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Oxidative Stress and Vascular Disease
Abstract
Growing evidence indicates that chronic and acute overproduction of reactive oxygen species (ROS) under pathophysiologic conditions is integral in the development of cardiovascular diseases (CVD). These ROS can be released from nicotinamide adenine dinucleotide (phosphate) oxidase, xanthine oxidase, lipoxygenase, mitochondria, or the uncoupling of nitric oxide synthase in vascular cells. ROS mediate various signaling pathways that underlie vascular inflammation in atherogenesis: from the initiation of fatty streak development through lesion progress to ultimate plaque rupture. Various animal models of oxidative stress support the notion that ROS have a causal role in atherosclerosis and other cardiovascular diseases. Human investigations also support the oxidative stress hypothesis of atherosclerosis. Oxidative stress is the unifying mechanism for many CVD risk factors, which additionally supports its central role in CVD. Despite the demonstrated role of antioxidants in cellular and animal studies, the ineffectiveness of antioxidants in reducing cardiovascular death and morbidity in clinical trials has led many investigators to question the importance of oxidative stress in human atherosclerosis. Others have argued that the prime factor for the mixed outcomes from using antioxidants to prevent CVD may be the lack of specific and sensitive biomarkers by which to assess the oxidative stress phenotypes underlying CVD. A better understanding of the complexity of cellular redox reactions, development of a new class of antioxidants targeted to specific subcellular locales, and the phenotype-genotype linkage analysis for oxidative stress will likely be avenues for future research in this area as we move toward the broader use of pharmacological and regenerative therapies in the treatment and prevention of CVD.
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“Additionally, studies show peroxynitrite can traverse cell membranes by both diffusion and through ion channels, suggesting that peroxynitrite can mediate oxidation/nitration distant from its site of formation (221, 611).”
From Sources of Vascular Nitric Oxide and Reactive Oxygen Species and Their Regulation (2019) · cites this paper as [611]
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“Additionally, studies show peroxynitrite can traverse cell membranes by both diffusion and through ion channels, suggesting that peroxynitrite can mediate oxidation/nitration distant from its site of formation (221, 611).”
From Sources of Vascular Nitric Oxide and Reactive Oxygen Species and Their Regulation (2019) · cites this paper as [611]
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BackgroundNotoginsenoside R1 Attenuates Atherosclerotic Lesions in ApoE Deficient Mouse Model
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“Several lines of evidence support a role for oxidative stress in the pathogenesis of both Alzheimer disease (AD) (4) and atherosclerosis (5).”
BackgroundHydrogen sulfide donors: Therapeutic potential in anti-atherosclerosis
Zhang, H., Bai, Z., Zhu, L., Liang, Y., Fan, X., Li, J., Wen, H., Shi, T., Zhao, Q., & Wang, Z. (2020) · European Journal of Medicinal Chemistry · doi:10.1016/j.ejmech.2020.112665 · Cited by 60
Fukuzawa, K., Saitoh, Y., Akai, K., Kogure, K., Ueno, S., Tokumura, A., Otagiri, M., & Shibata, A. (2004) · Biochimica et Biophysica Acta (BBA) - Biomembranes · doi:10.1016/j.bbamem.2004.12.006 · Cited by 59
Yu, Y., Thorpe, S. R., Jenkins, A. J., Shaw, J., Sochaski, M. A., McGee, D., Aston, C. E., Orchard, T. J., Silvers, N., Peng, Y., et al. (2006) · Diabetologia · doi:10.1007/s00125-006-0355-8 · Cited by 59
Redox proteomics and the dynamic molecular landscape of the aging brain
Marzia Perluigi, A., Swomley, A. M., & Butterfield, D. A. (2013) · Ageing Research Reviews · doi:10.1016/j.arr.2013.12.005 · Cited by 62
High Mean Corpuscular Volume Is a New Indicator of Prognosis in Acute Decompensated Heart Failure
Ueda, T., Kawakami, R., Horii, M., Sugawara, Y., Matsumoto, T., Okada, S., Nishida, T., Soeda, T., Okayama, S., Somekawa, S., et al. (2013) · Circulation Journal · doi:10.1253/circj.cj-13-0718 · Cited by 59
Kishimoto, M., Suenaga, J., Takase, H., Araki, K., Yao, T., Fujimura, T., Murayama, K., Okumura, K., Ueno, R., Shimizu, N., et al. (2019) · Scientific Reports · doi:10.1038/s41598-019-50073-8 · Cited by 59
Takabe, W., Li, R., Ai, L., Yu, F., Berliner, J. A., & Hsiai, T. K. (2010) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.109.202135 · Cited by 58
Role of DNA damage in atherosclerosis—Bystander or participant?
