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Forebrain Electroneutral Transporters in Salt-sensitive Hypertension: an MRI Study

Primary Purpose

Salt-Sensitivity of Blood Pressure

Status
Not yet recruiting
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Furosemide (Diuretic)
Hypertonic Saline Infusion
Sponsored by
University of Delaware
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional basic science trial for Salt-Sensitivity of Blood Pressure

Eligibility Criteria

40 Years - 60 Years (Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria: Age: > 40 years or < 60 years Blood pressure: > 120/80 mmHg or < 140/90 mmHg BMI: > 18.5 kg/m2 or < 30 kg/m2 Serum potassium: > 3.5 mmol/L or < 5.5 mmol/L No history of cardiovascular, renal, metabolic, or neurological disease Exclusion Criteria: Age: < 40 years or > 60 years Blood pressure: < 120/80 mmHg or > 140/90 mmHg BMI: < 18.5 kg/m2 or > 30 kg/m2 Serum potassium: < 3.5 mmol/L or > 5.5 mmol/L Abnormal ECG History of - cardiovascular, cancer, metabolic, respiratory, renal disease Hormone replacement therapy Current tobacco or nicotine use Pregnant or nursing mothers Major brain injury (concussions do not count) Clinically diagnosed psychiatric or neurological disorder Clinically diagnosed anxiety or depression Psychiatric, neurological, anxiety or depression medications Hypertension medications Sulfonamide drug allergy Contra-indications to MRI (implants, metal, etc) Claustrophobia

Sites / Locations

    Arms of the Study

    Arm 1

    Arm 2

    Arm Type

    Experimental

    Experimental

    Arm Label

    Salt Resistant Adults

    Salt Sensitive

    Arm Description

    Adults who experience minimal BP change during dietary sodium challenge

    Adults who experience increased BP (mean arterial pressures >5mmHg) during dietary sodium challenge

    Outcomes

    Primary Outcome Measures

    Bold fMRI
    Intensity of sodium sensing regions of the brain

    Secondary Outcome Measures

    Blood Pressure
    Systolic and Diastolic Blood pressure responses to hypertonic saline

    Full Information

    First Posted
    October 11, 2023
    Last Updated
    October 17, 2023
    Sponsor
    University of Delaware
    Collaborators
    National Heart, Lung, and Blood Institute (NHLBI)
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    1. Study Identification

    Unique Protocol Identification Number
    NCT06094816
    Brief Title
    Forebrain Electroneutral Transporters in Salt-sensitive Hypertension: an MRI Study
    Official Title
    Forebrain Electroneutral Transporters in Salt-sensitive Hypertension: an MRI Study
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    October 2023
    Overall Recruitment Status
    Not yet recruiting
    Study Start Date
    January 2024 (Anticipated)
    Primary Completion Date
    January 2028 (Anticipated)
    Study Completion Date
    July 2028 (Anticipated)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    University of Delaware
    Collaborators
    National Heart, Lung, and Blood Institute (NHLBI)

    4. Oversight

    Studies a U.S. FDA-regulated Drug Product
    No
    Studies a U.S. FDA-regulated Device Product
    No
    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    The overall objective of this project is to identify the key salt-sensing regions of the brain and determine the underlying mechanism of sodium sensing. The investigators will assess how the brain responds to an acute increase of salt in the blood using MRI. This will be done during a 30-minute infusion of a saline solution containing 3% salt. One trial will be conducted with a salt sensing channel blocker and one trial without the salt sensing channel blocker. This will help to assess the role of a specific salt sensing channel in the brain. Salt sensitivity of BP will be assessed using 7-day dietary feeding where participants will be given food to consume for 7-days. Comparisons will be made between salt resistant (no change in blood pressure going from low to high salt diets) and salt sensitive adults (a change in blood pressure going from low to high salt diets). The investigators think the changes in MRI will be greater in salt sensitive compared to salt resistant subjects.
    Detailed Description
    The ability of the brain to sense changing sodium levels in the blood is critical in mediating the neurohumoral responses to hypernatremia, however, the mechanisms underlying sodium sensing in humans is poorly understood. The purpose of this study is to identify key sodium-sensing regions of the human brain in middle-aged men and women with high blood pressure and determine if the Na-K-2Cl co-transporter (NKCC2) mediates the neurohumoral response to acute hypernatremia. The investigators plan on comparing these central sodium responses to acute hypernatremia between salt-sensitive and salt-resistant adults. In this randomized double-blinded crossover study subjects will have a 3% NaCl (hypertonic saline) infusion with or without NKCC2 antagonism (furosemide). Completion of this project will increase the understanding of blood pressure regulation, which has major public health implications.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Salt-Sensitivity of Blood Pressure

