# Targeting the Endothelial Glycocalyx to Enhance Vascular Function and Exercise-Induced Vascular Adaptations in Type 2 Diabetes

> **NIH VA I01** · HARRY S. TRUMAN MEMORIAL VA HOSPITAL · 2024 · —

## Abstract

PROJECT SUMMARY/ABSTRACT
 Cardiovascular disease (CVD) is the leading cause of death in Veterans with type 2 diabetes (T2D).
Lifestyle modifications, including increased physical activity, are recommended as first-line therapy for the
management of T2D. Unfortunately, the efficacy of these lifestyle interventions for preventing CVD morbidity
and mortality in patients with T2D is not well-established. Available evidence from our group and others
indicates that vascular adaptations to exercise training are impaired in subjects with T2D. We propose that
diminished vascular adaptations explain why increased physical activity does not lead to a robust reduction in
CVD morbidity and mortality in T2D. However, the mechanisms responsible for this deficit in vascular
adaptations to exercise in T2D remain unknown. This is a major limitation for identifying new adjuvant
therapeutics to maximize the cardiovascular benefits of exercise in the diabetic population. Exercise exerts
direct effects on the vasculature via repetitive exposure to hemodynamic stimuli or shear stress. The
increased blood flow and luminal shear stress attendant to each bout of exercise are primary mechanisms
contributing to vascular adaptations. Shear stress is detected by mechanosensitive endothelial luminal
structures, such as the glycocalyx, that convert mechanical forces into biochemical signals via
mechanotransduction. As such, we propose that an intact endothelial glycocalyx is required for the
mechanotransduction of increased shear stress and the subsequent chronic vascular adaptations associated
with exercise to occur. Notably, glycocalyx degradation is a classic feature of T2D. Accordingly, our
overarching hypothesis is that endothelial glycocalyx degradation is a key factor precluding shear stress
mechanotransduction and consequent exercise-induced vascular adaptations in T2D. The corollary to this
hypothesis is that restoration of the endothelial glycocalyx by dietary supplementation of glycocalyx precursors
(DSGP) will improve vascular adaptations to exercise in T2D. Specifically, in Aim 1 (Proof of Concept Clinical
Trial Phase), we will document that DSGP enhances endothelial glycocalyx integrity in patients with T2D.
Although we provide preliminary evidence that DSGP can increase glycocalyx thickness and endothelial
function in a mouse model of T2D, this will be the first study to demonstrate these effects in T2D subjects. The
effects of DSGP for eight weeks will be studied using a double-blinded randomized placebo control trial.
Subsequently, in Aim 2 (Expended Clinical Trial Phase), we will demonstrate the permissive role of the
endothelial glycocalyx in exercise-induced vascular adaptations in patients with T2D. Having shown that
restoration of the endothelial glycocalyx via DSGP is feasible in T2D subjects, we will now investigate whether
such supplementation will potentiate exercise training-induced improvements in endothelial function. This will
be accomplished in a ...

## Key facts

- **NIH application ID:** 10910977
- **Project number:** 5I01CX002399-03
- **Recipient organization:** HARRY S. TRUMAN MEMORIAL VA HOSPITAL
- **Principal Investigator:** Camila Margarita Manrique Acevedo
- **Activity code:** I01 (R01, R21, SBIR, etc.)
- **Funding institute:** VA
- **Fiscal year:** 2024
- **Award amount:** —
- **Award type:** 5
- **Project period:** 2022-04-01 → 2024-09-30

## Primary source

NIH RePORTER: https://reporter.nih.gov/project-details/10910977

## Citation

> US National Institutes of Health, RePORTER application 10910977, Targeting the Endothelial Glycocalyx to Enhance Vascular Function and Exercise-Induced Vascular Adaptations in Type 2 Diabetes (5I01CX002399-03). Retrieved via AI Analytics 2026-05-24 from https://api.ai-analytics.org/grant/nih/10910977. Licensed CC0.

---

*[NIH grants dataset](/datasets/nih-grants) · CC0 1.0*
