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Sex Differences in the Dilatory Response of Compound 21

A

Anna Stanhewicz, PhD

Status and phase

Completed
Early Phase 1

Conditions

Sex Differences

Treatments

Drug: Compound 21
Drug: Compound 21 + losartan

Study type

Interventional

Funder types

Other

Identifiers

NCT05576155
202206519

Details and patient eligibility

About

When blood pressure changes, Angiotensin II is produced and released into the bloodstream. This substance can make blood vessels smaller (i.e., vasoconstriction) by acting through Angiotensin II type I receptors (AT1R) to increase blood pressure. Or it can increase the diameter of vessels (i.e., vasodilation) through Angiotensin II type II receptors (AT2R) to decrease blood pressure. These two receptors normally work in balance to maintain blood pressure. However, excess Angiotensin II released in the bloodstream may reduce the sensitivity of AT2Rs, leading to excessive activation of AT1Rs. This results in increased constriction which plays a major role in diseases such as high blood pressure, hardening of the arteries, and heart failure. In the body, Angiotensin II production is reduced in the presence of estrogen, as seen in pre-menopausal women. Pre-menopausal women have a greater protection against cardiovascular diseases compared to age-matched males, likely due to the protective effects of estrogen. However, the extent that estrogen may impact the sensitivity of Angiotensin II receptors in pre-menopausal is unknown.

In this study, the investigators use the blood vessels in the skin as a representative vascular bed for examining mechanisms of microvascular dysfunction in humans. Using a minimally invasive technique (intradermal microdialysis for the local delivery of pharmaceutical agents), the blood vessels in a dime-sized area of the skin are studied in healthy young women and men. As a compliment to these measurements, blood is drawn from the subjects and circulating factors that may contribute to cardiovascular health are measured.

Enrollment

26 patients

Sex

All

Ages

18 to 35 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Young women or men,
  • 18-35 years old,
  • Body mass index between 18 and 30 kg/m2,
  • Systolic blood pressure <140,
  • Diastolic blood pressure <90 mmHg.

Exclusion criteria

  • Skin allergies, skin disorders, or skin diseases such as Raynaud's phenomenon or other history of cold intolerance,
  • History of metabolic or cardiovascular disease,
  • Taking medications that could alter vascular function, including antidepressants, anxiety medications, or cholesterol or blood pressure lowering drugs,
  • Women with oligo- or amenorrhea,
  • Women that are pregnant or nursing
  • current tobacco use,
  • Allergy to materials used during the experiment (e.g. latex).

Trial design

Primary purpose

Basic Science

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

26 participants in 2 patient groups

Local losartan perfusion
Experimental group
Description:
\~1 hour of losartan is perfused through an intradermal microdialysis fiber
Treatment:
Drug: Compound 21 + losartan
Local lactated Ringer's (control) perfusion
Other group
Description:
\~1 hour of lactated Ringer's is perfused through an intradermal microdialysis fiber
Treatment:
Drug: Compound 21

Trial documents
2

Trial contacts and locations

1

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Central trial contact

Kelsey Schwartz, BS; Kaila Brustkern, BS

Data sourced from clinicaltrials.gov

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