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Molecular Mechanisms of Angiotensin II–Mediated Mitochondrial Dysfunction: Linking Mitochondrial Oxidative Damage and Vascular Endothelial Dysfunction
Abstract
Mitochondrial dysfunction is a prominent feature of most cardiovascular diseases. Angiotensin (Ang) II is an important stimulus for atherogenesis and hypertension; however, its effects on mitochondrial function remain unknown. We hypothesized that Ang II could induce mitochondrial oxidative damage that in turn might decrease endothelial nitric oxide (NO · ) bioavailability and promote vascular oxidative stress. The effect of Ang II on mitochondrial ROS, mitochondrial respiration, membrane potential, glutathione, and endothelial NO · was studied in isolated mitochondria and intact bovine aortic endothelial cells using electron spin resonance, dihydroethidium high-performance liquid chromatography –based assay, Amplex Red and cationic dye fluorescence. Ang II significantly increased mitochondrial H 2 O 2 production. This increase was blocked by preincubation of intact cells with apocynin (NADPH oxidase inhibitor), uric acid (scavenger of peroxynitrite), chelerythrine (protein kinase C inhibitor), N G -nitro- l -arginine methyl ester (nitric oxide synthase inhibitor), 5-hydroxydecanoate (mitochondrial ATP-sensitive potassium channels inhibitor), or glibenclamide. Depletion of p22 phox subunit of NADPH oxidase with small interfering RNA also inhibited Ang II–mediated mitochondrial ROS production. Ang II depleted mitochondrial glutathione, increased state 4 and decreased state 3 respirations, and diminished mitochondrial respiratory control ratio. These responses were attenuated by apocynin, 5-hydroxydecanoate, and glibenclamide. In addition, 5-hydroxydecanoate prevented the Ang II–induced decrease in endothelial NO · and mitochondrial membrane potential. Therefore, Ang II induces mitochondrial dysfunction via a protein kinase C–dependent pathway by activating the endothelial cell NADPH oxidase and formation of peroxynitrite. Furthermore, mitochondrial dysfunction in response to Ang II modulates endothelial NO · and generation, which in turn has ramifications for development of endothelial dysfunction.
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In the citing paper
“This process appears to require the function of mitochondrial ATP-dependent potassium channels (KATP), as shown by the ability of KATP inhibitors to block the increase of mitochondrial ROS production after angiotensin II–induced activation of NOX (242, 507).”
From Sources of Vascular Nitric Oxide and Reactive Oxygen Species and Their Regulation (2019) · cites this paper as [242]
In the citing paper
“Of note, the activation of NOX via angiotensin II and the angiotensin II type 1 receptor is mediated by PKC; however, the isoform PKCε is also an activator of the KATP channel, which, as indicated, also stimulates mitochondrial ROS production (FIGURE 17) (187, 242).”
From Sources of Vascular Nitric Oxide and Reactive Oxygen Species and Their Regulation (2019) · cites this paper as [242]
In the citing paper
“Mitochondrial potassium channels were also implicated in enhanced mitochondrial ROS generation and increased uncoupling.”
From Redox regulation of mitochondrial function (2012) · cites this paper as [121]
In the citing paper
“peroxynitrite formation was shown to be involved in these pathways as uric acid, a peroxynitrite scavenger, blocked mitochondrial ROS generation and mitochondrial dysfunction, attenuating AII-mediated reduction of ΔΨ, and decreased the respiratory control ratio”
From Redox regulation of mitochondrial function (2012) · cites this paper as [121]
In the citing paper
“AII-activated NOXs were found to cause mitochondrial dysfunction and upregulate mitochondrial release of oxidants, in part, by stimulating ETC-mediated production of ROS (121).”
