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At least 433 records · Page 24Linked to original sources

Model of the proximal urethra: measurement of the urethral stress profile.

Research on the activity of the urinary tract has led to the creation of a theoretical mechanical model where elastic forces, affecting rigid segments represent the living tissue of the urethral walls whereby it is assumed that the tissue acts as an elastic material. Such a model provides a clearer picture of changes in the physical parameters of the elastic walls of the urethra and facilitates better analysis of measurement errors. Artefacts make it exceptionally difficult to accurately measure the urethral pressure profile. The known methods have a measurement error of at least 30%. We have been trying to eliminate the basic error caused by the size of the measuring sensor. The methods involves measuring the urethral pressure profile in one patients using several sensors of varying diameters. The problem was defined mathematically. By extrapolation of measuring points, the value of elastic force under normal conditions can be obtained. Preliminary results of pressure profile measurements in our patients are much more accurate than those of other currently known measuring techniques. It is too early, however, to predict the extent of increased objectivity in the results of the new method for measuring urethral pressure profile, with and without functional electrical stimulation. The parameters of stimuli produced by our electrical stimulators will be based upon these findings.

Electric Stimulation↗

[Effect of pyramidal tract stimulation on segmental spinal cord potentials].

The author reports his results of the effect of pyramidal tract stimulation on the segmental spinal cord potentials (seg-SCP) using a total of 50 Wistar rats. Forty two Wistar rats were used to observe the effects of a pyramidal tract stimulation on the seg-SCP evoked by hindpaw stimulation. Another 5 Wistar rats were used to observe dorsal column stimulation as the conditioning stimuli instead of pyramidal tract stimulation. And the other 3 Wistar rats were used for both pyramidal tract and dorsal column stimulation as a separate trial. The seg-SCP of the rats consisted of three major peaks, P1, N1 and P2. P2 was separated into a first (P2F) and second component (P2S). The P2F peak was constantly preceded by a small notch, considered to be the onset of P2F, and named the P2F initial peak. The P2F peak amplitude of the seg-SCP was significantly decreased by pyramidal tract stimulation, while the P2F initial peak amplitude remained unchanged. This effect persisted until the concentration of sevoflurane was reduced to below 1.5% or until the peak arterial blood pressure was decreased to below 80 mmHg. The amplitude of both the P2F initial peak and the P2F peak were decreased significantly by dorsal column stimulation. These findings indicated that inhibition of the P2F peak amplitude was a characteristic effect of the pyramidal tract stimulation on the seg-SCP, while inhibition of the overall P2F amplitude was characteristic of the dorsal column stimulation.

Animals↗

Stimulus eccentricity and spatial frequency interact to determine circular vection.

While early research suggested that peripheral vision dominates the perception of self-motion, subsequent studies found little or no effect of stimulus eccentricity. In contradiction to these broad notions of 'peripheral dominance' and 'eccentricity independence', the present experiments showed that the spatial frequency of optic flow interacts with its eccentricity to determine circular vection magnitude--central stimulation producing the most compelling vection for high-spatial-frequency stimuli and peripheral stimulation producing the most compelling vection for lower-spatial-frequency stimuli. This interaction appeared to be due, in part at least, to the effect that the higher-spatial-frequency moving pattern had on subjects' ability to organise optic flow into related motion about a single axis. For example, far-peripheral exposure to this high-spatial-frequency pattern caused many subjects to organise the optic flow into independent local regions of motion (a situation which clearly favoured the perception of object motion not self-motion). It is concluded that both high-spatial-frequency and low-spatial-frequency mechanisms are involved in the visual perception of self-motion--with their activities depending on the nature and eccentricity of the motion stimulation.

Adult↗

Stimulus-dependent oscillations in the cat visual cortex: differences between bar and grating stimuli.

