Hippocampal modulation of cingulo‐thalamic neuronal activity and discriminative avoidance learning in rabbits

Two experiments assessed the effects of 1) combined subicular complex and posterior cingulate cortical lesions on training‐induced neuronal activity (TIA) in the anterior ventral (AV) and medial dorsal (MD) thalamic nuclei; 2) hippocampal (Ammon's horn and dentate gyrus) lesions on TIA in cingulate cortex and in the AV and MD thalamic nuclei. The rabbits acquired a conditioned avoidance response (CR), stepping in an activity wheel upon hearing a 0.5‐s tone (CS+), in order to prevent a foot‐shock scheduled 5 s after tone onset. No response was required after a different, safety‐predictive tone (CS−). In experiment 1 the combined subicular and cingulate cortical lesions enhanced thalamic TIA during acquisition and increased CR incidence in the first session of acquisition. These results confirmed the hypothesis that subicular and cingulate cortical efferents are not essential for thalamic TIA or for avoidance learning. Hippocampal lesions (experiment 2) also enhanced thalamic TIA. However, unlike subicular lesions, hippocampal lesions enhanced posterior cingulate cortical TIA as well, especially during extinction training. Hippocampal lesions did not affect CR performance. The results suggested that subicular excitatory efferents are responsible for incrementing cingulate cortical TIA, which is viewed as subserving associative attention. Activity from hippocampus downregulates the cue‐elicited neuronal activity of the cingulo‐thalamic circuits by suppressing the excitatory influence of the subiculum. The hippocampal influence reduces cingulo‐thalamic cue‐elicited activation in particular circumstances, such as the onset of CR extinction, when an expected reinforcer is omitted. Hippocampus 1998;8:491–510. © 1998 Wiley‐Liss, Inc.

[1]  M. Gabriel,et al.  Impairment of cingulothalamic learning-related neuronal coding in rabbits exposed to cocaine in utero: general and sex-specific effects. , 1999, Behavioral neuroscience.

[2]  L. Swanson,et al.  The structural organization of connections between hypothalamus and cerebral cortex 1 Published on the World Wide Web on 2 June 1997. 1 , 1997, Brain Research Reviews.

[3]  Amanda Parker,et al.  The effect of anterior thalamic and cingulate cortex lesions on object-in-place memory in monkeys , 1997, Neuropsychologia.

[4]  M. Gabriel,et al.  Lesions of the entorhinal cortex disrupt behavioral and neuronal responses to context change during extinction of discriminative avoidance behavior , 1997, Experimental Brain Research.

[5]  H. Eichenbaum,et al.  The hippocampus and memory for orderly stimulus relations. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[6]  Michael S. Fanselow,et al.  Electrolytic Lesions of the Fimbria/Fornix, Dorsal Hippocampus, or Entorhinal Cortex Produce Anterograde Deficits in Contextual Fear Conditioning in Rats , 1997, Neurobiology of Learning and Memory.

[7]  Trevor W. Robbins,et al.  Dissociable effects of anterior and posterior cingulate cortex lesions on the acquisition of a conditional visual discrimination: Facilitation of early learning vs. impairment of late learning , 1996, Behavioural Brain Research.

[8]  G. Byatt,et al.  Both anteromedial and anteroventral thalamic lesions impair radial-maze learning in rats. , 1996, Behavioral neuroscience.

[9]  R. Knight Contribution of human hippocampal region to novelty detection , 1996, Nature.

[10]  M. Gabriel,et al.  Stimulus-related and movement-related single-unit activity in rabbit cingulate cortex and limbic thalamus during performance of discriminative avoidance behavior , 1996, Brain Research.

[11]  H. Eichenbaum,et al.  Conservation of hippocampal memory function in rats and humans , 1996, Nature.

[12]  M. Gallagher,et al.  Hippocampal lesions disrupt decrements but not increments in conditioned stimulus processing , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[13]  J. Aggleton,et al.  A comparison of the effects of anterior thalamic, mamillary body and fornix lesions on reinforced spatial alternation , 1995, Behavioural Brain Research.

[14]  M. Gabriel,et al.  Mamillothalamic tract transection blocks anterior thalamic training- induced neuronal plasticity and impairs discriminative offidance behavior in rabbits , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[15]  J. Taube Head direction cells recorded in the anterior thalamic nuclei of freely moving rats , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[16]  Yasuo Kubota,et al.  Afferent connections of the anterior thalamus in rabbits , 1994, Brain Research Bulletin.

[17]  M. Gluck,et al.  Context, conditioning, and hippocampal rerepresentation in animal learning. , 1994, Behavioral neuroscience.

[18]  R. C. Honey,et al.  Selective hippocampal lesions abolish the contextual specificity of latent inhibition and conditioning. , 1993, Behavioral neuroscience.

[19]  R. Sutherland,et al.  Posterior Cingulate Cortex and Spatial Memory: A Microlimnology Analysis , 1993 .

[20]  M. Gabriel,et al.  Discriminative Avoidance Learning: A Model System , 1993 .

[21]  D. Finch Hippocampal, Subicular, and Entorhinal Afferents and Synaptic Integration in Rodent Cingulate Cortex , 1993 .

[22]  D. Weinberger,et al.  Ibotenic acid lesion of the ventral hippocampus differentially affects dopamine and its metabolites in the nucleus accumbens and prefrontal cortex in the rat , 1992, Brain Research.

[23]  Joseph E LeDoux,et al.  Differential Contribution of Amygdala and Hippocampus to Cued and Contextual Fear Conditioning , 1992 .

[24]  J M Wyss,et al.  Connections of the retrosplenial dysgranular cortex in the rat , 1992, The Journal of comparative neurology.

