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Nitrite Regulates Hypoxic Vasodilation via Myoglobin-Dependent Nitric Oxide Generation
Open accessAbstract
BACKGROUND: Hypoxic vasodilation is a physiological response to low oxygen tension that increases blood supply to match metabolic demands. Although this response has been characterized for >100 years, the underlying hypoxic sensing and effector signaling mechanisms remain uncertain. We have shown that deoxygenated myoglobin in the heart can reduce nitrite to nitric oxide (NO·) and thereby contribute to cardiomyocyte NO· signaling during ischemia. On the basis of recent observations that myoglobin is expressed in the vasculature of hypoxia-tolerant fish, we hypothesized that endogenous nitrite may contribute to physiological hypoxic vasodilation via reactions with vascular myoglobin to form NO·. METHODS AND RESULTS: We show in the present study that myoglobin is expressed in vascular smooth muscle and contributes significantly to nitrite-dependent hypoxic vasodilation in vivo and ex vivo. The generation of NO· from nitrite reduction by deoxygenated myoglobin activates canonical soluble guanylate cyclase/cGMP signaling pathways. In vivo and ex vivo vasodilation responses, the reduction of nitrite to NO·, and the subsequent signal transduction mechanisms were all significantly impaired in mice without myoglobin. Hypoxic vasodilation studies in myoglobin and endothelial and inducible NO synthase knockout models suggest that only myoglobin contributes to systemic hypoxic vasodilatory responses in mice. CONCLUSIONS: Endogenous nitrite is a physiological effector of hypoxic vasodilation. Its reduction to NO· via the heme globin myoglobin enhances blood flow and matches O(2) supply to increased metabolic demands under hypoxic conditions.
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In the citing paper
“Inhaled NO induces vasodilation in PAH and is capable of reversing hypoxic pulmonary vasoconstriction[139–141].”
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 [141]
In the citing paper
“Nitrite as a reservoir can be further reduced to NO via numerous pathways in blood and tissue, and this process is indeed accelerated under hypoxic conditions.44 -47”
From Dietary nitrate supplementation improves revascularization in chronic ischemia (2012) · cites this paper as [44]
In the citing paper
“Nitrite may form NO either via deoxyhemoglobin (deoxyHb, Fe II Hb) [80,81], deoxymyoglobin [82] or xanthine oxidoreductase (XOR)-mediated reduction [83], or via spontaneous [84] and carbonic anhydrase-facilitated disproportionation [85].”
From On the chemical biology of the nitrite/sulfide interaction (2015) · cites this paper as [82]
In the citing paper
“Mb-mediated nitrite reduction has been reported to be important in both cardiomyocytes [55] and smooth muscle [56].”
From Mechanisms of nitrite bioactivation (2014) · cites this paper as [56]
In the citing paper
“As discussed below, a functional role for myoglobin in nitrite reduction and signaling is strongly supported by multiple studies in myoglobin knockout mice showing a reduction in nitrite mediated effects on mitochondrial respiration, cardiac function, ischemia reperfusion cytoprotection, and systemic hypoxic vasodilation [54–56].”
From Mechanisms of nitrite bioactivation (2014) · cites this paper as [56]
In the citing paper
“Smooth muscle myoglobin has also been implicated in modulating nitrite-dependent increases in blood flow [56, 113].”
From Mechanisms of nitrite bioactivation (2014) · cites this paper as [56]
In the citing paper
“In addition, NO formation from administered nitrite and associated vasorelaxation were much higher in wild type mice compared to knockouts .[56]”
From Mechanisms of nitrite bioactivation (2014) · cites this paper as [56]
In the citing paper
“Totzeck and coworkers conducted in vitro and in vivo experiments supporting a role for smooth muscle Mb in nitrite mediated vasodilation using wild type and Mb knockout mice [56].”
From Mechanisms of nitrite bioactivation (2014) · cites this paper as [56]
In the citing paper
“NO production from nitrite in aorta were greatly attenuated in the knockout compared to wild type and inhibition of XOR did not affect NO production in the wild type [56]”
From Mechanisms of nitrite bioactivation (2014) · cites this paper as [56]
In the citing paper
“A role for nitrite reduction by NOS was not supported by experiments using NOS knockout mice [56].”
