Temporal relationship between sniffing and the limbic theta rhythm during odor discrimination reversal learning

The temporal relationship between sniffing and the limbic 19 rhythm was studied in rats during odor discrimination reversal learning. The I3 rhythm was monitored as rhythmic slow wave activity (RSA) in the dorsal hippocampal formation, and cyclic nasal airflow (sniffing) was monitored with a thermocouple in the nasal cavity. The training procedures required animals to perform a sequence of whole body locomotion toward one wall of an arena, followed by investigatory sniffing of stimuli through a port while otherwise standing still. Hippocampal RSA was present reliably during the periods of investigatory sniffing. Analyses based on the fast Fourier transform (FFT) demonstrated that this RSA tended to be lower in frequency and amplitude than RSA which occurred during locomotory approach. Other analyses based on the FFT were developed to characterize the nature and parameters of the temporal relationship between rhythmic sniffing and hippocampal RSA as a function of the dominant sniffing frequency during the periods of stimulus sampling. The phase difference between sniffing and RSA tended to vary linearly with frequency so as to maintain a preferred latency relationship between the onset of each sniff cycle and a particular phase of the hippocampal RSA. The phase of RSA to which sniffing was related differed across animals and was correlated with electrode position relative to the phase reversal layers within the hippocampal formation. These results therefore are consistent with the interpretation that, during the periods of stimulus sampling, the sniffs were being timed to maintain a preferred latency relationship with the pacemaker activity which drives the 8 rhythm and the recorded RSA. The consistency with which the animals exhibited the preferred latency relationship varied during the course of training. Across animals, this correlation between sniffing and 8 activity was consistently high during the trials which immediately preceded the achievement of criterion level performance, and the correlation was reduced during the criterion run and/or subsequent trials of overtraining. Thus, the tendency of the animals to exhibit this relationship was not associated specifically with correct performance. Rather, the correlation tended to be highest when the animals were most likely to be evaluating the behavioral relevance of stimuli and were in the process of modifying their responses to those stimuli. The timing of investigatory sniffs as a function of 6’ cycle phase may be important for the neural processing of sensory and/or motor information of relevance for response modification. The mammalian limbic system exhibits a pronounced to as 0 activity, although its upper frequency range 4to 12-Hz electrographic rhythm during a variety of extends into the (Y band. I3 activity has been recorded as behavioral and drug states (cf., Vanderwolf, 1975; Komrhythmic single unit or slow wave activity in numerous isaruk, 1977). This neural rhythm commonly is referred limbic and related structures of the forebrain and is ’ This work was supported by National Institutes of Health Research prominent in waking animals during active exploration Grants NS12344 and AG00779, National Science Foundation Research of the environment (cf., Komisaruk, 1977). The limbic 0 Grants BNS77-24405 and BNS78-06248, and National Science Founrhythm can be monitored readily as rhythmic slow wave dation Equipment Grants PRM-COP81-6784 and BNS78-18113. We activity (RSA) in the hippocampal formation (cf., Winthank Karen Shedlack and Paul Murphy for technical assistance. son, 1974). Its pacemaker activity is thought to originate ’ To whom reprint requests should be sent at the Worcester Founin neurons of the medial septum-diagonal band complex dation for Experimental Biology, 222 Maple Avenue, Shrewsbury, MA (cf., Petsche et al., 1962, 1965), and its occurrence and 01545. frequency appear to be regulated through multisynaptic

[1]  J. Curray,et al.  The Analysis of Two-Dimensional Orientation Data , 1956, The Journal of Geology.

[2]  J. Greenwood,et al.  Modifications of the Rayleigh Test for Uniformity in Analysis of Two-Dimensional Orientation Data , 1958, The Journal of Geology.

[3]  W. R. Adey,et al.  Hippocampal slow waves. Distribution and phase relationships in the course of approach learning. , 1960, Archives of neurology.

[4]  H. Petsche,et al.  [The significance of the rabbit's septum as a relay station between the midbrain and the hippocampus. I. The control of hippocampus arousal activity by the septum cells]. , 1962, Electroencephalography and clinical neurophysiology.

