Concentration-dependent Effects of Nitric Oxide on Mitochondrial Permeability Transition and Cytochrome cRelease

PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENT

Lowry, O. H., Rosebrough, N., Farr, A. L., & Randall, R. (1951) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)52451-6 · Cited by 316,394

Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4

LAEMMLI, U. K. (1970) · Nature · doi:10.1038/227680a0 · Cited by 249,961

Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications.

Towbin, H., Staehelin, T., & Gordon, J. (1979) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.76.9.4350 · Cited by 53,218

Guide for the Care and Use of Laboratory Animals: Eighth Edition

(2011) · doi:10.17226/12910 · Cited by 16,199

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

Induction of Apoptotic Program in Cell-Free Extracts: Requirement for dATP and Cytochrome c

Liu, X., Kim, C. N., Yang, J., Jemmerson, R., & Wang, X. (1996) · Cell · doi:10.1016/s0092-8674(00)80085-9 · Cited by 5,167

The mitochondrial permeability transition pore and its role in cell death

CROMPTON, M. (1999) · Biochemical Journal · doi:10.1042/bj3410233 · Cited by 2,432

Bcl-2 family proteins regulate the release of apoptogenic cytochrome c by the mitochondrial channel VDAC

Shimizu, S., Narita, M., Tsujimoto, Y., & Tsujimoto, Y. (1999) · Nature · doi:10.1038/20959 · Cited by 2,178

An APAF-1·Cytochrome c Multimeric Complex Is a Functional Apoptosome That Activates Procaspase-9

Zou, H., Li, Y., Liu, X., & Wang, X. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.17.11549 · Cited by 2,089

Mitochondrial control of nuclear apoptosis.

Zamzami, N., Susín, S. A., Marchetti, P., Hirsch, T., Gomez-Monterrey, I. M., Castedo, M., & Kroemer, G. (1996) · The Journal of Experimental Medicine · doi:10.1084/jem.183.4.1533 · Cited by 1,360

Mitostasis, Calcium and Free Radicals in Health, Aging and Neurodegeneration

Godoy, J. A., Ríos, J. A., Picón-Pagès, P., Herrera-Fernández, V., Swaby, B., Crepin, G., Vicente, R., Fernández‐Fernández, J. M., & Muñoz, F. J. (2021) · Biomolecules · doi:10.3390/biom11071012 · Cited by 73

Protective effect of harmaline and harmalol against dopamine‐ and 6‐hydroxydopamine‐induced oxidative damage of brain mitochondria and synaptosomes, and viability loss of PC12 cells

Kim, D. H., Jang, Y. Y., Han, E. S., & Lee, C. S. (2001) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01563.x · Cited by 71

Nitric oxide promotes intracellular calcium release from mitochondria in striatal neurons

Horn, T. F. W., Wolf, G. L., Duffy, S. N., Weiss, S., Keilhoff, G., & MacVicar, B. A. (2002) · The FASEB Journal · doi:10.1096/fj.02-0126com · Cited by 71

Nitric oxide regulation of cellular metabolism: Adaptive tuning of cellular energy

Pappas, G., Wilkinson, M. L., & Gow, A. J. (2022) · Nitric Oxide · doi:10.1016/j.niox.2022.11.006 · Cited by 74

Differential effect of catecholamines and MPP+ on membrane permeability in brain mitochondria and cell viability in PC12 cells

Lee, C. S., Han, J. H., Jang, Y.-Y., Song, J. H., & Han, E. S. (2002) · Neurochemistry International · doi:10.1016/s0197-0186(01)00069-9 · Cited by 70

The end-effectors of preconditioning protection against myocardial cell death secondary to ischemia–reperfusion

GARCIADORADO, D., Rodríguez‐Sinovas, A., Ruiz‐Meana, M., Inserte, J., Agulló, L., & Cabestrero, A. (2006) · Cardiovascular Research · doi:10.1016/j.cardiores.2006.02.011 · Cited by 69

Sodium nitroprusside enhances TRAIL-induced apoptosis via a mitochondria-dependent pathway in human colorectal carcinoma CX-1 cells

Lee, Y. J., Lee, K. H., Kim, H.-R. C., Jessup, J. M., Seol, D., Kim, T., Billiar, T. R., & Song, Y. K. (2001) · Oncogene · doi:10.1038/sj.onc.1204225 · Cited by 69

