Abstract
Frontal cortical efferent fibers are thought to have important regulatory influence on cortico-basal ganglia (BG) circuits. The cortico-midbrain (substantia nigra/ventral tegmental area, SN/VTA) pathway has received particular attention in psychiatric diseases, most notably schizophrenia. Work in rodents demonstrates that the prefrontal cortico (PFC)-midbrain pathway plays a central role in regulating the firing pattern of dopamine (DA) neurons. These findings have led to some important hypotheses concerning PFC/BG interaction in schizophrenia. Descending PFC projections to the SN/VTA have been primarily documented in the rodent. The aim of this study was to determine the degree and organization of PFC afferents to these areas in the Macaque monkey. Anterograde tracer injections were made into discrete orbital, cingulate, and dorsolateral prefrontal areas. Projections were charted to the SN and VTA. Overall, there were very few fibers in the ventral midbrain following injections confined to specific areas of the PFC. To determine the relationship of the descending fibers to the midbrain DA neurons, sections were double stained for the tracer molecules and for tyrosine hydroxylase. In all cases, the prefrontal projections and the TH-positive cells did not appear to be in close juxtaposition. The results show a very limited projection from the PFC to the midbrain DA neurons in primates, terminating both within the SN proper as well as in the VTA. They arise from a broad region of the PFC, including the DLPF, cingulate, and orbital cortices. However, despite the relative lack of cortical input to the midbrain cells, these neurons are rich in glutamate receptors in primates. Thus, while, based on these anatomical studies, direct cortical control of DA neurons remains debatable in primates; the cortex may directly impact other sources of glutamatergic control.
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References
Abi-Dargham A, Gil R, Krystal J, Baldwin RM, Seibyl JP, Bowers M et al (1998). Increased striatal dopamine transmission in schizophrenia: confirmation in a second cohort. Am J Psychiatry 155: 761–767.
Abi-Dargham A, Rodenhiser J, Printz D, Zea-Ponce Y, Gil R, Kegeles LS et al (2000). From the cover: increased baseline occupancy of D2 receptors by dopamine in schizophrenia. Proc Natl Acad Sci USA 97: 8104–8109.
Afifi AK, Bahuth NB, Kaelber WW, Mikhael E, Nassar S (1974). The cortico-nigral fibre tract. An experimental Fink–Heimer study in cats. J Anat 118: 469–476.
An X, Bandler R, ngür D, Price JL (1998). Prefrontal cortical projections to longitudinal columns in the midbrain periaqueductal gray in macaque monkeys. J Comp Neurol 401: 455–479.
Berendse HW, Galisde Graaf Y, Groenewegen HJ (1992). Topographical organization and relationship with ventral striatal compartments of prefrontal corticostriatal projections in the rat. J Comp Neurol 316: 314–347.
Breier A, Su TP, Saunders R, Carson RE, Kolachana BS, deBartolomeis A et al (1997). Schizophrenia is associated with elevated amphetamine-induced synaptic dopamine concentrations: evidence from a novel positron emission tomography method. Proc Natl Acad Sci USA 94: 2569–2574.
Bunney BS, Aghajanian GK (1976). The precise localization of nigral afferents in the rat as determined by a retrograde tracing technique. Brain Res 117: 423–435.
Callicott J, Bertolino A, Mattay V, Langheim F, Duyn J, Coppola R et al (2000). Physiological dysfunction of the dorsolateral prefrontal cortex in schizophrenia revisited. Cereb Cortex 10: 1078–1092.
Carlsson A, Lindqvist M (1963). Effect of chlorpromazine or haloperidol on formation of 3-methoxytyramine and normetanephrine in mouse brain. Acta Pharmacol Toxicol 20: 140–144.
Carlsson A, Waters N, Carlsson ML (1999). Neurotransmitter interactions in schizophrenia—therapeutic implications. Biol Psychiatry 46: 1388–1395.
Carpenter MB, Baton III RR, Carleton SC, Keller JT (1981). Interconnections and organization of pallidal and subthalamic nucleus neurons in the monkey. J Comp Neurol 197: 579–603.