[5]  W. Welker Analysis of Sniffing of the Albino Rat 1) , 1964 .

[6]  H PETSCHE,et al.  RHYTHMICITY OF SEPTAL CELL DISCHARGES AT VARIOUS LEVELS OF RETICULAR EXCITATION. , 1965, Electroencephalography and clinical neurophysiology.

[7]  C. H. Vanderwolf,et al.  Hippocampal electrical activity and voluntary movement in the rat. , 1969, Electroencephalography and clinical neurophysiology.

[8]  B. Komisaruk,et al.  Synchrony between limbic system theta activity and rhythmical behavior in rats. , 1970, Journal of comparative and physiological psychology.

[9]  J. Gray,et al.  Medial septal lesions, hippocampal theta rhythm and the control of vibrissal movement in the freely moving rat. , 1971, Electroencephalography and clinical neurophysiology.

[10]  C. H. Vanderwolf,et al.  Limbic-diencephalic mechanisms of voluntary movement. , 1971, Psychological review.

[11]  Vanderwolf Ch Limbic-diencephalic mechanisms of voluntary movement. , 1971 .

[12]  G Dumermuth,et al.  Spectral analysis of EEG activity in different sleep stages in normal adults. , 1972, European neurology.

[13]  I. Whishaw Hippocampal electroencephalographic activity in the Mongolian gerbil during natural behaviours and wheel running and in the rat during wheel running and conditioned immobility. , 1972, Canadian journal of psychology.

[14]  J L McGaugh,et al.  Theta Rhythm: A Temporal Correlate of Memory Storage Processes in the Rat , 1972, Science.

[15]  B. Komisaruk,et al.  Responses of diencephalic neurons to olfactory bulb stimulation, odor, and arousal. , 1972, Brain research.

[16]  F. Macrides,et al.  Olfactory Bulb Units: Activity Correlated with Inhalation Cycles and Odor Quality , 1972, Science.

[17]  C. H. Vanderwolf,et al.  Hippocampal EEG and behavior: changes in amplitude and frequency of RSA (theta rhythm) associated with spontaneous and learned movement patterns in rats and cats. , 1973, Behavioral biology.

[18]  M. Murphy Effects of female hamster vaginal discharge on the behavior of male hamsters. , 1973, Behavioral biology.

[19]  J. Winson,et al.  Patterns of hippocampal theta rhythm in the freely moving rat. , 1974, Electroencephalography and clinical neurophysiology.

[20]  F. Macrides,et al.  Effects of exposure to vaginal odor and receptive females on plasma testosterone in the male hamster. , 1974, Neuroendocrinology.

[21]  F. Macrides,et al.  Temporal relationships between hippocampal slow waves and exploratory sniffing in hamsters. , 1975, Behavioral biology.

[22]  C. H. Vanderwolf,et al.  Two types of hippocampal rhythmical slow activity in both the rabbit and the rat: Relations to behavior and effects of atropine, diethyl ether, urethane, and pentobarbital , 1975, Experimental Neurology.

[23]  C. H. Vanderwolf Neocortical and hippocampal activation relation to behavior: effects of atropine, eserine, phenothiazines, and amphetamine. , 1975, Journal of comparative and physiological psychology.

[24]  T. L. Bennett The Electrical Activity of the Hippocampus and Processes of Attention , 1975 .

[25]  O. Steward,et al.  Topographic organization of the projections from the entorhinal area to the hippocampal formation of the rat , 1976, The Journal of comparative neurology.

[26]  Jonathan Winson,et al.  Hippocampal theta rhythm. II. Depth profiles in the freely moving rabbit , 1976, Brain Research.

[27]  J. Scott A measure of extracellular unit responses to repeated stimulation applied to observations of the time course of olfactory responses , 1977, Brain Research.

[28]  J. Velluti,et al.  Relationships of hippocampal theta cycles with bar pressing during self-stimulation , 1977, Physiology & Behavior.

[29]  Dynamic Aspects of Central Olfactory Processing , 1977 .

[30]  W. Cowan,et al.  An autoradiographic study of the organization of the efferet connections of the hippocampal formation in the rat , 1977, The Journal of comparative neurology.

