» Articles » PMID: 34129851

Motive Control of Unconscious Inference: The Limbic Base of Adaptive Bayes

Overview
Date 2021 Jun 15
PMID 34129851
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

Current computational models of neocortical processing, described as predictive coding theory, are providing new ways of understanding Helmholtz's classical insight that perception cannot proceed in a data-driven fashion, but instead requires unconscious inference based on prior experience. Predictive coding is a Bayesian process, in which the operations at each lower level of the cortical hierarchy are predicted by prior projections of expectancies from a higher level, and are then updated by error-correction with lower level evidence. To generalize the predictive coding model to the human neocortex as a whole requires aligning the Bayesian negotiation of prior expectancies with sensory and motor evidence not only within the connectional architecture of the neocortex (primary sensory/motor, unimodal association areas, and heteromodal association areas) but also with the limbic cortex that forms the base for the adaptive control of the heteromodal areas and thereby the cerebral hemisphere as a whole. By reviewing the current evidence on the anatomy of the human corticolimbic connectivity (now formalized as the Structural Model) we address the problem of how limbic cortex resonates to the homeostatic, personal significance of events to provide Bayesian priors to organize the operations of predictive coding across the multiple levels of the neocortex. By reviewing both classical evidence and current models of control exerted between limbic and neocortical networks, we suggest a neuropsychological theory of human cognition, the adaptive Bayes process model, in which prior expectancies are not simply rationalized propositions, but rather affectively-charged expectancies that bias the interpretation of sensory data and action affordances to support allostasis, the motive control of expectancies for future events.

Citing Articles

An active inference strategy for prompting reliable responses from large language models in medical practice.

Shusterman R, Waters A, ONeill S, Bangs M, Luu P, Tucker D NPJ Digit Med. 2025; 8(1):119.

PMID: 39987335 PMC: 11847020. DOI: 10.1038/s41746-025-01516-2.


Neural underpinnings of a two-phase memory suppression process in the neural response to self-related and observed perspective views.

Song X, Liu Q, Zhang X, Liu C, Lan C, Zhang X Int J Clin Health Psychol. 2025; 24(4):100509.

PMID: 39823094 PMC: 11735992. DOI: 10.1016/j.ijchp.2024.100509.


Cortical development in the structural model and free energy minimization.

Wright J, Bourke P Cereb Cortex. 2024; 34(10).

PMID: 39470397 PMC: 11520235. DOI: 10.1093/cercor/bhae416.


Feasibility of a Personal Neuromorphic Emulation.

Tucker D, Luu P Entropy (Basel). 2024; 26(9).

PMID: 39330092 PMC: 11431400. DOI: 10.3390/e26090759.


Measuring brain potentials of imagination linked to physiological needs and motivational states.

Proverbio A, Pischedda F Front Hum Neurosci. 2023; 17:1146789.

PMID: 37007683 PMC: 10050745. DOI: 10.3389/fnhum.2023.1146789.