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Heterozygous Cellular Glutathione Peroxidase Deficiency in the Mouse: Abnormalities in Vascular and Cardiac Function and Structure
Abstract
Background— Oxidant stress has been implicated in the pathogenesis of atherothrombosis and other vascular disorders accompanied by endothelial dysfunction. Glutathione peroxidases (GPx) play an important role in the cellular defense against oxidant stress by utilizing glutathione (GSH) to reduce lipid hydroperoxides and hydrogen peroxide to their corresponding alcohols. Cellular GPx (GPx-1) is the principal intracellular isoform of GPx. We hypothesized that GPx-1 deficiency per se induces endothelial dysfunction and structural vascular abnormalities through increased oxidant stress. Methods and Results— A murine model of heterozygous deficiency of GPx-1 (GPx +/−) was investigated to examine this hypothesis. Mesenteric arterioles in GPx-1 +/− mice demonstrated vasoconstriction to acetylcholine compared with vasodilation in wild-type mice (maximal change in vessel diameter, −13.0±2.8% versus 13.2±2.8%, P <0.0001). We also noted an increase in the plasma and aortic levels of the isoprostane iPF 2α -III, a marker of oxidant stress, in GPx-1 +/− mice compared with wild-type mice (170.4±23 pg/mL plasma versus 98.7±7.1 pg/mL plasma, P <0.03; 11.7±0.87 pg/mg aortic tissue versus 8.2±0.55 pg/mg aortic tissue, P <0.01). Histological sections from the coronary vasculature of GPx-1 +/− mice show increased perivascular matrix deposition, an increase in the number of adventitial fibroblasts, and intimal thickening. These structural abnormalities in the myocardial vasculature were accompanied by diastolic dysfunction after ischemia-reperfusion. Conclusions— These findings demonstrate that heterozygous deficiency of GPx-1 leads to endothelial dysfunction, possibly associated with increased oxidant stress, and to significant structural vascular and cardiac abnormalities. These data illustrate the importance of this key antioxidant enzyme in functional and structural responses of the mammalian cardiovascular system.
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“GPx-1-deficient mice manifest endothelial dysfunction, characterized by a lack of normal responses to endothelium-dependent vasoactive compounds (134, 135).”
From Redox regulation of mitochondrial function (2012) · cites this paper as [134]
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Metadata
- Authors
- Forgione, M. A., Cap, A., Liao, R., Moldovan, N. I., Eberhardt, R. T., Lim, C. C., Jones, J., Goldschmidt-Clermont, P. J., & Loscalzo, J.
- Affiliations
- Boston University (US)
- From Evans Department of Medicine (M.A.F., R.L., R.T.E., C.C.L., J.L.), Department of Surgery (J.J.), and Whitaker Cardiovascular Institute (M.A.F., A.C., R.L., C.C.L., R.T.E., J.J., J.L.), Boston University School of Medicine, Boston, Mass; Cardiology Section, Department of Medicine (N.M.), The Ohio State University, Columbus, Ohio; and Duke University School of Medicine (P.G.), Durham, NC.
- Venue
- Circulation
- Published
- 2002-08-27
- Volume
- 106
- Issue
- 9
- Pages
- 1154-1158
- ISSN
- 0009-7322 (ISSN-L)
- 1524-4539
- OpenAlex
- W2104128564
- Cited by
- 200
- References
- 31
- Citations by year
- 2026: 2 · 2025: 6 · 2024: 5 · 2023: 1 · 2022: 7 · 2021: 6 · 2020: 4 · 2019: 5 · 2018: 8 · 2017: 10 · 2016: 12 · 2015: 8 · 2014: 8 · 2013: 13 · 2012: 4
- FWCI
- 4.40
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Circulation (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- National Heart, Lung, and Blood Institute (HL61795, HL 55993, HL-07224-24, HL58976, R01HL058976, T32HL007224, P50HL055993)
- Topics
- Health Sciences › Medicine › Physiology (medical) › Nitric Oxide and Endothelin Effects
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Health Sciences › Medicine › Biochemistry (medical) › Antioxidant Activity and Oxidative Stress
- Keywords
- glutathione peroxidase 1, oxidative stress, endothelial dysfunction, atherothrombosis, mesenteric arterioles, acetylcholine-induced vasoconstriction, intimal thickening, myocardial ischemia-reperfusion injury, diastolic dysfunction, antioxidant enzymes, mouse model
- MeSH terms
- Glutathione Peroxidase GPX1, Animals, Antioxidants, Aorta, Thoracic, Bradykinin, Coronary Vessels, Disease Models, Animal, Dose-Response Relationship, Drug, Glutathione Peroxidase, Cyclic GMP, Heterozygote, Male, Mesentery, Metabolism, Inborn Errors, Microcirculation, Myocardial Contraction, Myocardium, Vasodilator Agents, Vasomotor System, Oxidative Stress, Gene Targeting, Muscarinic Agonists, Nitric Oxide Donors, Mice, In Vitro Techniques
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