From Redox regulation of mitochondrial function (2012) · cites this paper as [121]
Citations
Cites
Mitochondrial free radical generation, oxidative stress, and aging
Cadenas, E., & Davies, K. J. A. (2000) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(00)00317-8 · Cited by 3,010
Angiotensin II cell signaling: physiological and pathological effects in the cardiovascular system
Mehta, P. K., & Griendling, K. K. (2007) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00287.2006 · Cited by 1,924
Rubbo, H., Radí, R., Trujillo, M., Telleri, R., Kalyanaraman, B., Barnes, S., KIRK, M. C., & Freeman, B. Α. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)47160-8 · Cited by 1,350
Role of oxidative stress in atherosclerosis
Harrison, D., Griendling, K. K., Landmesser, U., Hornig, B., & Drexler, H. (2003) · The American Journal of Cardiology · doi:10.1016/s0002-9149(02)03144-2 · Cited by 1,275
Self-citationComplex iii releases superoxide to both sides of the inner mitochondrial membrane
Muller, F. L., Liu, Y., & Van Remmen, H. (2004) · Journal of Biological Chemistry · doi:10.1074/jbc.m407715200 · Cited by 1,036
Ide, T., Tsutsui, H., Hayashidani, S., Kang, D., Suematsu, N., Nakamura, K., Utsumi, H., Hamasaki, N., & Takeshita, A. (2001) · Circulation Research · doi:10.1161/01.res.88.5.529 · Cited by 733
Rego, A. C., & Oliveira, C. R. (2003) · Neurochemical Research · doi:10.1023/a:1025682611389 · Cited by 476
Mitochondrial reactive oxygen species-mediated signaling in endothelial cells
Zhang, D. X., & Gutterman, D. D. (2007) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.01283.2006 · Cited by 442
Mitochondrial dysfunction in cardiovascular disease
Ballinger, S. W. (2005) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2005.02.014 · Cited by 405
Protection of Cardiac Mitochondria by Overexpression of MnSOD Reduces Diabetic Cardiomyopathy
Shen, X., Zheng, S., Metreveli, N. S., & Epstein, P. N. (2006) · Diabetes · doi:10.2337/diabetes.55.03.06.db05-1039 · Cited by 375
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Items 301–400 of 710
Ortiz‐Avila, O., Sámano-García, C. A., Calderón‐Cortés, E., Pérez-Hernández, I. H., Mejía‐Zepeda, R., Rodríguez-Orozco, A. R., Saavedra‐Molina, A., & Cortés‐Rojo, C. (2013) · Journal of Bioenergetics and Biomembranes · doi:10.1007/s10863-013-9502-3 · Cited by 54
Ashby, E. L., & Kehoe, P. G. (2013) · Expert Opinion on Investigational Drugs · doi:10.1517/13543784.2013.812631 · Cited by 55
Stroke and the neurovascular unit: glial cells, sex differences, and hypertension
Morrison, H. W., & Filosa, J. A. (2019) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00333.2018 · Cited by 56
Dobi, A., Bravo, S. B., Veeren, B., Paradela‐Dobarro, B., Álvarez, E., Meilhac, O., Viranaïcken, W., Baret, P., Devin, A., & Rondeau, P. (2019) · Free Radical Research · doi:10.1080/10715762.2018.1529866 · Cited by 53
Colli, L. G., Belardin, L. B., Echem, C., Akamine, E. H., Antoniassi, M. P., Andretta, R. R., Mathias, L. S., Rodrigues, S. F., Bertolla, R. P., & de Carvalho, M. H. C. (2019) · Scientific Reports · doi:10.1038/s41598-019-47157-w · Cited by 53
Lee, H., Abe, Y., Lee, I., Shrivastav, S., Crusan, A. P., Hüttemann, M., Hopfer, U., Felder, R. A., Asico, L. D., Armando, I., et al. (2013) · Kidney International · doi:10.1038/ki.2013.397 · Cited by 52
