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Anthony K Jones

Publications and source records attributed to Anthony K Jones.

2 recordsLinked to original sources

'Prior entry' for pain: attention speeds the perceptual processing of painful stimuli.

We investigated whether the perception of simultaneity for pairs of nociceptive and visual stimuli was dependent upon the focus of participants' attention to a particular sensory modality (either pain or vision). Two stimuli (one painful and the other visual) were presented randomly at different stimulus onset asynchronies (SOAs) using the method of constant stimuli. Participants made unspeeded verbal responses as to which stimulus they perceived as having been presented first, or else responded that the two stimuli were presented simultaneously. This temporal discrimination task was repeated under three different attention conditions (blocks): divided attention, attend pain, and attend vision. The results showed that under conditions of divided attention, nociceptive stimuli had to be presented before visual stimuli in order for the two to be perceived as simultaneous. A comparison of the two focused attention conditions revealed that the painful stimulus was perceived as occurring earlier in time (relative to the visual stimulus) when attention was directed toward pain than when it was directed toward vision. These results provide the first empirical demonstration that attention can modulate the temporal perception of painful stimuli.

Adult↗

Temporal difference models describe higher-order learning in humans.

The ability to use environmental stimuli to predict impending harm is critical for survival. Such predictions should be available as early as they are reliable. In pavlovian conditioning, chains of successively earlier predictors are studied in terms of higher-order relationships, and have inspired computational theories such as temporal difference learning. However, there is at present no adequate neurobiological account of how this learning occurs. Here, in a functional magnetic resonance imaging (fMRI) study of higher-order aversive conditioning, we describe a key computational strategy that humans use to learn predictions about pain. We show that neural activity in the ventral striatum and the anterior insula displays a marked correspondence to the signals for sequential learning predicted by temporal difference models. This result reveals a flexible aversive learning process ideally suited to the changing and uncertain nature of real-world environments. Taken with existing data on reward learning, our results suggest a critical role for the ventral striatum in integrating complex appetitive and aversive predictions to coordinate behaviour.

Conditioning, Classical↗