Mitochondrial dysfunction in cardiovascular disease

Atherosclerosis--an inflammatory disease

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Risks and Benefits of Estrogen Plus Progestin in Healthy Postmenopausal Women: Principal Results From the Women's Health Initiative Randomized Controlled Trial

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Beyond Cholesterol

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Weight-Reducing Effects of the Plasma Protein Encoded by the obese Gene

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Normalizing mitochondrial superoxide production blocks three pathways of hyperglycaemic damage

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Orai inhibition modulates pulmonary ILC2 metabolism and alleviates airway hyperreactivity in murine and humanized models

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Differential regulation of metabolism by nitric oxide and S-nitrosothiols in endothelial cells

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Aconitine attenuates mitochondrial dysfunction of cardiomyocytes via promoting deacetylation of cyclophilin-D mediated by sirtuin-3

Wang, N., Xu, H., Zhou, W. J., Yang, H., Wang, J., Ma, Z.-C., & Gao, Y. (2021) · Journal of Ethnopharmacology · doi:10.1016/j.jep.2020.113765 · Cited by 26

Pandora's Box: mitochondrial defects in ischaemic heart disease and stroke

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Sex-dependent vulnerability of fetal nonhuman primate cardiac mitochondria to moderate maternal nutrient reduction

Pereira, S. P., Tavares, L. C., Duarte, A. I., Baldeiras, I., Cunha‐Oliveira, T., Martins, J. D., Santos, M. S., Maloyan, A., Moreno, A. J., Cox, L. A., et al. (2021) · Clinical Science · doi:10.1042/cs20201339 · Cited by 26

Targeting Mitochondrial Dysfunction for the Prevention and Treatment of Metabolic Disease by Bioactive Food Components

Kim, M., Lee, J., & Lee, J. (2024) · Journal of Lipid and Atherosclerosis · doi:10.12997/jla.2024.13.3.306 · Cited by 28

Endogenous 3,4-Dihydroxyphenylalanine and Dopaquinone Modifications on Protein Tyrosine

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A genome-wide trans-ethnic interaction study links the PIGR-FCAMR locus to coronary atherosclerosis via interactions between genetic variants and residential exposure to traffic

Ward-Caviness, C. K., Neas, L., Blach, C., Haynes, C. S., Larocque-Abramson, K. R., Grass, E. A., Dowdy, Z. E., Devlin, R. B., Díaz-Sánchez, D., Cascio, W. E., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0173880 · Cited by 24

Mitochondrial oxidative phosphorylation in peripheral blood mononuclear cells is decreased in chronic HIV and correlates with immune dysregulation

Gangcuangco, L. M. A., Mitchell, B. I., Siriwardhana, C., Kohorn, L. B., Chew, G. M., Bowler, S. A., Kallianpur, K. J., Chow, D. C., Ndhlovu, L. C., Gerschenson, M., et al. (2020) · PLoS ONE · doi:10.1371/journal.pone.0231761 · Cited by 24

Modulations of Cardiac Functions and Pathogenesis by Reactive Oxygen Species and Natural Antioxidants

Woo, S., Kim, J., Eslenur, N., Trinh, T. N., & Hoàng, L. N. (2021) · Antioxidants · doi:10.3390/antiox10050760 · Cited by 26

Protection of H9c2 rat cardiomyoblasts against oxidative insults by total paeony glucosides from Radix Paeoniae Rubrae

Luo, C. Y., Wang, H., Chen, X., Cui, Y., Li, H., Long, J., Mo, X., & Liu, J. (2013) · Phytomedicine · doi:10.1016/j.phymed.2013.08.002 · Cited by 23

Ursolic-Acid-Enriched Herba Cynomorii Extract Protects against Oxidant Injury in H9c2 Cells and Rat Myocardium by Increasing Mitochondrial ATP Generation Capacity and Enhancing Cellular Glutathione Redox Cycling, Possibly through Mitochondrial Uncoupling

Chen, J., & Ko, K. M. (2013) · Evidence-based Complementary and Alternative Medicine · doi:10.1155/2013/924128 · Cited by 23

Protective effects of shikonin on brain injury induced by carbon ion beam irradiation in mice.

