Persistent inhibition of cell respiration by nitric oxide: Crucial role of S -nitrosylation of mitochondrial complex I and protective action of glutathione

Apparent hydroxyl radical production by peroxynitrite: Implications for endothelial injury from nitric oxide and superoxide

Beckman, J. S., Beckman, T. W., Chen, J., Marshall, P. A., & Freeman, B. A. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.4.1620 · Cited by 7,029

Vascular endothelial cells synthesize nitric oxide from L-arginine

Palmer, R. M. J., Ashton, D., & Moncada, S. (1988) · Nature · doi:10.1038/333664a0 · Cited by 4,786

Nitric oxide. A macrophage product responsible for cytostasis and respiratory inhibition in tumor target cells

Stuehr, D. J., & Nathan, C. F. (1989) · The Journal of Experimental Medicine · doi:10.1084/jem.169.5.1543 · Cited by 1,744

Potent and specific inhibition of glutathione synthesis by buthionine sulfoximine (S-n-butyl homocysteine sulfoximine).

Griffith, O. W., & Meister, A. (1979) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)35980-5 · Cited by 1,683

The chemistry of peroxynitrite: A product from the reaction of nitric oxide with superoxide

Pryor, W. A., & Squadrito, G. L. (1995) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.1995.268.5.l699 · Cited by 1,511

Mitochondrial control of apoptosis

Kroemer, G., Zamzami, N., & Susín, S. A. (1997) · Immunology Today · doi:10.1016/s0167-5699(97)80014-x · Cited by 1,476

Reversible inhibition of cytochrome c oxidase, the terminal enzyme of the mitochondrial respiratory chain, by nitric oxide: Implications for neurodegenerative diseases

Cleeter, M. W. J., Cooper, J. M., Darley-Usmar, V. M., Moncada, S., & Schapira, A. H. V. (1994) · FEBS Letters · doi:10.1016/0014-5793(94)00424-2 · Cited by 1,241

Ubisemiquinone is the electron donor for superoxide formation by complex III of heart mitochondria

Turrens, J. F., Alexandre, A., & Lehninger, A. L. (1985) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(85)90293-0 · Cited by 1,214

Nanomolar concentrations of nitric oxide reversibly inhibit synaptosomal respiration by competing with oxygen at cytochrome oxidase

Brown, G. C., & Cooper, C. E. (1994) · FEBS Letters · doi:10.1016/0014-5793(94)01290-3 · Cited by 1,055

Activation of the Cardiac Calcium Release Channel (Ryanodine Receptor) by Poly-S-Nitrosylation

Xu, L., Eu, J. P., Meissner, G., & Stamler, J. S. (1998) · Science · doi:10.1126/science.279.5348.234 · Cited by 991

Neurotoxic nitric oxide rapidly depolarizes and permeabilizes mitochondria by dynamically opening the mitochondrial transition pore⋆

Kindler, D. (2003) · Molecular and Cellular Neuroscience · doi:10.1016/s1044-7431(03)00074-5 · Cited by 31

The flux of energy in critical illness and the obesity paradox

Jaitovich, A., & Hall, J. B. (2025) · Physiological Reviews · doi:10.1152/physrev.00029.2024 · Cited by 34

Nitric oxide synthase type-1 modulates cardiomyocyte contractility and calcium handling: association with low intrinsic aerobic capacity

ydal, M. A. H., Wisløff, U., Kemi, O. J., Britton, S. L., Koch, L. G., Smith, G. L., & Ellingsen, Y. (2007) · European Journal of Cardiovascular Prevention & Rehabilitation · doi:10.1097/hjr.0b013e3280128bef · Cited by 30

Indirect inhibition of mitochondrial dihydroorotate dehydrogenase activity by nitric oxide

Beuneu, C., Auger, R., Löffler, M., Guissani, A., Lemaire, G., & Lepoivre, M. (2000) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(00)00239-2 · Cited by 32

Nanomolar melatonin enhances nNOS expression and controls HaCaT‐cells bioenergetics

Arese, M., Magnifico, M. C., Mastronicola, D., Fabio Altieri, F., Grillo, C., Blanck, T. J. J., & Sarti, P. (2012) · IUBMB Life · doi:10.1002/iub.603 · Cited by 31

Multiple Organ Dysfunction Syndrome

Proulx, F., Leteurtre, S., Joyal, J., & Jouvet, P. A. (2014) · Springer eBooks · doi:10.1007/978-1-4471-6362-6_35 · Cited by 30

