L-DOPA improves extinction memory retrieval after successful fear extinction (Exp. 2)

ID 227 2 Reuses

Abstract

Rationale A promising strategy to prevent a return of fear after exposure-based therapy in anxiety disorders is to pharmacologically enhance the extinction memory consolidation presumed to occur after exposure. Accumulating evidence suggests that the effect of a number of pharmacological consolidation enhancers depends on a successful fear reduction during exposure. Here, we employed the dopamine precursor L-DOPA to clarify whether its documented potential to enhance extinction memory consolidation is dependent on successful fear extinction. Methods In two double-blind, randomized and placebo-controlled experiments (experiment 1: N = 79, experiment 2: N = 32) comprising fear conditioning (day 1), extinction followed by administration of 150 mg L-DOPA or placebo (day 2) and a memory test (day 3) in healthy male adults, conditioned responses were assessed as differential skin conductance responses. We tested whether the effect of L-DOPA on conditioned responses at test depended on conditioned responses at the end of extinction in an experiment with a short (10 trials, experiment 1) and long (25 trials, experiment 2) extinction session. Results In both experiments, the effect of L-DOPA was dependent on conditioned responses at the end of extinction. That is, post-extinction L-DOPA compared to placebo administration reduced conditioned responses at test only in participants showing a complete reduction of conditioned fear at the end of extinction. Conclusion The results support the potential use of L-DOPA as a pharmacological adjunct to exposure treatment, but point towards a common boundary condition for pharmacological consolidation enhancers: a successful reduction of fear in the exposure session.

Authors

Anna M. V. Gerlicher*, Johannes Gutenberg University Medical Center, Mainz, Germany; University of Amsterdam, Amsterdam, The Netherlands Oliver Tüscher, Johannes Gutenberg University Medical Center, Mainz, Germany Raffael Kalisch, Johannes Gutenberg University Medical Center, Mainz, Germany

Year

2019

DOI of the Publication

https://doi.org/10.1007/s00213-019-05301-4

Is Version of

https://doi.org/10.17605/OSF.IO/KEQRN

Location of Data Collection

Johannes Gutenberg University Medical Center, Germany

How to Cite

Gerlicher, A., Tüscher, O., & Kalisch, R. (2025, December 12). L-DOPA improves extinction memory retrieval after successful fear extinction. https://doi.org/10.17605/OSF.IO/KEQRN

Study Design

Contingency Instructions

Partially instructed (whole exp)

Outcome Measures

habituation
CS+
Trials
8000s
acquisition
5 different CS+
5 Trials
Reinforcement Rate
80%
8000s
5 different CS-
5 Trials
8000s
1 days
extinction
25 different CS+
25 Trials
8000s
25 different CS-
25 Trials
8000s
intervention
intervention
1 days
re-extinction
8 different CS+
8 Trials
8000s
8 different CS-
8 Trials
8000s

Participant Information

Participant Sex

Experimental Group

Administration of L-DOPA (150/37.5 mg levodopa-benserazide; L-DOPA group) or placebo (placebo group) on day 2 after extinction.

Stimuli

Drug Administration

Yes

Conditioning Protocol

Differential

Instructions Regarding CS–US Contingencies

Partially instructed (whole exp)

US scored separately

No

Number of Different US

1

US Modality

electrotactile

US Duration (ms)

106

Time Between CS and US Onset (ms)

7900

Number of Different CS+

1

CS+ Duration (ms)

8000

CS+ 1: Reinforcement Rate (%)

80

CS+ 2: Reinforcement Rate (%)

CS+ 3: Reinforcement Rate (%)

Number of Different CS-

1

CS- Duration (ms)

8000

CS Modality

visual

Data Collected During MRI

No

Measures

skin conductance response

trialwise & untransformed

Amplitude of skin conductance response to stimulus.

US intensity rating

Intensity rating of the US stimulus.

State Trait Anxiety Inventory (STAI-T)

State Trait Anxiety Inventory (STAI-S)

Anxiety Sensitivity Index (ASI)