From Mechanisms of nitrite bioactivation (2014) · cites this paper as [56]
In the citing paper
“NO production from nitrite in aorta were greatly attenuated in the knockout compared to wild type and inhibition of XOR did not affect NO production in the wild type [56]”
From Mechanisms of nitrite bioactivation (2014) · cites this paper as [56]
In the citing paper
“Blood pressure from wild type mice was substantially more reduced compared to Mb knockout mice when exposed to hypoxia in vivo [56].”
From Mechanisms of nitrite bioactivation (2014) · cites this paper as [56]
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Citations
Cites
Textbook of Medical Physiology
Guyton, A. C., & Hall, J. E. (1966) · Annals of Internal Medicine · doi:10.7326/0003-4819-64-6-1363_2 · Cited by 9,760
The L-Arginine-Nitric Oxide Pathway
Epstein, F. H., Moncada, S., & Higgs, A. (1993) · New England Journal of Medicine · doi:10.1056/nejm199312303292706 · Cited by 6,678
Nitrite reduction to nitric oxide by deoxyhemoglobin vasodilates the human circulation
Cosby, K., Partovi, K. S., Crawford, J. H., Patel, R. P., Reiter, C. D., Martyr, S., Yang, B. K., Waclawiw, M. A., Zalos, G., Xu, X., et al. (2003) · Nature Medicine · doi:10.1038/nm954 · Cited by 1,807
Self-citationIgnarro, L. J., Lippton, H., Edwards, J. C., Baricos, W. H., Hyman, A. L., Kadowitz, P. J., & Gruetter, C. A. (1981) · The Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)32738-2 · Cited by 1,633
Arnold, W. P., Mittal, C. K., Katsuki, S., & Murad, F. (1977) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.74.8.3203 · Cited by 1,459
Enzyme-independent formation of nitric oxide in biological tissues
Zweier, J. L., Wang, P., Samouilov, A., & Kuppusamy, P. (1995) · Nature Medicine · doi:10.1038/nm0895-804 · Cited by 788
Cytoprotective effects of nitrite during in vivo ischemia-reperfusion of the heart and liver
Duranski, M. R., Greer, J. J. M., Dejam, A., Jaganmohan, S., Hogg, N., Langston, W., Patel, R. P., Yet, S.-F., Wang, X., Kevil, C. G., et al. (2005) · Journal of Clinical Investigation · doi:10.1172/jci22493 · Cited by 674 · cited 2×
“the cardiopulmonary resuscitation syndrome(47) and for chronic and acute intervention regimens.(48,49) by gest on July (2)5, 2017 http://ciajournals.”
Self-citationFurchgott, R. F., & Bhadrakom, S. (1953) · The Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(25)05163-8 · Cited by 655 · cited 3×
“High concentrations of the inorganic anion, nitrite, has been known to be vasoactive for many years.(17) Indeed, millimolar to high micromolar pharmacological concentrations of exogenous nitrite have been demonstrated to relax preconstricted isolated vessels.”
Shiva, S., Huang, Z., Grubina, R., Sun, J., Ringwood, L. A., MacArthur, P. H., Xu, X., Murphy, E., Darley-Usmar, V. M., & Gladwin, M. T. (2007) · Circulation Research · doi:10.1161/01.res.0000260171.52224.6b · Cited by 599
Self-citationEffects of Dietary Nitrate on Blood Pressure in Healthy Volunteers
Larsen, F. J., Ekblom, B., Sahlin, K., Lundberg, J. O., & Weitzberg, E. (2006) · New England Journal of Medicine · doi:10.1056/nejmc062800 · Cited by 587
Cited by
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Items 101–200 of 201
Wajih, N., Liu, X., Shetty, P., Basu, S., Wu, H., Hogg, N., Patel, R. P., Furdui, C. M., & Kim‐Shapiro, D. B. (2016) · Redox Biology · doi:10.1016/j.redox.2016.04.004 · Cited by 25