Carpenter MB, Carlton SC, Keller JT, Conte P (1981). Connections of the subthalamic nucleus in the monkey. Brain Res 224: 1–29.
Carr DB, Sesack SR (2000a). Projections from the rat prefrontal cortex to the ventral tegmental area: target specificity in the synaptic associations with mesoaccumbens and mesocortical neurons. J Neurosci 20: 3864–3873.
Carr DB, Sesack SR (2000b). Projections from the rat prefrontal cortex to the ventral tegmental area: target specificity in the synaptic associations with mesoaccumbens and mesocortical neurons. J Neurosci 20: 3864–3873.
Carter CJ (1980). Glutamatergic pathways from the medial pre-frontal cortex to the anterior striatum, nucleus accumbens and substantia nigra. Br J Pharmacol 70: 50–51.
Charara A, Smith Y, Parent A (1996). Glutamatergic inputs from the pedunculopontine nucleus to midbrain dopaminergic neurons in primates: Phaseolus vulgaris-Leucoagglutinin antereograde labeling combined with postembedding glutamate and GABA immunohistochemistry. J Comp Neurol 364: 254–266.
Chiba T, Kayahara T, Nakano K (2001). Efferent projections of infralimbic and prelimbic areas of the medial prefrontal cortex in the Japanese monkey, Macaca fuscata. Brain Res 888: 83–101.
Christie MJ, Bridge S, James LB, Beart PM (1985). Excitotoxin lesions suggest an aspartatergic projection from rat medial prefrontal cortex to ventral tegmental area. Brain Res 333: 169–172.
Creese I, Burt DR, Snyder SH (1976). Dopamine receptor binding predicts clinical and pharmacological potencies of antischizophrenic drugs. Science 19: 481–483.
Davis KA, Gdowski GT, Voigt HF (1995). A statistically based method to generate response maps objectively. J Neurosci Methods 57: 107–118.
Dong HW, Swanson LW (2004). Organization of axonal projections from the anterolateral area of the bed nuclei of the stria terminalis. J Comp Neurol 468: 277–298.
Frankle W, Bennett S, Laruelle M, Haber S (2003). Prefrontal Cotical Projections to the Subthalamic Nucleua, VTA and Substantia Nigra in the Primate Society for Neuroscience Annual Meeting, New Orleans.
Freedman LJ, Insel TR, Smith Y (2000). Subcortical projections of area 25 (subgenual cortex) of the macaque monkey. J Comp Neurol 421: 172–188.
Fudge JL, Haber SN (2001). Bed nucleus of the stria terminalis and extended amygdala inputs to dopamine subpopulations in primates. Neuroscience 104: 807–827.
Georges F, Aston-Jones G (2002). Activation of ventral tegmental area cells by the bed nucleus of the stria terminalis: a novel excitatory amino acid input to midbrain dopamine neurons. J Neurosci 22: 5173–5187.
Goldman-Rakic PS (1999). The physiological approach: functional architecture of working memory and disordered cognition in schizophrenia. Biol Psychiatry 46: 650–661.
Goldman-Rakic PS, Muly III EC, Williams GV (2000). D(1) receptors in prefrontal cells and circuits. Brain Res Brain Res Rev 31: 295–301.
Goldman-Rakic PS, Selemon LD (1997). Functional and anatomical aspects of prefrontal pathology in schizophrenia. Schizophrenia Bull 23: 437–458.
Green MF (1996). What are the functional consequences of neurocognitive deficits in schizophrenia? Am J Psychiatry 153: 321–330.
Groenewegen HJ, Wright CI, Uylings HB (1997). The anatomical relationships of the prefrontal cortex with limbic structures and the basal ganglia. J Psychopharmacol 11: 99–106.
Haber SN (2003). The basal ganglia. In: The Human Nervous System. Paxinos G, Mai JK (eds). Academic Press: New York.
Haber SN, Lynd-Balta E, Mitchell SJ (1993). The organization of the descending ventral pallidal projections in the monkey. J Comp Neurol 329: 111–129.