Xiao, Y., Wigginton, J. G., Maass, D. L., Ma, L., Carlson, D., Wolf, S. E., Minei, J. P., & Zang, Q. S. (2014) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00475.2013 · Cited by 52
Ho, H., Liu, B., Snyder, J. S., Lou, Q., Brundage, E. A., Velez‐Cortes, F., Wang, H., Ziolo, M. T., Anderson, M. E., Sen, C. K., et al. (2013) · Cardiovascular Research · doi:10.1093/cvr/cvt233 · Cited by 52
MnSOD protects against COX1-mediated endothelial dysfunction in chronic heart failure
Miller, J. D., Peotta, V. A., Chu, Y., Weiss, R. M., Zimmerman, K., Brooks, R. M., & Heistad, D. D. (2010) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.01108.2009 · Cited by 51
Dual Pathways of Carbon Monoxide–Mediated Vasoregulation
Lamon, B. D., Zhang, F. F., Puri, N., Brodsky, S. V., Goligorsky, M. S., & Nasjletti, A. (2009) · Circulation Research · doi:10.1161/circresaha.109.197434 · Cited by 51
Wu, Y., Ma, K. L., Zhang, Y., Wen, Y., Wang, G. H., Hu, Z. B., Liu, L., Lü, J., Chen, P. P., Ruan, X. Z., et al. (2016) · Liver International · doi:10.1111/liv.13131 · Cited by 51
Leitner, L. M., Wilson, R. J., Yan, Z., & Gödecke, A. (2016) · Antioxidants and Redox Signaling · doi:10.1089/ars.2016.6942 · Cited by 54
Hariharan, A., Shetty, S., Shirole, T., & Jagtap, A. G. (2014) · NeuroToxicology · doi:10.1016/j.neuro.2014.10.004 · Cited by 50
de Cavanagh, E. M. V., Ferder, L., Ferder, M., Stella, I. Y., Toblli, J. E., & Inserra, F. (2010) · American Journal of Hypertension · doi:10.1038/ajh.2010.167 · Cited by 47
Effect of renin–angiotensin system on senescence
Mogi, M. (2020) · Geriatrics & Gerontology International · doi:10.1111/ggi.13927 · Cited by 48
Luo, S.-Y., 315211,中国, 宁. 宁., Liu, C., Ding, J., Gao, X., Wang, J., Zhang, Y., Du, C., Hou, C.-C., Zhu, J., et al. (2021) · 动物学研究 · doi:10.24272/j.issn.2095-8137.2021.079 · Cited by 51
Paradigm Shift in the Role of Uric Acid in Acute Kidney Injury
Shimada, M., Dass, B., & Ejaz, A. A. (2011) · Seminars in Nephrology · doi:10.1016/j.semnephrol.2011.08.010 · Cited by 49
Ohsaki, Y., O'Connor, P. M., Mori, T., Ryan, R. P., Dickinson, B. C., Chang, C. J., Lu, Y., Ito, S., & Cowley, A. W. (2011) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00469.2011 · Cited by 47
Kröller‐Schön, S., Jansen, T., Schüler, A., Oelze, M. W., Wenzel, P., Hausding, M., Kerahrodi, J. G., Beisele, M., Lackner, K. J., Daiber, A., et al. (2013) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.113.301717 · Cited by 49
Li, X., Yu, Y., Gorshkov, B. A., Haigh, S. B., Bordán, Z., Weintraub, D. S., Rudic, R. D., Chakraborty, T., Barman, S. A., Verin, A. D., et al. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01309 · Cited by 49
Simulated microgravity‐induced mitochondrial dysfunction in rat cerebral arteries
Zhang, R., Ran, H., Cai, L., Zhu, L., Sun, J., Peng, L., Liu, X., Zhang, L. Y., Fang, Z., Fan, Y., et al. (2014) · The FASEB Journal · doi:10.1096/fj.13-245654 · Cited by 48
Shiny, A., Regin, B., Narayanasamy, A., Chakroborty, A., Manickam, N., Dixit, M., Mohan, V., & Balasubramanyam, M. (2012) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-012-1478-5 · Cited by 47
Schiffer, T. A., Lundberg, J. O., Weitzberg, E., & Carlström, M. (2020) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2020.165811 · Cited by 49
Obstructive Sleep Apnea–induced Endothelial Dysfunction Is Mediated by miR-210