Nitric oxide as a regulator of tissue oxygen consumption

Wolin, M. S., Xie, Y.-W., & Hintze, T. H. (1999) · Current Opinion in Nephrology & Hypertension · doi:10.1097/00041552-199901000-00015 · Cited by 30

The Role Of Glial–Neuronal Metabolic Cooperation in Modulating Progression of Multiple Sclerosis and Neuropathic Pain

Robinson, R. R., Dietz, A. K., Maroof, A. M., Asmis, R., & Forsthuber, T. G. (2019) · Immunotherapy · doi:10.2217/imt-2018-0153 · Cited by 33

Cardiac mitochondrial function, nitric oxide sensitivity and lipid composition following hypoxia acclimation in sablefish

Gerber, L., Clow, K. A., Katan, T., Emam, M., Leeuwis, R. H. J., Parrish, C. C., & Gamperl, A. K. (2019) · Journal of Experimental Biology · doi:10.1242/jeb.208074 · Cited by 29

Therapeutic targeting of metabolic alterations in acute respiratory distress syndrome

Robinson, M. J., & Krasnodembskaya, A. D. (2020) · European Respiratory Review · doi:10.1183/16000617.0114-2020 · Cited by 29

The versatile biochemistry of iron in macrophage effector functions

Behmoaras, J. V. (2020) · FEBS Journal · doi:10.1111/febs.15682 · Cited by 30

The microcirculation in sepsis.

Tyagi, A., Sethi, A. K., Girotra, G., & Mohta, M. (2009) · PubMed Central · Cited by 29

Long-lasting inhibition of presynaptic metabolism and neurotransmitter release by protein S-nitrosylation

Rudkouskaya, A., Sim, V., Shah, A. A., Feustel, P. J., Jourd’heuil, D., & Mongin, A. A. (2010) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2010.05.032 · Cited by 29

Interactions of nitric oxide-derived reactive nitrogen species with peroxidases and lipoxygenases

Coffey, M. J., Coles, B., & O’Donnell, V. B. (2001) · Free Radical Research · doi:10.1080/10715760100301471 · Cited by 29

Soluble guanylate cyclase

Hobbs, A. J. (2000) · Emerging Therapeutic Targets · doi:10.1517/14728222.4.6.735 · Cited by 29

Spatial confinement of isoforms of cardiac nitric-oxide synthase: unravelling the complexities of nitric oxide's cardiobiology

Hare, J. M. (2004) · The Lancet · doi:10.1016/s0140-6736(04)16083-2 · Cited by 29

Imaging Axonal Degeneration and Repair in Preclinical Animal Models of Multiple Sclerosis

Yandamuri, S. S., & Lane, T. E. (2016) · Frontiers in Immunology · doi:10.3389/fimmu.2016.00189 · Cited by 27

Modulation of the conformational state of mitochondrial complex I as a target for therapeutic intervention

Galkin, A. S., & Moncada, S. (2017) · Interface Focus · doi:10.1098/rsfs.2016.0104 · Cited by 30

Inorganic nitrate, hypoxia, and the regulation of cardiac mitochondrial respiration—probing the role of PPARα

Horscroft, J. A., O’Brien, K. A., Clark, A. D., Lindsay, R. T., Steel, A. S., Procter, N. E. K., Devaux, J. B. L., Frenneaux, M. P., Harridge, S. D. R., & Murray, A. J. (2019) · The FASEB Journal · doi:10.1096/fj.201900067r · Cited by 26

Compartmentalized Nitrosation and Nitration in Mitochondria

Ghafourifar, P., & Colton, C. A. (2003) · Antioxidants and Redox Signaling · doi:10.1089/152308603322110913 · Cited by 28

Nitric oxide inhibits the mitochondrial carnitine/acylcarnitine carrier through reversible S -nitrosylation of cysteine 136

Tonazzi, A., Giangregorio, N., Console, L., Palma, A. D., & Indiveri, C. (2017) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2017.04.002 · Cited by 27

Dimeric structures of quinol-dependent nitric oxide reductases (qNORs) revealed by cryo–electron microscopy

Gopalasingam, C. C., Johnson, R. M., Chiduza, G. N., Tosha, T., Yamamoto, M., Shiro, Y., Antonyuk, S. V., Muench, S. P., & Hasnain, S. S. (2019) · Science Advances · doi:10.1126/sciadv.aax1803 · Cited by 27