Hurley KM, Herbert H, Moga MM, Saper CB (1991). Efferent projections of the infralimbic cortex of the rat. J Comp Neurol 308: 249–276.
Karreman M, Moghaddam B (1996). The prefrontal cortex regulates the basal release of dopamine in the limbic striatum: an effect mediated by ventral tegmental area. J Neurochem 66: 589–598.
Keefe KA, Gerfen CR (1999). Local infusion of the (+/−)-a-amino-3-hydroxy-5-methylisoxazole-4-propionate/kainate receptor antagonist 6-cyano-7-nitroquinoxaline-2,3-dione does not block D1 dopamine receptor-mediated increases in immediate early gene expression in the dopamine-depleted striatum. Neuroscience 89: 491–504.
Kitano H, Tanibuchi I, Jinnai K (1998). The distribution of neurons in the substantia nigra pars reticulata with input from the motor, premotor and prefrontal areas of the cerebral cortex in monkeys. Brain Res 784: 228–238.
Kolomiets BP, Deniau JM, Glowinski J, Thierry AM (2003). Basal ganglia and processing of cortical information: functional interactions between trans-striatal and trans-subthalamic circuits in the substantia nigra pars reticulata. Neuroscience 117: 931–938.
Kornhuber J (1984). The cortico-nigral projection: reduced glutamate content in the substantia nigra following frontal cortex ablation in the rat. Brain Res 322: 124–126.
Kunzle H (1978). An autoradiographic analysis of the efferent connections from premotor and adjacent prefrontal regions (areas 6 and 9) in macaca fascicularis. Brain Behav Evol 15: 185–234.
Laruelle M, Abi-Dargham A, van Dyck CH, Gil R, De Souza CD, Erdos J et al (1996). Single photon emission computerized tomography imaging of amphetamine-induced dopamine release in drug free schizophrenic subjects. Proc Natl Acad Sci USA 93: 9235–9240.
Leichnetz GR, Astruc J (1976). The efferent projections of the medial prefrontal cortex in the squirrel monkey (Saimiri sciureus). Brain Res 109: 455–472.
Manoach D, Press D, Thangaraj V, Searl M, Goff DC, Halpern E et al (1999). Schizophrenic subjects activate dorsolateral prefrontal cortex during a working memory task, as measured by fMRI. Biol Psychiatry 45: 1128–1137.
Manoach DS, Gollub RL, Benson ES, Searl MM, Goff DC, Halpern E et al (2000). Schizophrenic subjects show aberrant fMRI activation of dorsolateral prefrontal cortex and basal ganglia during working memory performance. Biol Psychiatry 48: 99–109.
Maurice N, Deniau JM, Glowinski J, Thierry AM (1999). Relationships between the prefrontal cortex and the basal ganglia in the rat: physiology of the cortico-nigral circuits. J Neurosci 19: 4674–4681.
McGeorge AJ, Faull RLM (1989). The organization of the projection from the cerebral cortex to the striatum in the rat. Neuroscience 29: 503–537.
Meissner W, Harnack D, Reese R, Paul G, Reum T, Ansorge M et al (2003). High-frequency stimulation of the subthalamic nucleus enhances striatal dopamine release and metabolism in rats. J Neurochem 85: 601–609.
Monakow KH, Akert K, Kunzle H (1978). Projections of the precentral motor cortex and other cortical areas of the frontal lobe to the subthalamic nucleus in the monkey. Exp Brain Res 33: 395–403.
Nambu A, Takada M, Inase M, Tokuno H (1996). Dual somatotopical representations in the primate subthalamic nucleus: evidence for ordered but reversed body-map transformations from the primary motor cortex and the supplimentary motor area. J Neurosci 16: 2671–2683.
Nambu A, Tokuno H, Inase M, Takada M (1997). Corticosubthalamic input zones from forelimb representations of the dorsal and ventral divisions of the premotor cortex in the macaque monkey: comparison with the input zones from the primary motor cortex and the supplementary motor area. Neurosci Lett 239: 13–16.