Shang, F., Wang, S., Gongol, B., Han, S. Y., Cho, Y., Schiavon, C. R., Chen, L., Xing, Y., Zhao, Y., Ning, M., et al. (2022) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.202202-0394oc · Cited by 46
The role of the brain renin-angiotensin system in Parkinson´s disease
Labandeira-García, J. L., Labandeira, C. M., Guerra, M. J., & Rodriguez-Perez, A. I. (2024) · Translational Neurodegeneration · doi:10.1186/s40035-024-00410-3 · Cited by 44
Mistry, Y., Poolman, T. M., Williams, B., & Herbert, K. E. (2013) · Redox Biology · doi:10.1016/j.redox.2013.08.004 · Cited by 46
Yu, Y., & Zheng, H. (2012) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-012-1264-4 · Cited by 46
Sharma, K., Lee, H.-H., Gong, D.-S., Park, S., Yi, E., Schini‐Kerth, V. B., & Oak, M. (2019) · Environmental Pollution · doi:10.1016/j.envpol.2019.05.066 · Cited by 46
Vascular dysfunction in retinopathy—An emerging role for arginase
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Mitochondrial Fission of Smooth Muscle Cells Is Involved in Artery Constriction
Liu, M., Jin, J., Li, S., Yan, J., Zhen, C., Gao, J., Zhang, Y.-H., Zhang, Y., Shen, X., Zhang, L., et al. (2016) · Hypertension · doi:10.1161/hypertensionaha.116.07974 · Cited by 45
Li, Q., Youn, J. Y., Siu, K. L., Murugesan, P., Zhang, Y., & Cai, H. “. (2019) · Redox Biology · doi:10.1016/j.redox.2019.101185 · Cited by 45
Lubrano, V., & Balzan, S. (2019) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-019-03656-y · Cited by 45
NADPH oxidase contributes to coronary endothelial dysfunction in the failing heart
Zhang, P., Hou, M., Li, Y., Xu, X., Barsoum, M. K., Chen, Y., & Bache, R. J. (2009) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00519.2008 · Cited by 44
Park, J.-B., Nagar, H., Choi, S., Jung, S.-B., Kim, H., Kang, S. K., Lee, J. W., Lee, J. H., Park, J., Irani, K., et al. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.02.017 · Cited by 47
Robinson, A. T., Franklin, N. C., Norkeviciute, E., Bian, J. T., Babana, J. C., Szczurek, M. R., & Phillips, S. A. (2016) · Journal of Hypertension · doi:10.1097/hjh.0000000000000946 · Cited by 44
Panov, A. V., Mayorov, V., & Dikalov, S. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23074047 · Cited by 47
Self-citationOxidative stress and endothelial dysfunction
de Dios, S. T., Sobey, C. G., & Drummond, G. R. (2010) · Springer eBooks · doi:10.1007/978-3-0346-0168-9_3 · Cited by 44
Metabolomics in Angiotensin II-Induced Cardiac Hypertrophy
Mervaala, E. M. A., Biala, A. K., Merasto, S., Lempiäinen, J., Mattila, I. M., Martonen, E., Eriksson, O., Louhelainen, M., Finckenberg, P., Kaheinen, P., et al. (2010) · Hypertension · doi:10.1161/hypertensionaha.109.145490 · Cited by 43
Hypertension and Insulin Resistance: Implications of Mitochondrial Dysfunction
Manucha, W. A., Ritchie, B., & Ferder, L. (2014) · Current Hypertension Reports · doi:10.1007/s11906-014-0504-2 · Cited by 43
Gupta, V., Dhull, D. K., Joshi, J., Kaur, S., & Kumar, A. (2019) · Neurochemistry International · doi:10.1016/j.neuint.2019.104604 · Cited by 43
Fa, H., Chang, W., Zhang, X.-J., Xiao, D., & Wang, J. (2020) · Acta Pharmacologica Sinica · doi:10.1038/s41401-020-0471-x · Cited by 43
Elevated mitochondrial superoxide contributes to enhanced chemoreflex in heart failure rabbits
Ding, Y., Li, Y., Zimmerman, M. C., & Schultz, H. D. (2009) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00629.2009 · Cited by 43
