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GENERAL COMMENTARY article

Front. Hum. Neurosci., 18 July 2017
Sec. Brain Imaging and Stimulation
Volume 11 - 2017 | https://doi.org/10.3389/fnhum.2017.00372

Commentary: Deficient approaches to human neuroimaging

  • Department of Biology and Psychology, University of Victoria, Victoria, BC, Canada

A commentary on
Deficient approaches to human neuroimaging

by Stelzer, J., Lohmann, G., Mueller, K., Buschmann, T., and Turner, R. (2014). Front. Hum. Neurosci. 8:462. doi: 10.3389/fnhum.2014.00462

The current pursuit of neuroscientist has seemingly and unendingly been to “localize function” and to attribute certain cognitive and behavioral activities with specific locations in the brain. Various neuroscientists have attempted to articulate this with regards to neuroimaging techniques such as one by Stelzer et al. (2014). To an extent, there has been innumerable successes in this field of research which are evident by the current advances in neuropharmalogical advances in treatments for psychiatric and neurological disorders (Arango, 2015; Millan et al., 2015). However, more recent research on localization of function has shown the ambiguity of functions as they pertain to specific brain areas, and while some areas remain attributed to one or two functions only, other areas have been attributed to multiple cognitive and behavioral processes. For instance, the anterior cingulate cortex (ACC), has been attributed to so many different cognitive functions that it seems absurd for the human brain to need any other brain area for its day to day function other than the ACC. Depression has been correlated with lower activity of the ACC (Artigas, 2015), while others have attributed its function to working memory, conflict monitoring, self-maintenance and self-monitoring (Botvinick et al., 2001, 2004; Schnur et al., 2009; Obeso et al., 2010; Melloni et al., 2012; Fonville et al., 2015). Personality differences among individuals along with neuroeconomical and emotional processing has also been associated to the ACC (Etkin et al., 2006, 2011; Gasquoine, 2013; Kurzban et al., 2013). Most recently research has tied the presence of mood disorders to reductions in gray matter in the ACC among other frontal lobe areas (Drevets, 2007). Meanwhile, the altered activity of the angular cingulate cortex, in which the rostral areas are more active and the dorsal areas are less so compared to control groups, were attributed to obsessive compulsive disorders (Cavanagh et al., 2010). Lastly, ACC has also been attributed to intentional decision making, with increased activation during intentional planning of actions, and attentional circuitry (Isoda and Noritake, 2013; van Veen and Carter, 2016).

The several functions of the ACC stated above, don't come close to the number of functions that have been attributed to the ACC. Clearly, it would be plausible for some of these functions to be part of what the ACC does, however, these functions should be attributed to different brain circuits, instead of being solely implicated on specific brain areas. The basal ganglia (BG) is another example of possible areas that have been implicated and has been attributed to multiple different functions. For instance, the basal ganglia has been attributed to movement disorders, including Parkinson's, Huntington's, and dyskinesia (Aron and Poldrack, 2005; Stoessl, 2012; Maurice et al., 2015). BG has also been attributed to memory, movement memory, planning of action, and the initiation of movement (Menon et al., 2000; Monchi et al., 2006; Vitay and Hamker, 2009; Nakayama et al., 2010; Fermin et al., 2016). BG has also been proven to be responsible for motivation and implicated in many addictive behaviors and disorders (Haber, 2008; Gaznick et al., 2014). Once again, there is a whole array of possibilities with multiple functions being attributed to this one area of the brain, which while it is possible for the BG to be responsible for these functions, it is highly unlikely for it to be the only structure that is involved in these cognitive and behavioral processes.

For areas such as the ACC and the BG, extensive circuitry studies and systematic interactions are very scarce. Both the ACC and the BG have been attributed to specific areas of the prefrontal and frontal cortex (respectively) (Luerding et al., 2008; Novak et al., 2015) but not to an extent where cohesive systems to be constructed and for models to be crafted for the explaining of such systems. The localization of functions to specific areas of the brain is only useful to the extent that it allows for understanding what circuits a structure is a part of, but such findings are treated as if the functions attributed to specific brain areas only belong to them and them alone. This distinction will perhaps be negligible for many, but the route to determining localization of function is through the understanding of the circuits and the functions of the individual structures in those circuits. Without understanding the circuits, the functions the individual structures serve will not be precise and will not provide a cohesive understanding of the human brain as an organ.

Author Contributions

The author confirms being the sole contributor of this work and approved it for publication.

