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OPINION article

Front. Neuroanat., 03 May 2024

Of artificial intelligence, machine learning, and the human brain. Celebrating Miklos Palkovits' 90th birthday

  • Department of Anatomy, Physiology and Genetics, Uniformed Services University, Bethesda, MD, United States

The promises and challenges of artificial intelligence (AI), machine learning (ML), and deep learning (DL) are based on the premise that we can build machines and write algorithms that will mimic and even surpass the capacity and capabilities of the human brain (Alzubaidi et al., 2021). AI uses artificial neural networks (ANNs) that intend to mimic the works of the neural networks of the human brain. In AI, the strength of the connection of each “neuron” to its “neighbor” is a parameter known as “weight”. The network starts with random “weights” and adjusts them until the output agrees with the correct answer during the “training,” which includes “reading” huge volumes of the text in which some words are masked and then “asking” the network to “guess” what those masked words are. Using over 3 billion words, the network “learns” what the masked words are (Jain et al., 1996). By comparison, an average child requires 3,000 times fewer words to learn and speak a language (Saenko, 2020). It should be noted, however, that a child needs much longer time, ~4 to 5 years to learn ~3,000 words. Regardless of this, as illustrated by generative AI, e.g., ChatGPT and Google's Bard, such “brute force” works well for certain brain functions, i.e., storing and analyzing and finding correlations in massive amounts of existing data (Polyportis and Pahos, 2024).

The current AI comes, however, with caveats. One is the abovementioned inefficiency of ANNs—even a large language model (LLM)—to “learn.” The other one is the currently limited ability of AI for intuition and creativity as compared to the human brain. This is despite the landmark 2016 victory of Google's AlphaGo that beat the South Korean Go champion, Lee Se-dol (Metz, 2016). A third and critical issue is the enormous energy required by generative AI (Saenko, 2020; de Vries, 2023). Training an ANN, i.e., reading through vast amounts of data until the system “understands it,” needs electricity that can be as much as a small country's electricity consumption. Currently, ~2% of the total and global electricity production is used by data centers. In addition, this is only the very beginning of AI. With the predicted growth of AI—assessed by counting the annual rate of increase in chip production, e.g., by NVIDIA—electricity demand for AI will increase dramatically. By some estimates, the global electricity demand for AI and related computing can increase by 85–134 TWh annually. Such an increase in electricity demand is similar to that in Sweden, which doubles its electricity consumption yearly (de Vries, 2023). The effect of such an increase in electricity demand on the “carbon footprint” with the current mix of electric power generation (natural gas: 38%; coal: 22%; nuclear: 19%; renewables: 20%; hydroelectric 6%) can be alarmingly high (Dhar, 2020; Heikkilä, 2023). For example, creating GPT-3 needs 1,287 MWh of electricity with an added 552 tons of CO2–or equivalent—and this is before any user has started any queries (Patterson et al., 2021). It is no surprise then that Microsoft has been interested—and has invested—in nuclear power generation, especially in small modular reactors (SMRs) that will not increase the carbon footprint (McFadden, 2023). Microsoft has also invested in Helion—a Sam Altman-backed company—that plans to generate electricity using futuristic, nuclear fusion-based power (Gardner, 2023).

We compare the massive hunger for energy by AI with that of the human brain. While it is hard to calculate the exact energy required by the human brain for its various functions including information processing and analysis, it is clearly only an insignificant fraction of that of AI. In 1989, Ralph Merkle published his study “Energy Limits to the Computational Power of the Human Brain” (Merkle, 1989). He estimated that the human brain uses only ~10 W of energy per second. However, he also estimated that the “computational power” of the human brain is limited to ~1013 to 1016 operations per second. Regardless of the exact energy “consumption” of the human brain per operation, which is rather challenging to determine even with magnetic resonance spectroscopy (MRS) and functional magnetic resonance spectroscopy (fMRS) (Rothman et al., 2011, 2019; Hyder and Rothman, 2012), the notion that the human brain is using less energy when compared to AI is hard to contest (Hughes, 2023).