Hendgen-Cotta, U. B., Esfeld, S., Rudi, K., Miinalainen, I., Klare, J. P., & Rassaf, T. (2017) · International Journal of Molecular Sciences · doi:10.3390/ijms18040687 · Cited by 26
Self-citationMannino, M. H., Patel, R. S., Eccardt, A. M., Perez-Magnelli, R., Robinson, C. L. C., Janowiak, B. E., Warren, D. E., & Fisher, J. S. (2019) · Comparative Biochemistry and Physiology Part B Biochemistry and Molecular Biology · doi:10.1016/j.cbpb.2019.04.005 · Cited by 24
Portella, R. D. L., Bickta, J., & Shiva, S. (2015) · Antioxidants and Redox Signaling · doi:10.1089/ars.2015.6260 · Cited by 21
Self-citationHuman Indoleamine 2,3-Dioxygenase 1 Is an Efficient Mammalian Nitrite Reductase
Lim, Y. J., Foo, T. C., Yeung, A. W. S., Tu, X., Ma, Y., Hawkins, C. L., Witting, P. K., Jameson, G. N. L., Terentis, A. C., & Thomas, S. R. (2018) · Biochemistry · doi:10.1021/acs.biochem.8b01231 · Cited by 21
Mechanisms for cellular NO oxidation and nitrite formation in lung epithelial cells
Zhao, X., Wang, L., Shiva, S., Tejero, J., Myerburg, M. M., Wang, J., Frizzell, S., & Gladwin, M. T. (2013) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2013.04.031 · Cited by 21
Self-citationRifkind, J. M., Nagababu, E., Dobrosielski, D. A., Salgado, M. T., Lima, M., Ouyang, P., & Silber, H. A. (2014) · Nitric Oxide · doi:10.1016/j.niox.2014.06.007 · Cited by 21
Nitric oxide generation from heme/copper assembly mediated nitrite reductase activity
Hematian, S., Siegler, M. A., & Karlin, K. D. (2014) · JBIC Journal of Biological Inorganic Chemistry · doi:10.1007/s00775-013-1081-6 · Cited by 20
Hypoxic potentiation of nitrite effects in human vessels and platelets
Dautov, R. F., Stafford, I., Liu, S., Cullen, H. C., Madhani, M., Chirkov, Y. Y., & Horowitz, J. D. (2014) · Nitric Oxide · doi:10.1016/j.niox.2014.05.005 · Cited by 22
Present and future pharmacotherapeutic agents in heart failure: an evolving paradigm
Loudon, B. L., Noordali, H., Gollop, N. D., Frenneaux, M. P., & Madhani, M. (2016) · British Journal of Pharmacology · doi:10.1111/bph.13480 · Cited by 20
Jung, H., Choi, E. K., Baek, S. I., Cho, C., Jin, Y., Kwak, K. H., Jeon, Y., Park, S.-S., Kim, S., & Lim, D. G. (2019) · Dose-Response · doi:10.1177/1559325819853651 · Cited by 19
Karmakar, S., Patra, S., Halder, R., Karmakar, S., & Majumdar, A. (2024) · Inorganic Chemistry · doi:10.1021/acs.inorgchem.4c03555 · Cited by 20
Atta, S., Mandal, A., Saha, R., & Majumdar, A. (2023) · Dalton Transactions · doi:10.1039/d3dt03768a · Cited by 18
Concepts of hypoxic NO signaling in remote ischemic preconditioning
Totzeck, M. (2015) · World Journal of Cardiology · doi:10.4330/wjc.v7.i10.645 · Cited by 18
Self-citationNitric Oxide and Oxidative Stress Changes at Depth in Breath-Hold Diving
Cialoni, D., Brizzolari, A., Samaja, M., Bosco, G., Paganini, M., Pieri, M., Lancellotti, V., & Marroni, A. (2021) · Frontiers in Physiology · doi:10.3389/fphys.2020.609642 · Cited by 18
Potential of dietary nitrate in angiogenesis
Rammos, C. (2015) · World Journal of Cardiology · doi:10.4330/wjc.v7.i10.652 · Cited by 17
Dietary Nitrate Is a Modifier of Vascular Gene Expression in Old Male Mice
Rammos, C., Totzeck, M., Deenen, R., Köhrer, K., Kelm, M., Rassaf, T., & Hendgen-Cotta, U. B. (2015) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2015/658264 · Cited by 17
