help button home button
AJRCCM
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS

Published ahead of print on May 29, 2009, doi:10.1164/rccm.200902-0300OC
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Online Supplement
Right arrow All Versions of this Article:
200902-0300OCv1
180/3/232    most recent
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Google Scholar
Right arrow Articles by von Leupoldt, A.
Right arrow Articles by Büchel, C.
PubMed
Right arrow PubMed Citation
Right arrow Articles by von Leupoldt, A.
Right arrow Articles by Büchel, C.
American Journal of Respiratory and Critical Care Medicine Vol 180. pp. 232-238, (2009)
© 2009 American Thoracic Society
doi: 10.1164/rccm.200902-0300OC


Original Article

Down-Regulation of Insular Cortex Responses to Dyspnea and Pain in Asthma

Andreas von Leupoldt1,2, Tobias Sommer2, Sarah Kegat1, Falk Eippert2, Hans Jörg Baumann3, Hans Klose3, Bernhard Dahme1 and Christian Büchel2

1 Department of Psychology, University of Hamburg; 2 Department of Systems Neuroscience, and 3 Department of Pneumology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany

Correspondence and requests for reprints should be addressed to Andreas von Leupoldt, Ph.D., Department of Psychology, University of Hamburg, Von-Melle-Park 5, 20146 Hamburg, Germany. E-mail: andreas.vonleupoldt{at}uni-hamburg.de

Rationale: Dyspnea is the impairing cardinal symptom of asthma but its accurate perception is also crucial for timely initiation of treatment. However, the underlying brain mechanisms of perceived dyspnea in patients with asthma are unknown.

Objectives: To study brain mechanisms of dyspnea in asthma.

Methods: By using functional magnetic resonance imaging we compared the neuronal responses to experimentally induced dyspnea in patients with asthma and healthy controls. These brain activations were compared with neuronal responses evoked by pain to study neuronal generalization processes to another, similarly unpleasant, physiological sensation.

Measurements and Main Results: While lying in the scanner, fourteen patients with mild-to-moderate asthma and fourteen matched healthy controls repeatedly underwent conditions of mild dyspnea, severe dyspnea, mild pain and severe pain. Dyspnea was induced by resistive loaded breathing. Heat pain of similar intensity was induced by a contact thermode.

Whereas the sensory intensity of both sensations was rated similar by patients and controls, ratings of the affective unpleasantness of dyspnea and pain were reduced in patients. This perceptual difference was mirrored by reduced insular cortex activity, but increased activity in the periaqueductal gray (PAG) in patients during both increased dyspnea and pain. Connectivity analyses showed that asthma-specific down-regulation of the insular cortex during dyspnea and pain was moderated by increased PAG activity.

Conclusions: The results suggest a down-regulation of affect-related insular cortex activity by the PAG during perceived dyspnea and pain in patients with asthma. This might represent a neuronal habituation mechanism reducing the affective unpleasantness of dyspnea in asthma, which generalizes to other unpleasant physiological sensations such as pain.

Key Words: asthma • brain • dyspnea • magnetic resonance imaging • perception


AT A GLANCE COMMENTARY

Scientific Knowledge on the Subject
Dyspnea is the cardinal symptom of asthma but its reduced perception can also lead to poor treatment outcomes including near fatal asthma attacks. However, the underlying brain mechanisms of perceived dyspnea in patients with asthma are not well characterized.

What This Study Adds to the Field
This study suggests a down-regulation of affect-related insular cortex activity by the periaqueductal grey during perceived dyspnea, and also pain, in patients with asthma. This might represent a neuronal habituation mechanism reducing the affective unpleasantness of dyspnea in asthma, which generalizes to other unpleasant physiological sensations such as pain.

 






HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Proc. Am. Thorac. Soc. Am. J. Respir. Cell Mol. Biol.
Copyright © 2009 American Thoracic Society
  New Orleans Int'l Conf