A possible role for cholinergic neurons of the basal forebrain and pontomesencephalon in consciousness.
N J Woolf
Consciousness and Cognition December 1, 1997 DOI: 10.1006/ccog.1997.0319 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Theoretical or philosophical paper Peer reviewed |
|---|---|
| Keywords | Mesencephalon Pons Prosencephalon Cholinergic fibers Humans Microtubule-associated proteins Consciousness |
| Key points | Proposes that cholinergic afferents to the cerebral cortex enhance activity at specific cortical circuits and determine the content of a conscious moment by activating certain combinations of postsynaptic sites in select cortical modules, with the underlying mechanism hypothetically involving cholinergic mediation of linkages between microtubules and MAP-2. Argues that learning-related restructuring adjusts the cytoskeletal matrix at specific postsynaptic constellations, and raises the possibility that muscarinic actions on MAP-2 could modulate microtubular coherence and self-collapse. |
Abstract
Excitation at widely dispersed loci in the cerebral cortex may represent a neural correlate of consciousness. Accordingly, each unique combination of excited neurons would determine the content of a conscious moment. This conceptualization would be strengthened if we could identify what orchestrates the various combinations of excited neurons. In the present paper, cholinergic afferents to the cerebral cortex are hypothesized to enhance activity at specific cortical circuits and determine the content of a conscious moment by activating certain combinations of postsynaptic sites in select cortical modules. It is proposed that these selections are enabled by learning-related restructuring that simultaneously adjusts the cytoskeletal matrix at specific constellations of postsynaptic sites giving all a similar geometry. The underlying mechanism of conscious awareness hypothetically involves cholinergic mediation of linkages between microtubules and microtubule-associated protein-2 (MAP-2). The first reason for proposing this mechanism is that previous studies indicate cognitive-related changes in MAP-2 occur in cholinoceptive cells within discrete cortical modules. These cortical modules are found throughout the cerebral cortex, measure 1-2 mm2, and contain approximately 10(3)-10(4) cholinoceptive cells that are enriched with MAP-2. The subsectors of the hippocampus may function similarly to cortical modules. The second reason for proposing the current mechanism is that the MAP-2 rich cells throughout the cerebral cortex correspond almost exactly with the cortical cells containing muscarinic receptors. Many of these cholinoceptive, MAP-2 rich cells are large pyramidal cell types, but some are also small pyramidal cells and nonpyramidal types. The third reason for proposing the current mechanism is that cholinergic afferents are module-specific; cholinergic axons terminate wholly within individual cortical modules. The cholinergic afferents may be unique in this regard. Finally, the tapering apical dendrites of pyramidal cells are proposed as primary sites for cholinergic mediation of linkages between MAP-2 and microtubules because especially high amounts of MAP-2 are found here. Also, the possibility is raised that muscarinic actions on MAP-2 could modulate microtubular coherence and self-collapse, phenomena that have been suggested to underlie consciousness.
Citations in the library
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- Consciousness Operates Beyond the Timescale for Discerning Time Intervals: Implications for Q-mind Theories and Analysis of Quantum Decoherence in Brain September 5, 2007
- The Ferrier Lecture 1998. The molecular biology of consciousness investigated with genetically modified mice. Philosophical transactions of the Royal Society of London. Series B, Biological sciences December 1, 2006
- Conduction pathways in microtubules, biological quantum computation, and consciousness. Biosystems 2002
- A quantum approach to visual consciousness. Trends in Cognitive Sciences November 1, 2001
- Consciousness, the brain, and spacetime geometry. Annals of the New York Academy of Sciences April 1, 2001
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