be more than one highly sensitive region. 4. Pairs of air-jet stimuli were used to investigate in-field afferent inhibition in LCN cells. One jet was used to condition the responses to another jet located at a different position within the excitatory receptive field and occurring 200 ms later. Sixteen units were tested and significant in-field inhibition was observed in all sixteen. 5. The in-field afferent inhibition was organized spatially in the sense that inhibition was generally strongest when the conditioning and testing stimuli were close together and became weaker as they were moved apart. The afferent inhibition was not simply a function of the response produced by the conditioning stimulus. Furthermore, increasing the strength of the stimuli did not in general lead to larger areas from which the inhibition could be produced. The inhibitory areas defined in these experiments were generally less than 120 mm in length in units with receptive fields much longer than 100 mm.(ABSTRACT TRUNCATED AT 400 WORDS)

Afferent Pathways↗
PubMed1990

Afferent inhibition and facilitation of transmission through the spinocervical tract in the anaesthetized cat.

1. Extracellular microelectrode recordings were made from single spinocervical tract (SCT) neurones in the lumbosacral spinal cord of cats anaesthetized with chloralose and paralysed with gallamine triethiodide. 2. Pairs of air-jet stimuli, 60 ms in duration, were used to investigate in-field afferent inhibition in SCT cells. One jet was used to condition the responses to another jet located at a different position within the excitatory receptive field and occurring at times from 100 to 1800 ms later. Fifteen neurones were tested and significant in-field inhibition was observed in all of them. 3. The in-field afferent inhibition was organized spatially in the sense that inhibition was generally strongest when conditioning and testing stimuli were close together and became weaker as they were moved apart. There was also a weak effect due to the strength of the conditioning response; when conditioning produced a strong response, from near the most excitable part of the receptive field, there was often a weak reduction in the test response from distant sites. The inhibitory areas defined in these experiments were generally less than 100 mm in length in units with excitatory receptive fields much longer than this. 4. The in-field afferent inhibition had a time course that lasted from 300 to about 1000 ms. 5. Afferent inhibition was also evoked by applying either air-jet stimuli to hairy skin outside, but close to, the excitatory receptive field or by applying a vibratory stimulus from a piezoelectric transducer (200 Hz) to glabrous skin of the toe pads or the central foot pad. These conditioning stimuli had durations of 20 or 60 ms. For convenience we call this inhibition 'out-of-field' afferent inhibition. 6. Out-of-field afferent inhibition was evoked from both glabrous and hairy skin areas outside the excitatory receptive field. It was common in neurones with receptive fields on the toes and of twenty-eight such neurones tested it was observed in twenty-four. This inhibition had a short latency (usually about 10 ms or less but occasionally up to 30 ms) and lasted for about the duration of the test stimulus (30 or 80 ms when the test stimulus was 20 or 60 ms respectively). It was often followed by a further period of inhibition, with a latency of between 50 and 100 ms and lasting for 60 up to 130 ms. 7. In thirteen SCT neurones more complex effects were seen.(ABSTRACT TRUNCATED AT 400 WORDS)

Action Potentials↗
PubMed1991

The effect of discrete stimulation of carotid body chemoreceptors on atrial natriuretic peptide in anaesthetized dogs.

1. In seven chloralose-anaesthetized and artificially ventilated beagles, the carotid sinus regions were vascularly isolated and perfused with either arterial or mixed (arterial and venous) blood (PO2 46.4 +/- 1.5 mmHg, mean +/- S.E.M.) to stimulate the chemoreceptors at constant flow and pressure. Cervical vagosympathetic trunks were ligated in all dogs, and gallamine triethiodide (2.0 mg kg-1 h-1, I.V.) was given in five dogs. Right atrial pressure was measured in all dogs, and left atrial pressure in four dogs. Mean aortic pressure was held constant (91.0 +/- 3.0 mmHg) by means of a reservoir connected to the animal via the common carotid and femoral arteries. Plasma atrial natriuretic peptide (ANP) was measured by radioimmunoassay and urinary sodium by flame photometry. 2. In seven dogs with mean carotid sinus pressure maintained at 96.0 +/- 4.3 mmHg, stimulation of the carotid chemoreceptors for 25 min produced significant increases in left atrial pressure of 41.2 +/- 3.3% (n = 4; P less than 0.005) from 5.4 +/- 0.6 cmH2O and of 30.9 +/- 4.5% (n = 7; P less than 0.002) in ANP from 31.6 +/- 2.1 pg ml-1. However, chemoreceptor stimulation produced significant decreases in urine flow rate of 26.1 +/- 1.9% (n = 9; P less than 0.001) from 0.29 +/- 0.03 ml min-1 (100 g kidney weight)-1 and sodium excretion of 29.0 +/- 2.3% (P less than 0.001) from 8.5 +/- 1.7 mumol min-1 (100 g kidney weight)-1 but right atrial pressure and heart rate did not change significantly. In three of the dogs, beta-adrenoceptor blockade by atenolol (2 mg kg-1, I.V.) greatly reduced the effects of chemoreceptor stimulation on plasma levels of ANP. 3. The results show, for the first time, that discrete stimulation of the carotid chemoreceptors caused an increase in plasma ANP levels, probably due to the reflex increase in atrial pressure that results from an inhibition of the cardiac sympathetic nerves, and an increase in venous return from a reduction of peripheral vascular capacitance.