Metabolic ROS Signaling: To Immunity and Beyond

Andreyev, A. Y., Kushnareva, Y. E., Starkova, N. N., & Starkov, A. A. (2020) · Biochemistry (Moscow) · doi:10.1134/s0006297920120160 · Cited by 28

Allosteric modulation by S-nitrosation in the low-O2affinity myoglobin from rainbow trout

Helbo, S., & Fago, A. (2010) · American Journal of Physiology-Regulatory, Integrative and Comparative Physiology · doi:10.1152/ajpregu.00374.2010 · Cited by 27

Response of mitochondrial antioxidant system and respiratory pathways to reactive nitrogen species in pea leaves

Martí, M. C., Florez‐Sarasa, I., Camejo, D. M., Pallol, B., Ortiz, A., Ribas‐Carbó, M., Jiménez, A., & Sevilla, F. (2012) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2012.01654.x · Cited by 27

The Emerging Role of Hepatocellular eNOS in Non-alcoholic Fatty Liver Disease Development

Cunningham, R. P., Sheldon, R. D., & Rector, R. S. (2020) · Frontiers in Physiology · doi:10.3389/fphys.2020.00767 · Cited by 28

Care of the critically ill neonate with hypoxemic respiratory failure and acute pulmonary hypertension: framework for practice based on consensus opinion of neonatal hemodynamics working group

Jain, A., Giesinger, R. E., Dakshinamurti, S., Elsayed, Y. N., Jankov, R. P., Weisz, D. E., Lakshminrusimha, S., Mitra, S., Mazwi, M., Ting, J. Y., et al. (2022) · Journal of Perinatology · doi:10.1038/s41372-021-01296-z · Cited by 26

Nitric Oxide and Superoxide Anion Differentially Activate Poly(ADP-ribose) Polymerase-1 and Bax to Induce Nuclear Translocation of Apoptosis-Inducing Factor and Mitochondrial Release of Cytochrome c after Spinal Cord Injury

Wu, K. L. H., Hsu, C., & Chan, J. Y. H. (2009) · Journal of Neurotrauma · doi:10.1089/neu.2008.0692 · Cited by 26

Ethanol and age enhances fluoride toxicity through oxidative stress and mitochondrial dysfunctions in rat intestine

Chauhan, S. S., Mahmood, A., & Ojha, S. (2013) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-013-1804-6 · Cited by 26

Modulation of nitrergic signalling pathway by American ginseng attenuates chronic unpredictable stress-induced cognitive impairment, neuroinflammation, and biochemical alterations

Rinwa, P., & Kumar, A. (2013) · Naunyn-Schmiedeberg s Archives of Pharmacology · doi:10.1007/s00210-013-0925-5 · Cited by 26

Mutual changes of thioredoxin and nitrosothiols during biliary cirrhosis: Results from humans and cholestatic rats

Grattagliano, I., Portincasa, P., Palmieri, V. O., & Palasciano, G. (2007) · Hepatology · doi:10.1002/hep.21519 · Cited by 26

Nitric Oxide and Oxidative Stress in Cardiovascular Aging

Raju, S. V. Y., Barouch, L. A., & Hare, J. M. (2005) · Science of Aging Knowledge Environment · doi:10.1126/sageke.2005.21.re4 · Cited by 27

Skeletal Muscle Vascular Control During Exercise

Ferguson, S. K., Glean, A. A., Holdsworth, C. T., Wright, J. L., Fees, A. J., Colburn, T. D., Stäbler, T., Allen, J. D., JONES, A. M., Musch, T. I., et al. (2015) · Journal of Cardiovascular Pharmacology and Therapeutics · doi:10.1177/1074248415599061 · Cited by 25

S-Nitrosylation-mediated dysfunction of TCA cycle enzymes in synucleinopathy studied in postmortem human brains and hiPSC-derived neurons

Doulias, P., Yang, H., Andreyev, A. Y., Dolatabadi, N., Scott, H. R., Raspur, C. K., Patel, P. R., Nakamura, T., Tannenbaum, S. R., Ischiropoulos, H., et al. (2023) · Cell chemical biology · doi:10.1016/j.chembiol.2023.06.018 · Cited by 24

Effects of Citrulline Malate and Beetroot Juice Supplementation on Energy Metabolism and Blood Flow During Submaximal Resistance Exercise

