Morten Kringelbach

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Morten L Kringelbach
MortenKringelbach Wikimedia.jpg
Professor Morten L Kringelbach
Born
Nationality Danish
AwardsScience Communication Prize 2006, Danish Ministry of Higher Education and Science. [1]
Scientific career
Fields Neuroscience, Cognitive Science
Institutions University of Oxford, University of Aarhus
Website hedonia.kringelbach.org

Morten L Kringelbach is a professor of neuroscience at University of Oxford, UK and Aarhus University, Denmark. [2] [3] He is the director of the 'Centre for Eudaimonia and Human Flourishing', fellow of Linacre College, Oxford and board member of the Empathy Museum. [4]

Contents

Research overview

Kringelbach has made contributions to a range of topics within neuroscience using neuroimaging, deep brain stimulation and whole-brain modelling. His research is focused on reverse-engineering the human brain and in particular he has identified some of the evolutionary principles and heuristics of teleological computation enabling us to survive and thrive, which depend on intact human brain systems related to emotion, pleasure and eudaimonia. Together with Kent Berridge he has identified brain mechanisms underlying the reward system and identified a network of hedonic hotspots essential for the fundamental pleasure cycle of 'wanting', 'liking' and learning. [5] [6] In a large series of neuroimaging studies of many rewards, he has elucidated the spatiotemporal organisation of the orbitofrontal cortex, [7] e.g. demonstrating a fast parental signature of infant cuteness even in adults who are not yet parents. [8] [9] [10] They have also investigated the close links between pleasure and happiness. [11]

Kringelbach has also worked with neurosurgeon Tipu Aziz to elucidate the neural mechanisms of deep brain stimulation for Parkinson's disease, essential tremor, dystonia and chronic pain [12]

Together with Peter Vuust, he founded the 'Center for Music in the Brain' [13] at University of Aarhus focused on better understanding the neuroscience of music and in particular the dual questions of how music is processed in the brain and how this can inform our understanding of fundamental principles behind brain functioning in general.

Furthermore, Kringelbach and Gustavo Deco have developed a research programme of whole-brain modelling for combining structural connectivity data Diffusion Tensor Imaging with functional neuroimaging data such as fMRI and magnetoencephalography. This allows for the discovery of causal mechanisms of brain function, and they have e.g. identified fundamental mechanisms and principles of integration and segregation, [14] as well as metastability and coherence. [15] In time, these findings might help open up for a better understanding and potential treatment of neuropsychiatric disorders [16] as well as the role of one of the cardinal symptoms, namely anhedonia, the lack of pleasure. [17]

See also

Related Research Articles

Pleasure refers to experience that feels good, that involves the enjoyment of something. It contrasts with pain or suffering, which are forms of feeling bad. It is closely related to value, desire and action: humans and other conscious animals find pleasure enjoyable, positive or worthy of seeking. A great variety of activities may be experienced as pleasurable, like eating, having sex, listening to music or playing games. Pleasure is part of various other mental states such as ecstasy, euphoria and flow. Happiness and well-being are closely related to pleasure but not identical with it. There is no general agreement as to whether pleasure should be understood as a sensation, a quality of experiences, an attitude to experiences or otherwise. Pleasure plays a central role in the family of philosophical theories known as hedonism.

The mesolimbic pathway, sometimes referred to as the reward pathway, is a dopaminergic pathway in the brain. The pathway connects the ventral tegmental area in the midbrain to the ventral striatum of the basal ganglia in the forebrain. The ventral striatum includes the nucleus accumbens and the olfactory tubercle.

<span class="mw-page-title-main">Dopaminergic pathways</span> Projection neurons in the brain that synthesize and release dopamine

Dopaminergic pathways in the human brain are involved in both physiological and behavioral processes including movement, cognition, executive functions, reward, motivation, and neuroendocrine control. Each pathway is a set of projection neurons, consisting of individual dopaminergic neurons.

Some philosophers, such as Jeremy Bentham, Baruch Spinoza, and Descartes, have hypothesized that the feelings of pain and pleasure are part of a continuum.

Brainwave entrainment, also referred to as brainwave synchronization or neural entrainment, refers to the observation that brainwaves will naturally synchronize to the rhythm of periodic external stimuli, such as flickering lights, speech, music, or tactile stimuli.

Affective neuroscience is the study of how the brain processes emotions. This field combines neuroscience with the psychological study of personality, emotion, and mood. The basis of emotions and what emotions are remains an issue of debate within the field of affective neuroscience.

<span class="mw-page-title-main">Orbitofrontal cortex</span> Region of the prefrontal cortex of the brain

The orbitofrontal cortex (OFC) is a prefrontal cortex region in the frontal lobes of the brain which is involved in the cognitive process of decision-making. In non-human primates it consists of the association cortex areas Brodmann area 11, 12 and 13; in humans it consists of Brodmann area 10, 11 and 47.

