1. In acute experiments, detailed grids of micro-electrode recordings were made from spinocervical tract (s.c.t.) cells in the lumbosacral cord of anaesthetized cats. These grids provided electrophysiological data on the location, distribution, density and somatotopic organization of s.c.t. neurones.2. In acute experiments lasting up to 48 hr, retrograde labelling of s.c.t. cells was carried out by injecting horseradish peroxidase into the lateral cervical nucleus in anaesthetized cats. The aim was to flood the nucleus with the enzyme so that all s.c.t. neurones would be labelled in order to provide an independent check on the location, density and distribution data obtained in the electrophysiological experiments.3. The electrophysiological and the anatomical experiments were sometimes performed on the same animal.4. The electrophysiological and anatomical results were in excellent agreement. (a) S.c.t. cells are located mainly in ipsilateral laminae III, IV and V. About 25% are in lamina III, 60% in lamina IV and 10% in lamina V. There are a few cells in laminae I, II and VI making up the remaining 5%. (b) There are about 550-800 s.c.t. cells in the lumbosacral enlargement (L4-S2 inclusive) on each side of the cord. Most cells are in L7-S1 where there are twenty to forty s.c.t. neurones in each millimetre length of cord.5. Many marginal (lamina I) cells were labelled with the retrograde horseradish peroxidase method and a few cells on the contralateral side in laminae III-V and VII-VIII were also labelled. The marginal cells formed 12-18% of labelled cells on the side of injection and, in addition, a similar absolute number of marginal cells was labelled on the side contralateral to the injection. The possible identity of these neurones is discussed.6. S.c.t. cells form a sheet of neurones across the dorsal horn. The sheet is organized somatotopically in a way which resembles the representation of the hind limb dermatomes in the dorsal columns (Werner & Whitsel, 1967). There is a relative enlargement of the L6-S1 dermatomes which encroach upon their neighbouring cord segments. The gradient of the map is very steep in the mediolateral direction but gradual in the rostrocaudal direction. The detailed somatotopic maps generated in the present work have revealed that s.c.t. cells are arranged so that their receptive fields form longitudinal columns and cells within the columns have overlapping fields.

SUMMARY1. Intracellular recordings were made from spinocervical tract (s.c.t.) neurones in cats anaesthetized with chloralose and paralysed with gallamine triethiodide.2. In one series of experiments the cells' receptive fields were examined with the use of natural stimuli. Hair movement within the impulse firing zone of the cell evoked excitatory post-synaptic potentials

SUMMARY1. Single axons innervating Pacinian corpuscles and rapidly adapting mechanoreceptors of the foot and toe pads were injected with horseradish peroxidase near their entrance to the lumbosacral spinal cord in cats anaesthetized with chloralose and paralysed with gallamine triethiodide. Subsequent histochemistry revealed the morphology of the intra-spinal parts of the axons.2. All Pacinian corpuscle axons that could be traced into the dorsal root bifurcated upon entering the cord into ascending and descending branches. All Pacinian corpuscle axons gave rise to collaterals that entered the dorsal horn.3. The collaterals of Pacinian corpuscle afferent fibres had a distinctive morphology. They provided two regions of termination, a larger dorsal region in laminae III and IV and a smaller ventral region in laminae V and VI. Within the dorsal region the terminal axons ran mainly in the longitudinal axis of the cord and carried many boutons en passant. Within the ventral region the axons ran dorso-ventrally in the transverse plane of the cord and although carrying some boutons en passant also gave rise to clusters of boutons.4. The collaterals of rapidly adapting afferent fibres had a distinctive morphology different from that of the Pacinian corpuscle afferent fibre collaterals. The termination region of rapidly adapting afferents was limited almost exclusively to lamina III, with only slight extension into lamina IV. Boutons were mainly of the en passant type and terminal axons were generally orientated within the longitudinal axis of the cord.5. The morphology of the afferent fibre collaterals is discussed in relation to the physiology of the dorsal horn.

1. The respiratory response to isocapnic hypoxia (inspired O2 fraction (FI,O1), 0.1-0.12) was measured in twelve vagotomized, paralysed, artificially ventilated young rabbits (aged 26.6 +/- 0.4 days), following pre-collicular decerebration. Phrenic nerve efferent activity was used as an index of central respiratory output (RO). In hypoxia RO increased after 1-2 min (phase 1) but decreased over the subsequent 3-4 min to, or below, the pre-hypoxic control level (phase 2). 2. We used electrical stimulation to target areas in the mesencephalon which inhibit RO. Profiles of the response to stimulation were determined in a grid of electrode penetrations made mediolaterally and rostrocaudally at the level of the superior colliculi, in normoxia. Histology confirmed that stimulation in the red nucleus (RN) inhibited RO profoundly. 3. Electrolytic lesions were made bilaterally in RN inhibitory sites or in adjacent areas. The respiratory response to isocapnic hypoxia was measured again post-lesioning. 4. In six rabbits with bilateral lesions in the RN, phase 2 of the respiratory response was abolished and RO remained elevated throughout the hypoxic exposure. However, in six rabbits with unilateral lesions in the RN, or with bilateral lesions placed in areas outside the RN that did not inhibit RO on electrical stimulation, the respiratory response remained biphasic. 5. In both groups of animals, blood pressure increased during 1-3 min of hypoxia before decreasing to pre-hypoxic levels. This cardiovascular response remained biphasic irrespective of whether animals showed a biphasic respiratory response or a sustained increase in RO after lesioning. 6. We conclude that structures within the RN are crucial to the mechanism producing a fall in RO during isocapnic hypoxaemia in the neonate.

SUMMARY1. In cats under chloralose anaesthesia single dorsal root ganglion cells with axons innervating hair follicles were stimulated intracellularly to produce single impulses. At the same time single spinocervical tract (s.c.t.) neurones were recorded extracellularly, from their axons in the upper lumbar cord.2. When the receptive field of the afferent fibre was contained within the impulse firing zone of the s.c.t. cell, a single afferent impulse increased the probability of firing of the neurone. In thirty-nine pairs of units, where the afferent fibre had a group II conduction velocity, coupling was very efficient and for seventeen pairs the single afferent impulse produced one or more impulses in the s.c.t. cell in at least 90 % of trials. The mean number of impulses evoked in s.c.t. cells by a single group II afferent impulse was 1-47. The latencies of the impulses ranged from 1-5 to 14-0 ms, with times to peak and total durations of 25--17'5 ms and 4'5-28'0 ms respectively. For two pairs of units where the afferent fibre had a group III conduction velocity the effectiveness of single afferent impulses was much less and the latencies, but not the durations, of the impulses were longer (12 and 17 ms).3. When the receptive field of the hair follicle afferent fibre was outside, but close to, the firing zone of the s.c.t. neurone there was no indication that single afferent impulses affected the probability of neuronal discharge for thirteen of fifteen pairs of units. Weak excitation was observed in two pairs and this was clear only when two or more afferent impulses were employed.4. There was a tendency for hair follicle afferent fibres with their receptive fields at or near the centre of the s.c.t. cell's firing zone to be most effective, producing shorter latency responses with more impulses at higher frequencies. When the afferent's field was peripherally located in the s.c.t. neurone's firing zone there was a wide range of responses but these included those with the longest latencies and very few impulses.5. The results are discussed with reference too previous work on the spinocervical tract and to the known actions of single impulses on other neuronal types.