Role of nitric oxide in liver regeneration

Carnovale, C. E., & Ronco, M. T. (2012) · Annals of Hepatology · doi:10.1016/s1665-2681(19)31436-x · Cited by 65

Induction of the permeability transition and cytochrome c release by 15-deoxy-Δ12,14-prostaglandin J2 in mitochondria

Landar, A. L., Shiva, S., Levonen, A., Oh, J., Zaragoza, C., Johnson, M. S., & Darley-Usmar, V. M. (2006) · Biochemical Journal · doi:10.1042/bj20051259 · Cited by 63

Inhibition of α‐ketoglutarate dehydrogenase complex promotes cytochrome c release from mitochondria, caspase‐3 activation, and necrotic cell death

Huang, H., Ou, H., Xu, H., Chen, H., Fowler, C., & Gibson, G. E. (2003) · Journal of Neuroscience Research · doi:10.1002/jnr.10756 · Cited by 64

Consumption of hydrogen-rich water alleviates renal injury in spontaneous hypertensive rats

Xin, H., Zhang, B., Wu, Z., Hang, X., Xu, W., Ni, W., Zhang, R., & Miao, X. (2014) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-014-2024-4 · Cited by 63

Addition of Adenosine Monophosphate-Activated Protein Kinase Activators to University of Wisconsin Solution

Mosbah, I. B., Massip‐Salcedo, M., Fernández-Monteiro, I., Xaus, C., Bartrons, R., Boillot, O., Roselló‐Catafau, J., & Peralta, C. (2007) · Liver Transplantation · doi:10.1002/lt.21059 · Cited by 63

Nitric oxide, mitochondrial hyperpolarization, and T cell activation

Nagy, G., Koncz, Á., Fernández, D., & Perl, A. (2007) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2007.02.026 · Cited by 63

Angiotensin II blockade: how its molecular targets may signal to mitochondria and slow aging. Coincidences with calorie restriction and mTOR inhibition

de Cavanagh, E. M. V., Inserra, F., & Ferder, L. (2015) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00459.2014 · Cited by 66

The short variant of optic atrophy 1 (OPA1) improves cell survival under oxidative stress

Lee, H., Smith, S. B., Sheu, S., & Yoon, Y. (2020) · Journal of Biological Chemistry · doi:10.1074/jbc.ra119.010983 · Cited by 67

Mechanisms of Hepatoprotection by Nitric Oxide

Wang, Y., Yoram Vodovotz, B., Kim, P. K. M., Zamora, R., & Billiar, T. R. (2002) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.2002.tb04085.x · Cited by 63

Mitochondrial apoptosis and proteolytic changes of myofibrillar proteins in two different pork muscles during aging

Zhang, J., Ma, D., & Kim, Y. H. B. (2020) · Food Chemistry · doi:10.1016/j.foodchem.2020.126571 · Cited by 62

Inhibition of the α-ketoglutarate dehydrogenase complex alters mitochondrial function and cellular calcium regulation

Huang, H.-M., Zhang, H., Xu, H., & Gibson, G. E. (2003) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/s0925-4439(02)00222-3 · Cited by 61

Severe life stress, mitochondrial dysfunction, and depressive behavior: A pathophysiological and therapeutic perspective

Allen, J., Caruncho, H. J., & Kalynchuk, L. E. (2020) · Mitochondrion · doi:10.1016/j.mito.2020.11.010 · Cited by 62

Cell Responses to Oxidative Stressors

Cataldi, A. (2010) · Current Pharmaceutical Design · doi:10.2174/138161210791033969 · Cited by 63

Relatively Small Increases in the Steady-State Levels of Nucleobase Deamination Products in DNA from Human TK6 Cells Exposed to Toxic Levels of Nitric Oxide

Dong, M., & Dedon, P. C. (2005) · Chemical Research in Toxicology · doi:10.1021/tx050252j · Cited by 60

Antineoplastic Effects of Bee Honey and Nigella sativa on Hepatocellular Carcinoma Cells

Hassan, M. I., Mabrouk, G. M., Shehata, H. H., & Aboelhussein, M. M. (2010) · Integrative Cancer Therapies · doi:10.1177/1534735410387422 · Cited by 59

