Pyridoxine, P2 Receptor Antagonism, and ATP-mediated Vasodilation in Young Adults

NCT03738943 · Status: COMPLETED · Phase: EARLY_PHASE1 · Type: INTERVENTIONAL · Enrollment: 9

Last updated 2021-07-27

No results posted yet for this study

Summary

Previous research has identified adenosine triphosphate (ATP) as an important vasodilator that is released from red blood cells during exercise and exposure to hypoxic environments in adult humans. Further, older adults appear to have lower blood flow during both of these stressors and also have lower amounts of ATP released from their red blood cells. However, the contribution of ATP to vasodilation in response to exercise and hypoxia is currently unknown due to the lack of an effective ATP receptor antagonist. We aim to determine whether Vitamin B6 or its metabolite, Pyridoxal-5-Phosphate (PLP) is an effective ATP receptor antagonist.

Conditions

  • Receptor Blockade

Interventions

DRUG

Adenosine Triphosphate

See arm/group descriptions

DRUG

Acetylcholine

See arm/group descriptions

DRUG

Sodium Nitroprusside

See arm/group descriptions

DRUG

Adenosine Diphosphate

See arm/group descriptions

DRUG

Adenosine Monophosphate

See arm/group descriptions

DRUG

Uridine Triphosphate

See arm/group descriptions

DRUG

Adenosine

See arm/group descriptions

DRUG

Vitamin B 6

See arm/group descriptions

DRUG

Pyridoxal 5'-Phosphate

See arm/group descriptions

Sponsors & Collaborators

  • Colorado State University

    lead OTHER

Principal Investigators

  • Frank Dinenno, PhD · Colorado State University

Study Design

Allocation
RANDOMIZED
Purpose
BASIC_SCIENCE
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
30 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-02-07
Primary Completion
2021-06-01
Completion
2021-06-01
FDA Drug
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03738943 on ClinicalTrials.gov