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Dorsolateral Prefrontal Cortex

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Structure

The dorsolateral prefrontal cortex (DLPFC) is located on the convexity of the prefrontal cortex, superior to orbital frontal cortex and anterior to the premotor cortex. Architectonically, it is composed of granular neurons distinct from the pyramidal cells of the adjacent motor cortex. The DLPFC includes at least Brodmann areas 9 and 46, the areas that are homologous to those surrounding the principal sulcus in lower primates, which have been shown to be important in working memory (WM) function (see below). Some researchers include other frontal zones in the DLPFC, including parts of Brodmann areas 8 through 12, 45, 46, and 47, though 44, 45, and 47/12 have also been characterized as ventrolateral prefrontal cortex (Diamond 2002).

Dendrites in the DLPFC reach full maturity by the age of 12 months, plateauing in length until at least age 27 years (Diamond 2002). Glucose metabolism also reaches adult levels by 12 months. However, synaptic density continues to decrease,...

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References and Reading

  • Abbruzzese, M., Ferri, S., & Scarone, S. (1995). Wisconsin Card Sorting Test performance in obsessive-compulsive disorder: No evidence for involvement of dorsolateral prefrontal cortex. Psychiatry Research, 58(1), 37–43.

    Article  PubMed  Google Scholar 

  • Altshuler, L., Bookheimer, S., Townsend, J., Proenza, M. A., Sabb, F., Mintz, J., et al. (2008). Regional brain changes in bipolar I depression: A functional magnetic resonance imaging study. Bipolar Disorders, 10(6), 708–717.

    Article  PubMed  PubMed Central  Google Scholar 

  • Basso, D., Lotze, M., Vitale, L., Ferreri, F., Bisiacchi, P., Olivetti Belardinelli, M., et al. (2006). The role of prefrontal cortex in visuo-spatial planning: A repetitive TMS study. Experimental Brain Research, 171(3), 411–415.

    Article  PubMed  Google Scholar 

  • Brooks, J. O., 3rd, Bonner, J. C., Rosen, A. C., Wang, P. W., Hoblyn, J. C., Hill, S. J., et al. (2009). Dorsolateral and dorsomedial prefrontal gray matter density changes associated with bipolar depression. Psychiatry Research, 172(3), 200–204.

    Article  PubMed  PubMed Central  Google Scholar 

  • Courtney, S. M., Ungerleider, L. G., Keil, K., & Haxby, J. V. (1996). Object and spatial visual working memory activate separate neural systems in human cortex. Cerebral Cortex, 6(1), 39–49.

    Article  PubMed  Google Scholar 

  • Cummings, J. L. (1994). Frontal-subcortical circuits and human behavior. Archives of Neurology, 8, 873–880.

    Google Scholar 

  • Dagher, A., Owen, A. M., Boecker, H., & Brooks, D. J. (1999). Mapping the network for planning: A correlational PET activation study with the Tower of London task. Brain, 122(Pt 10), 1973–1987.

    Article  PubMed  Google Scholar 

  • D’Esposito, M., Aguirre, G. K., Zarahn, E., Ballard, D., Shin, R. K., & Lease, J. (1998). Functional MRI studies of spatial and nonspatial working memory. Brain Research. Cognitive Brain Research, 7(1), 1–13.

    Article  PubMed  Google Scholar 

  • Diamond, A. (2002). Normal development of prefrontal cortex from birth to young adulthood: Cognitive functions, anatomy, and biochemistry. In D. T. K. Stuss & R. T. Knight (Eds.), Principles of frontal lobe function (pp. 466–503). New York: Oxford University Press.

    Chapter  Google Scholar 

  • Friston, K. J., Frith, C. D., Liddle, P. F., & Frackowiak, R. S. (1991). Investigating a network model of word generation with positron emission tomography. Proceedings of the Biological Sciences, 244(1310), 101–106.

    Article  Google Scholar 

  • Gansler, D. A., Fucetola, R., Krengel, M., Stetson, S., Zimering, R., & Makary, C. (1998). Are there cognitive subtypes in adult attention deficit/hyperactivity disorder? Journal of Nervous and Mental Disease, 186(12), 776–781.

    Article  Google Scholar 

  • Goghari, V. M., Sponheim, S. R., & MacDonald, A. W., 3rd. (2010). The functional neuroanatomy of symptom dimensions in schizophrenia: A qualitative and quantitative review of a persistent question. Neuroscience and Biobehavioral Reviews, 34(3), 468–486.

