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

NCT ID: NCT03738943

Last Updated: 2021-07-27

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

EARLY_PHASE1

Total Enrollment

9 participants

Study Classification

INTERVENTIONAL

Study Start Date

2019-02-07

Study Completion Date

2021-06-01

Brief Summary

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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.

Detailed Description

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Adenosine triphosphate (ATP) is an established vasodilator that is released from red blood cells during a variety of stimuli including exercise and exposure to hypoxic environments. Many studies have shown that infusion of ATP can lead to vasodilation similar to that which is achieved during exercise, and that plasma ATP concentrations increase in a graded fashion during graded exercise. Further, older adults have lower levels of blood flow during exercise and hypoxia compared to their younger counterparts, and the reduced blood flow is coupled with impaired release of ATP from red blood cells during these stimuli. Thus, ATP is believed to be an important vasodilator. However, the role of ATP in the regulation of blood flow is not fully understood due to the lack of an effective ATP receptor (P2Y2) antagonist. Development of an effective P2Y2 antagonist will allow researchers to determine the role of ATP in vasodilation to stimuli such as exercise by comparing blood flow during exercise with and without the blocker. Preliminary data from our laboratory suggests that Vitamin B6 (pyridoxine hydrochloride) or its metabolite Pyridoxal-5-Phosphate (PLP) may be an effective blocker of ATP-mediated vasodilation. As a result, the purpose of this study is to determine whether Vitamin B6 or PLP can inhibit vasodilation in response to intra-arterial infusions of ATP. This study also aims to determine the specificity of Vitamin B6 or PLP by measuring its effect on vasodilation in response to infusion of several other vasodilators.

Participants will be asked to complete one screening visit and one study visit. Once study eligibility has been determined, participants will report to the Human Performance Clinical Research Laboratory at Colorado State University following an overnight fast. A physician will then place a catheter in the brachial artery of the non-dominant arm, and participants will be randomized into one of three study arms to determine which drugs will be infused into the artery. Each arm includes ATP and two other vasodilators. The study will begin by measuring vasodilation in response to four standard doses of each vasodilator. Vasodilation in response to the vasodilators will then be assessed again following infusion of Vitamin B6 or PLP. Reduced vasodilation to any of the drugs during the second trial will suggest that Vitamin B6 or PLP is an antagonist to the channel through which the drug signals. Each study visit will last approximately 4-5 hours.

Conditions

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Receptor Blockade

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Participants will be assigned to one of three arms of the study. The arms of the study are based on the vasodilators being tested in order to determine the effect of pyridoxine or PLP on vasodilation in response to intra-arterial administration of the vasodilators.
Primary Study Purpose

BASIC_SCIENCE

Blinding Strategy

NONE

Study Groups

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ATP, Ach, SNP

All drugs will be administered via intra-arterial (brachial artery) infusion, and the dosages below will be administered two times: once before administration of Vitamin B6 (pyridoxine) and once following administration of the Vitamin B6 (pyridoxine) loading dose.

Adenosine Triphosphate: 1.25, 2.5, 5, and 10 μg/dl forearm volume/min for 3 minutes each.

Acetylcholine: 1, 4, 8, and 16 μg/dl forearm volume/min for 3 minutes each.

Sodium Nitroprusside: 0.25, 0.5, 1, and 2 μg/dl forearm volume/min for 3 minutes each.

Vitamin B6 (pyridoxine): up to 200 mg of pyridoxine will be infused over 20 minutes. A maintenance dose of 2.5 mg/min may be used throughout the remainder of the protocol.

Pyridoxal-5-Phosphate (PLP) may be used as an alternative blocker instead of pyridoxine. It will be infused at doses up to 200 µg/dl forearm volume/min.

Group Type EXPERIMENTAL

Adenosine Triphosphate

Intervention Type DRUG

See arm/group descriptions

Acetylcholine

Intervention Type DRUG

See arm/group descriptions

Sodium Nitroprusside

Intervention Type DRUG

See arm/group descriptions

Vitamin B 6

Intervention Type DRUG

See arm/group descriptions

Pyridoxal 5'-Phosphate

Intervention Type DRUG

See arm/group descriptions

ATP, ADP, AMP

All drugs will be administered via intra-arterial (brachial artery) infusion, and the dosages below will be administered two times: once before administration of Vitamin B6 (pyridoxine) and once following administration of the Vitamin B6 (pyridoxine) loading dose.