Anesthesia↗
PubMed1992

Effects of left atrial receptor stimulation on carotid chemoreceptor-induced renal responses in dogs.

1. Dogs were anaesthetized with thiopentone sodium and alpha-chloralose and artificially ventilated. The carotid sinus regions were vascularly isolated and perfused with arterial or venous blood to stimulate the chemoreceptors. Left atrial receptors were stimulated by distending four balloons, three in the left pulmonary vein-atrial junctions and one in the left atrial appendage. Mean aortic pressure was held constant by means of a pressure control device. Atenolol and atropine (2.0 and 0.5 mg kg-1, respectively), and gallamine triethiodide (3.0 mg kg-1 h-1) were given I.V. Renal blood flow was measured by an electromagnetic flowmeter, glomerular filtration rate by creatinine clearance, urinary sodium by flame photometry and solute excretion by osmometry. 2. In fifteen tests in eight dogs (in one dog responses of both left and right kidneys were determined), at a constant aortic pressure (AoP) of 92.0 +/- 3.2 mmHg, and carotid sinus pressure (CSP) of 95.0 +/- 2.0 mmHg, stimulation of left atrial receptors with balloon inflation resulted in significant increases in renal blood flow (RBF) by 8.3 +/- 0.9 from 255.0 +/- 14.6 ml min-1 (100 g kidney weight)-1 (n = 9), in glomerular filtration rate (GFR) by 4.1 +/- 0.6 from 21.2 +/- 1.9 ml min-1 (100 g)-1, in filtration fraction (FF) by 0.04 +/- 0.003 from 0.20 +/- 0.01, in urine flow rate (V) by 0.08 +/- 0.02 from 0.33 +/- 0.05 ml min-1 (100 g)-1, in sodium excretion (UNaV) by 4.4 +/- 0.9 from 27.7 +/- 4.2 mumol min-1 (100 g)-1, in osmolar excretion (UosmV) by 62.0 +/- 5.6 from 303.0 +/- 28.3 mu osmol min-1 (100 g)-1, and in a decrease in free water clearance (CH2O) by 0.13 +/- 0.03 from -0.63 +/- 0.04 ml min-1 (100 g)-1. Left atrial pressure (LAP) and heart rate (HR) did not change significantly from 6.9 +/- 0.3 cmH2O, and 133.0 +/- 3.4 beats min-1 respectively.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed2003

Purinergic signalling in the medullary mechanisms of respiratory control in the rat: respiratory neurones express the P2X2 receptor subunit.