Öngür D, An X, Price JL (1998). Prefrontal cortical projections to the hypothalamus in macaque monkeys. J Comp Neurol 401: 480–505.
Paquet M, Tremblay M, Soghomonian J-J, Smith Y (1997). AMPA and NMDA glutamate receptor subunits in midbrain dopaminergic neurons in the squirrel monkey: an immunohistochemical and in situ hybridization study. J Neurosci 17: 1377–1396.
Parent A (1986). Comparative Neurobiology of the Basal Ganglia. John Wiley and Sons: New York.
Reep RL, Corwin JV, Hashimoto A, Watson RT (1984). Afferent connections of medial precentral cortex in the rat. Neurosci Lett 44: 247–252.
Rosales MG, Flores G, Hernandez S, Martinez-Fong D, Aceves J (1994). Activation of subthalamic neurons produces NMDA receptor-mediated dendritic dopamine release in substantia nigra pars reticulata: a microdialysis study in the rat. Brain Res 645: 335–337.
Seeman P, Lee T (1975). Antipsychotic drugs: direct correlation between clinical potency and presynaptic action on dopamine neurons. Science 188: 1217–1219.
Sesack SR, Carr DB (2002). Selective prefrontal cortex inputs to dopamine cells: implications for schizophrenia. Physiol Behav 77: 513–517.
Sesack SR, Deutch AY, Roth RH, Bunney BS (1989a). Topographical organization of the efferent projections of the medial prefrontal cortex in the rat: an anterograde tract-tracing study with Phaseolus vulgaris leucoagglutinin. J Comp Neurol 290: 213–242.
Sesack SR, Deutch AY, Roth RH, Bunney BS (1989b). Topographical organization of the efferent projections of the medial prefrontal cortex in the rat: an anterograde tract-tracing study with Phaseolus vulgaris leucoagglutinin. J Comp Neurol 290: 213–242.
Sesack SR, Pickel VM (1992a). Prefrontal cortical efferents in the rat synapse on unlabeled neuronal targets of catecholamine terminals in the nucleus accumbens septi and on dopamine neurons in the ventral tegmental area. J Comp Neurol 320: 145–160.
Sesack SR, Pickel VM (1992b). Prefrontal cortical efferents in the rat synapse on unlabled neuronal targets of catecholamine terminals in the nucleus accumbens septi and on dopamine neurons in the ventral tegmental area. J Comp Neurol 320: 145–160.
Smith Y, Hazrati L-N, Parent A (1990). Efferent projections of the subthalamic nucleus in the squirrel monkey as studied by the PHA-L anterograde tracing method. J Comp Neurol 294: 306–323.
Smith Y, Shink E, Sidibe M (1998). Neuronal circuitry and synaptic connectivity of the basal ganglia. Neurosurg Clin N Am 9: 203–222.
Takagishi M, Chiba T (1991). Efferent projections of the infralimbic (area 25) region of the medial prefrontal cortex in the rat: an anterograde tracer PHA-L study. Brain Res 566: 26–39.
Takahata R, Moghaddam B (2000). Target-specific glutamatergic regulation of dopamine neurons in the ventral tegmental area. J Neurochem 75: 1775–1778.
Van Eden CG, Lamme VA, Uylings HB (1992). Heterotopic cortical afferents to the medial prefrontal cortex in the rat. A combined retrograde and anterograde tracer study. Eur J Neurosci 4: 77–97.
Weinberger DR (1987). Implications of the normal brain development for the pathogenesis of schizophrenia. Arch Gen Psychiatry 44: 660–669.
Acknowledgements
We thank April Whitbeck and Brian Bouverat for their excellent technical assistance. This work was supported by the Lieber Center for Schizophrenia Research at Columbia University College of Physicians & Surgeons and MH45573 to SNH.
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Frankle, W., Laruelle, M. & Haber, S. Prefrontal Cortical Projections to the Midbrain in Primates: Evidence for a Sparse Connection. Neuropsychopharmacol 31, 1627–1636 (2006). https://doi.org/10.1038/sj.npp.1300990
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DOI: https://doi.org/10.1038/sj.npp.1300990
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