Trexler, E. T., Keith, D. S., Lucero, A. A., Stoner, L. R., Schwartz, T. A., Persky, A. M., Ryan, E. D., & Smith‐Ryan, A. E. (2019) · Journal of Dietary Supplements · doi:10.1080/19390211.2019.1650866 · Cited by 25

Biology of macrophage fate decision: Implication in inflammatory disorders

Yadav, S., Dwivedi, A., & Tripathi, A. (2022) · Cell Biology International · doi:10.1002/cbin.11854 · Cited by 26

Pre- and post-treatment of α-Tocopherol on cognitive, synaptic plasticity, and mitochondrial disorders of the hippocampus in icv-streptozotocin-induced sporadic Alzheimer’s-like disease in male Wistar rat

Zadeh, F. N., Nazari, M., Amini, A., Adeli, S., Behrooz, A. B., & Fahanik‐Babaei, J. (2023) · Frontiers in Neuroscience · doi:10.3389/fnins.2023.1073369 · Cited by 24

Identification of mitochondrial deficits and melatonin targets in liver of septic mice by high-resolution respirometry

Doerrier, C., García, J. A. G., Volt, H., Díaz-Casado, M. E., Lima‐Cabello, E., Ortiz, F., Luna‐Sánchez, M., Escames, G., López, L. C., & Acuña-Castroviejo, D. (2014) · Life Sciences · doi:10.1016/j.lfs.2014.11.031 · Cited by 24

Age-related deficiencies in complex I endogenous substrate availability and reserve capacity of complex IV in cortical neuron electron transport

Jones, T. T., & Brewer, G. J. (2009) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2009.09.009 · Cited by 25

Post-Translational Oxidative Modifications of Mitochondrial Complex I (NADH: Ubiquinone Oxidoreductase): Implications for Pathogenesis and Therapeutics in Human Diseases

Bharath, M. M. S. (2017) · Journal of Alzheimer s Disease · doi:10.3233/jad-170117 · Cited by 23

Understanding the Metabolic Profile of Macrophages During the Regenerative Process in Zebrafish

Paredes, L. C., Câmara, N. O. S., & Braga, T. T. (2019) · Frontiers in Physiology · doi:10.3389/fphys.2019.00617 · Cited by 23

Differential Mechanisms of Nitric Oxide- and Peroxynitrite-Induced Cell Death

Meij, J. T. A., Haselton, C. L., Hillman, K. L., Dhanasekaran, M., Ebadi, M., & Yu, L. (2004) · Molecular Pharmacology · doi:10.1124/mol.104.001354 · Cited by 24

GSNOR Deficiency Enhances In Situ Skeletal Muscle Strength, Fatigue Resistance, and RyR1 S-Nitrosylation Without Impacting Mitochondrial Content and Activity

Moon, Y., Cao, Y., Zhu, J., Xu, Y., Balkan, W., Buys, E. S., Díaz, F., Kerrick, W. G. L., Hare, J. M., & Percival, J. M. (2016) · Antioxidants and Redox Signaling · doi:10.1089/ars.2015.6548 · Cited by 23

Attenuation of Oxidative Damage byBoerhaavia diffusa L.Against Different Neurotoxic Agents in Rat Brain Homogenate

Ayyappan, P., Palayyan, S. R., & Gopalan, R. K. (2015) · Journal of Dietary Supplements · doi:10.3109/19390211.2015.1036186 · Cited by 23

Caspase-6 mediated cleavage of guanylate cyclase alpha 1 during deoxycholate-induced apoptosis: Protective role of the nitric oxide signaling module

Payne, C. M., Waltmire, C. N., Crowley, C., Crowley-Weber, C. L., Dvorakova, K., Bernstein, H., Bernstein, C., Holubec, H., & Garewal, H. S. (2003) · Cell Biology and Toxicology · doi:10.1023/b:cbto.0000013331.70391.0e · Cited by 23

Contribution of glutamatergic signaling to nitrosative stress‐induced protein misfolding in normal brain aging and neurodegenerative diseases

Nakamura, T., Gu, Z., & Lipton, S. A. (2007) · Aging Cell · doi:10.1111/j.1474-9726.2007.00284.x · Cited by 23

Nitric oxide increases mitochondrial respiration in a cGMP-dependent manner in the callus from Arabidopsis thaliana

Wang, X., Li, J., Liu, J., He, W., & Bi, Y. (2010) · Nitric Oxide · doi:10.1016/j.niox.2010.07.004 · Cited by 23

