Sensitivity to edges of mechanoreceptive afferent units innervating the glabrous skin of the human hand

The impulse responses to perpendicular sinusoidal skin displacements were recorded from 4 different types of mechanoreceptive afferent units innervating the glabrous skin of the human hand. The Cycle responses, defined as the number of impulses evoked per sine wave cycle, were studied at a wide range of frequencies (0.5–400 Hz) and amplitudes (0.001–1 mm). The rapidly adapting units (RA) were most easily excited at stimulus frequencies between 8 and 64 Hz, whereas the corresponding frequencies for the Pacinian units (PC) were above 64 Hz. However, at high stimulus amplitudes, the RA and the PC units showed quite similar response profiles within the range of frequencies tested. The sensitivities of the slowly adapting unit types (SA I and SA II) were greatest at lower frequencies. A characteristic finding for all 4 types of units was that the higher the amplitude, the lower the frequency at which the cycle response was maximal.     

Participation of different groups of afferent fibers of mesenteric nerves in vasomotor reflexes]

The dependence of the magnitude and character of vasomotor reflexes on the amplitude of mesenteric nerve tetanic stimulation was studied in experiments with cats anesthetized with urethane and chloralose. A comparison of the stimulus amplitude reflex magnitude curves with the previously obtained data on electrical excitability of various groups of mesenteric nerves afferent fibres revealed that there are 3 groups of "vasomotor" afferents in mesenteric nerves: "fast" Adelta-fibres (conduction velocity above 8 m/s) the impulses of which evoke depressor or small pressor reflexes; "slow" Adelta-fibres (conduction velocity below 8 m/s) the impulses of which evoke pressor reflexes or interacting with impulses of lower-threshold "fast" Adelta-fibres, either decrease depressor reflexes evoked by impulses of these fibres or increase pressor reflexes evoked by these fibres impulses; C-fibres the impulses of which increase pressor reflexes evoked by impulses of "slow" Adelta-fibres.     

Reset of hippocampal rhythmical activities by afferent stimulation

Physostigmine induced theta rhythm and unit activity were recorded from the dorsal hippocampus in immobilized locally anesthetized rats. Correlations between theta and rhythmical unit activity and their modifications by hippocampal afferent stimulation were studied. The principal finding was that electrical stimulation of afferents reset theta and rhythmical unit activity in phase. Poststimulus theta displayed a variable frequency which depended upon the structure stimulated. Lower frequencies were evoked by septal, higher frequencies by entorhinal and reticular formation stimulations. When theta rhythms were absent either by spontaneous disappearance or as a consequence of lesions in the fornix superior of septum, the reset was not observed. The reset of the theta rhythms and unit activity by afferent stimulation, suggests that the hippocampus may participate in timing mechanisms.     

Characteristics of dorsal neck muscle afferent input to the cat frontal cortex before and after dorsal funiculus section

Electrical stimulation of a nerve branch to the biventer cervicis and complexus and of the suboccipital nerve to the rectus capitis dorsalis major and obliquus capitis caudalis muscles of the cat dorsal neck evoked field and single-cell activity in the frontal cortex at latencies of 5 to 46 ms. Inhibitory effects were also observed. Approximately 20% of the cells tested received their afferent input from electrophysiologically characterized group I afferent fibers, determined by recording threshold afferent volleys from the first and second dorsal rootlets. These cells had the shortest latencies (5 to 10 ms) and followed stimulus frequencies to as much as 2 Hz. The remainder of the neurons required intensities of stimulation greater than 1.5 times threshold for activation, and followed stimulus frequencies of 0.5 Hz or less. After unilateral dorsal funiculus transection, early evoked cell and field activity dependent on stimulation intensities of 1.1 to 1.3 times threshold was abolished in the contralateral frontal cortex. However, nerve stimulation with intensities of 1.8 to 3 times threshold was still effective in eliciting neuronal responses. Significant increase in mean cell latency was observed in coronal, in presylvian, and on the dorsal, but not the ventral, bank of the cruciate sulcus after the lesion. The results showed that the dorsal funiculus lesion resulted in selective removal of group I afferent input from the dorsal neck to the contralateral frontal cortex.     