A potential cue for such a highly energy-efficient “operation” may be the “wiring”; neuronal connectivity is a critical but not the only aspect of how the human brain operates (Gebicke-Haerter, 2023). In contrast to the computers— and thus AI's—binary modus operandi, the human brain is an incredibly complex “machine” using both analog and digital modes simultaneously (Guidolin et al., 2022; Marcoli et al., 2022). The seamless integration and utilization of digital and analog “modes” are likely the “secret” to the unparalleled capacity and abilities of the human brain. Its “operation” is not restricted to binary signaling but to a highly sophisticated and complex combination of electrical and chemical signaling within the networks. The dozens of neurotransmitters and neuromodulators along with their receptors, ion channels, and intracellular “effectors” promote the fact that the human brain is such an incredibly energy-efficient “computer.” In addition, neurons can use more than one neurotransmitter (Svensson et al., 2018), integrating various signaling modalities (e.g., Agoston et al., 1988, 1994). Knowledge of the neurotransmitters and neuromodulators utilized by various human brain regions and neuronal pathways—the chemical neuroanatomy—is fundamental to our understanding of how the human brain operates in health and the chemical changes underlying neuropsychiatric disorders (Hokfelt et al., 1984).

Miklos Palkovits has made an enormous contribution to this field. Miklos, along with Tomas Hokfelt, another significant contributor to the field of chemical neuroanatomy (Hokfelt, 2010) along with other giants of neuroscience—Kjell Fuxe (e.g., Steinbusch, 1981; Rakic, 1988; Sawchenko, 1998; Greengard, 2001; Agnati et al., 2011; Saper and Fuller, 2017; Swanson, 2018) to name a few—have majorly contributed to the “chemical mapping” of the human brain, thus helping us understand its majesty—and mysteries. The Handbook of Chemical Neuroanatomy, first published by editors Bjorklund and Hokfelt in 1983 has reached 22 volumes (Bjorklund and Hokfelt, 1996).

While celebrating Miklos' 80th birthday, 10 years ago, I wrote a short article entitled: “Great insight created by tiny holes; celebrating 40 years of brain micropunch technique” (Agoston, 2014) that summarized his immense contribution to neuroanatomy—up to December 2013. By 2013, Miklos had published more than 1,000 research papers—many of his papers are citation classics, 59 book chapters, and eight books, nominated twice for the Nobel prize. Ten years later, in December 2023, I had the honor of attending Miklos' 90th birthday celebration just to learn about his current and—yes—future projects. During the last 10 years, Miklos has published 57 peer-reviewed papers, numerous book chapters, and reviews and has written and constantly updated his book Practical Neurology and Neuroanatomy (co-written with Dr. S. Komoly) with the newest neuroimaging and neurophysiology findings.

Miklos' current research working with collaborators across the globe includes the characterization of the human brain (g)lymphatic system (Mezey and Palkovits, 2015; Mezey et al., 2021), identifying SARS-CoV-2 entry sites into the human brain (Vitale-Cross et al., 2022), identifying the role of neuropeptides and their signaling in neuropsychiatric disorders (Barde et al., 2016, 2024; Hökfelt et al., 2018; Zhong et al., 2022; Samardžija et al., 2023; Vas et al., 2023), and neurogenetics (Roy et al., 2017; Dóra et al., 2022; Hardwick et al., 2022).

The last decade of neuroscience research utilizing powerful imaging, electrophysiology, and such techniques has greatly expanded our knowledge; however, we are still far from a complete understanding of how the human brain works. What are the neurobiological, neuroanatomical, and chemical substrates of consciousness, inspiration, and intuition? What we do know is that Miklos' work has been paving the way toward a better understanding of the marvel, the human brain.

Miklós, thank you for teaching and inspiring so many of us, happy (belated) 90th birthday, and I am so much looking forward to learning much more from you!

Author contributions

DA: Writing – review & editing, Writing – original draft.

Funding

The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.

Acknowledgments

I thank Mr. Balint Tapai for the discussions about AI and ML.

Conflict of interest

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.

The author[s] declared that they were an editorial board member of Frontiers, at the time of submission. This had no impact on the peer review process and the final decision.

Publisher's note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

References

Agnati, L. F., Barlow, P. W., Baluška, F., Tonin, P., Guescini, M., Leo, G., et al. (2011). A new theoretical approach to the functional meaning of sleep and dreaming in humans based on the maintenance of 'predictive psychic homeostasis'. Commun. Integr. Biol. 4, 640–654. doi: 10.4161/cib.17602

PubMed Abstract | Crossref Full Text | Google Scholar

Agoston, D. V. (2014). Great insight created by tiny holes; celebrating 40 years of brain micropunch technique. Front. Neuroanat. 8:61. doi: 10.3389/fnana.2014.00061

