RecruitingEarly Phase 1NCT05301192

Angiotensin-(1-7) Cardiovascular Effects in Aging


Sponsor

Milton S. Hershey Medical Center

Enrollment

26 participants

Start Date

Dec 9, 2022

Study Type

INTERVENTIONAL

Conditions

Summary

Aging is an independent risk factor for developing hypertension and cardiovascular disease; however, the mechanisms underlying age-related cardiovascular disease remain poorly understood. One hallmark of aging is an increase in sympathetic nervous system activity, which can decrease the number and/or sensitivity of β2 adrenergic receptors to reduce dilation of blood vessels and increase blood pressure. Identifying new targets to restore vascular β2 adrenergic receptor signaling may help reduce cardiovascular risk in aging. This study will test the hypothesis that angiotensin-(1-7), a protective hormone of the renin-angiotensin system, can reduce cardiovascular sympathetic outflow and blood pressure and improve endothelial function in older healthy humans.


Eligibility

Min Age: 65 YearsMax Age: 80 Years

Inclusion Criteria7

  • Men and women of all races and ethnicities
  • Capable of giving informed consent
  • Fluent in written and spoken English
  • Age 65-80 years
  • Body mass index (BMI) between 18.5 and 30 kg/m2
  • Normotensive defined as seated blood pressure <130/80 mmHg and without hypertensive medications
  • Satisfactory history and physical exam

Exclusion Criteria19

  • Age < 65 or > 80 years
  • Women who are pregnant, nursing, or taking hormone replacement therapy
  • Decisional impairment
  • Prisoners
  • Current or recent (less than 6 months) recreational drug history or excessive alcohol abuse history (greater than 14 drinks per week)
  • Current smokers
  • Highly trained athletes
  • Evidence of type I or type II diabetes (fasting glucose > 126 mg/dL or use of anti-diabetic medications)
  • Hypertension or history of serious cardiovascular disease (e.g., myocardial infarction within 6 months, symptomatic coronary artery disease, presence of angina pectoris, significant arrhythmia, congestive heart failure, deep vein thrombosis, pulmonary embolism, second or third degree heart block, mitral valve stenosis, aortic stenosis, hypertrophic cardiomyopathy) or cerebrovascular disease (e.g., cerebral hemorrhage, stroke, transient ischemic attack).
  • History or presence of immunological or hematological disorders
  • Impaired hepatic function \[aspartate aminotransferase (AST) or alanine aminotransferase (ALT) levels >2 times upper limit of normal range\]
  • Impaired renal function (serum creatinine >2.0 mg/dl)
  • Anemia
  • Taking drugs known to influence sympathetic activity (e.g. serotonin-norepinephrine reuptake inhibitors, norepinephrine transporter inhibitors, stimulants).
  • Treatment with anticoagulants (e.g. warfarin)
  • Treatment with chronic systemic glucocorticoid therapy (>7 consecutive days in 1 month in the 1-month preceding the study)
  • Treatment with any investigational drug in the 1-month preceding the study
  • Known allergy or contraindication to angiotensin converting enzyme inhibitors or angiotensin receptor blockers, both of which increase endogenous angiotensin-(1-7) levels as part of their mechanism of action
  • Inability to give, or withdraw, informed consent

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Interventions

DRUGAngiotensin-(1-7)

This is a biologically active endogenous angiotensin peptide that may play an important role in regulation of blood pressure.

DRUGSaline

Saline will be used as the placebo comparator.


Locations(1)

Penn State Milton S. Hershey Medical Center

Hershey, Pennsylvania, United States

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NCT05301192


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