Gray, K., & Bennett, M. R. (2011) · Biochemical Pharmacology · doi:10.1016/j.bcp.2011.06.025 · Cited by 57
Roles of Oxidants, Nitric Oxide, and Asymmetric Dimethylarginine in Endothelial Function
Siekmeier, R., Grammer, T. B., & März, W. (2008) · Journal of Cardiovascular Pharmacology and Therapeutics · doi:10.1177/1074248408326488 · Cited by 59
“function up to now focused on XO, NADH/NADPHoxidase, and NO-synthase (eNOS).(10,35,47) Xanthine oxidoreductase is a molybdeniumcontaining enzyme catalyzing the oxidation of hypoxanthine and xanthine in the metabolism of purine.”
BackgroundInfluentialNovel markers of peripheral arterial disease
Khawaja, F. J., & Kullo, I. J. (2009) · Vascular Medicine · doi:10.1177/1358863x09106869 · Cited by 57
Lee, B. Y., Al-Waili, N., Stubbs, D., Wendell, K., Butler, G. J., Al-Waili, T. N., & Al-Waili, A. N. (2010) · International Journal of Medical Sciences · doi:10.7150/ijms.7.29 · Cited by 57
“It has been found that oxidative stress is associated with several cardiovascular diseases, including atherosclerosis, hypertension, heart failure, stroke, and diabetes, and plays a fundamental role in endothelial dysfunction associated with these diseases (1-6).”
BackgroundRedox Systems Biology of Nutrition and Oxidative Stress
Dennis, K. K., Go, Y., & Jones, D. P. (2018) · Journal of Nutrition · doi:10.1093/jn/nxy306 · Cited by 60
Zhu, J., Yi, X., Zhang, J., Chen, S., & Wu, Y. (2017) · Journal of Chromatography B · doi:10.1016/j.jchromb.2017.06.022 · Cited by 57
Chang, J., Chen, M., Liu, W., Yang, C., Chen, C.-J., Chen, Y., Pan, K., Tsai, T., & Chang, H. (2010) · Cardiovascular Pathology · doi:10.1016/j.carpath.2009.12.005 · Cited by 57
Vascular endothelial cells and dysfunctions role of melatonin
Rezzani, R. (2012) · Frontiers in Bioscience-Elite · doi:10.2741/e601 · Cited by 57
“The ROS may modify endothelial function by peroxidation of membrane lipids, activation of NF-κB, or by decreasing the NO availability (113).”
BackgroundMartinet, W., Schrijvers, D. M., & Meyer, G. R. Y. D. (2011) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2011.01342.x · Cited by 56
“Several reasons may account for antioxidant ineffectiveness including the administration of a nonoptimal dose and/or type of antioxidant, the complexity of redox reactions in vivo and the potential for a paradoxical increase in oxidant generation by antioxidants themselves (Madamanchi et al., 2005).”
BackgroundVitamin E Supplementation and Plasma 8‐Isoprostane and Adiponectin in Overweight Subjects
Sutherland, W. H. F., Manning, P. J., Walker, R. J., de Jong, S. A., Ryalls, A. R., & Berry, E. A. (2007) · Obesity · doi:10.1038/oby.2007.546 · Cited by 56
“They are at increased risk of cardiovascular disease and type 2 diabetes in which oxidant stress and 8-isoprostanes may play an important role (1,2).”
