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Altered anterior insula activation during anticipation and experience of painful stimuli in expert meditators.

Antoine Lutz, Daniel R McFarlin, David M Perlman, Tim V Salomons, Richard J. Davidson

Neuroimage January 1, 2013 DOI: 10.1016/j.neuroimage.2012.09.030 (opens in new tab) via PubMed

Summary

AI-generated from the abstract

Expert meditators with over 10,000 hours of practice experience pain as intensely as novices but find it less unpleasant. Brain imaging during a mindfulness-like meditation showed that experts had enhanced activity in the dorsal anterior insula and anterior mid-cingulate cortex—part of the salience network—during pain, alongside lower baseline activity in these regions and the amygdala before pain. This pattern was linked to faster neural habituation in pain-related areas. The findings suggest that cultivating experiential openness reduces anticipatory responses to aversive events and increases attentional engagement during pain, leading to quicker habituation.

Study at a glance

Characteristics Observational cohort Peer reviewed
Population Expert meditators (>10,000 h of practice) and novices
Intervention meditation practice similar to mindfulness
Key finding Expert meditators reported equal pain intensity but less unpleasantness compared to novices, associated with enhanced salience network activity during pain and reduced baseline activity in pain-related regions.

Abstract

Experientially opening oneself to pain rather than avoiding it is said to reduce the mind's tendency toward avoidance or anxiety which can further exacerbate the experience of pain. This is a central feature of mindfulness-based therapies. Little is known about the neural mechanisms of mindfulness on pain. During a meditation practice similar to mindfulness, functional magnetic resonance imaging was used in expert meditators (>10,000 h of practice) to dissociate neural activation patterns associated with pain, its anticipation, and habituation. Compared to novices, expert meditators reported equal pain intensity, but less unpleasantness. This difference was associated with enhanced activity in the dorsal anterior insula (aI), and the anterior mid-cingulate (aMCC) the so-called 'salience network', for experts during pain. This enhanced activity during pain was associated with reduced baseline activity before pain in these regions and the amygdala for experts only. The reduced baseline activation in left aI correlated with lifetime meditation experience. This pattern of low baseline activity coupled with high response in aIns and aMCC was associated with enhanced neural habituation in amygdala and pain-related regions before painful stimulation and in the pain-related regions during painful stimulation. These findings suggest that cultivating experiential openness down-regulates anticipatory representation of aversive events, and increases the recruitment of attentional resources during pain, which is associated with faster neural habituation.

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