Cortical areas involved in behavioral expression of external pallidum dysfunctions: A PET imaging study in non-human primates

Abstract The external pallidum (GPe) is a component of the indirect pathway centrally placed in the basal ganglia. Studies already demonstrated that the pharmacological disinhibition of the sensorimotor, associative, and limbic GPe produced dyskinesia, hyperactivity, and compulsive behaviors, respectively. The aim of this study was to investigate the cortical regions altered by the disinhibition of each GPe functional territory. Thus, 5 macaques were injected with bicuculline in sensorimotor, associative, and limbic sites of the GPe producing dyskinesia, hyperactivity, and compulsive behaviors, and underwent in vivo positron tomography with 18F‐2‐fluoro‐2‐deoxy‐D‐glucose to identify cortical dysfunctions related to GPe disinhibition. Blood cortisol levels were also quantified as a biomarker of anxiety for each condition. Our results showed that pallidal bicuculline injections in anesthetized animals reproducibly modified the activity of specific ipsilateral and contralateral cortical areas depending on the pallidal territory targeted. Bicuculline injections in the limbic GPe led to increased ipsilateral activations in limbic cortical regions (anterior insula, amygdala, and hippocampus). Injections in the associative vs. sensorimotor GPe increased the activity in the ipsilateral midcingulate vs. somatosensory and parietal cortices. Moreover, bicuculline injections increased blood cortisol levels only in animals injected in their limbic GPe. These are the first functional results supporting the model of opened cortico‐striato‐thalamo‐cortical loops where modifications in a functional pallidal territory can impact cortical activities of the same functional territory but also cortical activities of other functional territories. This highlights the importance of the GPe as a crucial node in the top‐down control of the cortico‐striato‐thalamo‐cortical circuits from the frontal cortex to influence the perception, attention, and emotional processes at downstream (or non‐frontal) cortical levels. Finally, we showed the implication of the ventral pallidum with the amygdala and the insular cortex in a circuit related to aversive processing that should be crucial for the production of anxious disorders. HighlightsPallidal activations impact preferentially cortical targets of opened loops.GPe is crucial for the top‐down control of cortico‐striato‐thalamo‐cortical loops.The ventral pallidum, amygdala and insula are parts of a circuit.This circuit is related to aversive processing.This circuit could be involved in the production of anxious disorders.

[1]  Jaskaran Singh,et al.  Regional Cerebral Glucose Metabolic Abnormalities in Bipolar II Depression , 2007, Biological Psychiatry.

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

[3]  T. Powell,et al.  An anatomical study of converging sensory pathways within the cerebral cortex of the monkey. , 1970, Brain : a journal of neurology.

[4]  M. Mesulam,et al.  Insula of the old world monkey. II: Afferent cortical input and comments on the claustrum , 1982, The Journal of comparative neurology.

[5]  Chantal François,et al.  Behavioural disorders induced by external globus pallidus dysfunction in primates: I. Behavioural study. , 2004, Brain : a journal of neurology.

[6]  A. Levey,et al.  Cholinergic innervation of cortex by the basal forebrain: Cytochemistry and cortical connections of the septal area, diagonal band nuclei, nucleus basalis (Substantia innominata), and hypothalamus in the rhesus monkey , 1983, The Journal of comparative neurology.

[7]  L. Tremblay,et al.  The pallidosubthalamic projection: An anatomical substrate for nonmotor functions of the subthalamic nucleus in primates , 2005, Movement disorders : official journal of the Movement Disorder Society.

[8]  Jonathan D. Cohen,et al.  Conflict monitoring and anterior cingulate cortex: an update , 2004, Trends in Cognitive Sciences.

[9]  M. Paulus,et al.  Interoception in anxiety and depression , 2010, Brain Structure and Function.

[10]  W. Marchand Cortico-basal ganglia circuitry: a review of key research and implications for functional connectivity studies of mood and anxiety disorders , 2010, Brain Structure and Function.

[11]  K H Sontag,et al.  Abnormalities of somatosensory evoked potentials in the quinolinic acid model of Huntington's disease: Evidence that basal ganglia modulate sensory cortical input , 1992, Annals of neurology.

[12]  M. Paulus,et al.  An Insular View of Anxiety , 2006, Biological Psychiatry.

[13]  Y. Smith,et al.  The subthalamic nucleus and the external pallidum: two tightly interconnected structures that control the output of the basal ganglia in the monkey , 1996, Neuroscience.

[14]  Martin Garwicz,et al.  Authenticity, Depression, and Deep Brain Stimulation , 2011, Front. Integr. Neurosci..

[15]  J. Penney,et al.  Differential loss of striatal projection neurons in Huntington disease. , 1988, Proceedings of the National Academy of Sciences of the United States of America.

[16]  M. Botvinick,et al.  Anterior cingulate cortex, error detection, and the online monitoring of performance. , 1998, Science.

[17]  T. Dalgleish,et al.  Can you feel the beat? Interoceptive awareness is an interactive function of anxiety- and depression-specific symptom dimensions , 2010, Behaviour research and therapy.

[18]  P. Strick,et al.  The temporal lobe is a target of output from the basal ganglia. , 1996, Proceedings of the National Academy of Sciences of the United States of America.