Self-citationNitrite circumvents canonical cGMP signaling to enhance proliferation of myocyte precursor cells
Totzeck, M., Schicho, A., Stock, P., Kelm, M., Rassaf, T., & Hendgen-Cotta, U. B. (2014) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-014-2305-y · Cited by 17
Self-citationUpdated Role of Nitric Oxide in Disorders of Erythrocyte Function
Kahn, M. J., Maley, J. H., Lasker, G. F., & Kadowitz, P. J. (2013) · Cardiovascular & Haematological Disorders - Drug Targets · doi:10.2174/1871529x11313010009 · Cited by 16
Hema, K., Sharma, K., Thinlas, T., Mohammad, G., & Pasha, M. A. Q. (2020) · Journal of Biomolecular Structure and Dynamics · doi:10.1080/07391102.2019.1711190 · Cited by 16
Hossain, M. K., Basak, A., & Majumdar, A. (2025) · Journal of the American Chemical Society · doi:10.1021/jacs.5c01529 · Cited by 15
Craig, J. C., Colburn, T. D., Hirai, D. M., Musch, T. I., & Poole, D. C. (2019) · Journal of Applied Physiology · doi:10.1152/japplphysiol.01004.2018 · Cited by 15
Role of aldehyde dehydrogenase in hypoxic vasodilator effects of nitrite in rats and humans
Arif, S., Borgognone, A., Lin, E., O'Sullivan, Á. G., Sharma, V., Drury, N. E., Menon, A., Nightingale, P., Mascaro, J. G., Bonser, R. S., et al. (2015) · British Journal of Pharmacology · doi:10.1111/bph.13122 · Cited by 14
Role of endothelial nitric oxide in pulmonary and systemic arteries during hypoxia
Nuñez, C., Víctor, V. M., Martí, M., & D’Ocón, P. (2013) · Nitric Oxide · doi:10.1016/j.niox.2013.12.008 · Cited by 14
Corti, P., Tejero, J., & Gladwin, M. T. (2013) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2013.09.020 · Cited by 13
Self-citationMouse cardiac mitochondria do not separate in subsarcolemmal and interfibrillar subpopulations
Hendgen-Cotta, U. B., Esfeld, S., Jastrow, H., Totzeck, M., Altschmied, J., Goy, C., Haendeler, J., Winterhager, E., & Rassaf, T. (2017) · Mitochondrion · doi:10.1016/j.mito.2017.07.005 · Cited by 13
Self-citationRole of blood and vascular smooth muscle in the vasoactivity of nitrite
Liu, T., Schroeder, H. J., Barcelo, L., Bragg, S. L., Terry, M. H., Wilson, S. M., Power, G. G., & Blood, A. B. (2014) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00138.2014 · Cited by 13
Reciprocal regulation of sulfite oxidation and nitrite reduction by mitochondrial sulfite oxidase
Kaczmarek, A. T., Strampraad, M. J. F., Hagedoorn, P., & Schwarz, G. (2019) · Nitric Oxide · doi:10.1016/j.niox.2019.04.004 · Cited by 13
Majerczak, J., Kij, A., Drzymała‐Celichowska, H., Kuś, K., Karasiński, J., Nieckarz, Z., Grandys, M., Celichowski, J., Szkutnik, Z., Hendgen-Cotta, U. B., et al. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23052686 · Cited by 13
Self-citationTotzeck, M., Hendgen-Cotta, U. B., French, B. A., & Rassaf, T. (2016) · Journal of Biological Methods · doi:10.14440/jbm.2016.149 · Cited by 12
Self-citationGuti�rrez-Camacho, L., Kormanovski, A., Castillo-Hern�ndez, M., Guevara‐Balcázar, G., & Lara‐Padilla, E. (2020) · Biomedical Reports · doi:10.3892/br.2020.1291 · Cited by 12
S -nitrosation of calpains is associated with cardioprotection in myocardial I/R injury
Totzeck, M., Korste, S., Miinalainen, I., Hendgen-Cotta, U. B., & Rassaf, T. (2017) · Nitric Oxide · doi:10.1016/j.niox.2017.04.003 · Cited by 12
Self-citationCardiac Effects of BRAF and MEK Inhibitors: Mechanisms and Clinical Management