PubMed Abstract | Crossref Full Text | Google Scholar

Agoston, D. V., Conlon, J. M., and Whittaker, V. P. (1988). Selective depletion of the acetylcholine and vasoactive intestinal polypeptide of the guinea-pig myenteric plexus by differential mobilization of distinct transmitter pools. Exp. Brain Res. 72, 535–542. doi: 10.1007/BF00250599

PubMed Abstract | Crossref Full Text | Google Scholar

Agoston, D. V., Komoly, S., and Palkovits, M. (1994). Selective up-regulation of neuropeptide synthesis by blocking the neuronal activity: galanin expression in septohippocampal neurons. Exp. Neurol. 126, 247–255. doi: 10.1006/exnr.1994.1062

PubMed Abstract | Crossref Full Text | Google Scholar

Alzubaidi, L., Zhang, J., Humaidi, A. J., Al-Dujaili, A., Duan, Y., Al-Shamma, O., et al. (2021). Review of deep learning: concepts, CNN architectures, challenges, applications, future directions. J. Big Data 8:53. doi: 10.1186/s40537-021-00444-8

PubMed Abstract | Crossref Full Text | Google Scholar

Barde, S., Aguila, J., Zhong, W., Solarz, A., Mei, I., Prud'homme, J., et al. (2024). Substance P, NPY, CCK and their receptors in five brain regions in major depressive disorder with transcriptomic analysis of locus coeruleus neurons. Eur. Neuropsychopharmacol. 78, 54–63. doi: 10.1016/j.euroneuro.2023.09.004

PubMed Abstract | Crossref Full Text | Google Scholar

Barde, S., Rüegg, J., Prud'homme, J., Ekström, T. J., Palkovits, M., Turecki, G., et al. (2016). Alterations in the neuropeptide galanin system in major depressive disorder involve levels of transcripts, methylation, and peptide. Proc. Natl. Acad. Sci. U. S. A. 113, E8472–e8481. doi: 10.1073/pnas.1617824113

PubMed Abstract | Crossref Full Text | Google Scholar

Bjorklund, A., and Hokfelt, T. (1996). Handbook of Chemical Neuroanatomy. Amsterdam: Elsevier.

Google Scholar

de Vries, A. (2023). The growing energy footprint of artificial intelligence. Joule 7, 2191–2194. doi: 10.1016/j.joule.2023.09.004

Crossref Full Text | Google Scholar

Dhar, P. (2020). The carbon impact of artificial intelligence. Nat. Mach. Intell. 2, 423–425. doi: 10.1038/s42256-020-0219-9

Crossref Full Text | Google Scholar

Dóra, F., Renner, É., Keller, D., Palkovits, M., and Dobolyi, Á. (2022). Transcriptome profiling of the dorsomedial prefrontal cortex in suicide victims. Int. J. Mol. Sci. 23. doi: 10.3390/ijms23137067

PubMed Abstract | Crossref Full Text | Google Scholar

Gardner, T. (2023). Microsoft Signs Power Purchase Deal With Nuclear Fusion Company Helion. Reuters.

Google Scholar

Gebicke-Haerter, P. J. (2023). The computational power of the human brain. Front. Cell. Neurosci. 17:1220030. doi: 10.3389/fncel.2023.1220030

PubMed Abstract | Crossref Full Text | Google Scholar

Greengard, P. (2001). The neurobiology of slow synaptic transmission. Science 294, 1024–1030. doi: 10.1126/science.294.5544.1024

PubMed Abstract | Crossref Full Text | Google Scholar

Guidolin, D., Tortorella, C., Marcoli, M., Maura, G., and Agnati, L. F. (2022). Intercellular communication in the central nervous system as deduced by chemical neuroanatomy and quantitative analysis of images: impact on neuropharmacology. Int. J. Mol. Sci. 23. doi: 10.3390/ijms23105805

PubMed Abstract | Crossref Full Text | Google Scholar

Hardwick, S. A., Hu, W., Joglekar, A., Fan, L., Collier, P. G., Foord, C., et al. (2022). Single-nuclei isoform RNA sequencing unlocks barcoded exon connectivity in frozen brain tissue. Nat. Biotechnol. 40, 1082–1092. doi: 10.1038/s41587-022-01231-3

PubMed Abstract | Crossref Full Text | Google Scholar

Heikkilä, M. (2023). AI's carbon footprint is bigger than you think. MIT Technology Review.

