Faculty Bibliography

Neonatal rats learn to approach odors associated with stimulation normally provided by their mother. The present report describes changes in olfactory bulb single-unit activity following olfactory learning in young rats. Rat pups were exposed from postnatal day 1 to 18 to either (1) peppermint-scented air while receiving tactile stimulation (Pepp-Stroked), (2) peppermint-scented air with no tactile stimulation (Pepp-Only), (3) clean air and tactile stimulation (Stroked-Only), or (4) clean air and no tactile stimulation (Naive). On day 19, single-unit activity was recorded from mitral/tufted cells in urethane-anesthetized, freely breathing pups in response to either peppermint or a novel orange odor. Mitral/tufted cell response patterns to peppermint were significantly altered in Pepp-Stroked animals compared to control pups. Peppermint exposure alone, not associated with tactile stimulation (Pepp-Only), did not affect subsequent single-cell response patterns to that odor. In addition, the modification of response patterns was specific to peppermint and was not associated with a change in respiration rate. Furthermore, Pepp-Stroked pups had a relative behavioral preference for peppermint on day 19 compared to control pups. These results demonstrate that postnatal olfactory learning selectively modifies the subsequent response patterns of olfactory bulb output cells to the attractive odor. Furthermore, these results indicate that the initial coding of an odor's attractive value occurs within the olfactory bulb

Lateral inhibitory circuits are found throughout the nervous system. While the neuroanatomical basis for lateral inhibitory interactions exists in the olfactory bulb of Norway rats, there has been no direct demonstration of lateral inhibition in the responses of olfactory bulb output neurons to odor stimulation. In this report we recorded the extracellular activity of a large number of sequentially recorded mitral/tufted cells in response to odor stimuli at two different concentrations, as well as the inter-cell distance between these cells. The probability of recording two cells with excitatory responses to the same odor was then determined for inter-cell distances up to 500 microns. For cells stimulated with high concentration odors, the probability of two cells 100-200 microns apart both being excited by the same odor was significantly lower than that predicted if all cells responded independently. Cells separated by greater or shorter inter-cell distances did not differ from the predicted value. Responses to the low odor concentration were not dependent on inter-cell distance. These results demonstrate that lateral synaptic interactions within the olfactory bulb influence output cell responses to odor stimulation

Olfactory bulb responses to paired-pulse stimulation of the lateral olfactory tract were examined in urethane-anesthetized rats, aged 5 days to adult. Brief inter-pulse intervals resulted in a depression of test responses at all ages. The magnitude of this depression decreased dramatically between postnatal days 19 and 20 to approach adult levels. Longer inter-pulse intervals resulted in a facilitation of test response amplitude in adult animals. This facilitation was evident at adult levels by postnatal day 10. These results suggest that both inhibitory and facilitatory synaptic mechanisms appear early in the course of rat olfactory bulb development. Furthermore, presumed granule cell-mediated inhibition is present at unusually high levels in the developing bulb, decreasing sharply between days 19 and 20

The functional development of inhibition in the rat olfactory bulb was examined in the present study. Inhibition of presumed mitral cell spontaneous activity following stimulation of the lateral olfactory tract was present by postnatal day 5, the youngest age tested. The duration of this inhibition was greatest in young animals, decreasing after postnatal day 15. Possible mechanisms of this enhanced inhibition in neonates were discussed

Previous studies have shown that rat pups have an enhanced metabolic activity to familiar odors in specific glomeruli of the olfactory bulb. The present study examined extracellularly recorded mitral cell responses to odors in this glomerular region, in odor-familiar and odor-unfamiliar pups. Mitral cells in odor-familiar pups had significantly fewer excitatory and more inhibitory responses to the familiar odor than controls. There were no differences between groups in responses to a novel odor. These results demonstrate that neonatal exposure to odors selectively alters subsequent mitral cell responsiveness to that odor

The postnatal development of short-term potentiation (STP) and long-term potentiation (LTP) was examined in the neocortex and dentate gyrus of rats aged 7 days to adult. STP and LTP of the transcallosal response in the neocortex could not be demonstrated until the third postnatal week. STP and LTP of the perforant path-dentate response could not be demonstrated until the second postnatal week. In both cases, STP appeared several days before LTP. Structural and neurochemical correlates of STP/LTP development, and their implications for possible STP/LTP mechanisms, are discussed

The postnatal development of short-term potentiation (STP) and long-term potentiation (LTP) of the transcallosal response (TCR) was examined in anesthetized rats, aged 7 days (PN7) to adult (greater than or equal to PN180). Stimulation of callosal fibers produced a biphasic, positive-negative TCR recorded at the surface of the anterior neocortex in all age groups. The TCR showed a decrease in threshold, latency and halfwidth, and an increase in peak amplitude with age. High frequency callosal stimulation produced marked STP and LTP of the mature TCR. STP in young animals, however, could not be reliably detected until after PN16. LTP was not detected until PN18. STP and LTP approached adult levels rapidly after their initial appearance. The correlations between STP/LTP onset and development and known structural developments such as initial synaptogenesis, spine formation and myelinogenesis were not particularly strong. The implications of these results for specific hypotheses of STP/LTP mechanisms were discussed