Adenosine Triphosphate: 1.25, 2.5, 5, and 10 μg/dl forearm volume/min for 3 minutes each.

Adenosine Diphosphate: 20, 40, 80, and 160 μg/dl forearm volume/min for 3 minutes each.

Adenosine Monophosphate: 25, 50, 100, and 200 μg/dl forearm volume/min for 3 minutes each.

Vitamin B6 (pyridoxine): up to 200 mg of pyridoxine will be infused over 20 minutes. A maintenance dose of 2.5 mg/min may be used throughout the remainder of the protocol.

Pyridoxal-5-Phosphate (PLP) may be used as an alternative blocker instead of pyridoxine. It will be infused at doses up to 200 µg/dl forearm volume/min.

Group Type EXPERIMENTAL

Adenosine Triphosphate

Intervention Type DRUG

See arm/group descriptions

Adenosine Diphosphate

Intervention Type DRUG

See arm/group descriptions

Adenosine Monophosphate

Intervention Type DRUG

See arm/group descriptions

Vitamin B 6

Intervention Type DRUG

See arm/group descriptions

Pyridoxal 5'-Phosphate

Intervention Type DRUG

See arm/group descriptions

ATP, UTP, Adenosine

All drugs will be administered via intra-arterial (brachial artery) infusion, and the dosages below will be administered two times: once before administration of Vitamin B6 (pyridoxine) and once following administration of the Vitamin B6 (pyridoxine) loading dose.

Adenosine Triphosphate: 1.25, 2.5, 5, and 10 μg/dl forearm volume/min for 3 minutes each.

Uridine Triphosphate: 1.25, 2.5, 5, and 10 μg/dl forearm volume/min for 3 minutes each.

Adenosine: 3.125, 6.25, 12.5, and 25 μg/dl forearm volume/min for 3 minutes each.

Vitamin B6 (pyridoxine): up to 200 mg of pyridoxine will be infused over 20 minutes. A maintenance dose of 2.5 mg/min may be used throughout the remainder of the protocol.

Pyridoxal-5-Phosphate (PLP) may be used as an alternative blocker instead of pyridoxine. It will be infused at doses up to 200 µg/dl forearm volume/min.

Group Type EXPERIMENTAL

Adenosine Triphosphate

Intervention Type DRUG

See arm/group descriptions

Uridine Triphosphate

Intervention Type DRUG

See arm/group descriptions

Adenosine

Intervention Type DRUG

See arm/group descriptions

Vitamin B 6

Intervention Type DRUG

See arm/group descriptions

Pyridoxal 5'-Phosphate

Intervention Type DRUG

See arm/group descriptions

Interventions

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Adenosine Triphosphate

See arm/group descriptions

Intervention Type DRUG

Acetylcholine

See arm/group descriptions

Intervention Type DRUG

Sodium Nitroprusside

See arm/group descriptions

Intervention Type DRUG

Adenosine Diphosphate

See arm/group descriptions

Intervention Type DRUG

Adenosine Monophosphate

See arm/group descriptions

Intervention Type DRUG

Uridine Triphosphate

See arm/group descriptions

Intervention Type DRUG

Adenosine

See arm/group descriptions

Intervention Type DRUG

Vitamin B 6

See arm/group descriptions

Intervention Type DRUG

Pyridoxal 5'-Phosphate

See arm/group descriptions

Intervention Type DRUG

Other Intervention Names

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ATP Ach SNP ADP AMP UTP Adenocard Pyridoxine Pyridoxine Hydrochloride PLP P5P pyridoxal phosphate monohydrate MC-1

Eligibility Criteria

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Inclusion Criteria

* Sedentary-moderately active
* Free of chronic disease

Exclusion Criteria

* Current smoker
* BMI \> 29.9 kg/m2
* Blood pressure equal to or greater than 140/90 mmHg
* Use of any medications including vitamin B6 supplements or antioxidants
Minimum Eligible Age

18 Years

Maximum Eligible Age

30 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

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Colorado State University

OTHER

Sponsor Role lead

Responsible Party

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Frank Dinenno

Professor

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

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Frank Dinenno, PhD

Role: PRINCIPAL_INVESTIGATOR

Colorado State University

Locations

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Human Performance and Clinical Research Laboratory

Fort Collins, Colorado, United States

Site Status

Countries

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United States

Other Identifiers

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17-7430H

Identifier Type: -

Identifier Source: org_study_id

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