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The Role of Aldosterone on Augmented Exercise Pressor Reflex in Hypertension

The Role of Aldosterone on Augmented Exercise Pressor Reflex in Hypertension

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01996449
Enrollment
14
Registered
2013-11-27
Start date
2013-07-31
Completion date
2021-04-30
Last updated
2022-03-18

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

Conditions

Hypertension

Keywords

Hypertension, blood pressure, Aldosterone, Eplerenone, Amlodipine, Primary aldosteronism, Exercise pressor reflex, handgrip exercise, passive arm cycling, active arm cycling

Brief summary

Hypertensive patients often show an exaggerated rise in blood pressure during exercise through overactivity of the exercise pressor reflex. An increasing body of evidence suggests a role for aldosterone in augmenting the exercise pressor reflex in hypertensive humans. We hypothesize that this effect of aldosterone is mediated by its direct action on the central nervous system and that administration of mineralocorticoid receptor antagonists constitute an effective treatment for EPR overactivity in hypertension, independent of reductions in resting BP.

Detailed description

Hypertensive patients are known to display exaggerated rise in blood pressure (BP) during exercise but the underlying mechanisms are poorly understood. Traditionally, muscle afferents were dichotomized as metaboreceptors, which are activated slowly and only during intense or ischemic muscle contraction, or mechanoreceptors, which respond quickly to even mild deformation of their receptive fields. The increase in sympathetic nerve activity and BP caused by activation of these receptors, known as exercise pressor reflex, is normally buffered by activation arterial baroreceptors, which are reset to operate at higher BP range but at the same level of sensitivity. Mechanisms responsible for overactive exercise pressor reflex in hypertension remain unknown, but an increasing body of evidence suggested a role for aldosterone in regulating resting central sympathetic outflow in both hypertensive rats and humans. Experiments will be performed on 3 groups of subjects 1) stage I (140-159/90-99 mmHg) subjects with essential hypertension, 2) stage I hypertensive subjects with Primary Aldosteronism (PA), and 3) normotensive controls. All participants will attend a baseline study visit, which will include a physical examination, a medical history review, vital sign measurements, and blood and urine collection. Small electrodes will be used to measure muscle nerve activity while the subjects perform a series of exercises that include passive arm cycling, active arm cycling, rhythmic hand grip, sustained hand grip and cold pressor test. Muscle blood flow will be measured before and after hand grip exercises. A subgroup of subjects with essential hypertension and PA will be assigned to receive Eplerenone or Amlodipine on a randomized, double-blinded design. Participants will attend two weeks visits over a period of 16 weeks. Study visits include measurement of vital signs and blood samples collection. After completing 8 weeks on each medication, muscle nerve activity will be measured while performing the same exercises described in the baseline study visit.

Interventions

DRUGEplerenone

The subject will be started on Eplerenone (Inspra) 50-200mg daily, which he or she will continue for a period of 8 weeks. Following the 8-week treatment period, the procedures listed below will be performed. After completion of the study procedures, the medication will be discontinued

DRUGAmlodipine

The subject will be started on Amlodipine (Norvasc) 2.5 -10mg daily, which he or she will continue for a period of 8 weeks. Following the 8-week treatment period, the procedures listed below will be performed. After completion of the study procedures, the medication will be discontinued.

Investigators will measure sympathetic nerve activity from the peroneal nerve by inserting a tiny needle directly into the nerve in the leg. Investigators will localize the nerve by electrical stimulation over the skin using a blunt probe. With this stimulation, subject will notice either involuntary twitching or a tingling sensation, which may be annoying but not painful. Investigators will then introduce a tiny, sterile wire needle (an electrode) through the skin at the same location. When the tip of the needle enters the nerve, subjects may again notice involuntary muscle twitches or tingling in the leg. Investigators will then turn the electrical stimulator off and make minor adjustments in the position of the needle until investigators begin to record the nerve signals. The recording needle will remain in position throughout the study.

Subjects will perform a rhythmic handgrip exercise at 30% or 45% of maximal voluntary contraction for 3 minutes. Investigators will measure cardiac output (non-invasive impedance plethysmography), blood pressure, and sympathetic nerve activity (SNA) at baseline and following this handgrip exercise

PROCEDURESustained hand grip

Subjects will perform a sustained handgrip exercise at 30% of maximal voluntary contraction for 3 minutes. Investigators will measure cardiac output (non-invasive impedance plethysmography), blood pressure, and sympathetic nerve activity (SNA) at baseline and following this handgrip exercise.

Using high-resolution ultrasound, investigators will measure skeletal muscle blood flow in the forearm at rest, following sustained handgrip exercise

Subjects will perform a cycling arm exercise with a stationary cycling device. Investigators will measure cardiac output (non-invasive impedance plethysmography), blood pressure, and sympathetic nerve activity (SNA) at baseline and following this exercise.