Modulation of the afferent input to the septal neurons by cholinergic drugs

The effects of cholinergic drugs upon the evoked activity of extracellularly recorded neurons of the medial septal nucleus-nucleus of the diagonal band (MS-DB complex) were tested in unanesthetized rabbits. Electrical stimulation of MFB resulted in entrainment of the background theta-cycles in the neurons with strong rhythmic discharge (types I and II). Phase-locking of the background theta-cycles to the stimulus occurred 'by the burst', or 'by the pause' within the theta-range of frequencies (3-12 Hz). Single-spike responses, following up to 30 Hz and more, were also evoked by MFB stimulation, especially in the cells with weak theta-modulation (type III) or without it (type IV). Injection of physostigmine increased background theta-modulation of neuronal activity and simultaneously blocked or diminished responses to repetitive MFB stimulation in 82% of the MS-DB units, independent of their type of response. Driving of theta-cycles both 'by the burst' and 'by the pause' was ineffective or drastically reduced. Single spike responses disappeared or became unstable, though their minimal latencies did not change. Initial inhibitory responses were blocked or became significantly shorter. Antimuscarinic drugs, scopolamine and atropine, which abolished theta-modulation in many MS-DB units, restored responses and sometimes enhanced them. Repetitive stimulation of the MFB in this condition was effective up to the high frequencies, well beyond the theta-range. Thus, the majority of the MS-DB units did not respond to the afferent stimuli during prominent theta-activity evoked by physostigmine. The role of the septal cholinergic system in gating of afferent input during the theta-state and its importance for learning and memory is suggested.     

Effect of stimulation in the periaqueductal grey matter on activity in ascending axons of the rat spinal cord: selective inhibition of activity evoked by afferent Aδ and C fibre stimulation and failure of naloxone to reduce inhibition

In rats with prenigral decerebration, the effect was studied of electrical stimulation of the periaqueductal grey matter (PAG) on the activity recorded from axons ascending in the spinal cord. These axons were activated by electrical stimulation of afferent Aβ, Aδ and C fibres in the ipsilateral sural nerve.Stimulation of the PAG with trains of impulses by itself evoked ascending activity, but strongly depressed the impulse transmission from C fibres to neurones with ascending axons. It exerted a weaker effect on impulse transmission from Aδ fibres and had no effect on impulse transmission from Aβ fibres to neurones with ascending axons. Intravenous naloxone, 1 mg/kg, did not diminish the depressant effect of PAG stimulation.Intravenous morphine depressed the activation of ascending axons from afferent C fibres (0.5 mg/kg) more markedly than that from afferent Aδ fibres (2 mg/kg), but did not modify the depression of ascending activity produced by PAG stimulation. Naloxone antagonized the depressant effect of morphine.The results indicate that PAG stimulation inhibits ascending activity evoked by noxious stimuli by a mechanism which does not necessarily involve endogenous opiates.     

Interaction of afferent impulses in the human primary sensorimotor cortex.

We recorded somatosensory evoked magnetic fields (SEFs) over the hand area of the primary sensorimotor cortex (SMI) in 6 healthy adults in 2 sets of experiments to study interaction of afferent impulses. In experiment 1, SEFs were elicited by contralateral median nerve (MC) stimuli presented alone and 40 msec after a conditioning stimulus to the contralateral ulnar (UC), ipsilateral median (MI) or contralateral tibial (TC) nerve. N20m, P30m and P60m deflections to MC stimulation were markedly attenuated by preceding UC stimulation whereas N40m was enhanced, and a novel P80m emerged. In contrast, MI or TC stimulation did not affect the responses to MC. In experiment 2, the time course of recovery of N20m to median nerve stimuli was studied after stimulation of the adjacent ulnar and of the same median nerve. The recovery curves were similar for both conditioning stimuli with nearly full recovery of N20m at 120 msec. The results indicate marked interaction of impulses from ipsilateral median and ulnar nerves in human SMI, but no evidence was found of interaction from the two hands or from ipsilateral hand and foot.     

Stimulation of group III and IV afferent nerves from the hindlimb by thromboxane A2

These experiments were designed to test the hypothesis that the TxA₂ mimetic, U46,619, would stimulate group III and IV afferent nerve endings from the hindlimb of the anesthetized cat. Nerve impulses were recorded from the dorsal rootlets of the L7-S1 segments of the spinal cord, and afferent units identified by measurement of conduction velocities, mechanical probing of hindlimb muscles, and local injection of chemical stimulants (capsaicin and bradykinin). Five of the 15 group III fibers were stimulated by U46,619 (2–10 μg injected into the abdominal aorta; mean baseline impulse frequency increasing from 7.3 (±3.2) impulses/s to 16.0 (±3.1)), while 7 of the 12 group IV fibers responded to U46,619 (impulse frequency increasing from 4.3 (±3.2) to 8.8 (±3.6)). The average latency for the response (20–30 s) did not differ between the two groups of afferent fibers. We conclude that group III and IV afferent fibers originating from the skeletal muscle of the hindlimb are stimulated by TxA₂ and that the release of TxA₂ in skeletal muscle could evoke cardiorespiratory reflexes known to be activated by stimulation of these afferent nerves.     