    Article  PubMed  Google Scholar 

  • Goldman-Rakic, P. S., & Leung, H.-C. (2002). Functional architecture of the dorsolateral prefrontal cortex. In D. T. K. Stuss & R. T. Knight (Eds.), Principles of frontal lobe function (pp. 85–95). New York: Oxford University Press.

    Chapter  Google Scholar 

  • Hassel, S., Almeida, J. R., Kerr, N., Nau, S., Ladouceur, C. D., Fissell, K., et al. (2008). Elevated striatal and decreased dorsolateral prefrontal cortical activity in response to emotional stimuli in euthymic bipolar disorder: No associations with psychotropic medication load. Bipolar Disorders, 10(8), 916–927.

    Article  PubMed  PubMed Central  Google Scholar 

  • Jaracz, J. (2008). The anatomy of depression in light of evidence from neuroimaging studies. Psychiatria Polska, 42(6), 875–888.

    PubMed  Google Scholar 

  • Jones-Gottman, M., & Milner, B. (1977). Design fluency: The invention of non-sense drawings after focal cortical lesions. Neuropsychologia, 15, 653–674.

    Article  Google Scholar 

  • Koenigs, M., & Grafman, J. (2009). The functional neuroanatomy of depression: Distinct roles for ventromedial and dorsolateral prefrontal cortex. Behavioural Brain Research, 201(2), 239–243.

    Article  PubMed  PubMed Central  Google Scholar 

  • Kondo, H., Osaka, N., & Osaka, M. (2004). Cooperation of the anterior cingulate cortex and dorsolateral prefrontal cortex for attention shifting. NeuroImage, 23(2), 670–679.

    Article  PubMed  Google Scholar 

  • Kostopoulos, P., & Petrides, M. (2003). The mid-ventrolateral prefrontal cortex: Insights into its role in memory retrieval. European Journal of Neuroscience, 17(7), 1489–1497.

    Article  Google Scholar 

  • Kumari, V., Peters, E. R., Fannon, D., Antonova, E., Premkumar, P., Anilkumar, A. P., et al. (2009). Dorsolateral prefrontal cortex activity predicts responsiveness to cognitive-behavioral therapy in schizophrenia. Biological Psychiatry, 66(6), 594–602.

    Article  PubMed  PubMed Central  Google Scholar 

  • Malloy, P., & Duffy, J. (1994). The frontal lobes in neuropsychiatric disorders. In F. Boller, D. P. Salmon, & J. M. Hamilton (Eds.), Handbook of neuropsychology. New York: Elsevier.

    Google Scholar 

  • Manoach, D. S., Gollub, R. L., Benson, E. S., Searl, M. M., Goff, D. C., Halpern, E., et al. (2000). Schizophrenic subjects show aberrant fMRI activation of dorsolateral prefrontal cortex and basal ganglia during working memory performance. Biological Psychiatry, 48(2), 99–109.

    Article  PubMed  Google Scholar 

  • McLaughlin, N. C. R., Moore, D. W., Fulwiler, C., Bhadelia, R., & Gansler, D. A. (2009). Differential contributions of lateral prefrontal cortex regions to visual memory processes. Brain Imaging and Behavior, 3(2), 202–211.

    Article  Google Scholar 

  • Nakao, T., Nakagawa, A., Nakatani, E., Nabeyama, M., Sanematsu, H., Yoshiura, T., et al. (2009). Working memory dysfunction in obsessive-compulsive disorder: A neuropsychological and functional MRI study. Journal of Psychiatric Research, 43(8), 784–791.

    Article  PubMed  Google Scholar 

  • Petrides, M. (1994). Frontal lobes and behaviour. Current Opinion in Neurobiology, 4(2), 207–211.

    Article  PubMed  Google Scholar 

  • Petrides, M. (2000). Dissociable roles of mid-dorsolateral prefrontal and anterior inferotemporal cortex in visual working memory. Journal of Neuroscience, 20(19), 7496–7503.

    Article  PubMed  Google Scholar 

  • Potkin, S. G., Turner, J. A., Brown, G. G., McCarthy, G., Greve, D. N., Glover, G. H., et al. (2009). Working memory and DLPFC inefficiency in schizophrenia: The FBIRN study. Schizophrenia Bulletin, 35(1), 19–31.

    Article  PubMed  Google Scholar 

  • Rao, S. C., Rainer, G., & Miller, E. K. (1997). Integration of what and where in the primate prefrontal cortex. Science, 276(5313), 821–824.

