Basal ganglia–hippocampal interactions support the role of the hippocampal formation in sensorimotor integration

Experiments were carried out to evaluate whether neural activity in the basal ganglia is functionally related to the neural activity underlying mechanisms of theta band oscillation and synchrony in the hippocampal formation. Experiment 1 demonstrated that electrical stimulation administered to the substantia nigra, globus pallidus (GP) and caudate-putamen (CPu) in urethane anesthetized rats elicited theta field activity in the hippocampal formation. Subsequent microinfusion of the local anesthetic procaine hydrochloride into the medial septum reversibly abolished this effect. In Experiment 2, single cell discharge profiles established for 152 cells recorded in nuclei of the basal ganglia resulted in 101 (66%) being classified as theta-related and 51 (34%) classified as nonrelated. Theta-related cells were further subclassified as tonic theta-ON cells (n = 79) and tonic theta-OFF (n = 22). Tonic theta-ON and tonic theta-OFF cells displayed irregular or regular (tonic) discharge patterns. Rhythmic discharge patterns did not occur in any theta-related cells in the nuclei of the basal ganglia. However, analyses using Kaneoke and Vitek's [J. Neurosci. Methods 68, (1996) 211] algorithms revealed that 51/101 (50%) theta-related cells displayed periodicity in their discharge patterns whereas 27/51 (53%) of the nonrelated cells displayed periodicity in their discharge patterns. The periodicities in the majority of cells were in frequency ranges above that of theta band oscillation and synchrony. The results support the following conclusions: (1) the cellular activity of the basal ganglia, composed of nuclei traditionally associated with motor functions, is functionally connected with the neural circuitry involved in the generation of theta band oscillation and synchrony in the hippocampal formation; (2) the observed functional connectivity provides support for the role of the hippocampal formation in sensorimotor integration.

[1]  B. H. Bland,et al.  Medial septal cell interactions in relation to hippocampal field activity and the effects of atropine , 1991, Hippocampus.

[2]  B. H. Bland,et al.  Theta band oscillation and synchrony in the hippocampal formation and associated structures: the case for its role in sensorimotor integration , 2001, Behavioural Brain Research.

[3]  B. H. Bland,et al.  Hippocampal formation neurons code the level of activation of the cholinergic septohippocampal pathway , 1987, Brain Research.

[4]  M. MacIver,et al.  Physiology, pharmacology, and topography of cholinergic neocortical oscillations in vitro. , 1997, Journal of neurophysiology.

[5]  B. H. Bland,et al.  Responses of phasic and tonic hippocampal theta-on cells to cholinergics: differential effects of muscarinic and nicotinic activation , 1988, Brain Research.

[6]  M. Sabatino,et al.  Striatonigral suppression of focal hippocampal epilepsy , 1989, Neuroscience Letters.

[7]  M. Alexander,et al.  Principles of Neural Science , 1981 .

[8]  Douglas L. Jones,et al.  From motivation to action: Functional interface between the limbic system and the motor system , 1980, Progress in Neurobiology.

[9]  B. H. Bland,et al.  State-dependent spike train dynamics of hippocampal formation neurons: evidence for theta-on and theta-off cells , 1987, Brain Research.

[10]  Charles J. Wilson,et al.  The generation of natural firing patterns in neostriatal neurons. , 1993, Progress in brain research.

[11]  I. Kirk,et al.  Classification of theta‐related cells in the entorhinal cortex: Cell discharges are controlled by the ascending brainstem synchronizing pathway in parallel with hippocampal theta‐related cells , 1995, Hippocampus.

[12]  M. Sabatino,et al.  Striatal and septal influence on hippocampal theta and spikes in the cat , 1985, Neuroscience Letters.

[13]  Brian H. Bland,et al.  Anatomical, Electrophysiological and Pharmacological Studies of Ascending Brainstem Hippocampal Synchronizing Pathways , 1998, Neuroscience & Biobehavioral Reviews.

[14]  G. Karmos,et al.  Electrical activity of the archicortex , 1986 .

[15]  B. H. Bland,et al.  Distribution and analysis of hippocampal theta‐related cells in the pontine region of the urethane‐anesthetized rat , 1999, Hippocampus.

[16]  B. H. Bland,et al.  In vivo intrahippocampal microinfusion of carbachol and bicuculline induces theta‐like oscillations in the septally deafferented hippocampus , 1991, Hippocampus.

[17]  C. Trepel,et al.  Extrinsic modulation of theta field activity in the entorhinal cortex of the anesthetized rat , 1994, Hippocampus.

[18]  I. Grofová,et al.  Origin of ascending and spinal pathways from the nucleus tegmenti pedunculopontinus in the rat , 1989, The Journal of comparative neurology.

[19]  R. Numan The Behavioral Neuroscience of the Septal Region , 2012, Springer New York.

[20]  C. Gerfen,et al.  The frontal cortex-basal ganglia system in primates. , 1996, Critical reviews in neurobiology.

[21]  R. Vertes,et al.  Brainstem-diencephalo-septohippocampal systems controlling the theta rhythm of the hippocampus. , 1997, Neuroscience.

