Targeting Endoplasmic Reticulum Stress in Human Hypertension

NCT ID: NCT06025630

Last Updated: 2025-03-28

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 70 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2023-08-15
• Study Completion Date: 2028-12-31

Brief Summary

There is strong evidence suggesting that endoplasmic reticulum stress contributes to neurogenic and vascular hypertension in various animal models, however this has never been explored in humans. Therefore, this project will fill this gap by performing a single-blind, placebo-controlled trial in humans with hypertension.

Detailed Description

The endoplasmic reticulum is a multipurpose organelle found in most human cells, including those in the brain and the endothelium of blood vessels. One of the primary functions of the endoplasmic reticulum is the posttranslational folding of new proteins and the reprocessing of misfolded or damaged proteins. Physiological and pathophysiological conditions can lead to the accumulation of unfolded/misfolded proteins, thus triggering the unfolded protein response which is a quality control system that maintains endoplasmic reticulum homeostasis. However, with prolonged or severe exposure to endoplasmic reticulum stress inducers, the unfolded protein response can augment the formation of reactive oxygen species, inflammatory mediators, and transcription factors that trigger sympathetic overactivity and induce endothelial dysfunction. There is strong evidence suggesting that endoplasmic reticulum stress contributes to neurogenic and vascular hypertension in various animal models, however this has never been explored in humans. This proposal builds on prior work in which the investigators pharmacologically augmented circulating concentrations of the potent endoplasmic reticulum stress inhibitor, tauroursodeoxycholic acid (TUDCA) and the development of an assay/test to quantify endoplasmic reticulum stress in cutaneous biopsy samples.

This study will accomplish the following Specific Aims:

1. Examine if endoplasmic reticulum stress inhibition, via chronic ingestion of tauroursodeoxycholic acid, will attenuate 24h blood pressure in humans with elevated (120-129/<80 mmHg) or stage 1 (130-140/80-90 mmHg) hypertension.

2. Examine the extent to which endoplasmic reticulum stress inhibition alters neurovascular control in the participants of Aim 1. Independent of the contribution to blood pressure regulation, neurovascular function is considered a key risk factor for cardiovascular morbidity and mortality. As such, the outcome of Aim 2, while providing mechanistic insight into the blood pressure lowering effect of endoplasmic reticulum stress inhibition, should be considered independent of the outcomes of Aim 1.

Conditions

Hypertension

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: SINGLE

Study Groups

Endoplasmic Reticulum Stress Inhibition

Group Type: EXPERIMENTAL

TUDCA

Intervention Type: DRUG

Endoplasmic reticulum stress will be inhibited by chronic (8 weeks) oral ingestion of the dietary supplement tauroursodeoxycholic acid (TUDCA; 1,750 mg/day)

Placebo

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DRUG

Placebo pills containing microcrystalline cellulose will be ingested over the course of the 8 week intervention.

Interventions

TUDCA

Endoplasmic reticulum stress will be inhibited by chronic (8 weeks) oral ingestion of the dietary supplement tauroursodeoxycholic acid (TUDCA; 1,750 mg/day)

Intervention Type: DRUG

Placebo

Placebo pills containing microcrystalline cellulose will be ingested over the course of the 8 week intervention.

Intervention Type: DRUG

Eligibility Criteria

Inclusion Criteria

1. 18 to 80 years of age

2. No tobacco/nicotine use within preceding 6 months (e.g., cigarettes, chewing tobacco, nicotine gum or patches)

3. Systolic blood pressure <140 mmHg; diastolic blood pressure <90 mmHg (obtained at the Screening and Familiarization Visit)

4. Normal 12-lead ECG (obtained at the Screening and Familiarization Visit and reviewed by a board-certified physician)

5. Normal clinical results from a medical exam reviewed by a board-certified physician (e.g., General Health Questionnaire obtained at the Screening and Familiarization Visit)