    Article  PubMed  Google Scholar 

  • Ravizza, S. M., & Carter, C. S. (2008). Shifting set about task switching: Behavioral and neural evidence for distinct forms of cognitive flexibility. Neuropsychologia, 46(12), 2924–2935.

    Article  PubMed  PubMed Central  Google Scholar 

  • Ruff, R. M., Allen, C. C., Farrow, C. E., Niemann, H., & Wylie, T. (1994). Figural fluency: Differential impairment in patients with left versus right frontal lobe lesions. Archives of Clinical Neuropsychology, 9(1), 41–55.

    Article  PubMed  Google Scholar 

  • Saint-Cyr, J. A., Bronstein, Y. L., & Cummings, J. L. (2002). Neurobehavioral consequences of neurosurgical treatments and focal lesions of frontal-subcortical circuits. In D. T. K. Stuss & R. T. Knight (Eds.), Principles of frontal lobe function (pp. 408–427). New York: Oxford University Press.

    Chapter  Google Scholar 

  • Seidman, L. J., Valera, E. M., Makris, N., Monuteaux, M. C., Boriel, D. L., Kelkar, K., et al. (2006). Dorsolateral prefrontal and anterior cingulate cortex volumetric abnormalities in adults with attention-deficit/hyperactivity disorder identified by magnetic resonance imaging. Biological Psychiatry, 60(10), 1071–1080.

    Article  PubMed  Google Scholar 

  • Shafritz, K. M., Kartheiser, P., & Belger, A. (2005). Dissociation of neural systems mediating shifts in behavioral response and cognitive set. NeuroImage, 25(2), 600–606.

    Article  PubMed  Google Scholar 

  • Stuss, D. T., Alexander, M. P., Hamer, L., Palumbo, C., Dempster, R., Binns, M., et al. (1998). The effects of focal anterior and posterior brain lesions on verbal fluency. Journal of the International Neuropsychological Society, 4(3), 265–278.

    PubMed  Google Scholar 

  • Stuss, D. T., Alexander, M. P., Floden, D., Binns, M. A., Levine, B., McIntosh, A. R., et al. (2002). Fractionation and localization of distinct frontal lobe processes: Evidence from focal lesions in humans. In D. T. K. Stuss & R. T. Knight (Eds.), Principles of frontal lobe function. New York: Oxford University Press.

    Chapter  Google Scholar 

  • van den Heuvel, O. A., Remijnse, P. L., Mataix-Cols, D., Vrenken, H., Groenewegen, H. J., Uylings, H. B., et al. (2009). The major symptom dimensions of obsessive-compulsive disorder are mediated by partially distinct neural systems. Brain, 132(Pt 4), 853–868.

    PubMed  Google Scholar 

  • Weinberger, D. R., Berman, K. F., & Zec, R. F. (1986). Physiologic dysfunction of dorsolateral prefrontal cortex in schizophrenia. I. Regional cerebral blood flow evidence. Archives of General Psychiatry, 43(2), 114–124.

    Article  PubMed  Google Scholar 

  • Yeo, R. A., Hill, D. E., Campbell, R. A., Vigil, J., Petropoulos, H., Hart, B., et al. (2003). Proton magnetic resonance spectroscopy investigation of the right frontal lobe in children with attention-deficit/hyperactivity disorder. Journal of the American Academy of Child and Adolescent Psychiatry, 42(3), 303–310.

    Article  PubMed  Google Scholar 

  • Yurgelun-Todd, D. A., Gruber, S. A., Kanayama, G., Killgore, W. D., Baird, A. A., & Young, A. D. (2000). fMRI during affect discrimination in bipolar affective disorder. Bipolar Disorders, 2(3 Pt 2), 237–248.

    Article  PubMed  Google Scholar 

  • Zamboni, G., Huey, E. D., Krueger, F., Nichelli, P. F., & Grafman, J. (2008). Apathy and disinhibition in frontotemporal dementia: Insights into their neural correlates. Neurology, 71(10), 736–742.

    Article  PubMed  PubMed Central  Google Scholar 

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Correspondence to Nicole C. R. McLaughlin .

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McLaughlin, N.C.R., Malloy, P. (2018). Dorsolateral Prefrontal Cortex. In: Kreutzer, J.S., DeLuca, J., Caplan, B. (eds) Encyclopedia of Clinical Neuropsychology. Springer, Cham. https://doi.org/10.1007/978-3-319-57111-9_1887

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