ATP is involved in central respiratory control and may mediate changes in the activity of medullary respiratory neurones during hypercapnia, thus playing an important role in central chemoreception. The main objective of this study was to explore further the role of ATP-mediated signalling in respiratory control and central chemoreception by characterising the profile of the P2X receptors expressed by physiologically identified respiratory neurones. In particular we determined whether respiratory neurones in the rostral ventrolateral medulla (VLM) express P2X2 receptor subunits of the ATP-gated ion channel, since ATP currents evoked at recombinant P2X2 receptors are potentiated by lowering extracellular pH. Experiments were performed on anaesthetised (pentobarbitone sodium 60 mg kg-1 I.P., then 10 mg kg-1 I.V. as required), gallamine-triethiodide-treated (10 mg kg-1 I.V., then 2-4 mg kg-1 h-1 I.V.) and artificially ventilated rats. The VLM respiratory neurones were classified according to the timing of their discharge pattern in relation to that of the phrenic nerve and by the exclusion of pump cells from the study population; these were labelled with Neurobiotin using the juxtacellular method, and visualised with fluorescence microscopy. It was found that a substantial proportion of the VLM respiratory neurones express the P2X2 receptor subunit. P2X2 receptor subunit immunoreactivity was detected in approximately 50 % (six out of 12) of expiratory neurones and in approximately 20 % (two out of 11) of neurones with inspiratory-related discharge (pre-inspiratory and inspiratory). In contrast, no Neurobiotin-labelled VLM respiratory neurones (n = 19) were detectably immunoreactive for the P2X1 receptor subunit. Microionophoretic application of ATP (0.2 M, 20-80 nA for 40 s) increased the activity of approximately 80 % (13 out of 16) of expiratory neurones and of approximately 30 % (five out of 18) of VLM neurones with inspiratory-related discharge. These effects were abolished by the P2 receptor blocker suramin (0.02 M, 80 nA), which also reduced the baseline firing in some expiratory neurones. These data indicate that modulation of P2X2 receptor function, such as that evoked by acidification of the extracellular environment during hypercapnia, may contribute to the changes in activity of the VLM respiratory neurones that express these receptors.

Adenosine Triphosphate↗
PubMed1975

Sympathetic afferent nerve activity of right heart origin.

Six mongrel dogs anesthetized with sodium pentobarbital and paralyzed with gallamine triethiodide were studied on total cardiopulmonary bypass. This study verified the existence of right heart mechanoreceptors whose afferent nerves traverse the upper thoracic white rami communicantes. these mechanoreceptors were studied by observing changes in average maximum, and total nerve spike frequency when right atrial and right ventricular systolic and diastolic pressures were altered by means of intracardiac balloons. Receptors that responded to volume and pressure changes were found in both the right atrium and right ventricle. Nerve activity in these afferents increased with increasing right atrial and right ventricular pressures. These mechanoreceptors were more responsive in the upper physiological ranges of right heart pressures. In most nerve fibers studied, maximum activity occurred during both right atrial and right ventricular diastole.

Animals↗
PubMed1990

GABAergic responses in ventrolateral medulla in spontaneously hypertensive rats.

Gamma-Aminobutyric acid (GABA) and the GABA antagonist bicuculline methiodide were used to investigate the role of GABAergic transmission in the rostral and caudal ventrolateral medulla in 12- to 13-wk-old spontaneously hypertensive (SH) (n = 7) and normotensive, control Wistar-Kyoto (WKY) (n = 7) rats. Animals were anesthetized with urethan (1.25 g/kg sc), paralyzed with gallamine triethiodide (10 mg/kg iv), and artificially ventilated. Femoral arterial and venous catheters were inserted for the measurement of mean arterial pressure (MAP) and heart rate responses and for intravenous infusions. The ventral surface of the brain stem then was exposed. The responsiveness of the rostral ventrolateral medulla to GABA was compared in SH and WKY rats using unilateral microinjections (30 nl) of GABA at 1, 10, and 100 mM concentrations, which produced significantly (P less than 0.05) larger decreases of MAP in SH rats compared with WKY at the 10 and 100 mM concentrations (-37.3 +/- 2.8 mmHg for SH vs. -27.3 +/- 2.7 mmHg for WKY at 100 mM). Tonic GABAergic inhibition was gauged using bilateral microinjections (30 nl) of bicuculline (2 and 4 mM) into the rostral ventrolateral medulla, which caused significantly larger increases in MAP in the WKY group (+84.8 +/- 8.5 mmHg at 4 mM) compared with the SH group (+14.9 +/- 5.8 mmHg at 4 mM). In contrast, the ability to drive sympathetic outflow by microinjection of L-glutamate in the rostral ventrolateral medulla was not significantly different between WKY and SH rats.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMed1995

Gestational effects on volume-sensitive cardiopulmonary receptor reflexes in the rat.