Conflict of Interest Statement

The author declares that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

References

Arango, C. (2015). Present and future of developmental neuropsychopharmacology. Eur. Neuropsychopharmacol. 25, 703–712. doi: 10.1016/j.euroneuro.2014.11.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Aron, A. R., and Poldrack, R. A. (2005). The cognitive neuroscience of response inhibition: relevance for genetic research in attention-deficit/hyperactivity disorder. Biol. Psychiatry 57, 1285–1292. doi: 10.1016/j.biopsych.2004.10.026

PubMed Abstract | CrossRef Full Text | Google Scholar

Artigas, F. (2015). Developments in the field of antidepressants, where do we go now? Eur. Neuropsychopharmacol. 25, 657–670. doi: 10.1016/j.euroneuro.2013.04.013

PubMed Abstract | CrossRef Full Text | Google Scholar

Botvinick, M. M., Cohen, J. D., and Carter, C. S. (2004). Conflict monitoring and anterior cingulate cortex: an update. Trends Cogn. Sci. 8, 539–546. doi: 10.1016/j.tics.2004.10.003

PubMed Abstract | CrossRef Full Text | Google Scholar

Botvinick, M., Braver, T., and Barch, D. (2001). Conflict monitoring and cognitive control. Psychol. Rev. 108, 624–652. doi: 10.1037/0033-295X.108.3.624

PubMed Abstract | CrossRef Full Text | Google Scholar

Cavanagh, J. F., Gründler, T. O. J., Frank, M. J., and Allen, J. J. B. (2010). Altered cingulate sub-region activation accounts for task-related dissociation in ERN amplitude as a function of obsessive-compulsive symptoms. Neuropsychologia 48, 2098–2109. doi: 10.1016/j.neuropsychologia.2010.03.031

PubMed Abstract | CrossRef Full Text | Google Scholar

Drevets, W. C. (2007). Orbitofrontal cortex function and structure in depression. Ann. N. Y. Acad. Sci. 1121, 499–527. doi: 10.1196/annals.1401.029

PubMed Abstract | CrossRef Full Text | Google Scholar

Etkin, A., Egner, T., and Kalisch, R. (2011). Emotional processing in anterior cingulate and medial prefrontal cortex. Trends Cogn. Sci. 15, 85–93. doi: 10.1016/j.tics.2010.11.004

PubMed Abstract | CrossRef Full Text | Google Scholar

Etkin, A., Egner, T., Peraza, D. M., Kandel, E. R., and Hirsch, J. (2006). Resolving emotional conflict: a role for the rostral anterior cingulate cortex in modulating activity in the amygdala. Neuron 51, 871–882. doi: 10.1016/j.neuron.2006.07.029

PubMed Abstract | CrossRef Full Text | Google Scholar

Fermin, A. S. R., Yoshida, T., Yoshimoto, J., Ito, M., Tanaka, S. C., and Doya, K. (2016). Model-based action planning involves cortico-cerebellar and basal ganglia networks. Sci. Rep. 6:31378. doi: 10.1038/srep31378

PubMed Abstract | CrossRef Full Text | Google Scholar

Fonville, L., Cohen Kadosh, K., Drakesmith, M., Dutt, A., Zammit, S., Mollon, J., et al. (2015). Psychotic experiences, working memory, and the developing brain: a multimodal neuroimaging study. Cereb. Cortex 25, 4828–4838. doi: 10.1093/cercor/bhv181

PubMed Abstract | CrossRef Full Text | Google Scholar

Gasquoine, P. G. (2013). Localization of function in anterior cingulate cortex: from psychosurgery to functional neuroimaging. Neurosci. Biobehav. Rev. 37, 340–348. doi: 10.1016/j.neubiorev.2013.01.002

PubMed Abstract | CrossRef Full Text | Google Scholar

Gaznick, N., Tranel, D., McNutt, A., and Bechara, A. (2014). Basal ganglia plus insula damage yields stronger disruption of smoking addiction than basal ganglia damage alone. Nicotine Tob. Res. 16, 445–453. doi: 10.1093/ntr/ntt172

PubMed Abstract | CrossRef Full Text | Google Scholar

Haber, S. (2008). Parallel and integrative processing through the basal ganglia reward circuit: lessons from addiction. Biol. Psychiatry 64, 173–174. doi: 10.1016/j.biopsych.2008.05.033

PubMed Abstract | CrossRef Full Text

Isoda, M., and Noritake, A. (2013). What makes the dorsomedial frontal cortex active during reading the mental states of others? Front. Neurosci. 7:232. doi: 10.3389/fnins.2013.00232

PubMed Abstract | CrossRef Full Text | Google Scholar

Kurzban, R., Duckworth, A., Kable, J. W., and Myers, J. (2013). An opportunity cost model of subjective effort and task performance. Behav. Brain Sci. 36, 661–679. doi: 10.1017/S0140525X12003196

PubMed Abstract | CrossRef Full Text | Google Scholar

Luerding, R., Weigand, T., Bogdahn, U., and Schmidt-Wilcke, T. (2008). Working memory performance is correlated with local brain morphology in the medial frontal and anterior cingulate cortex in fibromyalgia patients: structural correlates of pain-cognition interaction. Brain 131, 3222–3231. doi: 10.1093/brain/awn229