Phase-dependent Modulation of a Cutaneous Sensory Pathway by Glycinergic Inhibition from the Locomotor Rhythm Generator in Xenopus Embryos

In immobilized Xenopus laevis embryos two classes of sensory interneuron are excited by mechanosensory Rohon - Beard neurons and rhythmically inhibited during fictive swimming. Dorsolateral commissural (DLC) interneurons are inhibited in time with rhythmic motor discharge on the same side as their soma, while unidentified dorsolateral (DLX) interneurons are inhibited in the opposite phase of the swimming rhythm. The inhibition is abolished by bath application of strychnine sulphate at 1 - 10 microM, but not by the gamma-aminobutyric acid antagonists bicuculline (20 - 40 microM) or curare (70 - 100 microM). The inhibitory postsynaptic potentials (IPSPs) involve an increase in chloride conductance since they are reversed in sign to become depolarizing following intracellular injection of chloride ions. The conductance increase during inhibition was able to block impulses evoked by intracellular current in a phase-dependent manner, suggesting that postsynaptic inhibition is sufficient to account for the gating of afferent input to the spinal cord during swimming. An interneuron receives IPSPs that are predominantly in one phase of the rhythm, but most interneurons are also inhibited sporadically in the opposite phase. The amplitude and time course of the IPSPs closely follow the frequency of the swimming rhythm, with maximal inhibition occurring near the starts of episodes, when swimming frequency is at its highest. Towards the end of an episode, when swimming frequency declines, the level of inhibition is low, the membrane potential of the interneurons returns to rest between cycles, and IPSPs often fail to occur. Inhibition suppresses sensory excitation in a phase-dependent manner (cf. Sillar and Roberts, Nature, 331, 262 - 265, 1988). Sensory interneurons fire a single impulse in response to a brief sensory stimulus, but they will usually fire multiple impulses when depolarized with sufficient intracellular current. In some sensory interneurons a short-latency IPSP follows the impulse evoked by skin stimulation that could curtail impulse activity. However, when the inhibition is blocked by strychnine, sensory interneurons still fire a single short-latency impulse, favouring the conclusion that brief, synchronized afferent excitation elicits a single impulse in neurons that are capable of firing multiply. Since the inhibition of DLC interneurons occurs in phase with activity on the same side it probably originates from spiking in ipsilateral glycinergic commissural interneurons which have ipsilateral as well as contralateral projections. The inhibition of DLX interneurons in the opposite phase probably originates from the contralateral projections of commissural interneurons.     

Long-lasting neuronal activity in rat dorsal horn evoked by impulses in cutaneous C fibres during noxious mechanical stimulation

The responses of 44 nociceptive neurones in the lumbar dorsal horn evoked by controlled mechanical stimulation of the skin, with or without conduction block in myelinated afferent fibres, were studied in the halothane-anaesthetized rat, in order to evaluate the effects of impulses in cutaneous nociceptive C fibres on dorsal horn neurones. Continuous non-noxious pinch of the skin evoked a short-latency discharge (mean latency 15 ms) in all the 13 class 2 neurones (i.e. neurones responding to both non-noxious and noxious stimulation of the skin) tested. The short-latency discharge was followed by weak prolonged activity in 6 neurones. Following noxious pinch of the skin a prominent late discharge (peak latency 150 ms-2 s) was evoked, which in all but two class 2 neurones outlasted the stimulation period (5-10 s). The discharge evoked by noxious pinch in class 3 neurones (i.e. neurones responding to noxious stimulation only) did not usually outlast the stimulation period. In all but two nociceptive neurones tested (n = 26) the late activity evoked by noxious pinch remained, albeit at a lower frequency in some neurones, during a conduction block in A fibres2,3. Hence this late discharge is probably mainly generated by impulses in nociceptive C fibers. It is concluded that nociceptive C fibres have an important role in sustaining long-lasting activation of class 2 neurones during noxious stimulation of the skin and that long-lasting discharges in these neurones indicates tissue damage to their receptive fields.     