We have investigated the dependence of cortical oscillations on the type of visual stimulus. Single unit recordings were performed in areas 17 and 18 of the cat visual cortex. Among 217 cortical neurons oscillations in the frequency range of 22-102 Hz were found in 29 cells (13%). The proportion of oscillating cells was higher (16%) if both bar and grating stimuli were used to stimulate cortical neurons. It was found that gratings are more effective than bars in triggering oscillatory patterns in cortical cells. Among 21 oscillating cells which were stimulated with both bar and grating stimuli, oscillations evoked with gratings were found in 17 neurons (81%) while oscillations evoked with bar stimuli were triggered in 7 cells (33%). The distributions of oscillation frequencies were statistically different for oscillations evoked with bars and gratings. Frequencies of oscillations evoked with bars were in the lower and higher range than frequencies of oscillations evoked with gratings. In 3 cells (14%), rhythmic patterns could be evoked with both bar and grating stimuli. However, the oscillations were of different frequencies. No significant correlation was found between the strength of oscillations and firing rate of cortical neurons. Both simple and complex cells manifested the same dependence on stimulus type. However, complex cells mostly exhibited oscillations in the lower frequency range while simple cells did so when neurons were stimulated with bars. The results suggest that various classes of visual stimuli can be coded by a temporal pattern of cortical responses.

Animals↗

Interhemispheric asymmetries in the perception of unimanual and bimanual cutaneous stimuli. A study using transcranial magnetic stimulation.

Previous studies have shown that transcranial magnetic stimulation (TMS) of the sensorimotor cortex can induce a suppression of cutaneous perception from the fingers of the contralateral hand. In this work, 17 normal subjects were submitted to focal TMS of frontal and parietal scalp sites of each hemisphere. TMS was delivered at two interstimulus intervals (20 and 40 ms) following a cutaneous electrical stimulation of the first, third and fifth digits of either hand or both hands near the subjective threshold of perception. The aim of our study was to investigate whether TMS could detect an asymmetrical hemispheric specialization in the sensory perception of unimanual and bimanual, ipsilateral and contralateral sensory stimuli. At each interpulse interval, the right parietal cortex was significantly more sensitive to TMS interference with stimulus detection for both contralateral and ipsilateral stimuli compared with the left parietal cortex. These effects were mainly evident during bimanual discrimination tasks. Our results are indicative of an interhemispheric difference in the detection of cutaneous sensation, showing right hemispheric prevalence in the perception of contralateral as well as of ipsilateral stimuli. They provide neurophysiological support in normal humans to the clinical evidence which indicates that right hemisphere lesions can indeed produce deficits in the perception of ipsilateral sensory stimuli.

Adult↗

The antinociceptive effects of anterior pretectal stimulation in tests using thermal, mechanical and chemical noxious stimuli.

Four behavioural tests have been used to study the antinociceptive effects of electrical stimulation of the anterior pretectal nucleus (APtN) in the rat. The antinociceptive effects of stimulating this nucleus, which lies dorsally in the posterior diencephalon, have recently been studied extensively but always using briefly applied heat stimuli. It is reported here that APtN stimulation effectively inhibited responses to briefly applied noxious pressure and longer-lasting noxious chemical (formalin) stimuli. Although the tail-flick reflex to noxious heat was very potently depressed by APtN stimulation, responses to noxious heat in the hot-plate test were not. Three doses of morphine were also studied with each test and it was concluded that 15 sec of 35 microA r.m.s. current into the APtN was as effective as 3-5 mg/kg morphine s.c. in the rat.

Animals↗

Release of autonomic neuromediators by local ventricular electrical stimulation.

Trains of electrical stimuli were applied to the ventricular epicardium in pentobarbital-anesthetized dogs. The trains, delivered during the absolute refractory period via Walton-Brodie strain gauge arches, resulted in a highly localized potentiation of ventricular contractile force. The magnitude of the potentiation was directly related to the intensity of the trains. The positive inotropic response of either ventricle to trains of stimuli was abolished following chronic cardiac denervation or beta-adrenergic blockade with tolamolol, indicating that the response was probably mediated by the excitation of local sympathetic nerve fibers. Following the elimination of adrenergic influences, a slight negative inotropic response to trains of stimuli was observed in some animals. Administration of atropine blocked the negative inotropic response. When the adrenergic system was intact the administration of atropine resulted in a significant augmentation of the positive inotropic response of both ventricles to trains of stimuli. Thus in addition to norepinephrine release, it also appeared that electrical stimulation of the ventricles resulted in activation of local parasympathetic fibers with subsequent release of acetylcholine.