[19]  P. Lavallée,et al.  Single-axon tracing study of neurons of the external segment of the globus pallidus in primate. , 2000, The Journal of comparative neurology.

[20]  M. Novak,et al.  The anxiogenic drug FG7142 increases self-injurious behavior in male rhesus monkeys (Macaca mulatta). , 2009, Life sciences.

[21]  H. Kita,et al.  The morphology of globus pallidus projection neurons in the rat: an intracellular staining study , 1994, Brain Research.

[22]  M. Mesulam,et al.  Insula of the old world monkey. III: Efferent cortical output and comments on function , 1982, The Journal of comparative neurology.

[23]  K. Zilles,et al.  The "what" and "when" of self-initiated movements. , 2013, Cerebral cortex.

[24]  André Parent,et al.  Comparative neurobiology of the basal ganglia , 1986 .

[25]  Leslie G. Ungerleider,et al.  Organization of visual cortical inputs to the striatum and subsequent outputs to the pallido‐nigral complex in the monkey , 1990, The Journal of comparative neurology.

[26]  S. Haber,et al.  The organization of the descending ventral pallidal projections in the monkey , 1993, The Journal of comparative neurology.

[27]  N Mizushima,et al.  A case of hemichorea-hemiballism associated with parietal lobe infarction. , 1997, European neurology.

[28]  D L Rosene,et al.  Comparison of the efferents of the amygdala and the hippocampal formation in the rhesus monkey: II. Reciprocal and non‐reciprocal connections , 1988, The Journal of comparative neurology.

[29]  E. Bullmore,et al.  Integrating evidence from neuroimaging and neuropsychological studies of obsessive-compulsive disorder: The orbitofronto-striatal model revisited , 2008, Neuroscience & Biobehavioral Reviews.

[30]  W. Drevets Functional anatomical abnormalities in limbic and prefrontal cortical structures in major depression. , 2000, Progress in brain research.

[31]  C. Colby,et al.  Heterogeneity of extrastriate visual areas and multiple parietal areas in the Macaque monkey , 1991, Neuropsychologia.

[32]  Garima Shukla,et al.  Hemichorea-hemiballism associated with frontoparietal bleed , 2006, Journal of Neurology.

[33]  A. Parent,et al.  Functional anatomy of the basal ganglia. I. The cortico-basal ganglia-thalamo-cortical loop , 1995, Brain Research Reviews.

[34]  M. Delong,et al.  Primate models of movement disorders of basal ganglia origin , 1990, Trends in Neurosciences.

[35]  K. Yau,et al.  Interoception: the sense of the physiological condition of the body , 2003, Current Opinion in Neurobiology.

[36]  L. Tremblay,et al.  Activity of pallidal neurons in the monkey during dyskinesia induced by injection of bicuculline in the external pallidum , 1995, Neuroscience.

[37]  Heide Klumpp,et al.  Anterior cingulate cortex and insula response during indirect and direct processing of emotional faces in generalized social anxiety disorder , 2013, Biology of Mood & Anxiety Disorders.

[38]  T. P. S. Powell,et al.  The projection of the primary somatic sensory cortex upon area 5 in the monkey , 1985, Brain Research Reviews.

[39]  J. Obeso,et al.  The basal ganglia in Parkinson's disease: Current concepts and unexplained observations , 2008, Annals of neurology.

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

[41]  R. M. Stewart,et al.  Evoked potentials in Huntington's disease. A comparative and longitudinal study. , 1984, Archives of neurology.

[42]  L. Hazrati,et al.  Functional anatomy of the basal ganglia , 1995 .

[43]  John J. Foxe,et al.  Identifying a Network of Brain Regions Involved in Aversion-Related Processing: A Cross-Species Translational Investigation , 2011, Front. Integr. Neurosci..

[44]  W. Chai,et al.  Imaging the Effects of Propofol on Human Cerebral Glucose Metabolism Using Positron Emission Tomography , 2008, The Journal of international medical research.

[45]  G. E. Alexander,et al.  Parallel organization of functionally segregated circuits linking basal ganglia and cortex. , 1986, Annual review of neuroscience.

[46]  M. Goldberg,et al.  Space and attention in parietal cortex. , 1999, Annual review of neuroscience.

[47]  J. Bolam,et al.  Selective Innervation of Neostriatal Interneurons by a Subclass of Neuron in the Globus Pallidus of the Rat , 1998, The Journal of Neuroscience.

[48]  H. Fibiger,et al.  The organization and some projections of cholinergic neurons of the mammalian forebrain , 1982, Brain Research Reviews.

[49]  R. Morecraft,et al.  Segregated parallel inputs to the brachial spinal cord from the cingulate motor cortex in the monkey. , 1997, Neuroreport.

[50]  M. Rushworth,et al.  The left parietal and premotor cortices: motor attention and selection , 2003, NeuroImage.

[51]  A. Kleinschmidt,et al.  Anterior insula activations in perceptual paradigms: often observed but barely understood , 2010, Brain Structure and Function.