6. Body mass index (BMI) <35 unless athletic/muscular build; calculation = body weight (kg)/height (m2);

7. Females only: documentation of a negative pregnancy test prior to the familiarization and experimental sessions unless post-menopausal

Exclusion Criteria

1. Not meeting the defined age criteria

2. Body mass index (BMI) >35 unless athletic/muscular build; calculation = body weight (kg)/height (m2)

3. Any tobacco/nicotine use within the last 6 months (e.g., cigarettes, chewing tobacco, nicotine gum or patches)

4. Positive pregnancy test

5. Females with an erratic/irregular menstrual cycle

6. Females who are breastfeeding

7. Women who are prescribed a continually releasing hormonal contraceptive (e.g. NuvaRingTM or other hormone releasing vaginal rings, Depo Provera shot, or birth control implants such as Nexplanon)

8. Subjects who weigh less than 80 lbs.

9. Use of prescription drugs, non-prescription drugs, dietary supplements or herbal medicines known to alter vascular function unless cleared prior to the study

10. Use of beta blockers

11. Daily use of bronchodilators

12. Use of anti-coagulant therapy

13. Implanted medical devices (e.g. cardiac pacemaker)

14. Current or past history of hyperthyroidism, or other thyroid hormone-related disease

15. Current use of hormone replacement therapy (e.g., estrogen, testosterone)

16. HbA1c >5.6

17. Resting systolic blood pressure of <100 mmHg; >140mmHg or diastolic blood pressure >90mmHg

18. Abnormal 12-lead ECG or uncontrolled heart rhythm issues causing symptoms, or an unstable blood pressure

19. History of cerebrovascular abnormalities (e.g., prior stroke, transient ischemic attacks, epilepsy)

20. Known history of atherosclerosis of the carotid arteries (i.e., plaque formation)

21. History of concussion and or other loss of consciousness within the preceding 30 days

22. Autonomic dysfunction (e.g., Shy-Drager Syndrome, Bradbury-Eggleston syndrome, sinus arrhythmia, idiopathic orthostatic hypotension, fainting disorder)

23. Respiratory illnesses (e.g., chronic asthma (including exercise-induced asthma), Chronic Obstructive Pulmonary Disease, Reactive Airway Disease)

24. Any prior history of anaphylaxis, not just prior reactions to the materials used in this study

25. Severe phobia of needles

26. Latex allergy aa) Known allergies or sensitivities to substances used in the study (e.g., Lidocaine HCL, sodium nitroprusside, acetylcholine, phentolamine, L-NAME, TUDCA, or related drugs) bb) Donated blood within the last 60 days cc) History or family history of abnormal blood clotting, clots in deep veins in the legs or pelvis, or blood clots to the lungs dd) History of alcohol or drug abuse which inhibits the subject's ability to complete this study ee) Individuals who have had mastectomies ff) History of methemoglobinemia gg) Current diagnosis of anemia hh) Current Fever (oral temp >99.5 °F/ 37.5 °C) ii) Current use of PDE3 inhibitors (e.g., Viagra) or soluble guanylate cyclase (sGC) stimulators (e.g., riociguat), or unwillingness to withhold medication for 2 weeks prior to laboratory testing jj) Current diagnosis of cancer kk) Cardiac surgery or cardiac events (e.g., coronary artery bypass graft surgery, myocardial infarction, heart failure) ll) Diagnosis of neurological disease or cognitive dysfunction

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of North Texas Health Science Center

OTHER

Sponsor Role: lead

Responsible Party

Steven A. Romero

Associate Professor

Responsibility Role: PRINCIPAL_INVESTIGATOR

Locations

University of North Texas Health Science Center

Fort Worth, Texas, United States

Site Status: RECRUITING

Countries

United States

Facility Contacts

Steven A Romero, PhD

Role: primary

steven.romero@unthsc.edu

8177355159

Bella Ruiz, BS

Role: backup

YsabellaRuiz@my.unthsc.edu

8177352088

Other Identifiers

ERX:2023-063

Identifier Type: -

Identifier Source: org_study_id