BackgroundTabur, S., Torun, A. N., Sabuncu, T., Turan, M. N., Çelık, H., Ocak, A. R., & Aksoy, N. (2009) · European Journal of Endocrinology · doi:10.1530/eje-09-0732 · Cited by 56
Dianat, M., Radmanesh, E., Badavi, M., Goudarzi, G., & Mard, S. A. (2016) · Environmental Science and Pollution Research · doi:10.1007/s11356-016-7168-1 · Cited by 55
“Reducing cardiovascular disease with antioxidants may be due partly to the types of antioxidants customarily used and in part to the lack of particular and susceptible biomarkers which diagnose oxidative stress phenotypes that underlay CVD (Madamanchi et al. 2005).”
InfluentialAssociation of oxidative stress and PON1 with LDL and HDL particle size in middle‐aged subjects
Vekić, J., Kotur‐Stevuljevic, J., Jelić‐Ivanović, Z., Spasić, S., Spasojević‐Kalimanovska, V., Topić, A., Zeljković, A., Stefanović, A., & Zunic, G. (2007) · European Journal of Clinical Investigation · doi:10.1111/j.1365-2362.2007.01849.x · Cited by 55
Vassalle, C., Bianchi, S., Battaglia, D., Landi, P., Bianchi, F., & Carpeggiani, C. (2012) · Journal of Atherosclerosis and Thrombosis · doi:10.5551/jat.12740 · Cited by 55
Marine resources effective in controlling and treating diabetes and its associated complications
Nasab, S. B., Homaei, A. A., Pletschke, B. I., Salinas‐Salazar, C., Castillo-Zacarías, C., & Parra‐Saldívar, R. (2020) · Process Biochemistry · doi:10.1016/j.procbio.2020.01.024 · Cited by 56
Zhang, W., Qi, X., Zhao, Y., Liu, Y., Xu, L., Song, X., Xiao, C., Yuan, X., Zhang, J., & Hou, M. (2020) · International Journal of Pharmaceutics · doi:10.1016/j.ijpharm.2020.119543 · Cited by 55
The role of DNA damage and repair in atherosclerosis: A review
Shah, N. R., & Mahmoudi, M. (2015) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2015.07.005 · Cited by 56
“on the arterial wall [21,26], but intimated that it may be causative rather than just a late consequence of ROS mediated tissue damage.”
BackgroundMorita, M., Yano, S., Yamaguchi, T., & Sugimoto, T. (2012) · Journal of Diabetes and its Complications · doi:10.1016/j.jdiacomp.2012.07.006 · Cited by 55
“Vascular endothelial dysfunction is considered an early event of atherosclerosis, and recent growing evidences suggest an important role of ROS and TNF-α in the endothelial dysfunction (Cai and Harrison, 2000; Madamanchi et al., 2005; Picchi et al., 2006; Zhang et al., 2006).”
BackgroundShinde, S. A., Dhadke, V. N., & Suryakar, A. N. (2010) · Indian Journal of Clinical Biochemistry · doi:10.1007/s12291-010-0041-y · Cited by 55
“A well established correlation exists between development of macro and microvascular disease in diabetes mellitus [4].”
BackgroundThe Role of Nrf2 in the Attenuation of Cardiovascular Disease
Reuland, D. J., McCord, J. M., & Hamilton, K. L. (2013) · Exercise and Sport Sciences Reviews · doi:10.1097/jes.0b013e3182948a1e · Cited by 55
“Oxidative stress is evident in both the etiology and progression of myocardial infarction, congestive heart failure, atherosclerosis, and hypertension (24).”