[52]  Daniel S. Margulies,et al.  Recent advances in structural and functional brain imaging studies of attention-deficit/hyperactivity disorder , 2007, Current psychiatry reports.

[53]  F. Holsboer,et al.  Stress and the brain: from adaptation to disease , 2005, Nature Reviews Neuroscience.

[54]  D. Joel,et al.  The organization of the basal ganglia-thalamocortical circuits: Open interconnected rather than closed segregated , 1994, Neuroscience.

[55]  A. Toga,et al.  The Rhesus Monkey Brain in Stereotaxic Coordinates , 1999 .

[56]  S. Haber The primate basal ganglia: parallel and integrative networks , 2003, Journal of Chemical Neuroanatomy.

[57]  R. Davidson,et al.  The integration of negative affect, pain and cognitive control in the cingulate cortex , 2011, Nature Reviews Neuroscience.

[58]  J. Price,et al.  The organization of projections from the mediodorsal nucleus of the thalamus to orbital and medial prefrontal cortex in macaque monkeys , 1993, The Journal of comparative neurology.

[59]  T. Paus Primate anterior cingulate cortex: Where motor control, drive and cognition interface , 2001, Nature Reviews Neuroscience.

[60]  S. Haber,et al.  Parallel and Integrative Processing Through the Basal Ganglia Reward Circuit: Lessons from Addiction , 2008, Biological Psychiatry.

[61]  A. Berardelli,et al.  Sensorimotor integration in movement disorders , 2003, Movement disorders : official journal of the Movement Disorder Society.

[62]  H. Kita,et al.  Monkey globus pallidus external segment neurons projecting to the neostriatum. , 1999, Neuroreport.

[63]  Yulia Worbe,et al.  Selective dysfunction of basal ganglia subterritories: From movement to behavioral disorders , 2015, Movement disorders : official journal of the Movement Disorder Society.

[64]  Dottie M. Clower,et al.  Basal ganglia and cerebellar inputs to 'AIP'. , 2005, Cerebral cortex.

[65]  KouichiC . Nakamura,et al.  Dichotomous Organization of the External Globus Pallidus , 2012, Neuron.

[66]  W. T. Thach,et al.  Basal ganglia motor control. I. Nonexclusive relation of pallidal discharge to five movement modes. , 1991, Journal of neurophysiology.

[67]  J. Noth,et al.  Evoked potentials in patients with Huntington's disease and their offspring. I. Somatosensory evoked potentials. , 1984, Electroencephalography and Clinical Neurophysiology.

[68]  O. Hikosaka,et al.  The Primate Ventral Pallidum Encodes Expected Reward Value and Regulates Motor Action , 2012, Neuron.

[69]  A. Parent,et al.  Projection from the external pallidum to the reticular thalamic nucleus in the squirrel monkey , 1991, Brain Research.

[70]  B S Peterson,et al.  Neuroimaging studies of Tourette syndrome: a decade of progress. , 2001, Advances in neurology.

[71]  L. Tremblay,et al.  Behavioural disorders induced by external globus pallidus dysfunction in primates II. Anatomical study. , 2004, Brain : a journal of neurology.

[72]  E. D. Kloet,et al.  Hormones, brain and stress , 2003 .

[73]  Andrew Jenkins,et al.  Menthol shares general anesthetic activity and sites of action on the GABA(A) receptor with the intravenous agent, propofol. , 2008, European journal of pharmacology.

[74]  T. Paus,et al.  Functional connectivity of the anterior cingulate cortex within the human frontal lobe: a brain-mapping meta-analysis , 2000, Experimental Brain Research.

[75]  Walle J. H. Nauta,et al.  Light microscopic evidence of striatal input to intrapallidal neurons of cholinergic cell group Ch4 in the rat: a study employing the anterograde tracerPhaseolus vulgaris leucoagglutinin (PHA-L) , 1986, Brain Research.

[76]  M. Hennerici,et al.  Evoked potentials in patients with Huntington's disease and their offspring. II. Visual evoked potentials. , 1985, Electroencephalography and clinical neurophysiology.

[77]  M. E. Anderson,et al.  A quantitative analysis of pallidal discharge during targeted reaching movement in the monkey , 2004, Experimental Brain Research.

[78]  S. Haber Neuroanatomy of Reward: A View from the Ventral Striatum , 2011 .

[79]  P. Brotchie,et al.  Motor function of the monkey globus pallidus. 1. Neuronal discharge and parameters of movement. , 1991, Brain : a journal of neurology.

[80]  J. Yelnik,et al.  Topographic distribution of the axonal endings from the sensorimotor and associative striatum in the macaque pallidum and substantia nigra , 2004, Experimental Brain Research.

[81]  A Jackson,et al.  Chorea and myoclonus in the monkey induced by gamma-aminobutyric acid antagonism in the lentiform complex. The site of drug action and a hypothesis for the neural mechanisms of chorea. , 1988, Brain : a journal of neurology.

[82]  D. N. Pandya,et al.  Insular interconnections with the amygdala in the rhesus monkey , 1981, Neuroscience.

[83]  J. Penney,et al.  Striatal inhomogeneities and basal ganglia function , 1986, Movement disorders : official journal of the Movement Disorder Society.