We tested the hypothesis that augmented reflex sympathoinhibition mediated by volume-sensitive cardiopulmonary (CP) receptors contributes to the vasodilation of pregnancy by comparing responses to acute volume expansion in 21-day-pregnant and age-matched virgin rats (n = 7) that were anesthetized (pentobarbital sodium, 50 mg/kg ip), paralyzed (gallamine triethiodide, 25 mg/kg iv), ventilated, and had undergone bilateral sinoaortic denervation. CP receptors were stimulated with intra-atrial injections of saline (50, 100, 200, and 300 microliter), and the following variables were recorded: 1) mean right atrial pressure (MRAP) to index the afferent stimulus intensity; 2) cell discharge in the nucleus tractus solitarii (NTS), the primary central terminus for CP afferents; and 3) mean arterial pressure (MAP), heart rate (HR), and renal sympathetic nerve activity (RSNA) to assess efferent reflex effects. Basal MAP was significantly lower in pregnant (71.5 +/- 3.8 mmHg) than in virgin rats (86.6 +/- 3.1 mmHg), and plasma volume was expanded in the pregnant group (17.6 +/- 1.1 vs. 10.0 +/- 0.7 ml, P < 0.05). Baseline MRAP was similar between groups. Saline injections evoked graded increases in MRAP, which were larger in gravid animals (P < 0.05). Volume injections evoked similar changes in NTS cell discharge between groups, but the responses were nongraded. Despite larger changes in MRAP in gravid rats, reflex effects on RSNA and HR were similar to those in control animals, and effects on MAP were attenuated in the pregnant group. We conclude that larger changes in MRAP in pregnant rats during stimulation of CP receptors are not associated with larger changes in central or efferent components of this reflex.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMed1984

Chemical activation of group I and II muscle afferents has no cardiorespiratory effects.

Although stimulation of group III and IV muscle afferents is known to cause reflex changes in cardiorespiratory function, it has not been resolved whether group I and II afferents contribute to this reflex activation. Therefore, we measured the effects of intra-arterial nonparalyzing doses of succinylcholine (50-100 micrograms/kg) on the firing of muscle afferents from the gastrocnemius muscle in one group of cats, and heart rate, blood pressure, and integrated phrenic nerve activity in a second group of cats. In nonparalyzed cats, succinylcholine injections caused muscular fasciculations and firing of all four groups of muscle afferents. However, succinylcholine stimulated only group I and II afferents after paralysis with gallamine triethiodide. Succinylcholine caused increases in blood pressure, heart rate, and phrenic nerve activity before paralysis. After paralysis, succinylcholine had no effects on any of the cardiorespiratory measures. We conclude that activation of only group I and II afferent fibers from the gastrocnemius muscle has no reflex effects on blood pressure, heart rate, or phrenic nerve activity. These afferents, therefore, are unlikely to play a role in increasing cardiorespiratory function during exercise.

Afferent Pathways↗
PubMed1990

Responses of single phrenic motoneurons to altered ventilatory drives in anesthetized dogs.

We studied the effects of altered ventilatory drives on the activity of the whole phrenic nerve and single phrenic motoneurons in dogs anesthetized with alpha-chloralose and paralyzed with gallamine triethiodide. Single phrenic motoneurons were classified as either late-onset or early-onset motoneurons (LOM and EOM, respectively), depending on the time of onset of their activity during inspiration. Increase in ventilatory drive was induced by altering chemical drive with changes in arterial blood gases and also by altering the vagal afferent contribution to ventilatory drive. The latter was accomplished by inducing pulmonary gas embolism (PGE) during hyperoxia. Whole phrenic nerve activity was increased by both types of increase in ventilatory drive. In both cases, changes in the firing pattern of LOMs and EOMs were responsible for the increased phrenic output. The changes in post-PGE firing pattern of the LOMs generally consisted of a shift in the time of onset to an earlier point in inspiration and an increase in the number of spikes per inspiratory cycle. Vagotomy abolished the difference between the contributions of LOMs and EOMs to the phrenic response to PGE. Data from dogs studied while they were breathing spontaneously were qualitatively the same as those from the paralyzed animals, indicating no major role for phasic volume feedback in these responses. Our data regarding altered chemical drive are similar to those reported earlier in other species, whereas those regarding PGE demonstrate that vagally mediated increases in ventilatory drive affect both LOMs and EOMs, although LOMs are affected to a greater degree.(ABSTRACT TRUNCATED AT 250 WORDS)

Anesthesia↗
PubMed1993

Oxygen radicals in bronchoconstriction of guinea pigs elicited by isocapnic hyperpnea.

