Deutsch
 
Hilfe Datenschutzhinweis Impressum
  DetailsucheBrowse

Datensatz

DATENSATZ AKTIONENEXPORT
 
 
DownloadE-Mail
 Lokale TagsFreigabegeschichteDetailsÜbersicht
  Determining the neural substrate for encoding a memory of human pain and the influence of anxiety

Tseng, M.-T., Kong, Y., Eippert, F., & Tracey, I. (2017). Determining the neural substrate for encoding a memory of human pain and the influence of anxiety. The Journal of Neuroscience: The Official Journal of the Society for Neuroscience, 37(49), 11806-11817. doi:10.1523/JNEUROSCI.0750-17.2017.

Item is

 

einblenden: alle ausblenden: alle

Basisdaten

einblenden: ausblenden:
Datensatz-Permalink: https://hdl.handle.net/21.11116/0000-0001-6CA9-8 Versions-Permalink: https://hdl.handle.net/21.11116/0000-0003-B4BF-B
Genre: Zeitschriftenartikel

Dateien

einblenden: Dateien
ausblenden: Dateien
:
Tseng_Kong_2017.pdf (Verlagsversion), 2MB
Öffnen   Speichern
Datei-Permalink:
https://hdl.handle.net/21.11116/0000-0001-F8B9-7
Name:
Tseng_Kong_2017.pdf
Beschreibung:
-
OA-Status:
Sichtbarkeit:
Öffentlich
MIME-Typ / Prüfsumme:
application/pdf / [MD5]
Technische Metadaten:
Öffnen
Copyright Datum:
-
Copyright Info:
-
Lizenz:
-

Externe Referenzen

einblenden:

Urheber

einblenden:
ausblenden:
 Urheber:
Tseng, Ming-Tsung1, Autor
Kong, Yazhuo1, Autor
Eippert, Falk1, Autor           
Tracey, Irene1, Autor
Affiliations:
1External Organizations, ou_persistent22              

Inhalt

einblenden:
ausblenden:
Schlagwörter: -
 Zusammenfassung: To convert a painful stimulus into a briefly maintainable construct when the painful stimulus is no longer accessible is essential to guide human behavior and avoid dangerous situations. Because of the aversive nature of pain, this encoding process might be influenced by emotional aspects and could thus vary across individuals, but we have yet to understand both the basic underlying neural mechanisms as well as potential interindividual differences. Using fMRI in combination with a delayed-discrimination task in healthy volunteers of both sexes, we discovered that brain regions involved in this working memory encoding process were dissociable according to whether the to-be-remembered stimulus was painful or not, with the medial thalamus and the rostral anterior cingulate cortex encoding painful and the primary somatosensory cortex encoding nonpainful stimuli. Encoding of painful stimuli furthermore significantly enhanced functional connectivity between the thalamus and medial prefrontal cortex (mPFC). With regards to emotional aspects influencing encoding processes, we observed that more anxious participants showed significant performance advantages when encoding painful stimuli. Importantly, only during the encoding of pain, the interindividual differences in anxiety were associated with the strength of coupling between medial thalamus and mPFC, which was furthermore related to activity in the amygdala. These results indicate not only that there is a distinct signature for the encoding of a painful experience in humans, but also that this encoding process involves a strong affective component.SIGNIFICANCE STATEMENT To convert the sensation of pain into a briefly maintainable construct is essential to guide human behavior and avoid dangerous situations. Although this working memory encoding process is implicitly contained in the majority of studies, the underlying neural mechanisms remain unclear. Using fMRI in a delayed-discrimination task, we found that the encoding of pain engaged the activation of the medial thalamus and the functional connectivity between the thalamus and medial prefrontal cortex. These fMRI data were directly and indirectly related to participants' self-reported trait and state anxiety. Our findings indicate that the mechanisms responsible for the encoding of noxious stimuli differ from those for the encoding of innocuous stimuli, and that these mechanisms are shaped by an individual's anxiety levels.

Details

einblenden:
ausblenden:
Sprache(n): eng - English
 Datum: 2017-08-312017-03-192017-09-052017-12-06
 Publikationsstatus: Erschienen
 Seiten: -
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: -
 Identifikatoren: DOI: 10.1523/JNEUROSCI.0750-17.2017
BibTex Citekey: tseng_determining_2017
PMID: 29097595
PMC: PMC5719969
 Art des Abschluß: -

Veranstaltung

einblenden:

Entscheidung

einblenden:

Projektinformation

einblenden: ausblenden:
Projektname : -
Grant ID : 100-2917-I-564-028
Förderprogramm : -
Förderorganisation : National Science Council
Projektname : -
Grant ID : 103-2410-H-002-121-MY2
Förderprogramm : -
Förderorganisation : Ministry of Science and Technology
Projektname : -
Grant ID : NHRI-EX106–10615NC
Förderprogramm : -
Förderorganisation : National Health Research Institutes of Taiwan
Projektname : Neurobiological mechanisms of endogenous pain modulation / PAIN MODULATION
Grant ID : 273805
Förderprogramm : Funding Programme 7
Förderorganisation : European Commission (EC)
Projektname : -
Grant ID : -
Förderprogramm : -
Förderorganisation : National Institute for Health Research Oxford Biomedical Research Centre
Projektname : -
Grant ID : -
Förderprogramm : -
Förderorganisation : Medical Research Council of Great Britain and Northern Ireland
Projektname : -
Grant ID : -
Förderprogramm : -
Förderorganisation : Wellcome Trust

Quelle 1

einblenden:
ausblenden:
Titel: The Journal of Neuroscience: The Official Journal of the Society for Neuroscience
Genre der Quelle: Zeitschrift
 Urheber:
Affiliations:
Ort, Verlag, Ausgabe: -
Seiten: - Band / Heft: 37 (49) Artikelnummer: - Start- / Endseite: 11806 - 11817 Identifikator: ISSN: 1529-2401