Hostname: page-component-78c5997874-lj6df Total loading time: 0 Render date: 2024-11-18T01:28:34.184Z Has data issue: false hasContentIssue false

PW01-44 - Impact of Glyoxalase-1 Mrna Expression On Cck-4 Induced Anxiety

Published online by Cambridge University Press:  17 April 2020

D. Eser
Affiliation:
Department of Psychiatry and Psychotherapy, Ludwig-Maximilian-University, Munich, Germany
G. Leicht
Affiliation:
Department of Psychiatry and Psychotherapy, Ludwig-Maximilian-University, Munich, Germany
A. Laenger
Affiliation:
Department of Psychiatry and Psychotherapy, Ludwig-Maximilian-University, Munich, Germany
C. Schuele
Affiliation:
Department of Psychiatry and Psychotherapy, Ludwig-Maximilian-University, Munich, Germany
T. Baghai
Affiliation:
Department of Psychiatry and Psychotherapy, Ludwig-Maximilian-University, Munich, Germany
C. Mulert
Affiliation:
Department of Psychiatry and Psychotherapy, Ludwig-Maximilian-University, Munich, Germany
M. Uhr
Affiliation:
Max-Planck-Institute of Psychiatry, Munich, Germany
R. Rupprecht
Affiliation:
Department of Psychiatry and Psychotherapy, Ludwig-Maximilian-University, Munich, Germany

Abstract

Core share and HTML view are not available for this content. However, as you have access to this content, a full PDF is available via the ‘Save PDF’ action button.
Objectives

There is evidence that the antioxidant enzyme glyoxalase-1 (Glx-1) may play a role in anxiety-related behaviour. However, discordant findings between Glx-1 expression and anxiety-related behaviour have been observed in animal models. Because no data are available on the relation between Glx-1 mRNA expression and human anxiety so far, we investigated the expression of Glx-1 mRNA in peripheral red blood cells in relation to cholecystokinin-tetrapeptide (CCK-4) induced anxiety in healthy subjects.

Methods

Twenty-three healthy subjects underwent challenge with CCK-4. Glx-1 mRNA expression was assessed by quantitative real-time polymerase chain reaction prior to CCK-4 injection. Baseline anxiety was assessed with the State-Trait-Anxiety-Inventory (STAI) and panic response was measured with the Panic Symptom Scale (PSS).

Results

CCK-4 elicited a marked anxiety response accompanied by a significant increase in heart rate. Glx-1 mRNA expression correlated significantly with severity of CCK-4 induced anxiety. In contrast, Glx-1 activity did not correlate with state or trait anxiety.

Conclusions

The positive correlation between Glx-1 mRNA expression and CCK-4 induced panic severity suggests that Glx-1 is involved into the acute anxiety response to CCK-4. Our preliminary findings support preclinical findings and point towards a role of Glx-1 for human anxiety.

Type
Anxiety disorders
Copyright
Copyright © European Psychiatric Association 2010
Submit a response

Comments

No Comments have been published for this article.