Google Scholar

Hokfelt, T. (2010). Looking at neurotransmitters in the microscope. Prog. Neurobiol. 90, 101–118. doi: 10.1016/j.pneurobio.2009.10.005

PubMed Abstract | Crossref Full Text | Google Scholar

Hökfelt, T., Barde, S., Xu, Z. D., Kuteeva, E., Rüegg, J., Le Maitre, E., et al. (2018). Neuropeptide and small transmitter coexistence: fundamental studies and relevance to mental illness. Front. Neural Circ. 12:106. doi: 10.3389/fncir.2018.00106

PubMed Abstract | Crossref Full Text | Google Scholar

Hokfelt, T., Johansson, O., and Goldstein, M. (1984). Chemical anatomy of the brain. Science 225:6147896. doi: 10.1126/science.6147896

PubMed Abstract | Crossref Full Text | Google Scholar

Hughes, N. (2023). Are AI Systems More Energy Efficient and Sustainable than Humans? Technopedia.

Google Scholar

Hyder, F., and Rothman, D. L. (2012). Quantitative fMRI and oxidative neuroenergetics. Neuroimage 62, 985–994. doi: 10.1016/j.neuroimage.2012.04.027

PubMed Abstract | Crossref Full Text | Google Scholar

Jain, A. K., Jianchang, M., and Mohiuddin, K. M. (1996). Artificial neural networks: a tutorial. Computer 29, 31–44. doi: 10.1109/2.485891

PubMed Abstract | Crossref Full Text | Google Scholar

Marcoli, M., Agnati, L. F., Franco, R., Cortelli, P., Anderlini, D., Guidolin, D., et al. (2022). Modulating brain integrative actions as a new perspective on pharmacological approaches to neuropsychiatric diseases. Front. Endocrinol. 13:1038874. doi: 10.3389/fendo.2022.1038874

PubMed Abstract | Crossref Full Text | Google Scholar

McFadden, C. (2023). Microsoft Wants Small Modular Nuclear Reactors to Power AI. Available online at: https://interestingengineering.com/innovation/microsoft-small-modular-nuclear-ai (accessed April 17, 2024).

Google Scholar

Merkle, A. C. (1989). Energy Limits to the Computational Power of the Human Brain. Foresight Update. Amsterdam: Elsevier.

Google Scholar

Metz, C. (2016). In a Huge Breakthrough, Google's AI Beats a Top Player at the Game of Go. Wired.

Google Scholar

Mezey, É., and Palkovits, M. (2015). Neuroanatomy: forgotten findings of brain lymphatics. Nature 524, 415. doi: 10.1038/524415b

PubMed Abstract | Crossref Full Text | Google Scholar

Mezey, É., Szalayova, I., Hogden, C. T., Brady, A., Dósa, Á., Sótonyi, P., et al. (2021). An immunohistochemical study of lymphatic elements in the human brain. Proc. Natl. Acad. Sci. U. S. A. 118. doi: 10.1073/pnas.2002574118

PubMed Abstract | Crossref Full Text | Google Scholar

Patterson, D., Gonzalez, J., Le, Q., Liang, C., Munguia, L., Rothchild, D., et al. (2021). Carbon emissions and large neural network training. arXiv: 2104.10350. doi: 10.48550/arXiv.2104.10350

Crossref Full Text | Google Scholar

Polyportis, A., and Pahos, N. (2024). Navigating the perils of artificial intelligence: a focused review on ChatGPT and responsible research and innovation. Human. Soc. Sci. Commun. 11:107. doi: 10.1057/s41599-023-02464-6

Crossref Full Text | Google Scholar

Rakic, P. (1988). Specification of cerebral cortical areas. Science 241, 170–176. doi: 10.1126/science.3291116

PubMed Abstract | Crossref Full Text | Google Scholar

Rothman, D. L., De Feyter, H. M., De Graaf, R. A., Mason, G. F., and Behar, K. L. (2011). 13C MRS studies of neuroenergetics and neurotransmitter cycling in humans. NMR Biomed. 24, 943–957. doi: 10.1002/nbm.1772

PubMed Abstract | Crossref Full Text | Google Scholar

Rothman, D. L., De Graaf, R. A., Hyder, F., Mason, G. F., Behar, K. L., and De Feyter, H. M. (2019). In vivo (13) C and (1) H-[(13) C] MRS studies of neuroenergetics and neurotransmitter cycling, applications to neurological and psychiatric disease and brain cancer. NMR Biomed. 32:e4172. doi: 10.1002/nbm.4172

PubMed Abstract | Crossref Full Text | Google Scholar

Roy, B., Wang, Q., Palkovits, M., Faludi, G., and Dwivedi, Y. (2017). Altered miRNA expression network in locus coeruleus of depressed suicide subjects. Sci. Rep. 7:4387. doi: 10.1038/s41598-017-04300-9

PubMed Abstract | Crossref Full Text | Google Scholar

Saenko, K. (2020). It Takes a Lot of Energy for Machines to Learn – Here's Why AI Is so Power-Hungry. The Conversation.