Immunoregulatory and Antimicrobial Effects of Nitrogen Oxides

Mannick, J. B. (2006) · Proceedings of the American Thoracic Society · doi:10.1513/pats.200505-048bg · Cited by 59

NOing the heart: Role of nitric oxide synthase-3 in heart development

Liu, Y., & Feng, Q. (2012) · Differentiation · doi:10.1016/j.diff.2012.04.004 · Cited by 63

Effect of oxygen free radicals and nitric oxide on apoptosis of immune organ induced by selenium deficiency in chickens

Zhang, Z., Zhang, J., Zhang, Y., Wang, Q., Li, S., Wang, X., & Xu, S. (2013) · BioMetals · doi:10.1007/s10534-013-9612-8 · Cited by 58

Inhibition of mitochondrial protein synthesis results in increased endothelial cell susceptibility to nitric oxide-induced apoptosis

Ramachandran, A., Moellering, D. R., CEASER, E. K., Shiva, S., Xu, J., & Darley-Usmar, V. M. (2002) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.102019899 · Cited by 57

TNF-α-induced impairment of mitochondrial integrity and apoptosis mediated by caspase-8 in adult ventricular myocytes

Zhu, J., Liu, M., Kennedy, R. H., & Liu, S. J. (2006) · Cytokine · doi:10.1016/j.cyto.2006.04.010 · Cited by 56

Hypoxia Sensitizes Cells to Nitric Oxide-induced Apoptosis

Lee, V. Y., McClintock, D. S., Santore, M. T., Budinger, G. R. S., & Chandel, N. S. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m111177200 · Cited by 56

Nitric oxide increases IL-8 gene transcription and mRNA stability to enhance IL-8 gene expression in lung epithelial cells

Sparkman, L., & Boggaram, V. (2004) · American Journal of Physiology-Lung Cellular and Molecular Physiology · doi:10.1152/ajplung.00165.2004 · Cited by 55

Thresholds of Nitric Oxide-Mediated Toxicity in Human Lymphoblastoid Cells

Wang, C., Trudel, L. J., Wogan, G. N., & Deen, W. M. (2003) · Chemical Research in Toxicology · doi:10.1021/tx0340448 · Cited by 53

Forecasting elasmobranch survival following exposure to severe stressors

Renshaw, G. M. C., Kutek, A. K., Grant, G. D., & Anoopkumar‐Dukie, S. (2011) · Comparative Biochemistry and Physiology Part A Molecular & Integrative Physiology · doi:10.1016/j.cbpa.2011.08.001 · Cited by 54

Aspirin eugenol ester attenuates oxidative injury of vascular endothelial cells by regulating NOS and Nrf2 signalling pathways

Huang, M., Yang, Y., Liu, X., Qin, Z., & Li, J. (2019) · British Journal of Pharmacology · doi:10.1111/bph.14592 · Cited by 53

Protective effect of serotonin on 6-hydroxydopamine- and dopamine-induced oxidative damage of brain mitochondria and synaptosomes and PC12 cells

Park, J. W., Youn, Y. C., Kwon, O. S., Jang, Y.-Y., Han, E. S., & Lee, C. S. (2002) · Neurochemistry International · doi:10.1016/s0197-0186(01)00072-9 · Cited by 52

Nitric oxide: a potential inducer of adhesion-related apoptosis—anoikis

Monteiro, H. P., Silva, E. F., & Stern, A. (2004) · Nitric Oxide · doi:10.1016/j.niox.2004.02.002 · Cited by 51

The Triterpenoid 2-Cyano-3,12-dioxooleana-1,9-dien-28-oic Acid and Its Derivatives Elicit Human Lymphoid Cell Apoptosis through a Novel Pathway Involving the Unregulated Mitochondrial Permeability Transition Pore

Brookes, P. S., Morse, K. M., Ray, D. M., Tompkins, A. J., Young, S. M., Hilchey, S. P., Salim, S., Konopleva, M. Y., Andreeff, M., Phipps, R. P., et al. (2007) · Cancer Research · doi:10.1158/0008-5472.can-06-2678 · Cited by 51

Modulation of mitochondrial Ca2+ by nitric oxide in cultured bovine vascular endothelial cells

Dedkova, E. N., & Blatter, L. A. (2005) · American Journal of Physiology-Cell Physiology · doi:10.1152/ajpcell.00011.2005 · Cited by 50

Effects of Anesthetics on Mitochondrial Signaling and Function

Monaca, E. L., & Fodale, V. (2012) · Current Drug Safety · doi:10.2174/157488612802715681 · Cited by 52

Nitric-oxide-induced Bax integration into the mitochondrial membrane commits MDA-MB-468 cells to apoptosis: essential role of Akt.