<span class="mw-page-title-main">Reward system</span> Group of neural structures responsible for motivation and desire

The reward system is a group of neural structures responsible for incentive salience, associative learning, and positively-valenced emotions, particularly ones involving pleasure as a core component. Reward is the attractive and motivational property of a stimulus that induces appetitive behavior, also known as approach behavior, and consummatory behavior. A rewarding stimulus has been described as "any stimulus, object, event, activity, or situation that has the potential to make us approach and consume it is by definition a reward". In operant conditioning, rewarding stimuli function as positive reinforcers; however, the converse statement also holds true: positive reinforcers are rewarding.

<span class="mw-page-title-main">Frisson</span> Psychophysiological response to rewarding auditory or visual stimuli

Frisson, also known as aesthetic chills or psychogenic shivers is a psychophysiological response to rewarding stimuli that often induces a pleasurable or otherwise positively-valenced affective state and transient paresthesia, sometimes along with piloerection and mydriasis. The sensation commonly occurs as a mildly to moderately pleasurable emotional response to music with skin tingling; piloerection and pupil dilation not necessarily occurring in all cases.

<span class="mw-page-title-main">Default mode network</span> Large-scale brain network active when not focusing on an external task

In neuroscience, the default mode network (DMN), also known as the default network, default state network, or anatomically the medial frontoparietal network (M-FPN), is a large-scale brain network primarily composed of the dorsal medial prefrontal cortex, posterior cingulate cortex/precuneus and angular gyrus. It is best known for being active when a person is not focused on the outside world and the brain is at wakeful rest, such as during daydreaming and mind-wandering. It can also be active during detailed thoughts related to external task performance. Other times that the DMN is active include when the individual is thinking about others, thinking about themselves, remembering the past, and planning for the future.

Cultural neuroscience is a field of research that focuses on the interrelation between a human's cultural environment and neurobiological systems. The field particularly incorporates ideas and perspectives from related domains like anthropology, psychology, and cognitive neuroscience to study sociocultural influences on human behaviors. Such impacts on behavior are often measured using various neuroimaging methods, through which cross-cultural variability in neural activity can be examined.

The ventral pallidum (VP) is a structure within the basal ganglia of the brain. It is an output nucleus whose fibres project to thalamic nuclei, such as the ventral anterior nucleus, the ventral lateral nucleus, and the medial dorsal nucleus. The VP is a core component of the reward system which forms part of the limbic loop of the basal ganglia, a pathway involved in the regulation of motivational salience, behavior, and emotions. It is involved in addiction.

The parabrachial nuclei, also known as the parabrachial complex, are a group of nuclei in the dorsolateral pons that surrounds the superior cerebellar peduncle as it enters the brainstem from the cerebellum. They are named from the Latin term for the superior cerebellar peduncle, the brachium conjunctivum. In the human brain, the expansion of the superior cerebellar peduncle expands the parabrachial nuclei, which form a thin strip of grey matter over most of the peduncle. The parabrachial nuclei are typically divided along the lines suggested by Baxter and Olszewski in humans, into a medial parabrachial nucleus and lateral parabrachial nucleus. These have in turn been subdivided into a dozen subnuclei: the superior, dorsal, ventral, internal, external and extreme lateral subnuclei; the lateral crescent and subparabrachial nucleus along the ventrolateral margin of the lateral parabrachial complex; and the medial and external medial subnuclei

<span class="mw-page-title-main">Gustavo Deco</span>

Gustavo Deco is an Argentinian and Italian professor and scientist. He serves as Research Professor at the Catalan Institution for Research and Advanced Studies and Full Professor (Catedratico) at the Pompeu Fabra University, where he is Director of the Center of Brain and Cognition and head of the Computational Neuroscience Group. In 2001 Deco was awarded the international prize of Siemens "Inventor of the Year" for his contributions in statistical learning, models of visual perception, and fMRI based diagnosis of neuropsychiatric diseases..

<span class="mw-page-title-main">Angus Silver</span> English neuroscientist

Robin Angus Silver is Professor of Neuroscience and a Wellcome Trust Principal Research Fellow at University College London. His laboratory studies neurotransmission and artificial neural networks by combining in vitro and in vivo experimental approaches with quantitative analysis and computational models developed in silico.

Peter Milner was a British-born Canadian neuroscientist.

Brain–body interactions are patterns of neural activity in the central nervous system to coordinate the activity between the brain and body. The nervous system consists of central and peripheral nervous systems and coordinates the actions of an animal by transmitting signals to and from different parts of its body. The brain and spinal cord are interwoven with the body and interact with other organ systems through the somatic, autonomic and enteric nervous systems. Neural pathways regulate brain–body interactions and allow to sense and control its body and interact with the environment.

Social cognitive neuroscience is the scientific study of the biological processes underpinning social cognition. Specifically, it uses the tools of neuroscience to study "the mental mechanisms that create, frame, regulate, and respond to our experience of the social world". Social cognitive neuroscience uses the epistemological foundations of cognitive neuroscience, and is closely related to social neuroscience. Social cognitive neuroscience employs human neuroimaging, typically using functional magnetic resonance imaging (fMRI). Human brain stimulation techniques such as transcranial magnetic stimulation and transcranial direct-current stimulation are also used. In nonhuman animals, direct electrophysiological recordings and electrical stimulation of single cells and neuronal populations are utilized for investigating lower-level social cognitive processes.