PROCEDURECold Pressor test

Subjects will place hand in cold water with ice for 3 minutes. Investigators will measure cardiac output (non-invasive impedance plethysmography), blood pressure, and sympathetic nerve activity (SNA) at baseline, during and 2 minutes after the test.

Sponsors

University of Texas Southwestern Medical Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Experiments will be performed on 3 groups of nondiabetic human subjects: * 1\) stage I (140-159/90-99 mmHg) subjects with essential hypertension. * 2\) stage I hypertensive subjects with primary aldosteronism * 3\) normotensive controls.

Exclusion criteria

* 1\) Any evidence of cardiopulmonary disease, left ventricular hypertrophy or systolic dysfunction by echocardiography. * 2\) Blood pressure averaging ≥160/100 mmHg * 3\) Estimated glomerular filtration rate (eGFR) \< 90 mL/min/1.73m2 * 4\) Diabetes mellitus or other systemic illness * 5\) Pregnancy * 6\) Hypersensitivity to nitroprusside, phenylephrine, amlodipine or eplerenone * 7\) Any history of substance abuse or current cigarette use * 8\) Any history of psychiatric illness * 9\) History of malignancy

Design outcomes

Primary

MeasureTime frameDescription
Muscle Sympathetic Nerve Activity at Rest8 weeks post treatment initiationmeasurement of sympathetic nerve activity by microneurography (intraneural microelectrodes)

Secondary

MeasureTime frameDescription
Muscle Sympathetic Nerve Activity During Exercise8 weeks post treatment initiationmeasurement of sympathetic nerve activity by microneurography (intraneural microelectrodes) during arm cycling exercise

Countries

United States

Participant flow

Participants by arm

ArmCount
Amlodipine Then Eplerenone
The subject will be started on Amlodipine 2.5-10 mg daily, which he or she will continue for a period of 8 weeks. After completion of the study procedures, the medication will be discontinued. The subject will be started on Eplerenone 50 - 200 mg daily, which he or she will continue for a period of 8 weeks.
6
Eplerenone Then Amlodipine
The subject will be started on Eplerenone 50 - 200 mg daily, which he or she will continue for a period of 8 weeks. After completion of the study procedures, the medication will be discontinued. The subject will be started on Amlodipine 2.5-10 mg daily, which he or she will continue for a period of 8 weeks.
8
Total14

Baseline characteristics

CharacteristicAmlodipine Then EplerenoneTotalEplerenone Then Amlodipine
Age, Continuous53 years
STANDARD_DEVIATION 9
51 years
STANDARD_DEVIATION 9
50 years
STANDARD_DEVIATION 8
Race (NIH/OMB)
American Indian or Alaska Native
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Asian
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Black or African American
1 Participants5 Participants4 Participants
Race (NIH/OMB)
More than one race
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Native Hawaiian or Other Pacific Islander
0 Participants0 Participants0 Participants
Race (NIH/OMB)
Unknown or Not Reported
0 Participants0 Participants0 Participants
Race (NIH/OMB)
White
5 Participants9 Participants4 Participants
Region of Enrollment
United States
6 participants14 participants8 participants
Sex: Female, Male
Female
0 Participants3 Participants3 Participants
Sex: Female, Male
Male
6 Participants11 Participants5 Participants

Adverse events

Event typeEG000
affected / at risk
EG001
affected / at risk
deaths
Total, all-cause mortality
0 / 140 / 14
other
Total, other adverse events
0 / 140 / 14
serious
Total, serious adverse events
0 / 140 / 14

Outcome results

Primary

Muscle Sympathetic Nerve Activity at Rest

measurement of sympathetic nerve activity by microneurography (intraneural microelectrodes)

Time frame: 8 weeks post treatment initiation

ArmMeasureValue (MEAN)Dispersion
AmlodipineMuscle Sympathetic Nerve Activity at Rest41 bursts/minuteStandard Deviation 11.7
EplerenoneMuscle Sympathetic Nerve Activity at Rest43.8 bursts/minuteStandard Deviation 13
Secondary

Muscle Sympathetic Nerve Activity During Exercise

measurement of sympathetic nerve activity by microneurography (intraneural microelectrodes) during arm cycling exercise

Time frame: 8 weeks post treatment initiation

ArmMeasureValue (MEAN)Dispersion
AmlodipineMuscle Sympathetic Nerve Activity During Exercise47 bursts/minuteStandard Deviation 16
EplerenoneMuscle Sympathetic Nerve Activity During Exercise51 bursts/minuteStandard Deviation 18

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