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Oral Vasopressin Modulates Neural Responses to Looming Visual Stimuli: An Eye-tracking Study

Recruiting
18 - 40 years of age
Both
Phase N/A

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Overview

The main aim of the present study is to investigate the effects of orally administered vasopressin (AVP) on the perception of time-to-collision of threatening and non-threatening stimuli by combining a validated looming fear eye-tracking paradigm with a randomized between-subject placebo-controlled pharmacological trial design.

Description

Animal models and initial findings in humans suggest a role of the AVP signaling system in socio-emotional processes. At the same time, the visual system's remarkable ability to perceive and interpret impending threats, notably through the "looming" phenomenon- a distinct pattern of optical expansion on the retina as objects approach, theoretically allows for precise estimation of the time-to-collision (TTC). It was recently demonstrated that the affective content of looming stimuli influences perceived TTC, with threatening objects judged as approaching sooner than non-threatening objects, hinting at a nuanced interaction between emotional valence and temporal perception. Within this context the present study aims to validate the effects of orally administered on the perception of time-to-collision of threatening and non-threatening stimuli. To this end, healthy individuals will undergo a double-blind, between-subjects, placebo-controlled pharmaco-eye-tracking experiment and receive a single oral dose of vasopressin (20 IU) or placebo before performing a looming visual stimuli task 45 minutes after administration. The task paradigm will encompass threatening (butterfly, rabbit) and non-threatening (spider, snake) stimuli

Eligibility

Inclusion Criteria:

  • Healthy subjects who volunteer to participate and are able to fully understand and agree with this study by written informed consent.
  • Normal or corrected-normal version

Exclusion Criteria:

  • History of neuropsychiatric diseases.
  • History of cardiac disease, including arrhythmias, aortic stenosis, or congestive heart failure; history of syncope or unexplained loss of consciousness.
  • History of hepatic diseases, including cholestasis, biliary obstructive disease, or severe liver dysfunction.
  • History of renal diseases, including renal stones or renal failure.
  • History of hyponatremia(Serum sodium <135mmol/L) or hyperkalemia (Serum potassium>5.5mmol/L); history of diabetes mellitus or diabetes insipidus
  • Known hypersensitivity or allergic reaction to any medication or hormone; strong allergic reaction to food.
  • Infections such as COVID-19 or influenza, or unexplained fever.
  • Subjects with hypertension (BP ≥130/80mmHg) or hypotension (BP ≤ 90/60mmHg).
  • History of alcohol or drug abuse; smoker (≥ 10 cigarettes or ≥ 3 cigars or ≥ 3 pipes/day); smoker using e-cigarettes.

Study details

Healthy

NCT06329063

University of Electronic Science and Technology of China

14 April 2024

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