Nitric oxide and nitrite-based therapeutic opportunities in intimal hyperplasia
Abstract
Vascular intimal hyperplasia (IH) limits the long term efficacy of current surgical and percutaneous therapies for atherosclerotic disease. There are extensive changes in gene expression and cell signaling in response to vascular therapies, including changes in nitric oxide (NO) signaling. NO is well recognized for its vasoregulatory properties and has been investigated as a therapeutic treatment for its vasoprotective abilities. The circulating molecules nitrite (NO(2)(-)) and nitrate (NO(3)(-)), once thought to be stable products of NO metabolism, are now recognized as important circulating reservoirs of NO and represent a complementary source of NO in contrast to the classic L-arginine-NO-synthase pathway. Here we review the background of IH, its relationship with the NO and nitrite/nitrate pathways, and current and future therapeutic opportunities for these molecules.
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Dietary nitrate and nitrite confer protection from intimal hyperplasia in rodents.
“Further, dietary nitrate and nitrite confer protection from intimal hyperplasia in rodents[117–119]”
From Enterosalivary nitrate metabolism and the microbiome: Intersection of microbial metabolism, nitric oxide and diet in cardiac and pulmonary vascular health (2017) · cites this paper as [118]
Multiple preclinical studies suggest nitrite may be effective for prevention and/or treatment of many cardiovascular disorders or risk factors for cardiovascular disease including peripheral artery disease, atherosclerosis, chronic heart failure, stroke, diabetes, and hypertension.
“multiple studies in preclinical models suggest that nitrite also may be effective for the prevention and/or treatment of many cardiovascular disorders or risk factors for CVD including peripheral artery disease (4, 69, 146), atherosclerosis (2, 3, 5, 127), chronic heart failure (32, 122), stroke (50, 82, 150), diabetes (138), and hypertension (22, 57, 58, 128).”
From Inorganic nitrite supplementation for healthy arterial aging (2014) · cites this paper as [2]
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- Authors
- Alef, M. J., Tzeng, E., & Zuckerbraun, B. S.
- Affiliations
- University of Pittsburgh (US)
- Corresponding author
- Zuckerbraun, Brian S.
- Venue
- Nitric Oxide
- Publisher
- Elsevier BV
- Published
- 2012-05
- Volume
- 26
- Issue
- 4
- Pages
- 285-294
- ISSN
- 1089-8603 (ISSN-L)
- OpenAlex
- W2026972928
- Cited by
- 20
- References
- 167
- Citations by year
- 2025: 1 · 2022: 1 · 2020: 1 · 2018: 3 · 2017: 2 · 2016: 3 · 2015: 3 · 2014: 3 · 2013: 2 · 2012: 1
- FWCI
- 0.31
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Nitric Oxide (publishedVersion)
- PubMed (publishedVersion)
- Funders
- U.S. Department of Veterans Affairs (I01 BX000635)
- Topics
- Health Sciences › Medicine › Physiology › Nitric Oxide and Endothelin Effects
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiovascular Health and Disease Prevention
- Life Sciences › Immunology and Microbiology › Immunology › Atherosclerosis and Cardiovascular Diseases
- Keywords
- intimal hyperplasia, nitrite, nitrate, no-signaling, atherosclerosis, vascular protection, therapeutic target
- MeSH terms
- Animals, Humans, Hyperplasia, Nitrates, Nitric Oxide, Nitrites, Vascular Diseases, Xanthine Dehydrogenase, Signal Transduction, Tunica Intima
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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