Courand, P., Berger, M., Bouali, A., Harbaoui, B., Lantelme, P., & Dalle, S. (2022) · Current Oncology Reports · doi:10.1007/s11912-022-01205-3 · Cited by 11
Nitrite Prevents Right Ventricular Failure and Remodeling Induced by Pulmonary Artery Banding
HU, J. L., Sharifi‐Sanjani, M., & Tofovic, S. P. (2016) · Journal of Cardiovascular Pharmacology · doi:10.1097/fjc.0000000000000446 · Cited by 12
The reactive species interactome
Cortese-Krott, M. M., Santolini, J., Wootton, S. A., Jackson, A. A., & Feelisch, M. (2019) · Elsevier eBooks · doi:10.1016/b978-0-12-818606-0.00004-3 · Cited by 11
Atta, S., Mandal, A., Patra, S., & Majumdar, A. (2025) · Inorganic Chemistry · doi:10.1021/acs.inorgchem.5c00753 · Cited by 10
Sethumadhavan, S., Whitsett, J., Bennett, B., Ionova, I. A., Pieper, G. M., & Vasquez-Vivar, J. M. (2016) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2016.01.019 · Cited by 10
Vitturi, D. A., Maynard, C. C., Olsufka, M., Straub, A. C., Krehel, N., Kudenchuk, P. J., Nichol, G., Sayre, M. R., Kim, F., & Dezfulian, C. (2020) · Redox Biology · doi:10.1016/j.redox.2020.101463 · Cited by 10
Role of nitrite in regulation of fetal cephalic circulation in sheep
Truong, G. T., Schröder, H. J., Liu, T., Zhang, M., Kanda, E., Bragg, S. L., Power, G. G., & Blood, A. B. (2014) · The Journal of Physiology · doi:10.1113/jphysiol.2013.269340 · Cited by 10
The Effects of Dietary Nitrate (Beetroot Juice) Supplementation on Exercise Performance: A Review
Zafeiridis, A. (2014) · American Journal of Sports Science · doi:10.11648/j.ajss.20140204.15 · Cited by 10
Yuschen, X., Choi, J.-H., Seo, J., Sun, Y., Lee, E., Kim, S.-W., & Park, H. (2024) · Healthcare · doi:10.3390/healthcare12131240 · Cited by 9
Cunha, M. S., Lacchini, R., & Tanus-Santos, J. E. (2024) · Antioxidants · doi:10.3390/antiox13060691 · Cited by 9
A moonlighting job for α-globin in blood vessels
Abbineni, P. S., Baid, S., & Weiss, M. J. (2024) · Blood · doi:10.1182/blood.2023022192 · Cited by 9
Yang, M., Dart, C., Kamishima, T., & Quayle, J. M. (2020) · PeerJ · doi:10.7717/peerj.10344 · Cited by 9
Zoladz, J. A., Grandys, M., Smęda, M., Kij, A., Kurpińska, A., Kwiatkowski, G., Karasiński, J., Hendgen-Cotta, U. B., Chłopicki, S., & Majerczak, J. (2024) · The Journal of Physiology · doi:10.1113/jp285067 · Cited by 9
Self-citationLoss of resilience contributes to detrusor underactivity in advanced age
Ramasamy, R., Baker, D. S., Lemtiri‐Chlieh, F., Rosenberg, D. A., Woon, E., Al‐Naggar, I. M., Hardy, C. C., Levine, E. S., Kuchel, G. A., Bartley, J. M., et al. (2023) · Biogerontology · doi:10.1007/s10522-022-10005-y · Cited by 8
Sonoda, K., Ohtake, K., Kubo, Y., Uchida, H., Uchida, M., Natsume, H., Kobayashi, M., & Kobayashi, J. (2013) · Clinical and Experimental Hypertension · doi:10.3109/10641963.2013.846355 · Cited by 9
Impact of mitochondrial nitrite reductase on hemodynamics and myocardial contractility
Dungel, P., Penzenstadler, C., Ashmwe, M., Dumitrescu, S., Stögerer, T., Redl, H. R., Bahrami, S., & Kozlov, A. V. (2017) · Scientific Reports · doi:10.1038/s41598-017-11531-3 · Cited by 8
Mendoza, J. P., Passafaro, R. J., Baby, S. M., Young, A. P., Bates, J. N., Gaston, B. M., & Lewis, S. J. (2014) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00842.2013 · Cited by 8