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Mitochondrial-targeted liposome-based drug delivery – therapeutic potential and challenges

Sanchez-Aranguren, L. C., Tahan, M. A. A., Uppal, M., Juvale, P. S., & Marwah, M. K. (2024) · Journal of drug targeting · doi:10.1080/1061186x.2024.2437440 · Cited by 25

Construction of a Dual-Emissive Probe for Discriminative Visualization of Lysosomal and Mitochondrial Dysfunction

Ge, W., Wang, H., Wu, X., Dong, B., Zhang, R., & Tian, M. (2023) · Analytical Chemistry · doi:10.1021/acs.analchem.3c03024 · Cited by 22

Ionizing Radiation Effects on Cells, Organelles and Tissues on Proteome Level

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Presence of mutation m.14484T>C in a Chinese family with maternally inherited essential hypertension but no expression of LHON

Guo, H., Zhuang, X., Zhang, A., Zhang, W., Yuan, Y., Guo, L., Yu, D., Liu, J., Yang, D.-K., & Yao, Y. (2012) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2012.06.010 · Cited by 22

Prolonged Exposure to Insulin Induces Mitochondrion-Derived Oxidative Stress through Increasing Mitochondrial Cholesterol Content in Hepatocytes

Mei, S., Gu, H., Yang, X., Guo, H., Liu, Z., & Cao, W. (2012) · Endocrinology · doi:10.1210/en.2011-2119 · Cited by 22

Catalase ameliorates diabetes‐induced cardiac injury through reduced p65/RelA‐ mediated transcription of BECN1

Wang, X., Tao, Y., Huang, Y., Zhan, K.-G., Xue, M., Wang, Y., Ruan, D., Liang, Y., Huang, X., Lin, J., et al. (2017) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.13252 · Cited by 22

SOD2, the principal scavenger of mitochondrial superoxide, is dispensable for embryogenesis and imaginal tissue development but essential for adult survival

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A conditional knockout rat resource of mitochondrial protein-coding genes via a DdCBE-induced premature stop codon

Tan, L., Qi, X., Kong, W., Jin, J., Lü, D., Zhang, X., Wang, Y., Wang, S., Dong, W., Shi, X., et al. (2023) · Science Advances · doi:10.1126/sciadv.adf2695 · Cited by 21

Blood-based bioenergetics: a liquid biopsy of mitochondrial dysfunction in disease

Wilkinson, M., & Dunham‐Snary, K. J. (2023) · Trends in Endocrinology and Metabolism · doi:10.1016/j.tem.2023.06.004 · Cited by 21

Associations of Annual Ambient Fine Particulate Matter Mass and Components with Mitochondrial DNA Abundance

Peng, C., Çayır, A., Sánchez-Guerra, M., Di, Q., Wilson, A., Zhong, J., Kosheleva, A., Trevisi, L., Colicino, E., Brennan, K. J. M., et al. (2017) · Epidemiology · doi:10.1097/ede.0000000000000717 · Cited by 19

NADPH oxidase- and mitochondrion-derived superoxide at rostral ventrolateral medulla in endotoxin-induced cardiovascular depression

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The Role of Oxidative Stress in Endothelial Dysfunction and Vascular Inflammation

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Cardiovascular Health and Mitochondrial Function: Testing an Association

Zampino, M., Spencer, R. G., Fishbein, K. W., Simonsick, E. M., & Ferrucci, L. (2021) · The Journals of Gerontology: Series A · doi:10.1093/gerona/glaa297 · Cited by 20

A tunable pH probe scaffold based on sulfonamide rhodamine and its application in mitochondrial pH research

Qiu, J., Zhong, C., Liu, M., Xiong, X., Gao, Y., & Zhu, H. (2022) · Sensors and Actuators B Chemical · doi:10.1016/j.snb.2022.132606 · Cited by 20

Cardiac-specific catalase overexpression rescues anthrax lethal toxin-induced cardiac contractile dysfunction: role of oxidative stress and autophagy

Kandadi, M. R., Yu, X., Frankel, A. E., & Ren, J. T. (2012) · BMC Medicine · doi:10.1186/1741-7015-10-134 · Cited by 19