Pervin, S., Singh, R., & Chaudhuri, G. (2003) · PubMed · Cited by 49

Extremely low‐frequency magnetic fields modulate nitric oxide signaling in rat brain

Cho, S. I., Nam, Y. S., Chu, L. Y., Lee, J. H., Bang, J. S., Kim, H. R., Kim, H., Lee, Y. J., Kim, H., Sul, J. D., et al. (2012) · Bioelectromagnetics · doi:10.1002/bem.21715 · Cited by 48

Differentiation of cGMP-dependent and -independent nitric oxide effects on platelet apoptosis and reactive oxygen species production using platelets lacking soluble guanylyl cyclase

Rukoyatkina, N., Walter, U., Friebe, A., & Gambaryan, S. P. (2011) · Thrombosis and Haemostasis · doi:10.1160/th11-05-0319 · Cited by 49

Tumoricidal Activity of Endothelial Cells

Carretero, J., Obrador, E., Esteve, J. M., Ortega, Á., Pellicer, J. A., Vera-Sempere, F. J., & Estrela, J. M. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m101148200 · Cited by 48

Nitric oxide‐induced programmed cell death in human neuroblastoma cells is accompanied by the synthesis of Egr‐1, a zinc finger transcription factor

Cibelli, G., Policastro, V., Rößler, O. G., & Thiel, G. (2002) · Journal of Neuroscience Research · doi:10.1002/jnr.10141 · Cited by 48

Survival of TNF toxicity: Dependence on caspases and NO

Cauwels, A., & Brouckaert, P. (2007) · Archives of Biochemistry and Biophysics · doi:10.1016/j.abb.2007.01.021 · Cited by 47

Liver preservation: is there anything new yet?

Guarrera, J. V., & Karim, N. A. (2008) · Current Opinion in Organ Transplantation · doi:10.1097/mot.0b013e3282f63930 · Cited by 46

Nitric Oxide Ameliorates Hydrophobic Bile Acid-induced Apoptosis in Isolated Rat Hepatocytes by Non-mitochondrial Pathways

Gumpricht, E., Dahl, R., Yerushalmi, B., Devereaux, M. W., & Sokol, R. J. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m112305200 · Cited by 46

Nitric oxide at a low concentration protects murine macrophage RAW264 cells against nitric oxide‐induced death via cGMP signaling pathway

Yoshioka, Y., Yamamuro, A., & Maeda, S. (2003) · British Journal of Pharmacology · doi:10.1038/sj.bjp.0705206 · Cited by 45

Mitochondrial Nitric Oxide Synthase Participates in Septic Shock Myocardial Depression by Nitric Oxide Overproduction and Mitochondrial Permeability Transition Pore Opening

Xu, C., Yi, C., Wang, H., Bruce, I. C., & Xia, Q. (2011) · Shock · doi:10.1097/shk.0b013e3182391831 · Cited by 44

Effects of nitric oxide on mitochondrial permeability transition pore and thiol-mediated responses in cardiac myocytes

Ohtani, H., Katoh, H., Tanaka, T. L., Saotome, M., Urushida, T., Satoh, H., & Hayashi, H. (2011) · Nitric Oxide · doi:10.1016/j.niox.2011.12.007 · Cited by 43

Cdk2 nitrosylation and loss of mitochondrial potential mediate NO-dependent biphasic effect on HL-60 cell cycle

Kumar, S., Barthwal, M. K., & Dikshit, M. (2010) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2010.01.004 · Cited by 43

Intracellular glutathione is a cofactor in methylseleninic acid-induced apoptotic cell death of human hepatoma HEPG2 cells

Shen, H., Ding, W., & Ong, C. N. (2002) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(02)00918-8 · Cited by 43

Effect of dietary restriction and N-acetylcysteine supplementation on intestinal mucosa and liver mitochondrial redox status and function in aged rats