[31]  F. Macrides,et al.  Responses of the male golden hamster to vaginal secretion and dimethyl disulfide: attraction versus sexual behavior. , 1977, Behavioral biology.

[32]  F. Macrides,et al.  Efferents and centrifugal afferents of the main and accessory olfactory bulbs in the hamster , 1978, Brain Research Bulletin.

[33]  HIGH COHERENCE BETWEEN LIMBIC THETA RHYTHM AND SNIFFING IN THE HAMSTER: IMPLICATIONS FOR OLFACTORY-LIMBIC INTEGRATION AND HORMONAL REGULATION , 1978 .

[34]  E. Garcı́a-Austt,et al.  Reset of hippocampal rhythmical activities by afferent stimulation , 1978, Brain Research Bulletin.

[35]  L. Haberly,et al.  Association and commissural fiber systems of the olfactory cortex of the rat II. Systems originating in the olfactory peduncle , 1978, The Journal of comparative neurology.

[36]  L. Haberly,et al.  Association and commissural fiber systems of the olfactory cortex of the rat. I. Systems originating in the piriform cortex and adjacent areas , 1978, The Journal of comparative neurology.

[37]  R. M. Beckstead Afferent connections of the entorhinal area in the rat as demonstrated by retrograde cell-labeling with horseradish peroxidase , 1978, Brain Research.

[38]  S. D. Berry,et al.  Prediction of learning rate from the hippocampal electroencephalogram. , 1978, Science.

[39]  M. T. Shipley,et al.  Projections from the subiculum to the deep layers of the lpsilateral presubicular and entorhinal cortices in the guinea pig , 1979, The Journal of comparative neurology.

[40]  R. Passingham The hippocampus as a cognitive map J. O'Keefe & L. Nadel, Oxford University Press, Oxford (1978). 570 pp., £25.00 , 1979, Neuroscience.

[41]  J. B. Ranck,et al.  Hippocampal excitability phase-locked to the theta rhythm in walking rats , 1980, Experimental Neurology.

[42]  H Eichenbaum,et al.  Thalamocortical mechanisms in odor-guided behavior. I. Effects of lesions of the mediodorsal thalamic nucleus and frontal cortex on olfactory discrimination in the rat. , 1980, Brain, behavior and evolution.

[43]  Terry E. Robinson,et al.  Hippocampal rhythmic slow activity (RSA, theta): A critical analysis of selected studies and discussion of possible species-differences , 1980, Brain Research Reviews.

[44]  H. Eichenbaum A behaviorist in the neurophysiology lab , 1981, Behavioral and Brain Sciences.

[45]  Terry E. Robinson,et al.  Reticulo-cortical activity and behavior: A critique of the arousal theory and a new synthesis , 1981, Behavioral and Brain Sciences.

[46]  F. Macrides,et al.  Cholinergic and catecholaminergic afferents to the olfactory bulb in the Hamster: A neuroanatomical, biochemical, and histochemical investigation , 1981, The Journal of comparative neurology.

[47]  S. Deadwyler,et al.  Entorhinal and septal inputs differentially control sensory-evoked responses in the rat dentate gyrus. , 1981, Science.

[48]  G. V. Van Hoesen,et al.  Olfactory bulb projections to the parahippocampal area of the rat , 1981, The Journal of comparative neurology.

[49]  F. Macrides,et al.  The organization of centrifugal projections from the anterior olfactory nucleus, ventral hippocampal rudiment, and piriform cortex to the main olfactory bulb in the hamster: An autoradiographic study , 1981, The Journal of comparative neurology.

[50]  M. Luskin,et al.  The distribution of axon collaterals from the olfactory bulb and the nucleus of the horizontal limb of the diagonal band to the olfactory cortex, demonstrated by double retrograde labeling techniques , 1982, The Journal of comparative neurology.

[51]  O. Steward,et al.  Medial septal area lesions disrupt theta rhythm and cholinergic staining in medial entorhinal cortex and produce impaired radial arm maze behavior in rats , 1982, The Journal of neuroscience : the official journal of the Society for Neuroscience.