scholarly journals Painful stimuli evoke different stimulus–response functions in the amygdala, prefrontal, insula and somatosensory cortex: a single‐trial fMRI study

Brain ◽  
2002 ◽  
Vol 125 (6) ◽  
pp. 1326-1336 ◽  
Author(s):  
K. Bornhövd ◽  
M. Quante ◽  
V. Glauche ◽  
B. Bromm ◽  
C. Weiller ◽  
...  
2020 ◽  
Vol 15 (2) ◽  
pp. 165-174
Author(s):  
Sarah Hope Lincoln ◽  
Laura T Germine ◽  
Patrick Mair ◽  
Christine I Hooker

Abstract Social dysfunction is a risk indicator for schizophrenia spectrum disorders, with at-risk individuals demonstrating a range of social behavior impairments. Variability in social ability may be explained by individual differences in the psychological processes of social behavior. In particular, mental simulation, the process by which an individual generates an internal representation of the thoughts or feelings of another, may explain variation in social behavior. This study investigates the neural process of simulation in healthy individuals and individuals at risk for psychosis. Using a novel fMRI pain paradigm, individuals watch videos of another person’s hand or foot experiencing pain. After each video, individuals are asked to simulate the observed painful situation on their own hand or foot. Neural activity during simulation in the somatosensory cortex was associated with real-world self-reported social behavior, such that a stronger neural response in the somatosensory cortex was associated with greater rates of positive social experiences and affective empathy across all participants. These findings suggest that the neural mechanisms that underlie simulation are important for social behavior, and may explain individual variability in social functioning in healthy and at-risk populations.


2008 ◽  
Vol 294 (4) ◽  
pp. G963-G970 ◽  
Author(s):  
Amanda J. Page ◽  
Tracey A. O'Donnell ◽  
L. Ashley Blackshaw

Despite universal use of opioids in the clinic to inhibit pain, there is relatively little known of their peripheral actions on sensory nerve endings, where in fact they may be better targeted with more widespread applications. Here we show differential effects of μ-, κ-, and δ-opioids on mechanosensitive ferret esophageal vagal afferent endings investigated in vitro. The effects of selective agonists [d-Ala2,N-Me-Phe4,Gly-ol5]-enkephalin (DAMGO), 2-(3, 4-dichlorophenyl)- N-methyl- N-[(1S)-1phenyl-2-(1-pyrrolidinyl) ethyl] acetamide hydrochlorine (ICI 199441), and (+)-4-[(αR)-α-((2S,5R)-4-allyl-2,5-dimethyl-1-piperazinyl)-3-methoxybenzyl]- N, N-diethylbenzamide (SNC-80), respectively, on mechanosensory stimulus-response functions were quantified. DAMGO (10−7 to 10−5 M) reduced the responses of tension receptors to circumferential tension (1–5 g) by up to 50%, and the responses of mucosal receptors to mucosal stroking (10–1,000 mg von Frey hair) by >50%. DAMGO effects were reversed by naloxone (10−5 M). Tension/mucosal (TM) receptor responses to tension and stroking were unaffected by DAMGO. ICI 199441 (10−6 to 10−5 M) potently inhibited all responses except TM receptor responses to tension, and SNC-80 (10−5 to 10−3 M) had no effect other than a minor inhibition of mucosal receptor responses to intense stimuli at 10−3 M. We conclude that μ- and κ-opioids have potent and selective peripheral effects on esophageal vagal afferents that may have applications in treatment of disorders of visceral sensation.


2009 ◽  
Vol 21 (9) ◽  
pp. 1766-1781 ◽  
Author(s):  
Elizabeth A. Race ◽  
Shanti Shanker ◽  
Anthony D. Wagner

Past experience is hypothesized to reduce computational demands in PFC by providing bottom–up predictive information that informs subsequent stimulus-action mapping. The present fMRI study measured cortical activity reductions (“neural priming”/“repetition suppression”) during repeated stimulus classification to investigate the mechanisms through which learning from the past decreases demands on the prefrontal executive system. Manipulation of learning at three levels of representation—stimulus, decision, and response—revealed dissociable neural priming effects in distinct frontotemporal regions, supporting a multiprocess model of neural priming. Critically, three distinct patterns of neural priming were identified in lateral frontal cortex, indicating that frontal computational demands are reduced by three forms of learning: (a) cortical tuning of stimulus-specific representations, (b) retrieval of learned stimulus-decision mappings, and (c) retrieval of learned stimulus-response mappings. The topographic distribution of these neural priming effects suggests a rostrocaudal organization of executive function in lateral frontal cortex.


NeuroImage ◽  
2000 ◽  
Vol 11 (3) ◽  
pp. 243-255 ◽  
Author(s):  
Désirée Gonzalo ◽  
Tim Shallice ◽  
Raymond Dolan

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