Animals↗

Convergence of lingual and palatal gustatory neural activity in the nucleus of the solitary tract.

The responses of 54 neurons to independent sapid stimulation of 4 taste receptor subpopulations associated with: (1) anterior tongue; (2) nasoincisor ducts; (3) soft palate; and (4) foliate papillae were recorded from the nucleus of the solitary tract (NST) of the Rat. Neurons responding to stimulation of receptor subpopulations in the anterior oral cavity (anterior tongue or nasoincisor ducts) were located more rostrally in the NST than neurons responding to stimulation of receptor subpopulations in the posterior oral cavity (soft palate or foliate papillae). Half of the sampled neurons responded exclusively to stimulation of one receptor subpopulation with the remaining neurons responsive to stimulation of two or more receptor subpopulations. The most common pattern of convergence observed was between responses arising from stimulation of the taste buds on the anterior tongue and those associated with the nasoincisor ducts of the hard palate. The sensitivity of NST neurons to anterior tongue and nasoincisor duct stimulation with the 4 standard taste stimuli was determined. When stimulating the anterior tongue, the order of effectiveness was NaCl greater than HCl greater than sucrose greater than quinine hydrochloride (QHCl). When the nasoincisor ducts were tested, however, the order of stimulus effectiveness was strikingly different: sucrose was the best stimulus, followed by HCl, NaCl, and QHCl. If both the anterior tongue and nasoincisor ducts are included, stimulation of taste receptors in the anterior oral cavity of the rat produces good responses to stimuli representing 3 of the 4 classical taste qualities: sweet, salty, and sour.

Animals↗

Summation between acoustic and trigeminal stimuli evoking startle.

Electrical stimulation of the spinal trigeminal pathway evokes a short-latency startle-like response in rats. To explore the relationship between acoustic and tactile systems mediating startle, we studied temporal summation between pairs of startle-evoking stimuli in awake rats by varying the interstimulus interval. The stimuli were: (i) two noise bursts; (ii) two unilateral electrical stimuli near the principal nucleus of the trigeminal nerve; (iii) electrical stimulation of the left and right trigeminal nucleus; or (iv) a noise burst and unilateral stimulation of the trigeminal nucleus. Following two noise bursts, the amplitude of startle increased as the interval increased from 0 to 4 ms, then declined smoothly as the interval increased to 15 ms. Unilateral stimulation of the trigeminal nucleus resulted in a sharper summation effect, with maximal summation at 2 ms, and refractory periods estimated at 0.4-0.8 ms. Bilateral stimulation of the trigeminal nucleus resulted in broader summation without a refractory period, and maximal summation when the stimuli on both sides of the trigeminal nucleus were presented simultaneously. The combination of acoustic and trigeminal stimulation was most effective in enhancing startle amplitudes, and summation peaked when the noise burst preceded the trigeminal stimulation by 5 ms. Similarly, electromyogram latencies measured in the hindlimb were 3-4 ms shorter for trigeminal stimulation than for the noise burst. Startle appears to be optimally activated by simultaneous acoustic and tactile stimuli, as occurs during head blows.

Acoustic Stimulation↗

Effects of focal transcranial magnetic stimulation on simple reaction time to acoustic, visual and somatosensory stimuli.

In a simple reaction time (RT) paradigm, magnetic stimulation of different intensities was delivered over different scalp positions and at variable delays before (negative) or after (positive) the go-signal. Magnetic stimulation shortened RT to different go-signals (auditory, visual and somatosensory stimuli) by approximately 30 ms when delivered over the motor cortex contralateral to the responding arm at intensities below motor threshold. This effect was maximal at a delay of approximately +10 ms. A similar effect was found with suprathreshold stimulation to the ipsilateral motor cortex. Magnetic stimulation over other scalp areas did not affect RT regardless of the delay. No differences were found between the effects on elbow flexion and thumb abduction. The shortening of RT was not associated with changes in the timing development of premovement excitability increase in the motor cortex. We conclude that magnetic stimulation shortens RT by inducing an earlier initiation of this excitability increase.

