Asymmetric Dimethylarginine Is a Well Established Mediating Risk Factor for Cardiovascular Morbidity and Mortality—Should Patients with Elevated Levels Be Supplemented with Citrulline?
Open accessAbstract
The arginine metabolite asymmetric dimethylarginine (ADMA) is a competitive inhibitor and uncoupler of endothelial nitric oxide synthase (eNOS), an enzyme that acts in multifarious ways to promote cardiovascular health. This phenomenon likely explains, at least in part, why elevated ADMA has been established as an independent risk factor for cardiovascular events, ventricular hypertrophy, and cardiovascular mortality. Fortunately, the suppressive impact of ADMA on eNOS activity can be offset by increasing intracellular arginine levels with supplemental citrulline. Although the long-term impact of supplemental citrulline on cardiovascular health in patients with elevated ADMA has not yet been studied, shorter-term clinical studies of citrulline administration demonstrate effects suggestive of increased NO synthesis, such as reductions in blood pressure and arterial stiffness, improved endothelium-dependent vasodilation, increased erection hardness, and increased ejection fractions in patients with heart failure. Supplemental citrulline could be a practical option for primary or secondary prevention of cardiovascular events and mortality, as it is inexpensive, has a mild flavor, and is well tolerated in doses (3–6 g daily) that can influence eNOS activity. Large and long-term clinical trials, targeting patients at high risk for cardiovascular events in whom ADMA is elevated, are needed to evaluate citrulline’s potential for aiding cardiovascular health.
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Ser1177 phosphorylation activates electron flow through the reductase domain and increases NO synthesis in functional eNOS.
“Ser1177 phosphorylation activates electron flow through the reductase domain and, hence, increases NO synthesis in functional eNOS.”
From Sources of Vascular Nitric Oxide and Reactive Oxygen Species and Their Regulation (2019) · cites this paper as [631]
Ser1177 is located in the C-terminal portion of eNOS in a helical C-terminal tail element that blocks flavin reduction and regulates the conformational equilibrium of the reductase domain.
“Ser1177 is located in the C-terminal portion of eNOS in a helical C-terminal tail element that blocks flavin reduction and regulates the conformational equilibrium of the reductase domain”
From Sources of Vascular Nitric Oxide and Reactive Oxygen Species and Their Regulation (2019) · cites this paper as [631]
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References 118 · Cited by 25
Research works printed but not linked: 1
- [86]Oster K.A. Ross D.J. Dawkins H.H.R. The XO Factor Park City Press New York, NY, USA 1983
- Authors
- McCarty, M.
- Affiliations
- Catalytic Longevity (US)
- Corresponding author
- McCarty, Mark
- ORCID
- McCarty, Mark
- Venue
- Healthcare
- Publisher
- MDPI AG
- Published
- 2016-07-08
- Volume
- 4
- Issue
- 3
- Pages
- 40
- ISSN
- 2227-9032 (ISSN-L)
- PMC
- PMC5041041
- OpenAlex
- W2467818405
- Cited by
- 25
- References
- 118
- Citations by year
- 2026: 1 · 2025: 1 · 2023: 1 · 2022: 4 · 2021: 3 · 2020: 3 · 2019: 3 · 2018: 3 · 2017: 6
- FWCI
- 0.47
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Healthcare (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Topics
- Health Sciences › Medicine › Physiology › Nitric Oxide and Endothelin Effects
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiovascular Health and Disease Prevention
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Cancer-related gene regulation
- Keywords
- asymmetric dimethylarginine, citrulline supplementation, endothelial nitric oxide synthase, nitric oxide production, cardiovascular risk, cardiovascular mortality, cardiovascular morbidity, arginine metabolism, endothelial dysfunction, arterial stiffness, blood pressure, heart failure, cardiovascular disease prevention
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