Nitric oxide inhibits neonatal hepatocyte oxidative metabolism

Romeo, C., Eaton, S. D., Spitz, L., & Pierro, A. (2000) · Journal of Pediatric Surgery · doi:10.1016/s0022-3468(00)80011-1 · Cited by 23

Fructose overconsumption-induced reprogramming of microglia metabolism and function

Ting, K. K. Y. (2024) · Frontiers in Immunology · doi:10.3389/fimmu.2024.1375453 · Cited by 23

Acetyl-CoA production by Mediator-bound 2-ketoacid dehydrogenases boosts de novo histone acetylation and is regulated by nitric oxide

Russo, M., Gualdrini, F., Vallelonga, V., Prosperini, E., Noberini, R., Pedretti, S., Borriero, C., Chiaro, P. D., Polletti, S., Imperato, G., et al. (2024) · Molecular Cell · doi:10.1016/j.molcel.2023.12.033 · Cited by 21

Mitochondrial genome and human mitochondrial diseases

Mazunin, I., Volodko, N. V., Starikovskaya, E. B., & Sukernik, R. I. (2010) · Molecular Biology · doi:10.1134/s0026893310050018 · Cited by 23

Cocoa protective effects against abnormal fat storage and oxidative stress induced by a high-fat diet involve PPARα signalling activation

Fidaleo, M., Fracassi, A., Zuorro, A., Lavecchia, R., Moreno, S., & Sartori, C. (2014) · Food & Function · doi:10.1039/c4fo00616j · Cited by 22

Regulation of mitochondrial function and endoplasmic reticulum stress by nitric oxide in pluripotent stem cells

Caballano‐Infantes, E., Bautista, J., Beltrán-Povea, A., Cahuana, G. M., Soria, B., Hajji, N., Bedoya, F. J., & Tejedo, J. R. (2017) · World Journal of Stem Cells · doi:10.4252/wjsc.v9.i2.26 · Cited by 22

Nonylphenol and Octylphenol Differently Affect Cell Redox Balance by Modulating the Nitric Oxide Signaling

Magnifico, M. C., Xhani, M., Popov, M., Saso, L., Sarti, P., & Arese, M. (2018) · Oxidative Medicine and Cellular Longevity · doi:10.1155/2018/1684827 · Cited by 22

Refocusing the Brain: New Approaches in Neuroprotection Against Ischemic Injury

Rodriguez, C., Agulla, J., & Delgado‐Esteban, M. (2020) · Neurochemical Research · doi:10.1007/s11064-020-03016-z · Cited by 21

Nitric oxide reduces energy supply by direct action on the respiratory chain in isolated cardiomyocytes

Stumpe, T., Decking, U. K. M., & Schrader, J. (2001) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.2001.280.5.h2350 · Cited by 22

Nitric oxide and mitochondrial function in cardiovascular diseases

Li, H., Cheng, Z., Wu, D., & Hu, Q. (2024) · Nitric Oxide · doi:10.1016/j.niox.2024.11.007 · Cited by 21

Effects of Aliphatic Polyesters on Activation of the Immune System: Studies on Macrophages

Scislowska-Czarnecka, A., Pamuła, E., Tlalka, A., & Kołaczkowska, E. (2012) · Journal of Biomaterials Science Polymer Edition · doi:10.1163/092050611x559421 · Cited by 21

Simvastatin pre-treatment improves survival and mitochondrial function in a 3-day fluid-resuscitated rat model of sepsis

Morel, J., Hargreaves, I. P., Brealey, D. A., Neergheen, V., Backman, J. T., Lindig, S., Bläss, M., Bauer, M. W., McAuley, D. F., & Singer, M. (2017) · Clinical Science · doi:10.1042/cs20160802 · Cited by 21

Poly(diallydimethylammonium chloride)-Induced Dispersion and Exfoliation of Tungsten Disulfide for the Sensing of Glutathione and Catalytic Hydrogenation of p-Nitrophenol

Tseng, W., Lee, C.-H., & Tseng, W. (2018) · ACS Applied Nano Materials · doi:10.1021/acsanm.8b01592 · Cited by 21