Mitochondrial Function and Reactive Oxygen/Nitrogen Species in Skeletal Muscle
Chen, M., Li, Y., Deng, S., Zhao, Y., Lian, Z., & Yu, K. (2022) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2022.826981 · Cited by 49
Diabetic Retinopathy: New Treatment Approaches Targeting Redox and Immune Mechanisms
Tang, Q., Buonfiglio, F., Böhm, E. W., Zhang, L., Pfeiffer, N., Korb, C. A., & Gericke, A. (2024) · Antioxidants · doi:10.3390/antiox13050594 · Cited by 48
Nolly, M. B., Caldiz, C. I., Yeves, A. M., Villa‐Abrille, M. C., Morgan, P. E., Mondaca, N. A., Portiansky, E. L., de Cingolani, G. E. C., Cingolani, H. E., & Ennis, I. L. (2013) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2013.12.004 · Cited by 42
Vaka, V. R., Cunningham, M., Deer, E. M., Franks, M., Ibrahim, T., Amaral, L. M., Usry, N., Cornelius, D. C., Dechend, R., Wallukat, G., et al. (2019) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00179.2019 · Cited by 42
Kim, S., Subramanian, V., Abdel‐Latif, A., & Lee, S. (2020) · Metabolic Syndrome and Related Disorders · doi:10.1089/met.2019.0120 · Cited by 42
Hatinguais, R., Pradhan, A., Brown, G. D., Brown, A. J. P., Warris, A., & Shekhova, E. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.641495 · Cited by 41
Choi, H., Tostes, R. C., & Webb, R. C. (2011) · Journal of the American Society of Hypertension · doi:10.1016/j.jash.2011.02.005 · Cited by 42
Hung, C., Chan, S., Chu, P., & Tsai, K. (2015) · Toxicological Sciences · doi:10.1093/toxsci/kfv017 · Cited by 41
Cholan, P. M., Cartland, S. P., Dang, L., Rayner, B. S., Patel, S., Thomas, S. R., & Kavurma, M. M. (2018) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2018.08.031 · Cited by 41
Goette, A., Bukowska, A., Lillig, C. H., & Lendeckel, U. (2012) · Frontiers in Physiology · doi:10.3389/fphys.2012.00236 · Cited by 42
Chrissobolis, S., & Faraci, F. M. (2010) · Hypertension · doi:10.1161/hypertensionaha.109.147041 · Cited by 41
Oxidant stress and skeletal muscle microvasculopathy in the metabolic syndrome
Goodwill, A. G., & Frisbee, J. C. (2012) · Vascular Pharmacology · doi:10.1016/j.vph.2012.07.002 · Cited by 42
Khemais‐Benkhiat, S., Idris-Khodja, N., Ribeiro, T. P., da Silva, G. C., Abbas, M., Kheloufi, M., Lee, J.-O., Toti, F., Auger, C., & Schini‐Kerth, V. B. (2015) · The Journals of Gerontology Series A · doi:10.1093/gerona/glv213 · Cited by 40
Sharma, M., Kaur, T., & Singla, S. K. (2016) · Mitochondrion · doi:10.1016/j.mito.2016.01.002 · Cited by 40
Rubattu, S. D., Stanzione, R., & Volpe, M. (2016) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2016/1067801 · Cited by 41
Genetic Deletion of NADPH Oxidase 1 Rescues Microvascular Function in Mice With Metabolic Disease
Thompson, J. A., Larion, S., MINTZ, J. D., de Chantemèle, E. J. B., Fulton, D. J., & Stepp, D. W. (2017) · Circulation Research · doi:10.1161/circresaha.116.309965 · Cited by 43
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Wang, J., & Swanson, R. A. (2020) · Frontiers in Neuroscience · doi:10.3389/fnins.2020.00861 · Cited by 40
Targeted Antioxidants in Exercise-Induced Mitochondrial Oxidative Stress: Emphasis on DNA Damage
Williamson, J., & Davison, G. W. (2020) · Antioxidants · doi:10.3390/antiox9111142 · Cited by 43
An Outline of Renal Artery Stenosis Pathophysiology—A Narrative Review
