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Review
. 2023 Mar 15:226:109398.
doi: 10.1016/j.neuropharm.2022.109398. Epub 2022 Dec 27.

Canalization and plasticity in psychopathology

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Free article
Review

Canalization and plasticity in psychopathology

R L Carhart-Harris et al. Neuropharmacology. .
Free article

Abstract

This theoretical article revives a classical bridging construct, canalization, to describe a new model of a general factor of psychopathology. To achieve this, we have distinguished between two types of plasticity, an early one that we call 'TEMP' for 'Temperature or Entropy Mediated Plasticity', and another, we call 'canalization', which is close to Hebbian plasticity. These two forms of plasticity can be most easily distinguished by their relationship to 'precision' or inverse variance; TEMP relates to increased model variance or decreased precision, whereas the opposite is true for canalization. TEMP also subsumes increased learning rate, (Ising) temperature and entropy. Dictionary definitions of 'plasticity' describe it as the property of being easily shaped or molded; TEMP is the better match for this. Importantly, we propose that 'pathological' phenotypes develop via mechanisms of canalization or increased model precision, as a defensive response to adversity and associated distress or dysphoria. Our model states that canalization entrenches in psychopathology, narrowing the phenotypic state-space as the agent develops expertise in their pathology. We suggest that TEMP - combined with gently guiding psychological support - can counter canalization. We address questions of whether and when canalization is adaptive versus maladaptive, furnish our model with references to basic and human neuroscience, and offer concrete experiments and measures to test its main hypotheses and implications. This article is part of the Special Issue on "National Institutes of Health Psilocybin Research Speaker Series".

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Conflict of interest statement

Declaration of competing interest RCH, DE, AG, DJN report being a scientific advisor to a number of new companies and not-for-profits that are seeking to develop psychedelic therapy and bring it to market. RCH is grateful to Meg Spriggs for comments on an earlier draft of this manuscript, Courtney Gallen for guidance on referencing brain network modularity findings, Rayyan Zafar for references on dopamine, stimulants and Hebbian mechanisms, Lindsay Cameron for references on environmental enrichment and neuroplasticity, and Max Wolff for the connection to the ideas of Klaus Grawe.

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