Effect of serotonin transporter genotype on carbon dioxide-induced fear-related behavior in mice

Author:

Leibold Nicole K12ORCID,van den Hove Daniel LA134,Weidner Magdalena T1345,Buchanan Gordon F267,Steinbusch Harry WM138,Lesch Klaus-Peter1349,Schruers Koen RJ1310

Affiliation:

1. Department of Psychiatry and Neuropsychology, Maastricht University, Maastricht, The Netherlands

2. Department of Neurology, Yale School of Medicine, New Haven, USA

3. School for Mental Health and Neuroscience (MHeNs), Maastricht University, Maastricht, The Netherlands

4. Division of Molecular Psychiatry, Center of Mental Health, University of Wuerzburg, Wuerzburg, Germany

5. Department of Psychiatry and Psychotherapy, Medical Center University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany

6. Department of Neurology, University of Iowa, Iowa City, USA

7. University of Iowa Graduate College, Iowa City, USA

8. Department of Brain and Cognitive Sciences, Daegu Gyeongbuk Institute of Science and Technoglogy (DGIST), Daegu, South Korea

9. Laboratory of Psychiatric Neurobiology, I.M. Sechenov First Moscow State Medical University, Moscow, Russia

10. Department of Psychology, University of Leuven, Leuven, Belgium

Abstract

Background: Inhaling 35% carbon dioxide induces an emotional and symptomatic state in humans closely resembling naturally occurring panic attacks, the core symptom of panic disorder. Previous research has suggested a role of the serotonin system in the individual sensitivity to carbon dioxide. In line with this, we previously showed that a variant in the SLC6A4 gene, encoding the serotonin transporter, moderates the fear response to carbon dioxide in humans. To study the etiological basis of carbon dioxide-reactivity and panic attacks in more detail, we recently established a translational mouse model. Aim: The purpose of this study was to investigate whether decreased expression of the serotonin transporter affects the sensitivity to carbon dioxide. Methods: Based on our previous work, wildtype and serotonin transporter deficient (+/–, –/–) mice were monitored while being exposed to carbon dioxide-enriched air. In wildtype and serotonin transporter +/– mice, also cardio-respiration was assessed. Results: For most behavioral measures under air exposure, wildtype and serotonin transporter +/– mice did not differ, while serotonin transporter –/– mice showed more fear-related behavior. Carbon dioxide exposure evoked a marked increase in fear-related behaviors, independent of genotype, with the exception of time serotonin transporter –/– mice spent in the center zone of the modified open field test and freezing in the two-chamber test. On the physiological level, when inhaling carbon dioxide, the respiratory system was strongly activated and heart rate decreased independent of genotype. Conclusion: Carbon dioxide is a robust fear-inducing stimulus. It evokes inhibitory behavioral responses such as decreased exploration and is associated with a clear respiratory profile independent of serotonin transporter genotype.

Funder

Deutsche Forschungsgemeinschaft

National Institute of Neurological Disorders and Stroke

5-100 Russian Academic Excellence Project

Beth and Nate Tross Epilepsy Research Fund

horizon 2020

Boehringer Ingelheim Fonds

ERA-Net NEURON/RESPOND

ERA-Net NEURON/DECODE

Publisher

SAGE Publications

Subject

Pharmacology (medical),Psychiatry and Mental health,Pharmacology

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