Dobrek, Ł. (2021) · Life · doi:10.3390/life11030208 · Cited by 40
Cumpstey, A. F., Clark, A. D., Santolini, J., Jackson, A. A., & Feelisch, M. (2021) · Antioxidants and Redox Signaling · doi:10.1089/ars.2021.0017 · Cited by 40
Zheng, H., & Yu, Y. (2012) · Biochemical Pharmacology · doi:10.1016/j.bcp.2012.01.031 · Cited by 40
Daiber, A., Wenzel, P., Oelze, M. W., Schuhmacher, S., Jansen, T., & Münzel, T. F. (2008) · Chemico-Biological Interactions · doi:10.1016/j.cbi.2008.09.003 · Cited by 40
Gopallawa, I., & Uhal, B. D. (2015) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00187.2015 · Cited by 39
Márquez‐Ramírez, C. A., de la Paz, J. L. H., Ortiz‐Avila, O., Raya‐‐Farias, A., González‐Hernández, J. C., Rodríguez-Orozco, A. R., Salgado‐Garciglia, R., Saavedra‐Molina, A., Godínez‐Hernández, D., & Cortés‐Rojo, C. (2018) · Nutrition · doi:10.1016/j.nut.2018.02.024 · Cited by 42
Lijnen, P. J., van Pelt, J. F., & Fagard, R. H. (2010) · American Journal of Hypertension · doi:10.1038/ajh.2010.128 · Cited by 39
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Harrison, D. G. (2012) · Wiley eBooks · doi:10.1002/9781118355244.ch9 · Cited by 39
Self-citationEnvironmental Toxins and Oxidative Stress: The Link to Cardiovascular Diseases
Sule, R. O., Rivera, G. D. T., Vaidya, T., Gartrell, E., & Gomes, A. V. (2025) · Antioxidants · doi:10.3390/antiox14050604 · Cited by 41
Evidence for a mitochondrial angiotensin-(1–7) system in the kidney
Wilson, B. A., Nautiyal, M., Gwathmey, T. M., Rose, J. C., & Chappell, M. C. (2015) · American Journal of Physiology-Renal Physiology · doi:10.1152/ajprenal.00479.2015 · Cited by 38
Systems biology of antioxidants
Andriantsitohaina, R., Duluc, L., Rodríguez, J., del Valle, L. G., Guevara-García, M., Simard, G., Soleti, R., Su, D., Velázquez‐Pérez, L., Wilson, J. X., et al. (2012) · Clinical Science · doi:10.1042/cs20110643 · Cited by 42
Zhou, X., Bohlen, H. G., Unthank, J. L., & Miller, S. J. (2009) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00325.2009 · Cited by 38
Münzel, T. F., & Daiber, A. (2023) · Antioxidants and Redox Signaling · doi:10.1089/ars.2023.0006 · Cited by 40
Oxidative Stress and Endoplasmic Reticular Stress Interplay in the Vasculopathy of Hypertension
Camargo, L. L., Wang, Y., Rios, F. J. O., McBride, M., Montezano, A. C. I., & Touyz, R. M. (2023) · Canadian Journal of Cardiology · doi:10.1016/j.cjca.2023.10.012 · Cited by 35
Eirin, A., Saad, A., Woollard, J. R., Juncos, L. A., Calhoun, D. A., Tang, H. J., Lerman, A., Textor, S. C., & Lerman, L. O. (2017) · American Journal of Hypertension · doi:10.1093/ajh/hpx103 · Cited by 37
Rajamohan, S. B., Raghuraman, G., Prabhakar, N. R., & Kumar, G. (2012) · Antioxidants and Redox Signaling · doi:10.1089/ars.2011.4176 · Cited by 37
Fu, X., Huang, X., Li, P., Chen, W., & Xia, M. (2014) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2014.03.010 · Cited by 36
Takada, S., Kinugawa, S., Matsushima, S., Takemoto, D., Furihata, T., Mizushima, W., Fukushima, A., Yokota, T., Ono, Y., Shibata, H., et al. (2015) · Experimental Physiology · doi:10.1113/ep085251 · Cited by 37
Tracy, E. P., Hughes, W. E., Beare, J. E., Rowe, G., Beyer, A., & LeBlanc, A. J. (2021) · Antioxidants and Redox Signaling · doi:10.1089/ars.2021.0031 · Cited by 39
Brain angiotensin and dopaminergic degeneration: relevance to Parkinson's disease.