Acoustic Stimulation↗

Functional magnetic resonance imaging and evoked potential correlates of conscious and unconscious vision in parietal extinction patients.

We describe recent functional magnetic resonance imaging (fMRI) and event-related potential (ERP) studies of visual extinction in patients with right parietal damage who can detect isolated visual stimuli on either side, yet often miss contralesional (left) stimuli during bilateral stimulation. We consider the neural fate of such extinguished visual stimuli and how neural responses differ for consciously detected versus extinguished stimuli. fMRI findings indicate that extinguished stimuli evoke activity in striate and ventral extrastriate visual cortex, despite escaping awareness. Activations for extinguished stimuli can be found even in category-specific (face-responsive) areas of the fusiform gyrus. On the other hand, activations in visual cortex are stronger for consciously detected versus extinguished stimuli, with parietal and frontal areas of the intact left hemisphere also implicated in this comparison. Recent ERP data likewise suggest differential neural responses for consciously detected versus extinguished stimuli. We discuss these findings in relation to current speculations about the neural basis of conscious and unconscious perception.

Attention↗

Noninvasive evaluation of retrograde conduction times to avoid pacemaker-mediated tachycardia.

Pacemaker-mediated tachycardia is a potential complication of atrioventricular (AV) universal DDD pacemakers when retrograde ventriculoatrial (VA) conduction is slower than the postventricular-atrial refractory period of the pulse generator. The propensity for pacemaker-mediated tachycardia was noninvasively assessed in 17 patients with a unipolar DDD pacemaker using chest wall stimulation. Low amplitude stimuli were delivered to chest wall electrodes through a programmed stimulator. Using this method, 13 of the 17 patients were found to have absent VA conduction or VA conduction time less than the postventricular-atrial refractory period. In the four patients with noninvasively measured VA conduction time greater than the postventricular-atrial refractory period, sustained pacemaker-mediated tachycardia was induced. Reprogramming of pacemaker parameters prevented repeat induction of pacemaker-mediated tachycardia in only one of four patients. The three remaining patients had clinical pacemaker-mediated tachycardia and underwent pacemaker programming to the DVI mode. A total of 13 patients continue to use DDD mode after a mean follow-up period of 9.5 +/- 5.4 months. Invasive measurement of VA conduction was performed in 13 of the 17 patients. The noninvasive method accurately predicted the invasive measurement in each case. Noninvasive evaluation of VA conduction accurately predicts the propensity for pacemaker-mediated tachycardia under a variety of clinical conditions. Serial testing can be performed after pacemaker reprogramming or drug intervention. Noninvasive evaluation of retrograde VA conduction should predict most clinical episodes of pacemaker-mediated tachycardia.

Adult↗

A mechanism of cardiac pain suppression by spinal cord stimulation: implications for patients with angina pectoris.

Clinical reports show that electrical stimulation of the spinal cord reduces symptoms of angina pectoris, but so far have not provided evidence on the mechanisms involved. The hypothesis for this study was that inhibition of spinothalamic tract transmission may account for this result. Extracellular potentials of 28 spinothalamic tract neurons were recorded in anaesthetized monkeys, and the effects of dorsal column stimulation were determined on activity evoked by cardiac and somatic stimuli. Dorsal column stimulation reduced the number of cell potentials evoked by electrical stimulation of cardiopulmonary sympathetic afferent fibres in 11 spinothalamic tract cells tested. Activity evoked by intracardiac injection of bradykinin was decreased by dorsal column stimulation in six of seven neurons that responded to chemical stimulation of afferents. Differential effects of dorsal column stimulation were correlated to the cell responses to somatic field stimulation. Dorsal column stimulation inhibited activity in 12 of 12 neurons which were excited only by noxious pinch of somatic fields, whereas eight of 16 neurons which were excited by innocuous brushing of somatic fields were unaffected or excited. Transection of the dorsal column showed that the pathway transmitting inhibitory impulses descended from the stimulation site to the spinothalamic tract neurons examined. Results of this study are consistent with the concept that spinal cord stimulation reduces pain by decreasing the firing of spinothalamic tract cells which are activated by small fibre afferents. The paresthesias associated with nerve stimulation techniques may result from activation of spinothalamic tract cells which are excited by large fibre afferents. The clinical decision to employ spinal cord stimulation in patients with angina should balance the obvious benefit of pain relief against the risk of depriving the patient of an important warning signal while active myocardial ischaemia is in progress.