PubMed Abstract | CrossRef Full Text | Google Scholar

Maurice, N., Liberge, M., Jaouen, F., Ztaou, S., Hanini, M., Camon, J., et al. (2015). Striatal cholinergic interneurons control motor behavior and basal ganglia function in experimental parkinsonism. Cell Rep. 13, 657–666. doi: 10.1016/j.celrep.2015.09.034

PubMed Abstract | CrossRef Full Text | Google Scholar

Melloni, M., Urbistondo, C., Sedeño, L., Gelormini, C., Kichic, R., and Ibanez, A. (2012). The extended fronto-striatal model of obsessive compulsive disorder: convergence from event-related potentials, neuropsychology and neuroimaging. Front. Hum. Neurosci. 6:259. doi: 10.3389/fnhum.2012.00259

PubMed Abstract | CrossRef Full Text | Google Scholar

Menon, V., Anagnoson, R. T., Glover, G. H., and Pfefferbaum, A. (2000). Basal ganglia involvement in memory-guided movement sequencing. Neuroreport 11, 3641–3645. doi: 10.1097/00001756-200011090-00048

PubMed Abstract | CrossRef Full Text | Google Scholar

Millan, M. J., Goodwin, G. M., Meyer-Lindenberg, A., and Ogren, S. O. (2015). 60 Years of advances in neuropsychopharmacology for improving brain health, renewed hope for progress. Eur. Neuropsychopharmacol. 25, 591–598. doi: 10.1016/j.euroneuro.2015.01.015

PubMed Abstract | CrossRef Full Text | Google Scholar

Monchi, O., Petrides, M., Strafella, A. P., Worsley, K. J., and Doyon, J. (2006). Functional role of the basal ganglia in the planning and execution of actions. Ann. Neurol. 59, 257–264. doi: 10.1002/ana.20742

PubMed Abstract | CrossRef Full Text | Google Scholar

Nakayama, Y., Yamagata, T., Arimura, N., Tanji, J., and Hoshi, E. (2010). Comparison of movement-related neuronal activity recorded from six different areas in the frontal cortex of macaques. Neurosci. Res. 68:e265. doi: 10.1016/j.neures.2010.07.1175

CrossRef Full Text | Google Scholar

Novak, M. J. U., Seunarine, K. K., Gibbard, C. R., Mccolgan, P., Draganski, B., Friston, K., et al. (2015). Basal ganglia-cortical structural connectivity in Huntington's disease. Hum. Brain Mapp. 36, 1728–1740. doi: 10.1002/hbm.22733

PubMed Abstract | CrossRef Full Text | Google Scholar

Obeso, J. A., Rodriguez-Oroz, M. C., Lanciego, J. L., and Rodriguez Diaz, M. (2010). How does Parkinson's disease begin? The role of compensatory mechanisms. Neuron 31, 1–11. doi: 10.1038/nature12373

CrossRef Full Text | Google Scholar

Schnur, T. T., Schwartz, M. F., Kimberg, D. Y., Hirshorn, E., Coslett, H. B., and Thompson-Schill, S. L. (2009). Localizing interference during naming: convergent neuroimaging and neuropsychological evidence for the function of broca's area. Proc. Natl. Acad. Sci. U.S.A. 106, 322–327. doi: 10.1073/pnas.0805874106

PubMed Abstract | CrossRef Full Text | Google Scholar

Stelzer, J., Lohmann, G., Mueller, K., Buschmann, T., and Turner, R. (2014). Deficient approaches to human neuroimaging. Front. Hum. Neurosci. 8:462. doi: 10.3389/fnhum.2014.00462

PubMed Abstract | CrossRef Full Text | Google Scholar

Stoessl, A. J. (2012). Neuroimaging in Parkinson's disease: from pathology to diagnosis. Parkinsonism Relat. Disord. 18, S55–S59. doi: 10.1016/S1353-8020(11)70019-0

PubMed Abstract | CrossRef Full Text | Google Scholar

van Veen, V., and Carter, C. S. (2016). The anterior cingulated as a conflict monitor : fMRI and ERP studies. Physiol. Behav. 77, 477–482. doi: 10.1016/S0031-9384(02)00930-7

PubMed Abstract | CrossRef Full Text

Vitay, J., and Hamker, F. (2009). Basal ganglia and memory retrieval during delayed match-to-sample and non-match-to-sample tasks. BMC Neurosci. 10:P162. doi: 10.1186/1471-2202-10-S1-P162

CrossRef Full Text | Google Scholar

Keywords: localization of function, neural networks, neural circuits and behavior, basal Ganglia, anterior cingulate cortex

Citation: Bayati A (2017) Commentary: Deficient approaches to human neuroimaging. Front. Hum. Neurosci. 11:372. doi: 10.3389/fnhum.2017.00372

Received: 24 May 2017; Accepted: 03 July 2017;
Published: 18 July 2017.

Edited by:

Stephane Perrey, Université de Montpellier, France

Reviewed by:

Hidenao Fukuyama, Kyoto University, Japan

Copyright © 2017 Bayati. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

*Correspondence: Armin Bayati, arminbay@uvic.ca

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