Journal of neurophysiology
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1. The effects of type I (BZ1) and type II (BZ2) benzodiazepine receptor ligands on monosynaptic gamma-aminobutyric acid (GABA)A-mediated inhibitory postsynaptic potentials (IPSPs) and on responses to exogenously applied GABA were studied using intracellular recordings from CA3 pyramidal cells of rat hippocampal slices taken at different postnatal stages [postnatal day 4 (P4)-P35)]. 2. The effects of midazolam, a BZ1 and BZ2 receptor agonist, were tested on the monosynaptic IPSPs at different stages. ⋯ In all cases, full recovery was obtained after exposure to R0 15-1788 (10 microM). DMCM (300 nM-10 microM) failed to reduce GABA responses in cells from young (n = 3) or adult (n = 7) rats. 6. Results indicate that the regulation by benzodiazepine of GABAA-mediated IPSPs varies with the developmental stage.(ABSTRACT TRUNCATED AT 400 WORDS)
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1. The aim of this study was to develop a quantitative behavioral model of nociception. Electromyographic (EMG) recordings from a hamstring flexor muscle provided a measure of the magnitude of hindlimb withdrawals elicited by brief, graded noxious contact thermal stimuli applied to the hindpaw in conscious rats. 2. ⋯ The decrement in withdrawal magnitude was greater at lower stimulus intensities and shorter interstimulus intervals, and transferred to a nearby (7.5 mm) but not distant (2.5 cm) site. Evidence for dishabituation was also obtained. 5. The advantages of this method as an animal model of nociception are presented and discussed in terms of the underlying neural circuitry and its modulation.
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1. Peripheral nerve injury sometimes leads to the development of neuropathic pain. One of the symptoms of such neuropathic pain is mechanical allodynia, pain in response to normally innocuous mechanical stimuli. ⋯ The response characteristics of MRAs change to those of typical RAs after a systemic injection of phentolamine, an alpha-adrenergic receptor blocker. 5. We conclude that many RAs become abnormal under the influence of sympathetic efferents in neuropathic pain, so that their response patterns change to those of MRAs. We propose that this abnormality is responsible for signaling the mechanical allodynia that can be seen in neuropathic pain states such as causalgia.
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1. To quantitatively investigate a nocifensive behavioral response, we developed a method to measure the magnitude of the rat's tail flick reflex and its modulation. A radial array of force transducers measured forces of tail flicks (in rostral, horizontal, and vertical planes) elicited by graded noxious radiant thermal stimulation of the conscious rat's tail, from which the overall movement vector was calculated. 2. ⋯ These observations are consistent with habituation of the tail flick reflex. 5. This method, therefore, provides a quantitative and reproducible measure of tail flick reflex magnitude that is sensitive to morphine. The underlying neural circuitry of the tail flick reflex is discussed in relation to limb withdrawal reflexes.
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1. The possibility of temporal encoding in the spike trains of single neurons recorded in the temporal lobe visual cortical areas of rhesus macaques was analyzed with the use of principal component and information theory analyses of smoothed spike trains. The neurons analyzed had responses selective for faces. 2. ⋯ It was also found that 44.0% of the information calculated from the first three principal components is available in the firing rates calculated over epochs as short as 20 ms. 8. More information was available near the start of the neuronal response, and the information available from short epochs became less later in the neuronal response. 9. Taken together, these analyses provide evidence that a short period of firing taken close to the start of the neuronal response provides a reasonable proportion of the total information that would be available if a long period of neuronal firing (e.g., 400 ms) were utilized to extract it, even if temporal encoding were used.(ABSTRACT TRUNCATED AT 400 WORDS)