Afferent Pathways↗

Responses of diencephalic nociceptive neurones to orofacial stimuli and effects of internal capsule stimulation in the rat.

The effect of conditioning stimulation of the internal capsule on nociceptive neurones in the rat diencephalon was investigated. The animals were anaesthetised with N(2)O/O(2) (2:1) and 0.5% halothane, and immobilised with pancuronium bromide. Nociceptive neurones responding to noxious stimulation of the face and oral structures were recorded in the ventral posteromedial nucleus, posterior group and zona incerta. These neurones were classified into wide dynamic range and nociceptive-specific types. Functional segregation of these nociceptive neurones was not apparent within the nucleus or between nuclei. A test stimulus with a single rectangular pulse (5-70 V) was applied to the centre of the receptive field; the nociceptive neurones exhibited short- and/or long-latency responses. Both responses in about 45% of the nociceptive neurones were inhibited by conditioning stimuli to the contralateral internal capsule with trains of 33 pulses (300 microA) at 330 Hz. The percent inhibitory effects on the nociceptive neurones of each area were 68.0+/-14.8% (n = 6) in the ventral posteromedial nucleus, 72.8+/-12.4% (n = 4) in the posterior group and 61.5+/-7.5% (n = 4) in the zona incerta. Effective sites for conditioning stimulation were concentrated in the lateral side of the internal capsule, through which the corticofugal fibres from the somatosensory cortex pass. These findings suggest that the transmission of nociceptive information to the diencephalon is modulated by stimulation of the internal capsule at the level of the trigeminal sensory complex in the brainstem. They might provide a novel way to elucidate the neurophysiological basis for antinociception by stimulation of the internal capsule observed in clinical studies.

Animals↗

Single neurons in the nucleus of the solitary tract respond selectively to bitter taste stimuli.

Molecular data suggest that receptors for all bitter ligands are coexpressed in the same taste receptor cells (TRCs), whereas physiological results indicate that individual TRCs respond to only a subset of bitter stimuli. It is also unclear to what extent bitter-responsive neurons are stimulated by nonbitter stimuli. To explore these issues, single neuron responses were recorded from the rat nucleus of the solitary tract (NST) during whole mouth stimulation with a variety of bitter compounds: 10 microM cycloheximide, 7 mM propylthiouracil, 10 mM denatonium benzoate, and 3 mM quinine hydrochloride at intensities matched for behavioral effectiveness. Stimuli representing the remaining putative taste qualities were also tested. Particular emphasis was given to activating taste receptors in the foliate papillae innervated by the quinine-sensitive glossopharyngeal nerve. This method revealed a novel population of bitter-best (B-best) cells with foliate receptive fields and significant selectivity for bitter tastants. Across all neurons, multidimensional scaling depicted bitter stimuli as loosely clustered yet clearly distinct from nonbitter tastants. When neurons with posterior receptive fields were analyzed alone, bitter stimuli formed a tighter cluster. Nevertheless, responses to bitter stimuli were variable across B-best neurons, with cycloheximide the most, and quinine the least frequent optimal stimulus. These results indicate heterogeneity for the processing of ionic and nonionic bitter tastants, which is dependent on receptive field. Further, they suggest that neurons selective for bitter substances could contribute to taste coding.

Algorithms↗

Transcranial magnetic stimulation effects on one-trial learning and response to anxiogenic stimuli in adult male rats.