Short-term depression at primary afferent synapses in rat substantia gelatinosa region

Short-term synaptic depression is a widespread and predominant mechanism underlying the process of neural information. To study the short-term depression at primary afferent synapses between Adelta fibers and substantia gelatinosa (SG) neurons in the spinal cord, transverse spinal cord slices with dorsal root attached were made from young rats. With whole-cell voltage-clamp method, Adelta-fiber elicited excitatory post-synaptic currents (EPSCs) were recorded from SG neurons visualized by infrared microscope. Using the normalized peak amplitudes of EPSCs, the existence of short-term depression was examined at all six stimulus frequencies ranging from 0.5 to 20 Hz. Both paired-pulse and steady-state depressions became greater with the increasing stimulus frequency. External calcium concentration could significantly affect the degrees of paired-pulse and steady-state depressions, with paired-pulse depression more affected. Application of NMDA receptor antagonist had no significant effect on this depression. These results indicated that short-term synaptic depression exists at primary afferent neurotransmission in spinal cord and results from the presynaptic reduction in the number of quanta of transmitter released by impulses.     

Discharge of group IV phrenic afferent fibers increases during diaphragmatic fatigue

The discharge of single unit group III (n=7) and group IV (n=8) phrenic afferent fibers was recorded during rhythmic diaphragmatic contractions before and after the onset of fatigue. Compared to pre-fatigue impulse activity, group IV, but not group III, phrenic afferent fibers discharged more (p<0.05) during rhythmic diaphragmatic contractions when the diaphragm was fatigued. This increase in group IV fiber discharge during diaphragmatic fatigue provides electrophysiological evidence consistent with the notion that group IV phrenic afferent fibers comprise the afferent arm of a fatigue-induced inhibitory reflex originating in the diaphragm.     

Characterization in vivo of the NMDA receptor-mediated component of dentate granule cell population synaptic responses to perforant path input.

The NMDA receptor-mediated component of the hippocampal granule cell population excitatory postsynaptic potential response to low frequency (< 0.2 Hz) stimulation of the medial perforant path was characterized in vivo. Extracellular recordings were obtained from the dentate molecular layer in anesthetized rabbits, and glutamatergic and GABAergic antagonists were applied locally by pressure ejection. To measure the NMDA-mediated component, the NMDA receptor antagonist D-5-aminophosphonovalerate (APV) was applied during the constant ejection of physiological saline, 6-cyano-7-nitroquinoxaline-2,3-dione (CNQX), and/or bicuculline methiodide. In general agreement with the results of attempts by other investigators to identify NMDA responses in vivo, APV did not significantly reduce the response to a single stimulus impulse in the presence of saline. However, an NMDA-mediated response was revealed when alpha-amino-3-hydroxy-5-methyl-4-isoxazoleproprianate receptor-mediated current flow was eliminated by applying the non-NMDA receptor antagonist CNQX. The NMDA component was negative-going as predicted, but its duration was considerably less than indicated in other studies of the dentate in vitro. The relative magnitudes of the NMDA and non-NMDA components of the EPSP were found to vary as a function of stimulus intensity or frequency. The NMDA receptor-mediated component represented 12% of the control response and increased to over 25% in response to higher stimulus intensities. A brief, high-frequency burst of impulses evoked a larger NMDA component in the presence of CNQX and was able to evoke an NMDA component in the presence of saline. Surprisingly, short trains of stimulation at lower frequencies typically produced suppression of the NMDA component. In a final series of experiments, it was found that many characteristics of the NMDA component were substantially altered by GABAergic inhibition. In the presence of the GABAA antagonist bicuculline, the magnitude of NMDA receptor-mediated responses was increased and their duration was greatly extended. Additionally, in the presence of bicuculline, the NMDA component facilitated markedly in response to frequencies of stimulus input > 20 Hz. These results indicate in vivo that the initiation and duration of NMDA current flow depend strongly upon the intensity and frequency of perforant path stimulation. In addition, the NMDA response to a single impulse appears to be reduced and truncated by input from GABAA receptor-mediated feedback and/or feedforward inhibition, and this inhibition affects temporal summation of NMDA receptor-mediated responses over a wide range of input frequencies. It is suggested that such inhibition results from the activation of GABAA receptors located on granule cell dendritic shafts.(ABSTRACT TRUNCATED AT 400 WORDS)     