Irene Mary Carmel Tracey, is Vice-Chancellor of the University of Oxford and former Warden of Merton College, Oxford, her alma mater. She is also Professor of Anaesthetic Neuroscience in the Nuffield Department of Clinical Neurosciences and formerly Pro-Vice-Chancellor at the University of Oxford. She is a co-founder of the Oxford Centre for Functional Magnetic Resonance Imaging of the Brain (FMRIB) now the Wellcome Centre for Integrative Neuroimaging. Her team’s research is focused on the neuroscience of pain, specifically pain perception and analgesia as well as how anaesthetics produce altered states of consciousness. Her team uses multidisciplinary approaches including neuroimaging.

References

  1. "Forskningskommunikationsprisen — Uddannelses- og Forskningsministeriet".
  2. Theils, Lone (26 September 2008). "Professor i Nydelse". Berlingske Tidende. Retrieved 17 April 2018.
  3. Feltman, Rachel (8 June 2016). "The sneaky ways babies get inside our heads". Washington Post. Retrieved 17 April 2018.
  4. "Empathy Museum".
  5. Grayling, A.C. (27 November 2010). "Exchanges at the Frontier: Episode 5 Interview with Morten L Kringelbach". BBC World Service. Retrieved 17 April 2018.
  6. Berridge KC, Kringelbach ML (May 2015). "Pleasure systems in the brain". Neuron. 86 (3): 646–664. doi:10.1016/j.neuron.2015.02.018. PMC   4425246 . PMID   25950633.
  7. Kringelbach, Morten L. (2005). "The human orbitofrontal cortex: linking reward to hedonic experience". Nature Reviews Neuroscience. 6 (9): 691–702. doi:10.1038/nrn1747. ISSN   1471-003X. PMID   16136173. S2CID   205500365.
  8. Cunningham, Aimeel (1 April 2008). "Baby in the Brain". Scientific American. Retrieved 17 April 2018.
  9. Kringelbach, Morten L.; Lehtonen, Annukka; Squire, Sarah; Harvey, Allison G.; Craske, Michelle G.; Holliday, Ian E.; Green, Alexander L.; Aziz, Tipu Z.; Hansen, Peter C.; Cornelissen, Piers L.; Stein, Alan (2008). "A Specific and Rapid Neural Signature for Parental Instinct". PLOS ONE. 3 (2): e1664. Bibcode:2008PLoSO...3.1664K. doi: 10.1371/journal.pone.0001664 . ISSN   1932-6203. PMC   2244707 . PMID   18301742.
  10. Kringelbach, Morten L.; Stark, Eloise A.; Alexander, Catherine; Bornstein, Marc H.; Stein, Alan (2016). "On Cuteness: Unlocking the Parental Brain and Beyond". Trends in Cognitive Sciences. 20 (7): 545–558. doi:10.1016/j.tics.2016.05.003. ISSN   1364-6613. PMC   4956347 . PMID   27211583.
  11. Kringelbach ML, Berridge KC (2009). "Towards a functional neuroanatomy of pleasure and happiness". Trends in Cognitive Sciences. 13 (11): 479–487. doi:10.1016/j.tics.2009.08.006. PMC   2767390 . PMID   19782634.
  12. Kringelbach, Morten L.; Jenkinson, Ned; Owen, Sarah L.F.; Aziz, Tipu Z. (2007). "Translational principles of deep brain stimulation". Nature Reviews Neuroscience. 8 (8): 623–635. doi:10.1038/nrn2196. ISSN   1471-003X. PMID   17637800. S2CID   147427108.
  13. "Center for Music in the Brain".
  14. Deco, Gustavo; Tononi, Giulio; Boly, Melanie; Kringelbach, Morten L. (2015). "Rethinking segregation and integration: contributions of whole-brain modelling". Nature Reviews Neuroscience. 16 (7): 430–439. doi:10.1038/nrn3963. hdl: 10230/27083 . ISSN   1471-003X. PMID   26081790. S2CID   7962033.
  15. Deco, Gustavo; Kringelbach, Morten (2016). "Metastability and Coherence: Extending the Communication through Coherence Hypothesis Using a Whole-Brain Computational Perspective". Trends in Neurosciences. 39 (6): 432. doi: 10.1016/j.tins.2016.04.006 . ISSN   0166-2236. PMID   27131472.
  16. Deco, Gustavo; Kringelbach, Morten L. (2014). "Great Expectations: Using Whole-Brain Computational Connectomics for Understanding Neuropsychiatric Disorders". Neuron. 84 (5): 892–905. doi: 10.1016/j.neuron.2014.08.034 . ISSN   0896-6273. PMID   25475184.
  17. Roemer Thomsen, Kristine; Whybrow, Peter C.; Kringelbach, Morten L. (2015). "Reconceptualizing anhedonia: novel perspectives on balancing the pleasure networks in the human brain". Frontiers in Behavioral Neuroscience. 9: 49. doi: 10.3389/fnbeh.2015.00049 . ISSN   1662-5153. PMC   4356228 . PMID   25814941.

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