Actively Recruiting
Transduction of Sympathetic Neural Activity in Human Obesity Without Hypertension
Led by University of Kansas Medical Center · Updated on 2024-10-03
60
Participants Needed
1
Research Sites
265 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
In addition to chronically elevated MSNA, there is a growing recognition that hypertension in states of insulin resistance and obesity may also be attributed to an increased vascular sensitivity to MSNA (1, 2, 13, 36-38). To study this phenomenon, we quantify vascular sensitivity to MSNA using an innovative, moment-to-moment assessment of the blood pressure response following individual bursts of muscle sympathetic nerve activity (MSNA), (10, 11, 34, 37). This approach is termed 'sympathetic-vascular transduction (SVT).' We will examine the hypothesis that SVT is exaggerated in obesity and insulin resistance and is attenuated by suppression of oxidative stress. Oxidative stress is the overabundance of reactive oxygen species and is another hallmark of hypertension, obesity, and insulin resistance. Oxidative stress can be safely reduced via intravenous infusion of ascorbic acid (Vit C) (4, 28). Therefore, we will use a randomized, double-blinded, placebo-controlled approach to test the hypothesis that elevated SVT will be attenuated by suppression of oxidative stress via ascorbic acid I.V. infusion compared with saline I.V. infusion (placebo) in obese adults with insulin resistance. Our study will identify a unique mechanism that can be targeted to reduce the excessively high prevalence of hypertension and risk for CVD in obesity and insulin resistance.
CONDITIONS
Official Title
Transduction of Sympathetic Neural Activity in Human Obesity Without Hypertension
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Obese with a body mass index (BMI) greater than 25 m/kg2
- Elevated insulin resistance with HOMA-IR greater than 2.5 based on fasting glucose and insulin
- Middle-aged adults between 35 and 65 years old
- Willing and able to stop taking vitamin C, vitamin E supplements, or omega-3 fatty acids two weeks before the study
- Able and willing to provide written informed consent
You will not qualify if you...
- Currently taking statin or antihypertension medications
- Fasting triglycerides less than 250 mg/dL indicating hyperlipidemia
- Hypertension with blood pressure greater than 130/80 mmHg
- History of heart disease such as myocardial infarction or stent placement
- History of vascular disease including bypass surgery or stroke
- Diagnosis of narrow angle glaucoma
AI-Screening
AI-Powered Screening
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Trial Site Locations
Total: 1 location
1
University of Kansas Medical Center
Kansas City, Kansas, United States, 66160
Actively Recruiting
Research Team
S
Seth Holwerda
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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