BackgroundFranzeck, F. C., Hof, D., Spescha, R. D., Hasun, M., Akhmedov, A., Steffel, J., Shi, Y., Cosentino, F., Tanner, F. C., von Eckardstein, A., et al. (2012) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2011.10.035 · Cited by 54
“Oxidative stress plays an important role in the pathogensis of atherosclerosis, leading to cardiovascular complications uch as myocardial infarction and stroke [1].”
BackgroundThe Evolving Applications of Creatine Supplementation: Could Creatine Improve Vascular Health?
Clarke, H. E., Kim, D., Meza, C., Ormsbee, M. J., & Hickner, R. C. (2020) · Nutrients · doi:10.3390/nu12092834 · Cited by 58
“Despite the above described potential of creatine for the management of various metabolic, muscular, and neurological diseases, there is surprisingly very little information on the use of creatine supplementation to reduce the current leading cause of mortality in the United States (US): CVD. Major examples of CVDs ca…”
BackgroundInfluentialLiang, H., Huang, Y., & Pan, S. (2014) · American Heart Journal · doi:10.1016/j.ahj.2014.11.018 · Cited by 54
Nishigaki, I., Rajendran, P., Venugopal, R., Ekambaram, G., Sakthisekaran, D., & Nishigaki, Y. (2009) · Phytotherapy Research · doi:10.1002/ptr.2867 · Cited by 54
Nakajima, H., Unoda, K.-I., Ito, T., Kitaoka, H., Kimura, F., & Hanafusa, T. (2012) · The Open Neurology Journal · doi:10.2174/1874205x01206010051 · Cited by 54
“Oxidative stress is one of the mechanisms involved in ischemic brain injury induced by ischemia-reperfusion [1,2].”
BackgroundREACTIVE OXYGEN SPECIES AND ANTIOXIDANT IN SEMINAL PLASMA AND THEIR IMPACT ON MALE FERTILITY
Hammadeh, M. E., Filippos, A. A., & Hamad, M. F. K. (2009) · doi:10.22074/ijfs.2009.45769 · Cited by 54
Generation of reactive oxygen species by a sufficient, insufficient and varicose vein wall.
Krzyściak, W., & Kózka, M. (2011) · Acta Biochimica Polonica · doi:10.18388/abp.2011_2290 · Cited by 54
“The inflammatory reaction has a mechanism of positive feedback; exposure of plasma to action of activated phagocytes results in generation of chemotactic factors and activating new lymphocytes (Madamanchi et al., 2005).”
Background
Metadata
- Authors
- Madamanchi, N. R., Vendrov, A., & Runge, M. S.
- Affiliations
- University of North Carolina at Chapel Hill (US)
- Venue
- Arteriosclerosis, Thrombosis, and Vascular Biology
- Published
- 2005-01
- Volume
- 25
- Issue
- 1
- Pages
- 29-38
- ISSN
- 1079-5642 (ISSN-L)
- 1524-4636
- OpenAlex
- W2109698138
- Cited by
- 1,618
- References
- 135
- Citations by year
- 2026: 47 · 2025: 46 · 2024: 42 · 2023: 53 · 2022: 61 · 2021: 62 · 2020: 73 · 2019: 73 · 2018: 57 · 2017: 75 · 2016: 78 · 2015: 105 · 2014: 111 · 2013: 104 · 2012: 95
- FWCI
- 7.02
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Arteriosclerosis Thrombosis and Vascular Biology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Physiology (medical) › Nitric Oxide and Endothelin Effects
- Health Sciences › Medicine › Biochemistry (medical) › Antioxidant Activity and Oxidative Stress
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Keywords
- oxidative stress, reactive oxygen species, atherosclerosis, vascular disease, cardiovascular disease, NADPH oxidase, xanthine oxidase, lipoxygenase, nitric oxide synthase uncoupling, vascular inflammation, atherogenesis, antioxidants, redox signaling, biomarkers, cardiovascular risk factors
- MeSH terms
- Animals, Humans, Vascular Diseases, Oxidative Stress
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