Grattagliano, I., Portincasa, P., Cocco, T., Moschetta, A., Paola, M. D., Palmieri, V. O., & Palasciano, G. (2004) · Experimental Gerontology · doi:10.1016/j.exger.2004.06.001 · Cited by 43

Dose controlled nitric oxide-based strategies for antibacterial property in biomedical devices

Mendhi, J., Asgari, M. S., Ratheesh, G., Prasadam, I., Yang, Y., & Xiao, Y. (2020) · Applied Materials Today · doi:10.1016/j.apmt.2020.100562 · Cited by 43

Induction of apoptosis in testis of the marine teleost mummichog Fundulus heteroclitus after in vivo exposure to the antifouling biocide 4,5-dichloro-2-n-octyl-3(2H)-isothiazolone (Sea-Nine 211)

Ito, M., Mochida, K., Ito, K., Onduka, T., & Fujii, K. (2012) · Chemosphere · doi:10.1016/j.chemosphere.2012.08.052 · Cited by 42

Cysteine 202 of cyclophilin D is a site of multiple post-translational modifications and plays a role in cardioprotection

Amanakis, G., Sun, J., Fergusson, M. M., McGinty, S. J., Liu, C., Molkentin, J. D., & Murphy, E. (2020) · Cardiovascular Research · doi:10.1093/cvr/cvaa053 · Cited by 43

Recent developments in nitric oxide-releasing biomaterials for biomedical applications

Huang, N., Yang, Z., Yu, H., & Cui, L.-X. (2019) · Medical Gas Research · doi:10.4103/2045-9912.273956 · Cited by 40

Mitochondria generated nitric oxide protects against permeability transition via formation of membrane protein S-nitrosothiols

Leite, A. C. R., Oliveira, H. C. F., Utino, F. L., Garcia, R., Alberici, L. C., Fernandes, M. P., Castilho, R. F., & Vercesi, A. E. (2010) · Biochimica et Biophysica Acta (BBA) - Bioenergetics · doi:10.1016/j.bbabio.2010.01.034 · Cited by 42

Protective effect of boldine on dopamine-induced membrane permeability transition in brain mitochondria and viability loss in PC12 cells

Youn, Y. C., Kwon, O. S., Han, E. S., Song, J. H., Shin, Y. K., & Lee, C. S. (2002) · Biochemical Pharmacology · doi:10.1016/s0006-2952(01)00852-8 · Cited by 40

Reductive Gas-Phase Chemiluminescence and Flow Injection Analysis for Measurement of the Nitric Oxide Pool in Biological Matrices

Hendgen-Cotta, U. B., Grau, M., Rassaf, T., Gharini, P. P. R., Kelm, M., & Kleinbongard, P. (2008) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(08)01216-0 · Cited by 40

Locally Different Endothelial Nitric Oxide Synthase Protein Levels in Ascending Aortic Aneurysms of Bicuspid and Tricuspid Aortic Valve

Mohamed, S. A., Radtke, A., Saraei, R., BULLERDIEK, J., Sorani, H., Nimzyk, R., Karluß, A., Sievers, H. H., & Belge, G. (2012) · Cardiology Research and Practice · doi:10.1155/2012/165957 · Cited by 39

Coexistence of translocated cytochrome c and nitrated protein in neurons of the rat cerebral cortex after oxygen and glucose deprivation

Alonso, D. C., Encinas, J. M., UTTENTHAL, L. O., Boscá, L., Serrano, J., Fernández, A. P., Castro‐Blanco, S., Santacana, M., Bentura, M. L., Richart, A., et al. (2002) · Neuroscience · doi:10.1016/s0306-4522(01)00571-1 · Cited by 38

UCP2/3 — likely to be fundamental for mitochondrial Ca2+ uniport

Trenker, M., Fertschai, I., Malli, R., & Graier, W. F. (2008) · Nature Cell Biology · doi:10.1038/ncb1108-1237 · Cited by 37

A2Badenosine receptors inhibit superoxide production from mitochondrial complex I in rabbit cardiomyocytes via a mechanism sensitive toPertussistoxin

Yang, X., Xin, W., Yang, X., Kuno, A., Rich, T. C., Cohen, M. V., & Downey, J. M. (2011) · British Journal of Pharmacology · doi:10.1111/j.1476-5381.2011.01288.x · Cited by 37