The role of oxygen radicals in isocapnic hyperpnea-induced bronchoconstriction (HIB) of guinea pigs was investigated using scavengers of the radicals. In series 1, 50 young guinea pigs were randomly divided into seven groups: control 1, control 2, chlorisondamine, tetrodotoxin (TTX), acute dimethylthiourea (DMTU), tachykinin depletion, and 5% CO2 in air. Animals of the control 2 group received vehicle (saline) infusion while those of the control 1 group did not. Chlorisondamine was used to block ganglionic transmission, TTX to interrupt nerve conduction, DMTU to scavenge hydroxyl radicals, and chronic capsaicin pretreatment to deplete tachykinins. The animals in the last group were ventilated with dry 5% CO2 in air during hyperpnea. In series 2, 13 additional animals were used to test the effects of intratracheal administration of superoxide dismutase and catalase (SOD + CAT) on HIB. Each animal was anesthetized with pentobarbital sodium, cannulated with a tracheal cannula and venous catheter, paralyzed with gallamine triethiodide, and mechanically ventilated. During the baseline period, each animal was ventilated normally with humidified air. Then it was hyperventilated 15 min with a dry gas mixture of 95% O2-5% CO2, except animals in the last group of series 1. Subsequently, all animals returned to normal ventilation with humidified air for 45 min (recovery period). The maximal expiratory flow and dynamic compliance were obtained periodically during the recovery period. The isocapnic hyperpnea using 95% O2-5% CO2, but not 5% CO2 in air, caused bronchoconstriction that was significantly blocked by acute DMTU, acute SOD + CAT, and tachykinin depletion. In an additional group of six animals, acute DMTU did not significantly alter acetylcholine-induced airway constriction.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMed1988

Organization and properties of neurons in a visual area within the insular cortex of the cat.

1. Extracellular recordings from 304 neurons were obtained with carbon fiber-containing multibarrel micropipettes. The cells were isolated in the insula in cats anesthetized with barbiturate and immobilized with gallamine triethiodide. Cells were tested with visual stimuli in the form of bars of light, moving edges, and square-wave, drifting grating patterns. 2. The spatial extent of the visually responsive region of insular cortex was assessed and was found to be limited to a surface area of approximately 6-8 mm2, the perimeter being delimited caudally by visually unresponsive cortex of the anterior sylvian gyrus, rostrally by the cortex surrounding the posterior third of the orbital sulcus (ventral bank), dorsally by the rostral extension of the dorsal bank of the anterior ectosylvian sulcus, and ventrally by a visually unresponsive zone bounded by a region about 2 mm2 ventrolateral from the anterior ectosylvian sulcal infolding. Furthermore, a group of unimodal, visually responsive cells often was found in the upper bank of the anterior rhinal sulcus. 3. The possibility of there being a visuotopic organization of insular neurons was examined by analyzing the distribution of receptive-field representation of neurons in sequential penetrations, as well as by searching for spatial progressions in the locations of visually responsive areas within the region. No such clear-cut organization was found among the cells of the insula. 4. Visually responsive neurons were encountered in groups, within electrode penetrations. These groupings were roughly segregated into three distinct levels within the depth of the cortex: the first between the pial surface and 600 micron, the second between 1,100 micron and 1,800 micron, and the third between 2,000 micron and 2,500 micron. 5. Neurons were classified according to their velocity sensitivity, directional preference, orientation sensitivity, length preference, modality specificity, response to electrical stimulation of extrageniculostriate regions, and response to light stimulation in the presence of microiontophoretically administered bicuculline methiodide (BMI). 6. Cells of superficial layers tended to exhibit a preference for high-velocity movements of light bars (600 degrees s-1), whereas those of deeper laminae generally preferred relatively lower velocity movements (60 degrees s-1). The clear preferences of many cells for certain directions of movement within the 360 degrees arc suggested the presence of a dynamic orientation sensitivity. 7. Proportionately more cells preferred moving bars (57%) to small moving spots (43%).(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗
PubMed1988

Modality specificity of neuronal responses within the cat's insula.