Monocyte glycolysis determines CD8+ T cell functionality in human Chagas disease

Sanmarco, L. M., Eberhardt, N., Bergero, G., Palacio, L. P. Q., Adami, P. V. M., Visconti, L. M., Minguez, Á. R., Hernández-Vásquez, Y., Silva, E. A. C., Morelli, L., et al. (2019) · JCI Insight · doi:10.1172/jci.insight.123490 · Cited by 21

Endothelial nitric oxide synthase upregulation in the cochlea of the guinea pig after intratympanic gentamicin injection

Heinrich, U., Selivanova, O., Brieger, J., & Mann, W. J. (2005) · European Archives of Oto-Rhino-Laryngology · doi:10.1007/s00405-005-0949-7 · Cited by 21

Mitochondria and Cancer

Owens, K. M., Modica-Napolitano, J. S., & Singh, K. K. (2008) · Springer eBooks · doi:10.1007/978-0-387-84835-8_1 · Cited by 21

Hemodynamic and metabolic responses to moderate asphyxia in brain and skeletal muscle of late-gestation fetal sheep.

Newman, J., Peebles, D., Harding, S. R., Springett, R., & Hanson, M. (2000) · Journal of applied physiology · doi:10.1152/jappl.2000.88.1.82 · Cited by 20

Til cell death do us part: nitric oxide and mechanisms of hepatotoxicity

Kim, P. K., Zuckerbraun, B. S., Otterbein, L. E., Yoram Vodovotz, B., & Billiar, T. R. (2004) · Biological Chemistry · doi:10.1515/bc.2004.002 · Cited by 21

Innate immunity champions: The diverse functions of macrophages

Biscu, F., Zouzaf, A., Cicia, D., Pridans, C., & Matteoli, G. (2024) · European Journal of Immunology · doi:10.1002/eji.202451139 · Cited by 25

Reactive oxygen species production by BP-1,6-quinone and its effects on the endothelial dysfunction: Involvement of the mitochondria

Shukla, H., Chitrakar, R., Bibi, H. A., Gaje, G., Koucheki, A., Trush, M. A., Zhu, H., Li, Y. R., & Jia, Z. (2020) · Toxicology Letters · doi:10.1016/j.toxlet.2020.01.011 · Cited by 21

Differential effects of the nonsteroidal antiinflammatory drug flurbiprofen and its nitric oxide‐releasing derivative, nitroflurbiprofen, on prostaglandin E2, interleukin‐1β, and nitric oxide synthesis by activated microglia

Ajmone‐Cat, M. A., Nicolini, A., & Minghetti, L. (2001) · Journal of Neuroscience Research · doi:10.1002/jnr.10038 · Cited by 20

Effects of nitrosopropofol on mitochondrial energy-converting system

Stevanato, R., Momo, F., Marian, M., Rigobello, M. P., Bindoli, A., Bragadin, M., Vincenti, E., & Scutari, G. (2002) · Biochemical Pharmacology · doi:10.1016/s0006-2952(02)01253-4 · Cited by 20

Nitric oxide, nitric oxide synthase, and hypertensive vascular disease

Busse, R., & Fleming, I. (1999) · Current Hypertension Reports · doi:10.1007/s11906-999-0078-6 · Cited by 20

Differential cytostatic effects of NO donors and NO producing cells

Lemaire, G., Alvarez-Pachon, F.-J., Beuneu, C., Lepoivre, M., & Petit, J. F. (1999) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(98)00331-1 · Cited by 20

Aerobic glycolysis of vascular endothelial cells: a novel perspective in cancer therapy

Xu, S., Liao, J., Liu, B., Zhang, C., & Xu, X. (2024) · Molecular Biology Reports · doi:10.1007/s11033-024-09588-1 · Cited by 20

Immuno-metabolic interfaces in cardiac disease and failure

Bertero, E., Dudek, J., Cochain, C., Delgobo, M., Ramos, G. C., Gerull, B., Higuchi, T., Vaeth, M., Zernecke, A., Frantz, S., et al. (2021) · Cardiovascular Research · doi:10.1093/cvr/cvab036 · Cited by 19

Comparative Transcriptome Analysis of Head Kidney of Aeromonas hydrophila-infected Hypoxia-tolerant and Normal Large Yellow Croaker

Zhang, Y., Shen, W., Ding, J., Gao, X., Wu, X., & Zhu, J. (2022) · Marine Biotechnology · doi:10.1007/s10126-022-10158-4 · Cited by 19

Extracellular Nitric Oxide Release Mediates Soluble Guanylate Cyclase-Independent Vasodilator Action of Spermine NONOate: Comparison with Other Nitric Oxide Donors in Isolated Rat Femoral Arteries

