ArticleFrontiers in human neuroscience2014
Equal pain-Unequal fear response: enhanced susceptibility of tooth pain to fear conditioning.
Article in Frontiers in human neuroscience, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
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Who cites it
8 citing papers in PubMed, 22 citations in OpenAlex.
- Review
- In patients' words: natural language processing of reports from patients experiencing orofacial pain and dysfunction.The journal of headache and pain · 2025Article
- Brain Functional Changes before, during, and after Clinical Pain.Journal of dental research · 2018Article
- The grimace scale reliably assesses chronic pain in a rodent model of trigeminal neuropathic pain.Neurobiology of pain (Cambridge, Mass.) · 2017Article
- Tracking local anesthetic effects using a novel perceptual reference approach.Journal of neurophysiology · 2016Article
- [Distinctive features of orofacial pain perception].Schmerz (Berlin, Germany) · 2015Review
- Amplified parabrachial nucleus activity in a rat model of trigeminal neuropathic pain.Neurobiology of pain (Cambridge, Mass.)Article
- Article
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Authors and funding
8 authors at 4 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Experimental fear conditioning in humans is widely used as a model to investigate the neural basis of fear learning and to unravel the pathogenesis of anxiety disorders. It has been observed that fear conditioning depends on stimulus salience and subject vulnerability to fear. It is further known that the prevalence of dental-related fear and phobia is exceedingly high in the population. Dental phobia is unique as no other body part is associated with a specific phobia. Therefore, we hypothesized that painful dental stimuli exhibit an enhanced susceptibility to fear conditioning when comparing to equal perceived stimuli applied to other body sites. Differential susceptibility to pain-related fear was investigated by analyzing responses to an unconditioned stimulus (UCS) applied to the right maxillary canine (UCS-c) vs. the right tibia (UCS-t). For fear conditioning, UCS-c and USC-t consisted of painful electric stimuli, carefully matched at both application sites for equal intensity and quality perception. UCSs were paired to simple geometrical forms which served as conditioned stimuli (CS+). Unpaired CS+ were presented for eliciting and analyzing conditioned fear responses. Outcome parameter were (1) skin conductance changes and (2) time-dependent brain activity (BOLD responses) in fear-related brain regions such as the amygdala, anterior cingulate cortex, insula, thalamus, orbitofrontal cortex, and medial prefrontal cortex. A preferential susceptibility of dental pain to fear conditioning was observed, reflected by heightened skin conductance responses and enhanced time-dependent brain activity (BOLD responses) in the fear network. For the first time, this study demonstrates fear-related neurobiological mechanisms that point toward a superior conditionability of tooth pain. Beside traumatic dental experiences our results offer novel evidence that might explain the high prevalence of dental-related fears in the population.
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