    7. Study Design

    Primary Purpose
    Basic Science
    Study Phase
    Not Applicable
    Interventional Study Model
    Crossover Assignment
    Model Description
    Double blind randomized cross-over
    Masking
    ParticipantInvestigator
    Allocation
    Randomized
    Enrollment
    120 (Anticipated)

    8. Arms, Groups, and Interventions

    Arm Title
    Salt Resistant Adults
    Arm Type
    Experimental
    Arm Description
    Adults who experience minimal BP change during dietary sodium challenge
    Arm Title
    Salt Sensitive
    Arm Type
    Experimental
    Arm Description
    Adults who experience increased BP (mean arterial pressures >5mmHg) during dietary sodium challenge
    Intervention Type
    Drug
    Intervention Name(s)
    Furosemide (Diuretic)
    Other Intervention Name(s)
    Lasix
    Intervention Description
    The diuretic furosemide will be given during a 3% hypertonic saline infusion to examine blockade of the NKCC2.
    Intervention Type
    Other
    Intervention Name(s)
    Hypertonic Saline Infusion
    Intervention Description
    3% Hypertonic saline infusion to acutely increase sodium and osmolality
    Primary Outcome Measure Information:
    Title
    Bold fMRI
    Description
    Intensity of sodium sensing regions of the brain
    Time Frame
    1 hour
    Secondary Outcome Measure Information:
    Title
    Blood Pressure
    Description
    Systolic and Diastolic Blood pressure responses to hypertonic saline
    Time Frame
    1 hour
    Other Pre-specified Outcome Measures:
    Title
    Sympathetic Nerve Activity
    Description
    sympathetic bursts per minute
    Time Frame
    1 hour

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    40 Years
    Maximum Age & Unit of Time
    60 Years
    Accepts Healthy Volunteers
    Accepts Healthy Volunteers
    Eligibility Criteria
    Inclusion Criteria: Age: > 40 years or < 60 years Blood pressure: > 120/80 mmHg or < 140/90 mmHg BMI: > 18.5 kg/m2 or < 30 kg/m2 Serum potassium: > 3.5 mmol/L or < 5.5 mmol/L No history of cardiovascular, renal, metabolic, or neurological disease Exclusion Criteria: Age: < 40 years or > 60 years Blood pressure: < 120/80 mmHg or > 140/90 mmHg BMI: < 18.5 kg/m2 or > 30 kg/m2 Serum potassium: < 3.5 mmol/L or > 5.5 mmol/L Abnormal ECG History of - cardiovascular, cancer, metabolic, respiratory, renal disease Hormone replacement therapy Current tobacco or nicotine use Pregnant or nursing mothers Major brain injury (concussions do not count) Clinically diagnosed psychiatric or neurological disorder Clinically diagnosed anxiety or depression Psychiatric, neurological, anxiety or depression medications Hypertension medications Sulfonamide drug allergy Contra-indications to MRI (implants, metal, etc) Claustrophobia
    Central Contact Person:
    First Name & Middle Initial & Last Name or Official Title & Degree
    Megan Wenner
    Phone
    3028317343
    Email
    mwenner@udel.edu

    12. IPD Sharing Statement

    Plan to Share IPD
    No

    Learn more about this trial

    Forebrain Electroneutral Transporters in Salt-sensitive Hypertension: an MRI Study

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