[22]  J. Vitek,et al.  Burst and oscillation as disparate neuronal properties , 1996, Journal of Neuroscience Methods.

[23]  Brian H. Bland,et al.  The medial septum: Node of the ascending brainstem hippocampal synchronizing pathways. , 2000 .

[24]  J. Penney,et al.  The functional anatomy of basal ganglia disorders , 1989, Trends in Neurosciences.

[25]  Y. Smith,et al.  Microcircuitry of the direct and indirect pathways of the basal ganglia. , 1998, Neuroscience.

[26]  C. Trepel,et al.  Intraseptal Microinfusion of Muscimol: Effects on Hippocampal Formation Theta Field Activity and Phasic Theta-ON Cell Discharges , 1996, Experimental Neurology.

[27]  J. Bolam,et al.  Cholinergic, GABAergic, and glutamate-enriched inputs from the mesopontine tegmentum to the subthalamic nucleus in the rat , 1995, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[28]  J. Walters,et al.  Multisecond oscillations in the subthalamic nucleus: Effects of apomorphine and dopamine cell lesion , 2000, Synapse.

[29]  B. H. Bland,et al.  Responses of septal θ-on and θ-off cells to activation of the dorsomedial-posterior hypothalamic region , 1990, Brain Research Bulletin.

[30]  R. Vertes,et al.  Extrinsic modulation of medial septal cell discharges by the ascending brainstem hippocampal synchronizing pathway , 1994, Hippocampus.

[31]  B. H. Bland,et al.  Preliminary observations on the physiology and pharmacology of hippocampal θ-off cells , 1989, Brain Research.

[32]  Ehren L. Newman,et al.  Human θ Oscillations Related to Sensorimotor Integration and Spatial Learning , 2003, The Journal of Neuroscience.

[33]  William H. Press,et al.  Numerical recipes in C , 2002 .

[34]  B. Christie,et al.  Cingulate cell discharge patterns related to hippocampal EEG and their modulation by muscarinic and nicotinic agents , 1988, Brain Research.

[35]  B. Cristie,et al.  Hippocampal theta field activity and theta-on/theta-off cell discharges are controlled by an ascending hypothalamo-septal pathway , 1991, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[36]  J. Bolam,et al.  Relationship of Activity in the Subthalamic Nucleus–Globus Pallidus Network to Cortical Electroencephalogram , 2000, The Journal of Neuroscience.

[37]  G Buzsáki,et al.  Ultra-slow oscillation (0.025 Hz) triggers hippocampal afterdischarges in Wistar rats , 1999, Neuroscience.

[38]  I. Kirk,et al.  Evidence for Differential Control of Posterior Hypothalamic, Supramammillary, and Medial Mammillary Theta-Related Cellular Discharge by Ascending and Descending Pathways , 1996, The Journal of Neuroscience.

[39]  Philip M. Groves,et al.  Statistical properties of neuronal spike trains in the substantia nigra: Cell types and their interactions , 1977, Brain Research.

[40]  George V Rebec,et al.  Behavior-related changes in the activity of substantia nigra pars reticulata neurons in freely moving rats , 1999, Brain Research.

[41]  M. Witter,et al.  Organization of the projections from the subiculum to the ventral striatum in the rat. A study using anterograde transport of Phaseolus vulgaris leucoagglutinin , 1987, Neuroscience.

[42]  B. McNaughton,et al.  Behavioral correlates of theta-on and theta-off cells recorded from hippocampal formation of mature young and aged rats , 1990, Experimental Brain Research.

[43]  B H Bland,et al.  Discharge patterns of hippocampal theta-related cells in the caudal diencephalon of the urethan-anesthetized rat. , 1995, Journal of neurophysiology.

[44]  B. H. Bland,et al.  The classification of medial septum-diagonal band cells as σ-on or σ-off in relation to hippocampal EEG states , 1989, Brain Research.

[45]  Y Kaneoke,et al.  Multisecond oscillations in firing rate in the basal ganglia: robust modulation by dopamine receptor activation and anesthesia. , 1999, Journal of neurophysiology.

[46]  M. Sabatino,et al.  Effects of substantia nigra and pallidum stimulation on hippocampal interictal activity in the cat , 1986, Neuroscience Letters.

[47]  B H Bland,et al.  Hippocampal theta‐related cellular activity in the superior colliculus of the urethane‐anesthetized rat , 1999, Hippocampus.

[48]  B. H. Bland The physiology and pharmacology of hippocampal formation theta rhythms , 1986, Progress in Neurobiology.

[49]  D. A. Bergstrom,et al.  Multisecond periodicities in basal ganglia firing rates correlate with theta bursts in transcortical and hippocampal EEG. , 2002, Journal of neurophysiology.

[50]  S. Oddie,et al.  In vivo intracellular correlates of hippocampal formation theta-on and theta-off cells , 1992, Brain Research.

[51]  A. Mcgeorge,et al.  The organization of the projection from the cerebral cortex to the striatum in the rat , 1989, Neuroscience.