Miller, M. R., Okubo, K., Roseberry, M. J., Webb, D. J., & Megson, I. L. (2004) · Journal of Cardiovascular Pharmacology · doi:10.1097/00005344-200403000-00016 · Cited by 18

The Peculiar Facets of Nitric Oxide as a Cellular Messenger: From Disease-Associated Signaling to the Regulation of Brain Bioenergetics and Neurovascular Coupling

Laranjinha, J. A. N., Nunes, C., Ledo, A., Lourenço, C. F., Rocha, B. S., & Barbosa, R. M. (2020) · Neurochemical Research · doi:10.1007/s11064-020-03015-0 · Cited by 18

Lymphoid Tissue–Resident Alcaligenes Establish an Intracellular Symbiotic Environment by Creating a Unique Energy Shift in Dendritic Cells

Hosomi, K., Shibata, N., Shimoyama, A., Uto, T., Nagatake, T., Tojima, Y., Nishino, T., Takeyama, H., Fukase, K., Kiyono, H., et al. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.561005 · Cited by 19

Effects of inhalation of low-dose nitrite or carbon monoxide on post-reperfusion mitochondrial function and tissue injury in hemorrhagic shock swine

Haugaa, H., Gómez, H., Maberry, D. R., Holder, A. L., Ogundele, O., Quintero, A. M. B., Escobar, D. A., Tønnessen, T. I., Airgood, H., Dezfulian, C., et al. (2015) · Critical Care · doi:10.1186/s13054-015-0903-z · Cited by 19

S-Nitrosation and thiol switching in the mitochondrion: a new paradigm for cardioprotection in ischaemic preconditioning

Hill, B. G., & Darley-Usmar, V. M. (2008) · Biochemical Journal · doi:10.1042/bj20080716 · Cited by 19

The Evolution of Nitric Oxide Function: From Reactivity in the Prebiotic Earth to Examples of Biological Roles and Therapeutic Applications

Shepherd, M., Giordano, D., Verde, C., & Poole, R. K. (2022) · Antioxidants · doi:10.3390/antiox11071222 · Cited by 20

Effect of Melittin on Metabolomic Profile and Cytokine Production in PMA-Differentiated THP-1 Cells

Alqarni, A. M., Ferro, V. A., Parkinson, J. A., Dufton, M. J., & Watson, D. G. (2018) · Vaccines · doi:10.3390/vaccines6040072 · Cited by 18

Selective Vulnerability of Synaptic Signaling and Metabolism to Nitrosative Stress

Mongin, A. A., Dohare, P., & Jourd’heuil, D. (2012) · Antioxidants and Redox Signaling · doi:10.1089/ars.2012.4559 · Cited by 19

Nitrosyl heme production compared in endotoxemic and hemorrhagic shock

Davies, N. A., Brealey, D. A., Stidwill, R. P., Singer, M., Svistunenko, D. A., & Cooper, C. E. (2004) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2004.09.026 · Cited by 18

Septic cardiomyopathy: characteristics, evaluation, and mechanism

Xue, W., Pang, J., Liu, J., Wang, H., Guo, H., & Chen, Y. (2022) · Emergency and Critical Care Medicine · doi:10.1097/ec9.0000000000000060 · Cited by 17

Pro-inflammatory macrophage activation does not require inhibition of oxidative phosphorylation

Ball, A. B., Jones, A. E., Nguyễn, K. B., Rios, A., Marx, N., Hsieh, W. Y., Yang, K., Desousa, B. R., Kim, K. K. O., Veliova, M., et al. (2025) · EMBO Reports · doi:10.1038/s44319-024-00351-y · Cited by 22

Increased mitochondrial prooxidant activity mediates up-regulation of Complex I S-glutathionylation via protein thiyl radical in the murine heart of eNOS−/−

Kang, P. T., Chen, C., & Chen, Y. (2014) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2014.11.016 · Cited by 17

Cardioprotective effects of ozone oxidative preconditioning in an in vivo model of ischemia/reperfusion injury in rats

Ahmed, L. A., Salem, H. A., Mawsouf, M. N., Attia, A. S., & Agha, A. M. (2012) · Scandinavian Journal of Clinical and Laboratory Investigation · doi:10.3109/00365513.2012.663100 · Cited by 17