[25]  M. Gabriel,et al.  Training-stage related neuronal plasticity in limbic thalamus and cingulate cortex during learning: a possible key to mnemonic retrieval , 1991, Behavioural Brain Research.

[26]  P. Solomon,et al.  Hippocampus, context, and conditioning. , 1991, Behavioral neuroscience.

[27]  J. Aggleton,et al.  Both fornix and anterior thalamic, but not mammillary, lesions disrupt delayed non-matching-to-position memory in rats , 1991, Behavioural Brain Research.

[28]  T. Otto,et al.  Analysis of aversively conditioned learning and memory in rats recovered from pyrithiamine-induced thiamine deficiency. , 1991, Behavioral neuroscience.

[29]  G. Lynch,et al.  Hippocampus and olfactory discrimination learning: effects of entorhinal cortex lesions on olfactory learning and memory in a successive-cue, go-no-go task. , 1991, Behavioral neuroscience.

[30]  T. van Groen,et al.  Extrinsic projections from area CA1 of the rat hippocampus: Olfactory, cortical, subcortical, and bilateral hippocampal formation projections , 1990, The Journal of comparative neurology.

[31]  M. Gabriel,et al.  Neuronal encoding of conditional stimulus duration in the cingulate cortex and the limbic thalamus of rabbits. , 1990, Behavioral neuroscience.

[32]  T. van Groen,et al.  The postsubicular cortex in the rat: characterization of the fourth region of the subicular cortex and its connections , 1990, Brain Research.

[33]  T. van Groen,et al.  The connections of presubiculum and parasubiculum in the rat , 1990, Brain Research.

[34]  M P Witter,et al.  The subiculum: cytoarchitectonically a simple structure, but hodologically complex. , 1990, Progress in brain research.

[35]  D. Finch,et al.  Feedforward inhibition of the rat entorhinal cortex and subicular complex , 1988, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[36]  G. Winocur,et al.  The hippocampus and conditioning to contextual cues. , 1987, Behavioral neuroscience.

[37]  M. Gabriel,et al.  Posterior cingulate cortical lesions eliminate learning-related unit activity in the anterior cingulate cortex , 1987, Brain Research.

[38]  D. V. von Cramon,et al.  A contribution to the anatomical basis of thalamic amnesia. , 1985, Brain : a journal of neurology.

[39]  N. Schmajuk Psychological theories of hippocampal function , 1984 .

[40]  T. Babb,et al.  Excitatory projection of the rat subicular complex to the cingulate cortex and synaptic integration with thalamic afferents , 1984, Brain Research.

[41]  R. Isaacson Hippocampal damage: effects on dopaminergic systems of the basal ganglia. , 1984, International review of neurobiology.

[42]  E. Irle,et al.  Differential effects of double and triple lesions of the cat's limbic system on subsequent learning behavior. , 1983, Behavioral neuroscience.

[43]  M. Gabriel,et al.  Anterior thalamic lesions and neuronal activity in the cingulate and retrosplenial cortices during discriminative avoidance behavior in rabbits. , 1983, Behavioral neuroscience.

[44]  Elizabeth K. Warrington,et al.  Amnesia: A disconnection syndrome? , 1982, Neuropsychologia.

[45]  L. Devenport,et al.  Reward-induced stereotypy: modulation by the hippocampus. , 1981, Science.

[46]  M. Girgis,et al.  A new stereotaxic atlas of the rabbit brain , 1981 .

[47]  T. Babb,et al.  Inhibition in subicular and entorhinal principal neurons in response to electrical stimulation of the fornix and hippocampus , 1980, Brain Research.

[48]  L. Cermak,et al.  Alcoholic Korsakoff's Syndrome: An Information-Processing Approach to Amnesia , 1980 .

[49]  L. Cermak,et al.  Clinical Symptoms, Neuropathology, and Etiology , 1980 .

[50]  L. Swanson The hippocampus — new anatomical insights , 1979, Trends in Neurosciences.

[51]  L Weiskrantz,et al.  Memory disorder in Korsakoff's psychosis: a neuropathological and neuropsychological investigation of two cases. , 1979, Brain : a journal of neurology.

[52]  A. Black,et al.  Hippocampal function in avoidance learning and punishment. , 1977, Psychological bulletin.

[53]  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.

[54]  H. Huynh,et al.  Estimation of the Box Correction for Degrees of Freedom from Sample Data in Randomized Block and Split-Plot Designs , 1976 .

[55]  R. Chronister,et al.  The Septo-Hippocampal System: Significance of the Subiculum , 1976 .

[56]  W. Cowan,et al.  Hippocampo-hypothalamic connections: origin in subicular cortex, not ammon's horn. , 1975, Science.

[57]  R. Isaacson,et al.  Activity changes related to the location of lesion in the hippocampus. , 1975, Behavioral biology.

[58]  R. Hirsh The hippocampus and contextual retrieval of information from memory: a theory. , 1974, Behavioral biology.

[59]  P J Donovick,et al.  A metachromatic stain for neural tissue. , 1974, Stain technology.

[60]  J. Altman,et al.  The hippocampus and behavioral maturation. , 1973, Behavioral biology.

[61]  C. Netley Dichotic listening performance of hemispherectomized patients. , 1972, Neuropsychologia.

[62]  Seymour Geisser,et al.  Statistical Principles in Experimental Design , 1963 .

[63]  C. Fox,et al.  A rapid method for locating intracerebral electrode tracks. , 1959, Stain technology.

[64]  W. Scoville,et al.  LOSS OF RECENT MEMORY AFTER BILATERAL HIPPOCAMPAL LESIONS , 1957, Journal of neurology, neurosurgery, and psychiatry.

[65]  E. Culler,et al.  DEVICE FOR THE MOTOR CONDITIONING OF SMALL ANIMALS. , 1936, Science.