Taurine provides a time-dependent amelioration of the brain damage induced by γ-irradiation in rats

El-Maraghi, E. F., Abdel-Fattah, K. I., Soliman, S. M., & El-Sayed, W. M. (2018) · Journal of Hazardous Materials · doi:10.1016/j.jhazmat.2018.07.005 · Cited by 36

Enhancement of apoptosis by nitric oxide released from α‐phenyl‐tert‐butyl nitrone under hyperthermic conditions

Cui, Z., Kondo, T., & Matsumoto, H. (2005) · Journal of Cellular Physiology · doi:10.1002/jcp.20482 · Cited by 35

Cardioprotective actions of nitrite therapy and dietary considerations

Nathan, S. B. (2009) · Frontiers in bioscience · doi:10.2741/3568 · Cited by 34

Role of S-nitrosothiol transport in the cardioprotective effects of S-nitrosocysteine in rat hearts

Hogg, N., Broniowska, K. A., Novalija, J., Kettenhofen, N. J., & Novalija, E. (2007) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2007.06.016 · Cited by 33

Gelatin–siloxane nanoparticles to deliver nitric oxide for vascular cell regulation: Synthesis, cytocompatibility, and cellular responses

Zhang, Q., Wang, Z., Wen, F., Ren, L., Li, J., Teoh, S. H., & Thian, E. S. (2014) · Journal of Biomedical Materials Research Part A · doi:10.1002/jbm.a.35239 · Cited by 33

Cyclosporin A ameliorates mitochondrial ultrastructural injury in the ileum during acute endotoxemia*

Crouser, E. D., JULIAN, M. W., Joshi, M. S., Bauer, J. A., Wewers, M. D., Hart, J., & Pfeiffer, D. R. (2002) · Critical Care Medicine · doi:10.1097/00003246-200212000-00017 · Cited by 33

Signaling Pathways Involved in the Cardioprotective Effects of Cannabinoids

Lépicier, P., Bibeau-Poirier, A., Lagneux, C., Servant, M. J., & Lamontagne, D. (2006) · Journal of Pharmacological Sciences · doi:10.1254/jphs.crj06011x · Cited by 33

Increased expressions of ADAMTS‐13 and apoptosis contribute to neuropathology during Toxoplasma gondii encephalitis in mice

Dinçel, G. Ç., & Atmaca, H. (2015) · Neuropathology · doi:10.1111/neup.12263 · Cited by 32

Anabolic–androgenic steroids induce apoptosis and NOS2 (nitric-oxide synthase 2) in adult rat Leydig cells following in vivo exposure

Janjic, M. M., Stojkov, N. J., Andrić, S. A., & Kostic, T. S. (2012) · Reproductive Toxicology · doi:10.1016/j.reprotox.2012.10.003 · Cited by 32

Nitric-oxide-induced depolarization of neuronal mitochondria: implications for neuronal cell death

Solenski, N. J., Kostecki, V. K., Dovey, S. L., & Periasamy, A. (2003) · Molecular and Cellular Neuroscience · doi:10.1016/j.mcn.2003.08.011 · Cited by 32

Fasting-induced intestinal apoptosis is mediated by inducible nitric oxide synthase and interferon-γ in rat

Ito, J., Uchida, H., Yokote, T., Ohtake, K., & Kobayashi, J. (2010) · American Journal of Physiology-Gastrointestinal and Liver Physiology · doi:10.1152/ajpgi.00429.2009 · Cited by 31

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

Biphasic effect of nitric oxide on the cardiac voltage-dependent anion channel

Cheng, Q., Sedlić, F., Pravdić, D., Bosnjak, Z. J., & Kwok, W. (2010) · FEBS Letters · doi:10.1016/j.febslet.2010.12.008 · Cited by 30

Cocaine-Mediated Apoptosis in Bovine Coronary Artery Endothelial Cells: Role of Nitric Oxide

He, J., Xiao, Y., & Zhang, L. (2001) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1016/s0022-3565(24)29366-6 · Cited by 31

Role of angiotensin II in aging

Yi, W., Chen, F., Zhang, H., Tang, P., Yuan, M., Wen, J., Wang, S., & Cai, Z. (2022) · Frontiers in Aging Neuroscience · doi:10.3389/fnagi.2022.1002138 · Cited by 31