Transcranial magnetic stimulation (TMS) is a relatively new technique for inducing small, localized, and reversible changes in living brain tissue and has been suggested to have antidepressant properties in humans and animal models of depression. Memory function generally has been found to be unaffected by TMS, although some studies have raised the possibility of memory interference from TMS. Additionally, there have been indirect indications that TMS may possess anxiolytic features. This study examines the effects of TMS in animal models of one-trial learning and anxiety. In this study, short-term treatment with TMS compared with identically handled animals not given TMS in adult rats resulted in no significant differences in memory as assessed both by a one-time learning paradigm and by components of an elevated-plus maze task, that TMS does not impair memory as assessed by these tasks. In addition, no changes were found in anxiety-like behavior on the elevated plus maze task. In summary, these findings support previous reports that TMS does not interfere with memory function. There was no evidence of an anxiolytic response from TMS in rats as assessed by the elevated plus maze test.

Age Factors↗

Effect of digital nerve stimuli on responses to electrical or magnetic stimulation of the human brain.

1. Reflexes were elicited in the first dorsal interosseous muscle of seven normal subjects by electrical stimulation of the digital nerves of the index finger at 3 times perceptual threshold while subjects maintained a constant voluntary contraction of the muscle. The average response in the surface-rectified electromyogram (EMG) consisted of an early inhibitory (I1) component followed by a later excitation (E2). 2. Low intensity anodal electrical or magnetic scalp stimuli were given over the motor cortex in order to elicit muscle responses within the period of the I1 and E2 reflex components. 3. Compared with control responses elicited in the absence of digital nerve stimulation, responses to electrical cortex stimulation were suppressed in the I1 period and facilitated during the E2 period of the reflex. In contrast, responses evoked by magnetic stimulation were suppressed during I1 and also for the first 10 ms or so of the E2 response. Magnetically evoked responses were facilitated during the later part of the E2 reflex. 4. Similar effects were seen when the probability of firing of single motor units was studied. 5. In three subjects, small taps were given to the abducted index finger in order to stretch the first dorsal interosseous muscle and evoke reflexes which were of comparable size to the E2 reflex evoked by digital nerve stimulation. In contrast to the experiments in which digital nerve stimuli were given, responses evoked by magnetic stimulation over motor cortex were facilitated at all times during the course of the reflex evoked when the muscle was stretched. 6. We conclude that single electrical stimuli applied to the digital nerves can reduce for a short period the excitability of motor cortex to magnetic stimulation. This occurs at a time when the same stimulus is evoking an excitatory (E2) reflex in the average surface-rectified EMG.

Adult↗

Responses of units in the mesolimbic system to olfactory and somatosensory stimuli: modulation of sensory input by ventral tegmental stimulation.

It is well known that neurons of the nigrostriatal dopamine (DA) system respond to sensory stimuli, and our primary objective here was to ascertain if neurons in the terminal regions of the mesolimbic DA system respond to sensory input also. In addition, the effects of electrical stimulation of the ventral tegmentum, which contains the DA cells of origin of the mesolimbic system, on sensory-evoked responses in mesolimbic neurons was studied. In rats anesthetized with chloral hydrate, responses of single units to olfactory and somatosensory stimuli were recorded in 6 forebrain regions including nucleus accumbens and olfactory tubercle. Both increases and decreases in spontaneous firing rates were evoked in 225 of 336 units by one or more of the 8 types of sensory stimuli employed (5 olfactory, 3 somatosensory). Excitatory responses occurred twice as frequently as inhibitory responses, but a few units responded with excitatory responses to some stimuli and inhibitory responses to others. The proportions of units responsive to olfactory and/or somatosensory stimuli were different in different regions. After electrical stimulation of the ventral tegmentum, sensory-evoked responses were changed in 30 of the 49 units tested (61%). There were increases, decreases or combinations of a decrease followed by an increase in sensory-evoked responses, which persisted for 1-10 min after the application of a single electrical stimulus train. Haloperidol (0.3 mg/kg, i.p.) either blocked the effect of tegmental stimulation or decreased all responses. The present results demonstrated that units in the terminal regions of the mesolimbic DA system are responsive to sensory input and that these responses can be affected by prior electrical stimulation of the ventral tegmentum.

Action Potentials↗