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Losartan Effects on Emotion-memory Interaction

The Role of the Renin-angiotensin System in Emotion-memory Interactions

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04606225
Enrollment
60
Registered
2020-10-28
Start date
2020-10-10
Completion date
2022-03-31
Last updated
2020-10-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy

Keywords

Losartan, Emotion-memory interaction

Brief summary

The purpose of this study is to investigate whether a single dose of losartan (50 mg) can affect emotion-memory interaction in healthy humans and its underlying neural mechanisms.

Detailed description

Animal models and initial findings in humans suggest a role of the renin-angiotensin system in cognitive and emotional processes. Accumulating evidence demonstrates modulatory effects of the angiotensin antagonist losartan in the domains of memory and emotional processing. Against this background the present study aims to investigate the behavioral and neural effects of a single dose of losartan on emotional processing and emotion-memory integration in healthy subjects. In a double-blind, between-subject, placebo-controlled pharmaco-fMRI experiment, 60 male participants will be randomized to a single dose of losartan (50 mg) or placebo, and encode emotional pictures during fMRI (scheduled 90 minutes after drug administration). Then 24 hours post fMRI participants will finish a surprise recognition memory test to estimate the emotion effects on subsequent memory.

Interventions

DRUGLosartan

administration of losartan (50 mg) (oral) Cozaar Oral Tablet

DRUGPlacebo Oral Tablet

administration of placebo (oral)

Sponsors

University of Electronic Science and Technology of China
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
DOUBLE (Subject, Investigator)

Eligibility

Sex/Gender
MALE
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* Healthy subjects without past or current psychiatric or neurological disorders * Right-handedness * Normal or corrected-normal version

Exclusion criteria

* History of head injury * Medical or psychiatric illness * Hypertension * General cardio-vascular alteration or diseases * Allergy against medications * Visual or motor impairments * Claustrophobia * Drug addiction * Nicotine dependence * FMRI contradictions

Design outcomes

Primary

MeasureTime frameDescription
fMRI-based indices of neural activity during processing of emotional stimuli will be compared between the treatment groups120 to 150 minutes after treatmentNeural activation during processing of emotional pictures will be assessed by functional magnetic resonance imaging (fMRI). The fMRI data will be analyzed by a Generalized Linear Model approach. Effects of treatment will be determined by comparing the losartan-treated group with the placebo-treated group.
fMRI-based indices of neural activity for subsequently successfully remembered as compared to non-remembered stimuli will be compared between the treatment groups120 to 150 minutes after treatmentNeural activation for stimuli that are successfully remembered after an interval of 24hours will be compared to stimuli that are not successfully remembered. Neural activity between the subsequently remembered and non-remembered stimuli will be assessed by functional magnetic resonance imaging (fMRI) acquired during the initial encoding of the stimuli. The fMRI data will be analyzed by a Generalized Linear Model approach. Effects of treatment will be determined by comparing the losartan-treated group with the placebo-treated group.

Secondary

MeasureTime frameDescription
Self-Assessment Manikin (SAM) ratings of arousal of the stimuli will be compared between the treatment groups120 to 150 minutes after treatmentDuring the fMRI participants will rate the emotional arousal of each presented picture by means of the Self-Assessment Manikin (SAM). The assessment ranges from 1-5, with 1 referring to very low arousal while 5 refers to a very high arousal. The effects of treatment on arousal will be examined by comparing the losartan-treated with the placebo-treated group by means of a Generalized Linear Model approach.
Self-Assessment Manikin (SAM) ratings of valence of the stimuli will be compared between the treatment groups120 to 150 minutes after treatmentDuring the fMRI participants will rate the emotional valence of each presented picture by means of the Self-Assessment Manikin (SAM). The assessment ranges from 1-5, with 1 referring to very negative valence, while 5 refers to a very positive valence. The effects of treatment on valence will be examined by comparing the losartan-treated with the placebo-treated group by means of a Generalized Linear Model approach.
Memory performance in terms of correctly recognized stimuli will be compared between the treatment groups24 hours after treatment24 hours after the fMRI assessment subjects will be re-exposed to the stimuli that were presented during the fMRI and new stimuli. Subjects have to indicate for each stimulus whether it has been shown during fMRI. Memory performance in terms of correct responses will be computed and compared between the losartan-treated with the placebo-treated group by means of a Generalized Linear Model approach.

Countries

China

Contacts

Primary ContactWeihua Zhao, PhD
zarazhao.uestc@outlook.com86-28-61830811

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026