L-type Ca 2+ channel–mediated Ca 2+ influx adjusts neuronal mitochondrial function to physiological and pathophysiological conditions

Hoťka, M., Cagalinec, M., Hilber, K., Hool, L. C., Boehm, S., & Kubista, H. (2020) · Science Signaling · doi:10.1126/scisignal.aaw6923 · Cited by 29

Magnetic Stimulation as a Therapeutic Approach for Brain Modulation and Repair: Underlying Molecular and Cellular Mechanisms

Dufor, T., Lohof, A. M., & Sherrard, R. M. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242216456 · Cited by 28

Bradykinin Preconditioning Improves the Profile of Cell Survival Proteins and Limits Apoptosis After Cardioplegic Arrest

Feng, J., Bianchi, C. F., Sandmeyer, J. L., & Sellke, F. W. (2005) · Circulation · doi:10.1161/circulationaha.104.524454 · Cited by 27

Reversible Inhibition of Cytochrome c Oxidase by Peroxynitrite Proceeds through Ascorbate-dependent Generation of Nitric Oxide

Barone, M. C., Darley-Usmar, V. M., & Brookes, P. S. (2003) · Journal of Biological Chemistry · doi:10.1074/jbc.m304129200 · Cited by 27

Analysis of Mitochondrial Function, Structure, and Intracellular Organization In Situ in Cardiomyocytes and Skeletal Muscles

Kuznetsov, A. V., Javadov, S. A., Margreiter, R., Hagenbuchner, J., & Ausserlechner, M. J. (2022) · International Journal of Molecular Sciences · doi:10.3390/ijms23042252 · Cited by 26

Pancreastatin, a chromogranin A-derived peptide, inhibits DNA and protein synthesis by producing nitric oxide in HTC rat hepatoma cells

Sánchez‐Margalet, V., González-Yanes, C., & Najib, S. (2001) · Journal of Hepatology · doi:10.1016/s0168-8278(01)00071-x · Cited by 24

Oxidative stress and susceptibility to mitochondrial permeability transition precedes the onset of diabetes in autoimmune non-obese diabetic mice

Malaguti, C., Guardia, P. G. L., Leite, A. C. R., de Oliveira, D. N., Zollner, R. D. L., Catharino, R. R., Vercesi, A. E., & Oliveira, H. C. F. (2014) · Free Radical Research · doi:10.3109/10715762.2014.966706 · Cited by 23

The Role of Oxidative Stress in the Development and Persistence of Pressure Ulcers

Taylor, R. P., & James, T. J. (2005) · Springer eBooks · doi:10.1007/3-540-28804-x_13 · Cited by 24

Caspase‐1 and poly (ADP‐ribose) polymerase inhibitors may protect against peroxynitrite‐induced neurotoxicity independent of their enzyme inhibitor activity

Zhang, Y., & Rosenberg, P. A. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03651.x · Cited by 24

The mitochondrial NO‐synthase/guanylate cyclase/protein kinase G signaling system underpins the dual effects of nitric oxide on mitochondrial respiration and opening of the permeability transition pore

Dynnik, V. V., Grishina, E. V., & Fedotcheva, N. I. (2019) · FEBS Journal · doi:10.1111/febs.15090 · Cited by 23

The role of nitric oxide in the radiation-induced effects in the developing brain.

Gisone, P. A., Dubner, D., del Rosario Pérez, M., Michelin, S., & Puntarulo, S. (2004) · PubMed · Cited by 23

Resveratrol reduces light and electron microscopic changes in acetaminophen-induced hepatotoxicity in rats: Role of iNOS expression

Elbe, H., Gül, M., Çetin, A., Taşlıdere, E., Özyalın, F., Türköz, Y., & Otlu, A. (2017) · Ultrastructural Pathology · doi:10.1080/01913123.2017.1374313 · Cited by 23

The potential mediation of nitric oxide in the activation of mitochondrion-dependent apoptosis and yak meat tenderness during postmortem aging

Wang, L. L., Du, R. S., Li, J., Cai, Z.-J., Han, L., Mao, Y. J., Zhou, Y., Yu, Q., & Chen, L. H. (2021) · Food Bioscience · doi:10.1016/j.fbio.2021.101131 · Cited by 22

