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Extracellular recordings of 209 neurons were obtained with carbon fiber-containing multibarrel micropipettes. The cells were isolated in the primary somatosensory cortex of cats anesthetized with barbiturate and classified according to the nature of their response to natural stimuli, the nature of the surrounding multiunit responses to the same stimuli, the response to thalamic stimulation, and their depth in the cortex. To study factors controlling the excitability of somatosensory neurons, their receptive fields were examined in the presence of iontophoretically administered gamma-aminobutyric acid (GABA), glutamate, and bicuculline methiodide (BMI). Even when the neurons were depolarized to perithreshold levels with glutamate, or when local inhibitory influences mediated by GABA were antagonized by BMI, the apparent specificity for one class of afferent input was maintained. Neurons responding to stimulation of either cutaneous or deep receptors maintained their modality specificity, and neurons in cutaneous rapidly adapting regions never took on slowly adapting properties. When ejected at currents that did not elicit action potentials, glutamate lowered the threshold for activation by cutaneous stimuli but did not enlarge the receptive field. With larger ejecting currents, the neurons developed an on-going discharge, but even at these higher doses, glutamate did not produce an increase in the receptive-field size. Some neurons in regions of cortex exhibiting slowly adapting multiunit responses were relatively insensitive to glutamate. These cells required four to five times more glutamate to evoke discharges than did most neurons. Other cells, previously unresponsive to somatic stimuli, could be shown to possess distinct cutaneous receptive fields when either glutamate or BMI was ejected in their vicinity. Iontophoretically administered BMI altered the firing pattern of somatosensory neurons, causing them to discharge in bursts of 3-15 impulses. BMI enlarged the receptive-field size of neurons in regions displaying rapidly adapting multiunit background discharges but not in those regions with slowly adapting multiunit discharges. This differential effect of BMI, suggesting that GABA controls receptive-field size in rapidly adapting regions, also indicates that neurons in rapidly adapting regions differ pharmacologically from those in other submodality regions. In all cortical regions, BMI blocked the poststimulus inhibitory period that normally followed thalamic stimulation.(ABSTRACT TRUNCATED AT 400 WORDS)

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BackgroundThe human red nucleus (Nr) is comparatively less well-studied than that of cats or monkeys. Given the functional importance of reticular and midbrain structures in control of movement and locomotion as well as from an evolutionary perspective, we investigated the nature and extent of any differences in Nr projections to the olivary complex in quadrupedal and bipedal species. Using neuroanatomical tract-tracing techniques we developed a “neural sheet” hypothesis allowing us to propose how rubro-olivary relations differ among the three species.Methods and FindingsWheat germ agglutinin-horseradish peroxidase staining supports findings that the cat's nucleus accessories medialis of Bechtrew (NB) projects mainly to the lateral bend of the principal olive. We clarified boundaries among nucleus of Darkschewitsch (ND), NB and parvicellular red nucleus (pNr) of the cat's neural sheet. The macaque's ND-medial accessory olivary projection is rostro-caudally organized and the dorsomedial and ventrolateral parts of the macaque's pNr may project to the principal olive's rostral and caudal dorsal lamella; in cat it projects as well to pNr. Myelin- and Nissl-stained sections show that a well-developed dorsomedial part of the human Nr consists of densely packed cells, deriving small myelinated fibers that continue into the medial central tegmental tract.ConclusionsBased on these findings we suggest there are distinct bipedal-quadrupedal differences for Nr projections to the olivary complex. We propose the Nr of cats and monkeys comprise the ND, NB and pNr in a zonal sheet-like structure, retaining clear nuclear boundaries and an isolated, well-developed mNr. The human NB may be distinguished from its more specialised ND (ND lies alongside a well-developed pNr) in the human central gray. Phylogenetically, the NB may have been translocated into a roll-shaped Nr in the reticular formation, the dorsomedial portion of which might correspond to the cat's and monkey's NB.

Long‐term potentiation (LTP) of hippocampal population spike responses and excitatory postsynaptic potentials (EPSPs) from area CA1 stratum pyramidale was induced in slices of rat hippocampus maintained in vitro following brief high‐frequency stimulation (HFS) of the Schaffer collateral‐commissural pathway. When administered to slices prior to HFS, 17β‐oestradiol (OE2), at a concentration as low as 0.1 nm, suppressed the magnitude of the resultant HFS‐induced potentiation in slices from prepubertal animals (3 and 4 weeks old) of both sexes. OE2 did not suppress the induction of LTP in slices taken from the hippocampus of adult animals of either sex. There was no similar suppressant effect of 17α‐oestradiol (OE1), progesterone (PRG) or testosterone (TST) on LTP in the young animals, even at a concentration 100 times greater than was effective for OE2. The anti‐oestrogen compound tamoxifen (TMX; 1.0 and 10.0 μm), which acts principally at intracellular binding sites within the nucleus, was without effect in diminishing the suppressant effect of OE2 on LTP in slices from young animals. The LTP observed in slices from both 3‐week‐old and adult rats was AP5 sensitive and thus was shown to be dependent on activation of NMDA receptors. Results from whole‐cell recording experiments suggested that OE2 caused the LTP‐suppressant effect through an action on NMDA‐mediated currents. These data suggest an age‐dependent and possibly a surface membrane receptor‐mediated role for oestrogens in modulating the efficacy of input‐output properties of CA1 neurones produced by HFS during a critical period in development.

The effect of antagonism of GABA(A) receptors on the receptive fields of raccoon primary somatosensory cortical neurons was tested using microiontophoretic administration of bicuculline methiodide (BMI). The size of cutaneous receptive fields was examined using minimal suprathreshold mechanical stimulation before, during, and after BMI administration. In 65 of 102 rapidly adapting neurons, BMI produced a clear expansion of the receptive field. The mean increase in receptive-field size was 286%. The receptive fields on the distal digit, which were initially smaller, showed smaller increases in absolute area than more proximal receptive fields, but the percentage increase did not vary with location. Greater expansion was seen in superficially located neurons than in those below 800 microm. Of particular significance was the finding that the expansion of receptive fields produced by BMI never extended from one digit onto an adjacent digit or onto the palm, even when the original receptive field was at the base of a digit. This finding indicates that intracortical GABAergic inhibition is insufficient to explain cortical reorganization following digit amputation.

Visually responsive neurones of the cat's suprageniculate nucleus were categorized according to their responses to a variety of different types of light stimuli. Their velocity preferences were assessed quantitatively and have been found to predominate in the high range. The positions and dimensions of their receptive fields were determined and these tended to be found within a zone between the vertical meridian and 30-35 degrees. Receptive fields had mean diameters smaller than those reported by others for the pulvinar-LP complex. From these and other electrophysiological data, inferences have been made of the likely sources of afferents providing visual driving. A proposal is offered for SGn visuotopic organization based on correlations of receptive field location with cell position, as determined through electrode track reconstructions.