Effect of Brewing Duration on the Antioxidant and Hepatoprotective Abilities of Tea Phenolic and Alkaloid Compounds in a t-BHP Oxidative Stress-Induced Rat Hepatocyte Model

Braud, L., Peyre, L., de Sousa, G., Armand, M., Rahmani, R., & Maixent, J. M. (2015) · Molecules · doi:10.3390/molecules200814985 · Cited by 19

Ursolic Acid-Enriched Herba Cynomorii Extract Induces Mitochondrial Uncoupling and Glutathione Redox Cycling Through Mitochondrial Reactive Oxygen Species Generation: Protection Against Menadione Cytotoxicity in H9c2 Cells

Chen, J., Wong, H. S., & Ko, K. M. (2014) · Molecules · doi:10.3390/molecules19021576 · Cited by 19

Multiple measures of functionality exhibit progressive decline in a parallel, stochastic fashion in Drosophila Sod2 null mutants

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Mitochondrial Protection and Anti-inflammatory Effects Induced by Emodin in the Human Neuroblastoma SH-SY5Y Cells Exposed to Hydrogen Peroxide: Involvement of the AMPK/Nrf2 Signaling Pathway

de Oliveira, M. R., de Souza, I. C. C., & Brasil, F. B. (2020) · Neurochemical Research · doi:10.1007/s11064-020-03181-1 · Cited by 19

New Molecular and Organelle Alterations Linked to Down Syndrome Heart Disease

Venegas-Zamora, L., Bravo-Acuña, F., Sigcho, F., Gómez, W., Bustamante-Salazar, J., Pedrozo, Z., & Parra, V. (2022) · Frontiers in Genetics · doi:10.3389/fgene.2021.792231 · Cited by 19

Mitochondria can orchestrate sex differences in cell fate of vascular smooth muscle cells from rats

Straface, E., Vona, R., Campesi, I., & Franconi, F. (2015) · Biology of Sex Differences · doi:10.1186/s13293-015-0051-9 · Cited by 18

The role of reactive oxygen species derived from different NADPH oxidase isoforms and mitochondria in oxalate-induced oxidative stress and cell injury

Qian, X., Wu, W., Hu, H., Yu, X., Wang, S., Zhu, J., & Zhang, J. (2022) · Urolithiasis · doi:10.1007/s00240-022-01309-2 · Cited by 18

Mitochondria: how eminent in ageing and neurodegenerative disorders?

Bamshad, C., Najafi-Ghalehlou, N., Pourmohammadi-Bejarpasi, Z., Tomita, K., Kuwahara, Y., Sato, T., Feizkhah, A., Roushnadeh, A. M., & Roudkenar, M. H. (2022) · Human Cell · doi:10.1007/s13577-022-00833-y · Cited by 20

Cell-free chromatin particles released from dying cells inflict mitochondrial damage and ROS production in living cells

Raghuram, G. V., Tripathy, B. K., Avadhani, K., Shabrish, S., Khare, N. K., Lopes, R. S., Pal, K., & Mittra, I. (2024) · Cell Death Discovery · doi:10.1038/s41420-023-01728-z · Cited by 17

Experimental acute pancreatitis induces mitochondrial dysfunction in rat pancreas, kidney and lungs but not in liver

Trumbeckaitė, S., Kuliavienė, I., Deduchovas, O., Kinčius, M., Banienė, R., Virketyte, S., Bukauskas, D., Jansen, E. H. J. M., Kupčinskas, L., Borutaitė, V., et al. (2013) · Pancreatology · doi:10.1016/j.pan.2013.04.003 · Cited by 18

Le stress oxydant, composante physiopathologique de l'athérosclérose

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Diazoxide Pretreatment Prevents Aβ1–42 Induced Oxidative Stress in Cholinergic Neurons Via Alleviating NOX2 Expression

Fu, Q., Gao, N., Yu, J., Ma, G., Du, Y., Wang, F., Su, Q., & Che, F. (2014) · Neurochemical Research · doi:10.1007/s11064-014-1313-3 · Cited by 18

Effect of reactive oxygen, nitrogen, and sulfur species on signaling pathways in atherosclerosis