Labandeira-García, J. L., Rodríguez‐Pallares, J., Rodriguez-Perez, A. I., Garrido‐Gil, P., Villar‐Cheda, B., Valenzuela, R., & Guerra, M. J. (2012) · Europe PMC (PubMed Central) · Cited by 36
Dikalova, A., Mayorov, V., Xiao, L., Panov, A. V., Amarnath, V., Zagol-Ikapitte, I. A., Vergeade, A., Ao, M., Yermalitsky, V. N., Nazarewicz, R. R., et al. (2020) · Hypertension · doi:10.1161/hypertensionaha.120.15236 · Cited by 36
Self-citationLi, Y., Kračun, D., Dustin, C. M., Massry, M. E., Yuan, S. S., Goossen, C., DeVallance, E., Sahoo, S., Hilaire, C. S., Gurkar, A. U., et al. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2015666118 · Cited by 36
Perspectives and challenges of antioxidant therapy for atrial fibrillation
Gašparová, I., Kubatka, P., Opatřilová, R., Čaprnda, M., Filipová, S., Rodrigo, L., Malan, L., Mozos, I. M., Rabajdová, M., Nosáľ, V., et al. (2016) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-016-1320-9 · Cited by 36
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Shi, S., Zhang, B., Li, Y., Xu, X., Lv, J., Jia, Q., Chai, R., Xue, W., Li, Y., Wang, Y., et al. (2022) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2022.837270 · Cited by 35
Queisser, N., Fazeli, G., & Schupp, N. (2010) · Biological Chemistry · doi:10.1515/bc.2010.136 · Cited by 35
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Leskov, I. L., Neville, A., Shen, X., Pardue, S., Kevil, C. G., Granger, D. N., & Krzywanski, D. M. (2016) · Journal of the American Society of Hypertension · doi:10.1016/j.jash.2016.12.002 · Cited by 35
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Rader, F., Wagoner, D. R. V., Gillinov, A. M., & Blackstone, E. H. (2010) · American Heart Journal · doi:10.1016/j.ahj.2010.05.033 · Cited by 32
Toral, M., Romero, M., Jiménez, R., Robles‐Vera, I., Tamargo, J. L., Martínez, M. C., Pérez‐Vizcaíno, F., & Duarte, J. (2016) · Biochemical Pharmacology · doi:10.1016/j.bcp.2016.05.004 · Cited by 32
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Li, X., Zhang, X., Li, F., Chen, L., Li, L., Qin, X., Gao, J., Su, T., Zeng, Y., & Liao, D. (2010) · Acta Biochimica et Biophysica Sinica · doi:10.1093/abbs/gmq036 · Cited by 32
Metadata
- Authors
- Doughan, A. K., Harrison, D. G., & Dikalov, S. I.
- Affiliations
- United States Department of Veterans Affairs (US)
- Venue
- Circulation Research
- Published
- 2008-02-29
- Volume
- 102
- Issue
- 4
- Pages
- 488-496
- ISSN
- 0009-7330 (ISSN-L)
- 1524-4571
- OpenAlex
- W2164444293
- Cited by
- 710
- References
- 43
- Citations by year
- 2026: 24 · 2025: 24 · 2024: 19 · 2023: 32 · 2022: 33 · 2021: 44 · 2020: 39 · 2019: 31 · 2018: 31 · 2017: 36 · 2016: 54 · 2015: 29 · 2014: 58 · 2013: 51 · 2012: 50
- FWCI
- 25.60
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Circulation Research (publishedVersion)
- PubMed (publishedVersion)
- Funders
- American Heart Association
- National Institutes of Health (5p01hl075209-05)
- National Heart, Lung, and Blood Institute (P0-1 HL-075209, R01HL094469, P01HL058000)
- Topics
- Health Sciences › Medicine › Physiology (medical) › Nitric Oxide and Endothelin Effects
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Mitochondrial Function and Pathology
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Renin-Angiotensin System Studies
- Keywords
- angiotensin II, mitochondrial dysfunction, endothelial nitric oxide, NADPH oxidase, peroxynitrite, protein kinase C, mitochondrial reactive oxygen species, mitochondrial glutathione, mitochondrial respiration, endothelial dysfunction, oxidative stress, atherogenesis, hypertension
- MeSH terms
- Angiotensin II, Animals, Aorta, Cattle, Cells, Cultured, Glutathione, Hydrogen Peroxide, Mitochondria, Nitric Oxide, Superoxides, Vascular Diseases, Vasoconstrictor Agents, Oxidative Stress, Cell Respiration, Mitochondrial Diseases, Endothelial Cells, Membrane Potential, Mitochondrial
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