Latency of gustatory neural impulses initiated in frog tongue

Latencies of gustatory neural impulses evoked by stimulation of the bullfrog tongue with the 4 basic taste substances (NaCl, acetic acid, quinine-HCl(Q-HCl), sucrose), CaCl2 and water were studied by recording antidromic impulses conducted to the fungiform papillae. Mean latencies of the impulses ranged from 58 to 107 ms when very strong stimuli, such as 2 M NaCl, 0.1 M acetic acid, 0.1 M Q-HCl, 2 M sucrose and 1 M CaCl2, were applied. Mean latency in response to water was 2.41 s. The time required for arrival of an applied taste stimulus on the taste receptor membrane was a mean of 20.1 ms. The time required for antidromic conduction from the impulse initiation site to the recording site was a mean of 2.4 ms. Electrical stimulation of the fungiform papilla with a strong intensity produced the impulse with a long and fluctuating latency. The mean minimum latency of the fluctuating impulse, from which the conduction time was subtracted, was 5.3 ms. Mechanical destruction of the taste disk situated at the top of the fungiform papilla resulted in a disappearance of the fluctuating impulse, suggesting that this was initiated synaptically via a depolarization of taste cells by electrical current. The minimum 5.3-ms latency was likely to be the time required from the onset of taste cell depolarization to the initiation of an impulse at the first node of Ranvier of myelinated gustatory fiber. These results indicate that the latencies of 58-107 ms by strong taste stimulation were composed of the 30- to 79-ms latency of taste cell receptor potential and the remaining 28 ms latency, which was the sum of the time of stimulant diffusion, the time from taste cell depolarization to the first impulse and the time of impulse conduction.     

Interactions between cutaneous and muscle afferent projections to cerebral cortex in man

In order to demonstrate interactions between cutaneous and muscle afferent volleys in the ascending somatosensory pathways, different nerves of the lower limb were stimulated together in a conditioning-test paradigm, the changes in the earliest component of the cerebral potential evoked by the test stimulus being taken to indicate such an interaction. It was first confirmed that the cerebral potential evoked by stimulation of the posterior tibial nerve at the ankle is derived from muscle afferents in the mixed nerve and has shorter latencies than the cerebral potential evoked by purely cutaneous volleys in the sural nerve (see Burke et al. 1981). Complete suppression of the cerebral potential evoked by stimulation of muscle or cutaneous afferents was produced by conditioning volleys in a different nerve or in a different fascicle of the same nerve. The major factors determining the degree of suppression were found to be the relative sizes of the conditioning and test volleys and their timing, rather than whether the volleys were of cutaneous or muscular origin. It is concluded that the transmission of cutaneous or muscle afferent volleys to cortex can be profoundly altered in normal subjects by conditioning activity. The possibility that normal background afferent activity can similarly modify afferent transmission has implications for diagnostic studies, particularly when they are performed under non-standard conditions, such as in the operating theatre or intensive care unit. It is also concluded that, although a subject may perceive cutaneous paraesthesiae when the posterior tibial nerve is stimulated at the ankle, there may be no cutaneous component to the evoked cerebral potential.     

Sinusoidal movement of a grating across the monkey's fingerpad: temporal patterns of afferent fiber responses

Responses were recorded from cutaneous afferents innervating mechanoreceptors in the monkey's fingerpad, while gratings of alternating grooves and ridges were moved sinusoidally across their receptive fields. The gratings were specified by their spatial period and the movement by its peak speed: together these determined the peak temporal frequency at which grating ridges passed over the receptive field. During the central 42 degrees of each half cycle of movement, the speed and thus the temporal frequency of the grating ridges remained constant to within 6.6% of their peak values. In this region the responses of all afferents were phase-locked to the temporal sequence of grating ridges. The number of impulses elicited by each grating ridge was a function of the stimulus variables. For all 3 afferent classes--namely, slowly adapting afferents (SAs), rapidly adapting afferents (RAs), and Pacinian afferents (PCs)--the number of impulses per grating ridge increased as the spatial period of the grating increased (while the peak speed of movement was held constant). Similarly, for all 3 classes, the number of impulses per ridge decreased as the peak speed of movement increased (while the spatial period of the grating remained constant). When the peak temporal frequency of the grating ridges was held constant, for SAs and RAs the number of impulses per ridge increased with an increase in the spatial period of the grating and thus with an increase in the peak speed. These phase-locked responses provided information about the peak temporal frequency of the grating ridges independent of the grating spatial period and of the peak speed of movement. The shape of the response profile during a half cycle of movement was different for different afferents. Many of the RA response profiles were close to sinusoidal. The SA and PC profiles tended to have reduced peaks or raised troughs, resulting in flatter profiles. Other departures from sinusoidal profiles were also seen.     

