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Updated: Jun 23, 2026

Non-invasive Assessment of Microvascular and Endothelial Function
Published on: January 29, 2013
Impaired vasodilation of forearm resistance vessels in hypercholesterolemic humans
M A Creager1, J P Cooke, M E Mendelsohn
1Division of Vascular Medicine and Atherosclerosis, Brigham and Women's Hospital, Boston, Massachusetts 02115.
Insights
High cholesterol (hypercholesterolemia) impairs blood vessel function in humans. This study found reduced vasodilator responses to endothelium-derived relaxing factor and nitrovasodilators in hypercholesterolemic individuals.
Area of Science:
- Cardiovascular Physiology
- Metabolic Disorders
Background:
- Hypercholesterolemia is a significant risk factor for cardiovascular disease.
- Understanding its direct impact on vascular function, independent of atherosclerosis, is crucial.
Purpose of the Study:
- To investigate the effect of hypercholesterolemia on vascular reactivity in human forearm resistance vessels.
- To assess the roles of endothelium-derived relaxant factor and direct smooth muscle stimulation in hypercholesterolemia.
Main Methods:
- Vascular reactivity was measured in normal and hypercholesterolemic subjects using forearm venous occlusion plethysmography.
- Intrabrachial artery infusions of methacholine and nitroprusside were administered to assess vasodilation.
- Phenylephrine infusion was used to examine vasoconstrictive responsiveness.
Main Results:
- Basal and reactive hyperemia blood flow were comparable between groups.
- Hypercholesterolemic subjects showed blunted forearm blood flow responses to both methacholine and nitroprusside.
- Vasoconstrictive response to phenylephrine was not different between groups.
Conclusions:
- Hypercholesterolemia impairs vasodilator function in human forearm resistance vessels.
- This impairment affects both endothelium-dependent (endothelium-derived relaxant factor) and endothelium-independent (nitrovasodilator) pathways.
- Reduced vasodilator response in hypercholesterolemia may contribute to endothelial dysfunction.
Abstract:
The effect of hypercholesterolemia on vascular function was studied in humans. To eliminate the potential confounding effects of atherosclerosis, vascular reactivity was measured in the forearm resistance vessels of 11 normal subjects (serum LDL cholesterol = 111 +/- 7 mg/dl) and 13 patients with hypercholesterolemia (serum LDL cholesterol = 211 +/- 19 mg/dl, P less than 0.05). Each subject received intrabrachial artery infusions of methacholine, which releases endothelium-derived relaxant factor, and nitroprusside which directly stimulates guanylate cyclase in vascular smooth muscle. Maximal vasodilatory potential was determined during reactive hyperemia. Vasoconstrictive responsiveness was examined during intra-arterial phenylephrine infusion. Forearm blood flow was determined by venous occlusion plethysmography. Basal forearm blood flow in normal and hypercholesterolemic subjects was comparable. Similarly, reactive hyperemic blood flow did not differ between the two groups. In contrast, the maximal forearm blood flow response to methacholine in hypercholesterolemic subjects was less than that observed in normal subjects. In addition, the forearm blood flow response to nitroprusside was less in hypercholesterolemic subjects. There was no difference in the forearm vasoconstrictive response to phenylephrine in the two groups. Thus, the vasodilator responses to methacholine and nitroprusside were blunted in patients with hypercholesterolemia. We conclude that in humans with hypercholesterolemia, there is a decreased effect of nitrovasodilators, including endothelium-derived relaxing factor, on the vascular smooth muscle of resistance vessels.
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