1. Electrophysiological recordings of single-unit responses, multiunit responses, and electrically evoked field potentials have been made using carbon fiber-containing micropipettes in cats anesthetized with barbiturate and immobilized with gallamine triethiodide. Recording sites sampled cortical regions throughout the insula, including zones more ventrally situated and more rostral and caudal than those described in the preceding, companion paper. One-hundred eleven cells in total were tested with a battery of different types of stimuli. 2. Stimuli were divided into two classes, according to either the intensity of the stimulus or its form. These are called physiological forms, or levels of stimulation, and nonphysiological forms or levels. The nonphysiological forms of stimuli for visual, somatosensory, and auditory modalities consisted of (for visual stimuli): 1) electrical stimulation of the optic nerve or 2) bright flashes light at 100% contrast; for somatosensory, electrical stimulation of the radial nerve by implanted cuff electrodes; and for auditory, stimulation with bursts of white noise generated at high intensities (80-100 dB) or with a loud click stimulus. Physiologically relevant levels of stimuli for these same modalities were: moving bars of light projected onto a tangent screen in front of the animal (visual); light cutaneous deformation, hair displacement, and light pressure delivered to various regions on the surface of the cat's body with hand-held probes, or delivered manually (somatosensory); and white noise generated at low intensities (ca. 40 dB) (auditory). 3. Cells situated in dorsal insular regions responded to visual stimuli when levels of sensory activation were employed using natural means, within normal, physiologically relevant limits. Responses to auditory or somatosensory stimulation were observed in this region only when very intense forms of "natural" stimulation, or when electrical stimulation (nonphysiologically relevant levels of stimulation) was delivered. In this latter case, the same cells in several instances could be made to appear polymodally responsive. With cells situated in ventral insular regions, some polymodal responses to physiologically relevant levels of stimulation were noted, although it was considerably more common to obtain unimodal responses. Nonphysiological levels of activation yielded evidence for a polymodal convergence onto the greater proportion of cells recorded. 4. Field potential recordings with microelectrodes revealed widely overlapping representations of all modalities in both dorsal and ventral regions of the insula, irrespective of the sensitivity displayed by the local neuronal r

Animals↗
PubMedDate not supplied

Response of respiratory-related hypoglossal nerve activity to capsaicin-induced pulmonary C-fiber activation in rats.

This study was designed to examine respiratory-related hypoglossal nerve activity in response to activation of pulmonary C-fibers by capsaicin. Rats were anesthetized with urethane (1.2 g/kg, i.p.). Tracheostomy was performed. Catheters were introduced into the femoral vein and artery. Another catheter was placed near the entrance of the right atrium via the right jugular vein. Rats were paralyzed with gallamine triethiodide (5 mg/kg, i.v.), and ventilated artificially. Activities of the phrenic nerve (PNA) and the hypoglossal nerve (HNA) were recorded simultaneously. Varied doses of capsaicin (0.625, 1.25, and 5 microg/kg) were delivered into the right atrium to activate pulmonary C-fibers. Before bilateral vagotomy, apnea, decreases in PNA and HNA were observed in response to pulmonary C-fiber activation by the low and moderate doses of capsaicin. The high dose of capsaicin evoked an increase in PNA, an immediate tonic discharge of the hypoglossal nerve, and a decrease in phasic HNA. The onset time of HNA preceding PNA was abolished and replaced by a time lagged pattern as pulmonary C-fibers were activated. Raising CO(2) concentration did not attenuate the inhibitory effect of pulmonary C-fiber activation upon PNA and HNA. After bilateral sectioning of the vagi, administration of the moderate dose of capsaicin to activate non-vagal C-fibers produced increases in PNA and HNA. These results suggest that pulmonary vagal C-fiber activation may narrow the diameter at the oropharyngeal level by a decrease in phasic HNA, which may be disadvantageous for the maintenance of a patent upper airway.

Animals↗
PubMed1993

Effects of graded muscle contractions on spinal cord substance P release, arterial blood pressure, and heart rate.

