Human Cerebral Blood Flow Regulation

Cerebral Arterial Diseases Clinical Trial

— Gas Challenge  

Official title:

Human Cerebral Blood Flow Regulation: Sex, Mechanism, and Stress Differences

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT04265053
• Other study ID #: 2020-0336
• Secondary ID: A176000EDUC/KINE
• Status: Recruiting
• Phase: Early Phase 1
• Start date: April 12, 2021
• Est. completion date: May 31, 2026

Study information

• Verified date: March 2024
• Source: University of Wisconsin, Madison
• Contact: Shawn E Bolin, MS
• Phone: 608-263-6308
• Email: sbolin[@]wisc.edu
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study tests basic differences in how men and women control brain (cerebral) blood flow (CBF), at rest and under stress. The stress is low oxygen or high carbon dioxide. The investigators hypothesize that sex differences per se, plus sex hormone differences, drive different signals in blood vessels that change the way CBF is regulated. The investigators will test these mechanisms with medicine infusions during stress, and measure CBF using state-of-the-art MRI approaches. Research confounding variables like aging and disease will be mitigated by comparing younger adults (18-40 years old).

Description:

Cerebrovascular disease is the third leading killer in the U.S., and contributes to decreased quality of life and increased long-term care spending. The risk of cerebrovascular disease is inversely associated with resting cerebral blood flow (CBF). Men exhibit a lower resting CBF and have twice the risk of cerebrovascular disease when compared to premenopausal women. The ability of cerebral vessels to respond to challenges is also inversely related to disease risk, and may be useful in identifying at-risk patients pre-clinically. However, these studies are often confounded by aging and/or comorbidities, and the associations provide little insight into physiologic mechanisms responsible for sexually dimorphic cerebrovascular disease risk. Conversely, animal studies use supraphysiologic levels of hormone treatment in primarily young animals, which limits the translational relevance of animal CBF mechanisms. While there is general agreement that estrogen is protective in healthy adults, the basic impact of sex, and physiologic fluctuations in sex hormones, on mechanisms of CBF control remains unclear. The overall goal of this research program is to investigate the mechanisms which actively control cerebral blood flow (CBF) in humans, particularly how men and women differ in control mechanisms on a regional basis throughout the brain circulation. The investigators propose to study CBF control mechanisms in healthy younger (18-40 yrs) adult men and women. The overall hypothesis is that female sex and sex hormones contribute to larger stress-induced increases in CBF, due to greater prostanoid (COX) and nitric oxide (NOS) dilation. A key technological innovation of this proposal derives from multi-mode, high-resolution, flow sensitive MRI to quantify CBF at macrovascular and microvascular levels, at rest, and in response to environmental challenges (stress test for the brain). Additionally, the research design allows for quantification of sex differences in two vascular control mechanisms across all brain regions. Preliminary data demonstrate: hypoxic cerebral vasodilation is 60-100% higher in women compared to men, COX inhibition reduces dilation in women but not men, NOS inhibition reduces vasodilation more in women. Those concepts will be tested in Aims 1-2 of the grant in this current proposal, covered in Phase 1 using technical innovative MRI and pharmacologic tools to test potential sex specific mechanisms of CBF control. The conceptual innovation is planned in Aim 3 of the grant (or Phase 2). Participants must complete Phase 1 studies to continue to Phase 2. Study procedures in Phase 1 and 2 are identical, but we conduct them twice: once in the context of sex hormone suppression, and a second time during a single hormone replacement (during suppression), to study the independent impact of testosterone (men) and estrogen (women) on CBF control mechanisms. Substantial preliminary findings support these hypotheses, and integrated physiologic, pharmacologic, and MRI approaches are available to test them. This state-of-the-art approach will yield previously unattainable insight into not only maintaining basal CBF, but actively controlling it during physiologic demands for increased flow. These novel, high resolution, regionally-specific, sex-specific, and mechanism-specific findings will serve as a knowledge platform, for designing sex-specific CBF studies in high risk disease populations (e.g. diabetes, hypertension, Alzheimer's) which exhibit strong sex-specific etiology and important vascular contributions. Three Specific Aims will be addressed in this study: Aim 1: Test the hypothesis that healthy males exhibit reduced cerebral vasodilation compared to healthy females despite exhibiting similar vasodilation to hypercapnia. - Aim 1A: Vasodilation to hypoxia will be markedly lower in males, more so in anterior brain regions. - Aim 1B: Vasodilation to hypercapnia will be similar between sexes. Aim 2: Test the hypothesis that acute inhibition of COX or NOS will reduce sex differences in hypoxia-mediated cerebral vasodilation. - Aim 2A: COX-mediates vasodilation primarily in females. - Aim 2B: NOS mediates vasodilation more in females than males. Aim 3: Test the hypothesis that manipulating sex steroids can abolish or magnify sex differences in vasodilation. - Aim 3A: Short-term suppression of sex steroids will abolish sex differences in resting and hypoxic CBF via greater losses of COX- and NOS-mediated vasodilation in females than males. - Aim 3B: Short-term supplementation of unopposed testosterone in males will magnify sex differences by driving COX vasoconstriction (TXA2) and uncoupled NOS vasoconstriction. - Aim 3C: Short-term supplementation of unopposed estradiol in females will magnify sex differences via increased NOS and COX vasodilation.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 111
• Est. completion date: May 31, 2026
• Est. primary completion date: March 31, 2025
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 18 Years to 40 Years

Eligibility

Inclusion Criteria:

