2 Weeks of Citrulline Supplementation on Arterial Function in Postmenopausal Women With Elevated Blood Pressure or Hypertension

Sponsor
Texas Tech University (Other)
Overall Status
Recruiting
CT.gov ID
NCT06025383
Collaborator
(none)
19
1
2
11.4
1.7

Study Details

Study Description

Brief Summary

The objective of this project is to elucidate the effect of L-Citrulline (L-CIT) supplementation on vascular function at rest and during rhythmic handgrip exercise and functional sympatholysis via lower-body negative pressure in postmenopausal women with elevated blood pressure and hypertension.

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: L-Citrulline
  • Dietary Supplement: Placebo
N/A

Detailed Description

Using a double-blind, randomized, placebo-controlled, and crossover design, overweight or obese postmenopausal women with elevated blood pressure (BP) or hypertension will receive CIT (6 grams/day) or placebo for 2 weeks, separated by a two-week washout period.

There will be a total of 5 laboratory visits. The 1st visit will take approximately 1 hour. The 2nd - 5th visits will take about 2 hours and 15 minutes. Visit 1 will be a screening visit, visits 2 and 4 will be considered baseline visits, and visits 3 and 5 will be following the participants' two weeks of supplementation. Arterial stiffness (carotid-femoral and femoral-dorsalis pedis pulse wave velocity) and endothelial function will be assessed at rest. Additionally, brachial artery blood flow, forearm muscle oxygenation, cardiovascular hemodynamics (stroke volume, cardiac output, systemic vascular resistance), and BP will be assessed at rest, during 6 minutes of rhythmic handgrip exercise at 30% of a predetermined maximal voluntary contraction, and 2 minutes of superimposed lower body negative pressure to increase sympathetic activity.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
19 participants
Allocation:
Randomized
Intervention Model:
Crossover Assignment
Intervention Model Description:
Cross-Over Assignment Double (Participant, Investigator) randomized, double-blind, placebo-controlled, cross-over study designCross-Over Assignment Double (Participant, Investigator) randomized, double-blind, placebo-controlled, cross-over study design
Masking:
Double (Participant, Investigator)
Primary Purpose:
Basic Science
Official Title:
2 Weeks of L-Citrulline Supplementation Improves Arterial Function and Systolic Blood Pressure at Rest and During Exercise in Postmenopausal Women With Elevated Blood Pressure and Hypertension
Actual Study Start Date :
Jul 20, 2023
Anticipated Primary Completion Date :
Jul 1, 2024
Anticipated Study Completion Date :
Jul 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: L-Citrulline

L-Citrulline: 6 grams/day divided in 2 equal doses

Dietary Supplement: L-Citrulline
2 weeks of L-Citrulline supplementation (6 grams/day)

Placebo Comparator: Placebo

Microcrystalline cellulose: 8 capsules/day divided into 2 equal doses

Dietary Supplement: Placebo
2 weeks of microcrystalline cellulose supplementation (8 capsules/day)

Outcome Measures

Primary Outcome Measures

  1. Macrovascular endothelial function at rest [2 weeks of each intervention]

    Endothelial function will be assessed via brachial artery flow-mediated vasodilation (ultrasonography) during reactive hyperemia at baseline and after 2 weeks of each supplementation.

  2. Microvascular endothelial function at rest [2 weeks of each intervention]

    Endothelial function will be assessed via peripheral arterial tonometry (endoPAT) during reactive hyperemia at baseline and after 2 weeks of each supplementation.

  3. Microvascular endothelial function at rest [2 weeks of each intervention]

    Endothelial function will be assessed using forearm muscle oxygen saturation (near-infrared spectroscopy) during reactive hyperemia before and after 2 weeks of each supplementation.

  4. Brachial artery blood flow at rest and during rhythmic handgrip exercise with and without lower-body negative pressure [2 weeks of each intervention]

    Blood flow will be measured via Doppler ultrasound before and after 2 weeks of each intervention.

  5. Forearm muscle oxygenation at rest and during rhythmic handgrip exercise with and without lower-body negative pressure [2 weeks of each intervention]

    Muscle oxygen saturation will be measured via near-infrared spectroscopy before and after 2 weeks of each intervention.