Protective effect of Coptidis Rhizoma on S-nitroso-N-acetylpenicillamine (SNAP)-induced apoptosis and necrosis in pancreatic RINm5F cells

Kwon, K., Kim, E.-K., Lim, J.-G., Shin, B., Han, S.-C., Song, B.-K., Kim, K., Seo, E.-A., & Ryu, D. (2004) · Life Sciences · doi:10.1016/j.lfs.2004.10.008 · Cited by 22

Taurine abates the liver damage induced by γ-irradiation in rats through anti-inflammatory and anti-apoptotic pathways

El-Maraghi, E. F., Abdel-Fattah, K. I., Soliman, S. M., & El-Sayed, W. M. (2020) · International Journal of Radiation Biology · doi:10.1080/09553002.2020.1828656 · Cited by 23

Inhibition of the nitric oxide/cyclic guanosine monophosphate pathway limited the cardioprotective effect of post-conditioning in hearts with apical myocardial infarction

Correa, F., Buelna‐Chontal, M., de Sánchez, V. C., García‐Rivas, G., Vigueras, R. M., Pedraza‐Chaverrí, J., García‐Niño, W. R., Hernández‐Pando, R., León‐Contreras, J. C., & Zazueta, C. (2015) · European Journal of Pharmacology · doi:10.1016/j.ejphar.2015.09.018 · Cited by 21

Effect of IBD sera on expression of inducible and endothelial nitric oxide synthase in human umbilical vein endothelial cells

Palatka, K. (2006) · World Journal of Gastroenterology · doi:10.3748/wjg.v12.i11.1730 · Cited by 21

Detection of apoptotic cells in intestines from horses with and without gastrointestinal tract disease

Rowe, E. L., White, N. A., Buechner‐Maxwell, V., Robertson, J. L., & Ward, D. L. (2003) · American Journal of Veterinary Research · doi:10.2460/ajvr.2003.64.982 · Cited by 21

ALKBH7 mediates necrosis via rewiring of glyoxal metabolism

Kulkarni, C. A., Nadtochiy, S. M., Kennedy, L., Zhang, J., Chhim, S., Alwaseem, H., Murphy, E., Fu, D., & Brookes, P. S. (2020) · eLife · doi:10.7554/elife.58573 · Cited by 19

The Effect Of NO Donor on Calcium Uptake and Reactive Nitrogen Species Production in Mitochondria

Ov, A., Kotsiuruba, A., Korkach, Y. P., Kolchinskaya, L. I., Nosar, V. I., Gavenauskas, B. L., Serebrovska, Z. O., Im, M., & Sagach, V. F. (2016) · Cellular Physiology and Biochemistry · doi:10.1159/000445616 · Cited by 20

Mitochondrial Nitric-oxide Synthase Stimulation Causes Cytochrome c Release from Isolated Mitochondria

Ghafourifar, P., Schenk, U., Klein, S. D., & Richter, C. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.44.31185 · Cited by 328

Nitric oxide induces apoptosis via triggering mitochondrial permeability transition

Hortelano, S., Dallaporta, B., Zamzami, N., Hirsch, T., Susín, S. A., Marzo, I., Boscá, L., & Kroemer, G. (1997) · FEBS Letters · doi:10.1016/s0014-5793(97)00623-6 · Cited by 234

Nitric Oxide Inhibits Execution of Apoptosis at Two Distinct ATP-Dependent Steps Upstream and Downstream of Mitochondrial CytochromecRelease

Leist, M., Single, B., Naumann, H., Fava, E., Simon, B., Kühnle, S., & Nicotera, P. (1999) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1999.0491 · Cited by 64

Nitric Oxide and Differential Effects of ATP on Mitochondrial Permeability Transition

Piantadosi, C. A., Tatro, L. G., & Whorton, A. R. (2002) · Nitric Oxide · doi:10.1006/niox.2001.0368 · Cited by 33

Nitric oxide induces tyrosine nitration and release of cytochrome c preceding an increase of mitochondrial transmembrane potential in macrophages

Hortelano, S., Alvarez, A. M., & Boscá, L. (1999) · The FASEB Journal · doi:10.1096/fasebj.13.15.2311 · Cited by 132