• All participants will be healthy adults between 18-40 years old, matched for age and aerobic fitness
• Participants will be non-hypertensive (<125/80mm Hg)
• Participants will be non-obese (BMI 19-25 kg/m2)
• Participants will have normal blood glucose (<100 g/dl)
• Participants will have normal lipids (LDL cholesterol <130 mg/dl, triglycerides <150 mg/dl)
• Women must have a natural regular menstrual cycle

Exclusion Criteria:

• Participants with a history of:
• peripheral vascular disease
• hepatic disease
• renal disease
• hematologic disease
• stroke
• obesity
• prediabetes
• diabetes
• sleep apnea
• Participants with current BP>130/85 mmHg
• Regular smokers
• Taking cardiovascular medications
• Women who take hormonal birth control
• Women who are pregnant or have polycystic ovarian syndrome [Hormonal birth control will not be allowed in women]
• Contradictions to MRI
• Lactose intolerance

Related Conditions & MeSH terms

• Cerebral Arterial Diseases

Intervention

Drug:
• Indomethacin 25 MG/50 MG
Indomethacin is a nonsteroidal anti-inflammatory drug commonly used to reduce fever, pain, stiffness, and swelling from inflammation. It prevents the production of prostaglandins, endogenous signaling molecules known to cause symptoms from inflammation. We will use Indomethacin to test COX as a potential mechanism explaining sex differences in CBF control. Indomethacin usage is IND exempt.
• Placebo - Lactose
Subjects will be screened for lactose intolerance. Total dosing will be calculated to match the mg needed for the indomethacin study visit. Placebo usage is IND exempt.
• Ganirelix Acetate
Gonadotropin-Releasing Hormone (GnRH) antagonist ganirelix acetate as a model to isolate estrogen and testosterone effects on the cerebrovascular system. Participants receive daily injections of ganirelix for 12-14 days for Aim 3 studies only. This will be overseen by clinical endocrinologists. Both males and females receive this treatment in Aim 3.
• Testosterone Transdermal Product
In Aim 3, males receive this for 7-9 days of the ganirelix treatment.
• Estradiol Topical
In Aim 3, females receive this for 7-9 days of the ganirelix treatment.
• Antacid
Subjects will also be given a dose of over-the-counter antacid to combat the gastrointestinal distress expected from Indomethacin. Subjects will also be given a dose of over-the-counter antacid during the placebo visit to mimic the indomethacin study visit. Antacid is IND exempt.

Locations

Country	Name	City	State
United States	University of Wisconsin, Madison	Madison	Wisconsin

Sponsors (2)

Lead Sponsor	Collaborator
University of Wisconsin, Madison	National Heart, Lung, and Blood Institute (NHLBI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Cerebrovascular Conductance (CVC) in response to Hypoxia	CVC is the ratio between Cerebral Blood Flow (CBF) and blood pressure (BP). Change in CVC in response to hypoxia between male and female groups, where baseline CVC is subtracted from hypoxia CVC. Hypoxia typically lasts about 20 minutes. The hypothesis is that women will exhibit 50-60% more vasodilation in response to hypoxia [Aim 1].	up to 75 minutes for entire visit, but hypoxia lasts about 20 minutes
Primary	CVC in response to Hypercapnia	CVC is the ratio between Cerebral Blood Flow (CBF) and blood pressure (BP). Change in CVC in response to hypercapnia between male and female groups, where CBF is normalized for BP. Baseline CVC will be subtracted from hypercapnia CVC. Hypercapnia typically lasts about 10-15 minutes.The hypothesis is that hypercapnic vasodilation will be similar between groups [Aim 1B].	up to 75 minutes for entire visit, but hypercapnia lasts about 10-15 minutes
Primary	CVC change in response to Drug Infusion	CVC is the ratio between Cerebral Blood Flow (CBF) and blood pressure (BP). Change in CVC in response to drug infusion between male [NOS or COX] and female [NOS or COX] groups. The hypothesis is that acute inhibition of COX or NOS will reduce sex differences in hypoxia-mediated cerebral vasodilation [Aim 2].	approximately 10 minutes in the middle of 75 minute study visit
Primary	Change in hypoxia CVC in response to Ganirelix compared to no ganirelix Baseline (Aim 3a)	Change in hypoxia CVC response to ganirelix compared to baseline within male and female groups, where CVC is CBF is normalized for BP. The hypothesis is that GnRH suppression will abolish hypoxic CBF differences, indicating sex steroids play a vital role in CBF control [Aim 3].	baseline and up to 7 days during ganirelix treatment
Primary	Change in hypoxia CVC response to sex hormone suppression with single sex hormone add-back	Change in hypoxia CVC response to ganirelix+testosterone (in males Aim 3B) or ganirelix+estradiol (in females, Aim 3C) compared to baseline within male and female groups, where CVC is CBF is normalized for BP. The hypothesis is that adding a sex steroid will magnify hypoxic CVC differences, indicating sex steroids play a vital role in CBF control [Aim 3].	baseline and up to 14 days
Primary	Change in hypoxia CVC response to NOS or COX inhibition during ganirelix+single sex hormone add-back	Change in hypoxia CVC drug response to NOS or COX inhibition during ganirelix+testosterone (in males Aim 3B) or ganirelix+estradiol (in females, Aim 3C) compared to baseline hypoxia studies from Aim 2. The hypothesis is that adding a sex steroid will magnify hypoxic CVC differences in drug effects, indicating sex steroids play a vital role in CBF control [Aim 3].	baseline and up to 14 days