A Mononitrosyl Diiron(II) Compound Catalyzes the Reduction of Nitrite to Nitric Oxide
Mandal, A., Atta, S., & Majumdar, A. (2025) · Inorganic Chemistry · doi:10.1021/acs.inorgchem.5c02388 · Cited by 7
Catalase-Like Antioxidant Activity is Unaltered in Hypochlorous Acid Oxidized Horse Heart Myoglobin
Ahmad, G., Chami, B., Kazzi, M. E., Wang, X., Moreira, M. T. S., Hamilton, N. A., Maw, A. M., Hambly, T. W., & Witting, P. K. (2019) · Antioxidants · doi:10.3390/antiox8090414 · Cited by 6
Impact of mitochondria on nitrite metabolism in HL-1 cardiomyocytes
Dungel, P., Teuschl, A., Banerjee, A., Paier-Pourani, J., Redl, H., & Kozlov, A. V. (2013) · Frontiers in Physiology · doi:10.3389/fphys.2013.00101 · Cited by 7
Conjugated linoleic acid and nitrite attenuate mitochondrial dysfunction during myocardial ischemia
Hoose, P. M. V., Kelm, N. Q., Piell, K. M., & Cole, M. P. (2016) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2016.04.001 · Cited by 7
Unraveling the General Trend of the Reaction of Nitrite with Diiron(II)-polychalcogenides
Hossain, M. K., Basak, A., Choudhury, A. R., & Majumdar, A. (2025) · Journal of the American Chemical Society · doi:10.1021/jacs.5c14543 · Cited by 6
Targeted treatment for craniopharyngioma
Stec, N. E., Barker, F. G., & Brastianos, P. K. (2025) · Journal of Neuro-Oncology · doi:10.1007/s11060-025-04942-0 · Cited by 6
Tyrosine kinase inhibitors and atherosclerosis: A close but complicated relationship
Xu, K., Tang, H. T., Xiong, J., Ban, X., Duan, Y., & Tu, Y. (2023) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2023.175869 · Cited by 6
Nitrate as Warden of Nitric Oxide Homeostasis in Mammals
Piknova, B., Park, J. W., & Schechter, A. N. (2025) · Nutrients · doi:10.3390/nu17091544 · Cited by 6
Johnson, A. R., Rao, K., Zhang, B. B., Mullett, S. J., Goetzman, E. S., Gelhaus, S. L., Tejero, J., & Shiva, S. (2024) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2024.10.258 · Cited by 8
Self-citationLiu, Y., Buerk, D. G., Barbee, K. A., & Jaron, D. (2017) · Microvascular Research · doi:10.1016/j.mvr.2017.03.009 · Cited by 5
Heme Protein Metabolism of NO and Nitrite
Kim‐Shapiro, D. B., & Gladwin, M. T. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-804273-1.00006-5 · Cited by 5
Self-citationBuerk, D. G., Liu, Y., Zaccheo, K. A., Barbee, K. A., & Jaron, D. (2017) · Frontiers in Physiology · doi:10.3389/fphys.2017.01053 · Cited by 6
Aleksenko, L., Åkerström, B., Hansson, E., Erlandsson, L., & Hansson, S. R. (2020) · Scientific Reports · doi:10.1038/s41598-020-77561-6 · Cited by 5
Tissue Perfusion and Diffusion and Cellular Respiration: Transport and Utilization of Oxygen
Hsia, C. C. W. (2023) · Seminars in Respiratory and Critical Care Medicine · doi:10.1055/s-0043-1770061 · Cited by 8
Cortese-Krott, M. M., Kramer, C. M., & Kelm, M. (2017) · Elsevier eBooks · doi:10.1016/b978-0-12-804273-1.00014-4 · Cited by 5
Self-citationProtection by nitrite against the ischemic effects induced by acute myocardial infarction in mice
Wang, Y. (2017) · The Anatolian Journal of Cardiology · doi:10.14744/anatoljcardiol.2017.7952 · Cited by 5
Montmorency cherry supplement does not affect aerobic exercise performance in healthy men
Davis, G. R., & Bellar, D. M. (2019) · International Journal for Vitamin and Nutrition Research · doi:10.1024/0300-9831/a000575 · Cited by 5
Allergic activation of mast cells.