Google Scholar

Samardžija, B., Juković, M., Zaharija, B., Renner, É., Palkovits, M., and Bradshaw, N. J. (2023). Co-aggregation and parallel aggregation of specific proteins in major mental illness. Cells 12. doi: 10.3390/cells12141848

PubMed Abstract | Crossref Full Text | Google Scholar

Saper, C. B., and Fuller, P. M. (2017). Wake-sleep circuitry: an overview. Curr. Opin. Neurobiol. 44, 186–192. doi: 10.1016/j.conb.2017.03.021

PubMed Abstract | Crossref Full Text | Google Scholar

Sawchenko, P. E. (1998). Toward a new neurobiology of energy balance, appetite, and obesity: the anatomists weigh in. J. Comp. Neurol. 402, 435–441. doi: 10.1002/(SICI)1096-9861(19981228)402:4<435::AID-CNE1>3.0.CO;2-M

PubMed Abstract | Crossref Full Text | Google Scholar

Steinbusch, H. W. (1981). Distribution of serotonin-immunoreactivity in the central nervous system of the rat-cell bodies and terminals. Neuroscience 6, 557–618. doi: 10.1016/0306-4522(81)90146-9

PubMed Abstract | Crossref Full Text | Google Scholar

Svensson, E., Apergis-Schoute, J., Burnstock, G., Nusbaum, M. P., Parker, D., and Schiöt, H. H. B. (2018). General principles of neuronal co-transmission: insights from multiple model systems. Front. Neural Circuits 12:117. doi: 10.3389/fncir.2018.00117

PubMed Abstract | Crossref Full Text | Google Scholar

Swanson, L. W. (2018). Brain maps 4.0-Structure of the rat brain: an open access atlas with global nervous system nomenclature ontology and flatmaps. J. Comp. Neurol. 526, 935–943. doi: 10.1002/cne.24381

PubMed Abstract | Crossref Full Text | Google Scholar

Vas, S., Papp, R. S., Könczöl, K., Bogáthy, E., Papp, N., Ádori, C., et al. (2023). Prolactin-releasing peptide contributes to stress-related mood disorders and inhibits sleep/mood regulatory melanin-concentrating hormone neurons in rats. J. Neurosci. 43, 846–862. doi: 10.1523/JNEUROSCI.2139-21.2022

PubMed Abstract | Crossref Full Text | Google Scholar

Vitale-Cross, L., Szalayova, I., Scoggins, A., Palkovits, M., and Mezey, E. (2022). SARS-CoV-2 entry sites are present in all structural elements of the human glossopharyngeal and vagal nerves: clinical implications. bioRxiv. doi: 10.1016/j.ebiom.2022.103981

PubMed Abstract | Crossref Full Text | Google Scholar

Zhong, W., Barde, S., Mitsios, N., Adori, C., Oksvold, P., Feilitzen, K. V., et al. (2022). The neuropeptide landscape of human prefrontal cortex. Proc. Natl. Acad. Sci. U. S. A. 119:e2123146119. doi: 10.1073/pnas.2123146119

PubMed Abstract | Crossref Full Text | Google Scholar

Keywords: machine learning (ML), artificial neuronal network (ANN), neurotransmitters, energy consumption, efficiency

Citation: Agoston DV (2024) Of artificial intelligence, machine learning, and the human brain. Celebrating Miklos Palkovits' 90th birthday. Front. Neuroanat. 18:1374864. doi: 10.3389/fnana.2024.1374864

Received: 22 January 2024; Accepted: 25 March 2024;
Published: 03 May 2024.

Edited by:

Jackson Cioni Bittencourt, University of São Paulo, Brazil

Reviewed by:

Csaba Adori, Karolinska Institutet (KI), Sweden
Daniella Sabino Battagello, Federal University of ABC, Brazil

Copyright © 2024 Agoston. 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) and the copyright owner(s) 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: Denes V. Agoston, denes.agoston@usuhs.edu

Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.