Secondary Outcome Measures

  1. Beat-to-beat blood pressure at rest and during rhythmic handgrip exercise with and without lower-body negative pressure [2 weeks of each intervention]

    Blood pressure will be measured via a finger cuff (finometer) before and after 2 weeks of each intervention.

  2. Aortic hemodynamics at rest and during rhythmic handgrip exercise with and without lower body negative pressure [2 weeks of each intervention]

    Aortic blood pressure and pressure waves will be assessed using radial applanation tonometry before and after 2 weeks of each intervention.

  3. Stroke volume at rest and during rhythmic handgrip exercise with and without lower body negative pressure [2 weeks of each intervention]

    Stroke volume will be assessed via impedance cardiography before and after 2 weeks of each intervention.

  4. Heart rate at rest and during rhythmic handgrip exercise with and without lower body negative pressure [2 weeks of each intervention]

    Heart rate will be assessed via impedance cardiography before and after 2 weeks of each intervention.

  5. Systemic vascular resistance at rest and during rhythmic handgrip exercise with and without lower body negative pressure [2 weeks of each intervention]

    Systemic vascular resistance will be assessed via impedance cardiography before and after 2 weeks of each intervention.

  6. Central and peripheral arterial stiffness at rest [2 weeks of each intervention]

    Carotid-femoral and femoral-dorsalis pedis pulse wave velocity will be measured using arterial applanation tonometry before and after 2 weeks of each intervention.

  7. Forearm muscle strength [2 weeks of each intervention]

    Maximal forearm muscle strength will be measured using a handgrip dynamometer before and after 2 weeks of each intervention.

  8. L-arginine levels [2 weeks of each intervention]

    Serum levels of l-arginine will be assessed before and after 2 weeks of each intervention.

  9. Nitric oxide levels [2 weeks of each intervention]

    Serum levels of nitric oxide will be assessed before and after 2 weeks of each intervention.

  10. L-citrulline levels [2 weeks of each intervention]

    Serum levels of l-citrulline will be assessed before and after 2 weeks of each intervention.

  11. L-ornithine levels [2 weeks of each intervention]

    Serum levels of l-ornithine will be assessed before and after 2 weeks of each intervention.

Eligibility Criteria

Criteria

Ages Eligible for Study:
50 Years to 70 Years
Sexes Eligible for Study:
Female
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Postmenopausal women (defined as the absence of menstruation for at least 1 year).

  • Resting systolic blood pressure 120-150 mmHg.

  • Between the ages of 50 - 70 years.

  • Sedentary (< 120 minutes of exercise/week).

  • Body mass index of 25 - 39.9 kg/m2.

  • Fasting glucose < 126 mg/dL and HbA1c < 6.5%.

Exclusion Criteria:
  • Body mass index ≥ 40 or < 25 kg/m2.

  • Systolic blood pressure > 150 mmHg.

  • Taking more than two antihypertensive medications.

  • Cardiovascular diseases, type I/II diabetes, musculoskeletal disorders, or cancer.

  • Changes in hypertensive medication in the past three months.

  • Began or changed hormone replacement therapy in the past 6 months.

  • Current smoker.

  • Heavy drinking (> 7 alcoholic drinks/week).

  • Participants on beta-blockers or other vasodilatory supplements (nitrates).

  • Incorporated in a weight loss program and/or aerobic or resistance training program.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Texas Tech University Lubbock Texas United States 79409

Sponsors and Collaborators

  • Texas Tech University

Investigators

  • Principal Investigator: Arturo Figueroa, Texas Tech University

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Arturo Figueroa, Arturo Figueroa, Principal Investigator, Texas Tech University
ClinicalTrials.gov Identifier:
NCT06025383
Other Study ID Numbers:
  • IRB2022-1055
First Posted:
Sep 6, 2023
Last Update Posted:
Sep 6, 2023
Last Verified:
Aug 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Arturo Figueroa, Arturo Figueroa, Principal Investigator, Texas Tech University
Additional relevant MeSH terms:

Study Results

No Results Posted as of Sep 6, 2023