The release of substance P (SP)-like immunoreactivity (SP-LI) in the dorsal horn of the spinal cord and the cardiovascular changes to both high-tension (HT) and low-tension (LT) contractions were determined using alpha-chloralose-anesthetized cats. Over a 10-minute period, seven contractions (HT or LT) were induced. Each contraction was 20 seconds in duration and was followed by an 80-second quiescent period. The tension-time index (TTI) for the HT contractions was 2751 +/- 348 kg.s (mean +/- SD), which was greater than the TTI of 813 +/- 167 kg.s for the LT contractions. The HT contractions caused a greater release of SP-LI than the LT contractions: SP-LI increased from 0.18 +/- 0.02 to 0.32 +/- 0.03 fmol/100 microL and from 0.18 +/- 0.02 to 0.25 +/- 0.04 fmol/100 microL for the two types of contractions, respectively. Concomitant with this greater SP-LI release, HT contractions caused larger increases in mean arterial pressure (34 +/- 16 versus 11 +/- 4 mm Hg) and heart rate (18 +/- 7 versus 8 +/- 4 beats per minute) than did the LT contractions. These changes in SP-LI, mean arterial pressure, and heart rate were virtually abolished when the contractions were repeated after sectioning the L-5-S-2 dorsal and ventral roots or when the electrical stimulation of the ventral roots was repeated after muscle paralysis with gallamine triethiodide. These results demonstrate that contraction-evoked SP-LI release in the dorsal horn is related to the developed tension. Furthermore, these data provide additional support for the hypothesis that the release of SP from the central terminations of muscle afferents plays a role in mediating the cardiovascular responses to static contraction of skeletal muscle.

Animals↗
PubMed1994

Responses of neurons in the nucleus tractus solitarius to stimulation of heart and lung receptors in the rat.

To characterize central integration of reflex responses to stimulation of mechanically and chemically sensitive receptors in the heart and lung, male rats (350 to 425 g) were anesthetized (pentobarbital, 50 mg/kg IP) and paralyzed (gallamine triethiodide, 25 mg/kg IV) and then they underwent bilateral sinoaortic denervation. Extracellular activity of neurons in the nucleus tractus solitarius (NTS) was recorded in response to bolus intra-atrial saline (50, 100, 200, or 300 microL) or phenylbiguanide (PBG, 16 micrograms/kg in 100 microL) administered in random sequence. Changes in mean arterial pressure (MAP), mean right atrial pressure, and right atrial systolic pressure (RASP) were measured as correlates of stimulus intensity, and heart rate (HR) and renal sympathetic nerve activity (RSNA) were used to assess efferent reflex effects of cardiac and pulmonary receptor stimulation. NTS neurons with possible afferent input from stretch and chemically sensitive receptors were identified by an excitatory evoked response to electrical stimulation of the ipsilateral vagus nerve (1 Hz, 500 microA, 1-millisecond duration). Thirty-eight vagus nerve-evoked NTS units with onset latencies of 25.3 +/- 0.9 milliseconds displayed excitatory or inhibitory responses to saline or PBG injections or to both interventions. Saline administration elicited volume-dependent transient increases in MAP and RASP, which were followed by reflex decreases in MAP, HR, and RSNA. PBG injections also evoked hypotension, bradycardia, and sympathoinhibition.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMed1977

[Effects of morphine on the single unit activity of nucleus dorsal raphe].

Effects of morphine were studied in 36 gallamine triethiodide immobilized adult cats under light N2O anesthesia. Single units were recorded from the nucleus dorsal raphe using a stainless steel microelectrode. Dorsal raphe neurons were divided into two types; one was a clock-like (CL) neuron which was typically slow in rate, rhythmic and stable throughout recording time, and the other was a non-clock like (NCL) neuron which was relatively irregular in pattern as compared with CL neuron. Out of 36 neurons recorded in this experiment, 13 were CL neurons and 23 were NCL neurons. Mean discharge rates (spikes per sec) of CL neuron and NCL neuron were 2.84 (range of 2.01 approximately 3.68) and 4.11 (range of 0.10 approximately 35.09), respectively. None of the 13 CL neurons responded to the nociceptive (pinch and/or brdaykinin) and non-nociceptive (hair bending and/or tapping) stimuli. On the contrary, out of 23 NCL neurons, 13 responded to both nociceptive and non-nociceptive stimuli, 4 were responsive to only non-nociceptive stimuli and 6 were not responsive to these stimuli. Receptive fields of NCL neurons were wide with various somatic modalities. The latency for bradykinin (3 microgram) was 6.46 +/- 0.77 sec. Effects of morphine were examined in 6 CL neurons and 12 NCL neurons. After morphine, no nociceptive neuron responded to nociceptive stimuli, although there was no appreciable change in the responsiveness to non-nociceptive stimuli. Firing frequency and pattern of all CL neurons were unaffected by morphine. Out of 12 NCL neurons, 7 were unaffected in firing frequency and 5 were decreased after morphine.

Action Potentials↗