Neural organization of the viscero-cardiac reflexes

The reflex responses evoked in the postganglionic nerves to the heart were tested in chloralose-anaesthetized cats. Electrical stimulation of the A delta afferent fibres from the left inferior cardiac nerve evoked spinal and supraspinal reflex responses with the onset latencies of 36 ms and 77 ms respectively. The most effective stimulus was a train of 3-4 electrical pulses with the intratrain frequency of 200-300 Hz. Electrical stimulation of the high threshold afferent fibres (C-fibres) from the left inferior cardiac nerve evoked the reflex response with the onset latency of 200 ms. The C-reflex was present in intact animals and disappeared after spinalization. The most effective stimulus to evoke this reflex was a train of electrical pulses delivered at a frequency of 1-2 Hz with an intratrain frequency of 20-30 Hz. The most prominent property of the C-reflex was its marked increase after prolonged repeated electrical stimulation. We conclude that: (1) viscero-cardiac sympathetic reflexes may be organized at the spinal and supraspinal level; (2) viscero-cardiac sympathetic reflexes evoked by stimulation of the A delta and C afferent fibres from the left inferior cardiac nerve have different central organization.     

Vestibular afferent responses to microrotational stimuli

Intracellular microelectrode recording/labelling techniques were used to investigate vestibular afferent responses in the bullfrog, to very small amplitude (less than 0.5 degree p-p) sinusoidal rotations in the vertical plane over the frequency range of 0.063-4 Hz. The axis of rotation was congruent with the axis of the anterior semicircular canal. Robust responses to peak accelerations as low as 0.031 degree/S2 were obtained from units subsequently traced to either the central portion of the anterior canal crista or the striolar region of the utricle. All of these microrotationally sensitive afferent neurons had irregular resting discharge rates and the majority had transfer ratios (relative to rotational velocity) of 1-40 spikes/s per degree/s. Individual utricular afferent velocity transfer ratios were nearly constant over the frequency range of 0.125-4 Hz. Canal units generally displayed decreasing response transfer ratios as stimulus frequencies increased. These findings indicate that although utricular striolar and central crista afferent velocity transfer ratios to microrotations were very similar, utricular striolar afferent neurons were more faithful sensors of very small amplitude rotational velocity in the vertical plane.     

Long-term adaptation of crayfish neurons depends on the frequency and number of impulses

Increasing the impulse activity of crustacean neurons for a few days causes long-lasting changes in transmitter release, which are termed 'long-term adaptation' (LTA) in previous studies. Both the amount of transmitter released at the beginning of a stimulus train, and synaptic fatigue during repetitive stimulation, are reduced. The present study examines the dependence of these synaptic changes on the frequency and number of impulses used to elicit LTA. Fatigue resistance develops consistently when crayfish phasic motor neurons are stimulated for 3 days with as few as 9,000 impulses per day, and occurs in response either to low frequency stimulation (0.2 or 0.5 Hz), or to stimulation in short bursts at a moderate average frequency (2.5 Hz). In contrast, the reduction in initial transmitter release does not appear consistently when the frequency and number of impulses are both low (9,000 impulses per day delivered at 0.2 Hz), but does occur at the moderate stimulus frequency (2.5 Hz) and when a larger number of impulses (18,000) are delivered at a low frequency (0.5 Hz). The data suggest that the two changes in synaptic transmission that comprise LTA have different stimulus requirements.     

Inspiratory coupling to cardiac activity and to somatic afferent nerve stimulation in the anaesthetised rat

We examined the ability of somatic afferent nerve stimulation to entrain inspiratory onset in the anaesthetized spontaneously breathing rat, and compared features of this stimulus-ventilatory coupling to entrainment of inspiratory onset by cardiac activity. In 14 rats prior to stimulation, we commonly observed a constant temporal alignment between ECG R waves and inspiratory onset (cardioventilatory coupling). Stimulation of a hamstring nerve at rates close to the heart rate also caused coupling (a constant stimulus to inspiratory onset interval), although this was highly dependent upon frequency of stimulation, with small changes in frequency causing a loss of coupling. In experiments where stimuli were given at constant intervals after ECG R waves, we observed no augmentation of coupling. Our results indicate that both cardiac and somatic afferent nerve activity is able to entrain inspiratory onset. We have suggested that coupling causes respiratory frequency to increase, and it is possible that this is a general mechanism whereby non-respiratory afferents act as stimulants or pacemakers to respiratory rhythm. The role of non-respiratory activity in initiating inspiration needs to be more fully recognised and studied.