Parker, C. W. (1986) · PubMed · Cited by 5
Mandal, A., Atta, S., & Majumdar, A. (2025) · Inorganic Chemistry · doi:10.1021/acs.inorgchem.5c04413 · Cited by 4
Nitric oxide application for myocardial protection in coronary artery disease
Podoksenov, Y. K., Олегович, К. Н., & Аркадьевна, М. И. (2019) · Russian Journal of Anesthesiology and Reanimatology · doi:10.17116/anaesthesiology201902134 · Cited by 4
A new role for myoglobin in cardiac and skeletal muscle function
Кулева, Н. В., & Krasovskaia, I. E. (2016) · BIOPHYSICS · doi:10.1134/s000635091605016x · Cited by 4
Cytoglobin at the Crossroads of Vascular Remodeling
Amdahl, M. B., DeMartino, A. W., Tejero, J., & Gladwin, M. T. (2017) · Arteriosclerosis Thrombosis and Vascular Biology · doi:10.1161/atvbaha.117.310058 · Cited by 4
Self-citationLiubertas, T., Poderys, L. J., Zigmantaitė, V., Čapkauskienė, S., Trakimas, G., Pukėnas, K., & Viškelis, P. (2022) · Applied Sciences · doi:10.3390/app13010177 · Cited by 3
Mitochondrias' sense of SNO: pathway to cardioprotection in ischaemic preconditioning
Rassaf, T., & Schulz, R. (2015) · Cardiovascular Research · doi:10.1093/cvr/cvv115 · Cited by 3
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Hoose, P. M. V. (2015) · ThinkIR: The University of Louisville's Institutional Repository (University of Louisville) · doi:10.18297/etd/2293
Craig, J. C. (2015) · K-State Research Exchange (Kansas State University)
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Rassaf, T., & Schadendorf, D. (2022) · Elsevier eBooks · doi:10.1016/b978-0-323-68135-3.00053-2
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Editors, T. (2013) · Circulation · doi:10.1161/circulationaha.113.004990
Gao, Y. (2017) · Springer eBooks · doi:10.1007/978-981-10-4810-4_18
Gao, Y. (2022) · Springer eBooks · doi:10.1007/978-981-19-7122-8_20
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Holmes, A. P. (2013) · University of Birmingham Institutional Research Archive (University of Birmingham)
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Bickta, J. (2015) · D-Scholarship@Pitt (University of Pittsburgh)
Metadata
- Authors
- Totzeck, M., Hendgen-Cotta, U. B., Luedike, P., Berenbrink, M., Klare, J. P., Steinhoff, H.-J., Semmler, D., Shiva, S., Williams, D., Kipar, A., Gladwin, M. T., Schrader, J., Kelm, M., Cossins, A. R., & Rassaf, T.
- Affiliations
- University of Liverpool (GB)
- From the Department of Medicine, Division of Cardiology, Pulmonology, and Vascular Medicine, Medical Faculty, University Hospital Duesseldorf, Duesseldorf, Germany (M.T., U.B.H.-C., P.L., D.S., M.K., T.R.); Institute of Integrative Biology (M.B., D.W., A.R.C.) and Department of Veterinary Pathology (A.K.), University of Liverpool, Liverpool, United Kingdom; Department of Physics, University Osnabrueck, Osnabrueck, Germany (J.P.K., H.S.); Departments of Pharmacology and Chemical Biology (S.S.) and...
- ORCID
- Venue
- Circulation
- Published
- 2012-07-17
- Volume
- 126
- Issue
- 3
- Pages
- 325-334
- ISSN
- 0009-7322 (ISSN-L)
- 1524-4539
- PMC
- PMC3410747
- OpenAlex
- W2165218367
- Cited by
- 202
- References
- 58
- Citations by year
- 2026: 2 · 2025: 9 · 2024: 7 · 2023: 6 · 2022: 10 · 2021: 6 · 2020: 15 · 2019: 16 · 2018: 13 · 2017: 21 · 2016: 19 · 2015: 17 · 2014: 27 · 2013: 28 · 2012: 5
- FWCI
- 11.66
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Circulation (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Deutsche Forschungsgemeinschaft (RA969/4-2])
- Deutsche Herzstiftung
- Deutsche Gesellschaft für Kardiologie-Herz und Kreislaufforschung.
- National Institutes of Health
- Directorate for Biological Sciences
- Biotechnology and Biological Sciences Research Council
- National Heart, Lung, and Blood Institute (R01HL096973, P01HL103455, R01HL098032)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Hemoglobin structure and function
- Health Sciences › Medicine › Physiology (medical) › Nitric Oxide and Endothelin Effects
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Heme Oxygenase-1 and Carbon Monoxide
- Keywords
- hypoxic vasodilation, nitrite, nitric oxide, myoglobin, vascular smooth muscle, soluble guanylate cyclase, cGMP signaling, hypoxia sensing, inducible nitric oxide synthase, endothelial nitric oxide synthase, oxygen supply and demand
- MeSH terms
- Soluble Guanylyl Cyclase, Adaptation, Physiological, Animals, Hypoxia, Cardiac Output, Guanylate Cyclase, Mice, Mutant Strains, Muscle, Smooth, Vascular, Myoglobin, Nitric Oxide, Nitrites, Oxygen, Vasodilation, Signal Transduction, Receptors, Cytoplasmic and Nuclear, Mice, Nitric Oxide Synthase Type II, Nitric Oxide Synthase Type III
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