Mechanism of nitrite-dependent NO synthesis by human sulfite oxidase

Bender, D. A., Kaczmarek, A. T., Niks, D., Hille, R., & Schwarz, G. (2019) · Biochemical Journal · doi:10.1042/bcj20190143 · Cited by 18

Signature of high altitude adaptation in the gluteus proteome of the yak

Xin, J., Chai, Z., Zhang, C., Zhang, Q., Zhu, Y., Cao, H., Cidan, Y., Chen, X., Jiang, H., Zhong, J., et al. (2020) · Journal of Experimental Zoology Part B Molecular and Developmental Evolution · doi:10.1002/jez.b.22995 · Cited by 18

Cellular and Exosomal Regulations of Sepsis-Induced Metabolic Alterations

Appiah, M. G., Park, E. J., Akama, Y., Nakamori, Y., Kawamoto, E., Gaowa, A., & Shimaoka, M. (2021) · International Journal of Molecular Sciences · doi:10.3390/ijms22158295 · Cited by 19

Inhibition of Nitric-Oxide-Mediated Apoptosis in Jurkat Leukemia Cells despite Cytochrome c Release

Umansky, V., Ratter, F., Lampel, S., Bucur, M., Schirrmacher, V., & Ushmorov, A. (2001) · Experimental Cell Research · doi:10.1006/excr.2001.5188 · Cited by 17

Formation of nitric oxide from nitroxyl anion: role of quinones and ferricytochrome c

Büyükafşar, K., Nelli, S., & Martin, W. (2001) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0703812 · Cited by 17

The mechanism of the nitric oxide‐mediated enhancement of tert‐butylhydroperoxide‐induced DNA single strand breakage

Guidarelli, A., Clementi, E., Sciorati, C., & Cantoni, O. (1998) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0702159 · Cited by 17

Effect of sodium nitrite on local control of contracting skeletal muscle microvascular oxygen pressure in healthy rats

Colburn, T. D., Ferguson, S. K., Holdsworth, C. T., Craig, J. C., Musch, T. I., & Poole, D. C. (2016) · Journal of Applied Physiology · doi:10.1152/japplphysiol.00367.2016 · Cited by 16

Nitric oxide‐induced adenosine inhibition of hippocampal synaptic transmission depends on adenosine kinase inhibition and is cyclic GMP independent

Arrigoni, E., & Rosenberg, P. A. (2006) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2006.05124.x · Cited by 16

Clinical course and outcome for critically ill children with Down syndrome: a retrospective cohort study

Tibby, S. M., Durward, A., Goh, C. T., Thorburn, K., Morris, K., Broadhead, M., & Peters, M. J. (2012) · Intensive Care Medicine · doi:10.1007/s00134-012-2589-x · Cited by 16

Ischemic Preconditioning Reduces Caspase-Related Intestinal Apoptosis

Aban, N., Cinel, L., Tamer, L., Aktas, A. L., & Aban, M. (2005) · Surgery Today · doi:10.1007/s00595-004-2918-y · Cited by 16

Nitric oxide-evoked glutamate release and cGMP production in cerebellar slices: Control by presynaptic 5-HT1D receptors

Marcoli, M., Cervetto, C., Paluzzi, P., Guarnieri, S., Raiteri, M., & Maura, G. (2006) · Neurochemistry International · doi:10.1016/j.neuint.2005.12.010 · Cited by 16

Proteomic characterization of nitrated cell targets after hypobaric hypoxia and reoxygenation in rat brain

Peinado, M. Á., Hernández, R., Peragón, J., Ovelleiro, D., Pedrosa, J. Á., & Blanco, S. (2014) · Journal of Proteomics · doi:10.1016/j.jprot.2014.07.015 · Cited by 16

Nitric oxide and cell respiration: physiology and pathology.

Moncada, S. (2000) · PubMed · Cited by 37

Oxidative stress and S‐nitrosylation of proteins in cells

Beltrán, B., Orsi, A., Clementi, E., & Moncada, S. (2000) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0703147 · Cited by 196

Physiological regulation and pathological inhibition of tissue respiration by nitric oxide

Orsi, A. (2000) · UCL Discovery (University College London)

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Nitric oxide-induced persistent inhibition and nitrosylation of active site cysteine residues of mitochondrial cytochrome-c oxidase in lung endothelial cells

Zhang, J., Jin, B., Li, L., Block, E. R., & Patel, J. M. (2005) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00325.2004 · Cited by 102