Solanki, K., Bezsonov, E. E., Orekhov, A. N., Parihar, S. P., Vaja, S., White, F. A., Obukhov, A. G., & Baig, M. S. (2024) · Vascular Pharmacology · doi:10.1016/j.vph.2024.107282 · Cited by 17

Mitochondrial DNA integrity and function are critical for endothelium-dependent vasodilation in rats with metabolic syndrome

Kiyooka, T., Ohanyan, V. A., Yin, L., Pung, Y. F., Chen, Y., Chen, C., Kang, P. T., Hardwick, J. P., Yun, J. S., Janota, D., et al. (2022) · Basic Research in Cardiology · doi:10.1007/s00395-021-00908-1 · Cited by 17

Candesartan cilexetil attenuated cardiac remodeling by improving expression and function of mitofusin 2 in SHR

Wang, Z., Niu, Q., Peng, X., Li, M., Liu, K., Liu, Y., Liu, J., Jin, F., Li, X., & Wei, Y. (2016) · International Journal of Cardiology · doi:10.1016/j.ijcard.2016.04.007 · Cited by 17

Understanding the Role of Oxidative Stress in Platelet Alterations and Thrombosis Risk among Frail Older Adults

Arauna, D., Navarrete, S., Cecilia Albala, B., Wehinger, S., Pizarro-Mena, R. A., Palomo, I. F., & Eduardo Fuentes, Q. (2024) · Biomedicines · doi:10.3390/biomedicines12092004 · Cited by 15

Selected hydroxycoumarins as antioxidants in cells: physicochemical and reactive oxygen species scavenging studies

Pérez‐Cruz, F., Villamena, F. A., Zapata‐Torres, G., Das, A. K., Headley, C. A., Quezada, E., López‐Alarcón, C., & Olea‐Azar, C. (2013) · Journal of Physical Organic Chemistry · doi:10.1002/poc.3155 · Cited by 16

Psychological distress and lack of PINK1 promote bioenergetics alterations in peripheral blood mononuclear cells

Grigoruţă, M., Dagda, R. K., Díaz‐Sánchez, Á. G., & Martı́nez-Martı́nez, A. (2020) · Scientific Reports · doi:10.1038/s41598-020-66745-9 · Cited by 16

Photobiomodulation and estrogen stabilize mitochondrial membrane potential in angiotensin– II challenged porcine aortic smooth muscle cells

Gavish, L., Gilon, D., Beeri, R., Zuckerman, A., Nachman, D., & Gertz, S. D. (2020) · Journal of Biophotonics · doi:10.1002/jbio.202000329 · Cited by 17

Kidney protective potential of lactoferrin: pharmacological insights and therapeutic advances

Zahan, M. S., Ahmed, K. A., Moni, A., Sinopoli, A., Ha, H., & Uddin, M. J. (2021) · Korean Journal of Physiology and Pharmacology · doi:10.4196/kjpp.2022.26.1.1 · Cited by 16

A new duplication in themitochondrially encoded tRNA prolinegene in a patient with dilated cardiomyopathy

Cardena, M. M. S. G., Mansur, A. J., Pereira, A. C., & Fridman, C. (2012) · Mitochondrial DNA · doi:10.3109/19401736.2012.717933 · Cited by 15

Assessment of microvascular function and pharmacological regulation in genetically confirmed familial hypercholesterolemia

Pajkowski, M., Dudziak, M., Chlebus, K., & Hellmann, M. (2021) · Microvascular Research · doi:10.1016/j.mvr.2021.104216 · Cited by 15

Tramadol ameliorates behavioural, biochemical, mitochondrial and histological alterations in ICV-STZ-induced sporadic dementia of Alzheimer’s type in rats

Dhull, D. K., & Kumar, A. (2017) · Inflammopharmacology · doi:10.1007/s10787-017-0431-3 · Cited by 15

Critical Pathways in Heart Function: Bis(2-chloroethoxy)methane-Induced Heart Gene Transcript Change in F344 Rats

Dunnick, J. K., Blackshear, P. E., Kissling, G. E., Cunningham, M. L., Parker, J. S., & Nyska, A. (2006) · Toxicologic Pathology · doi:10.1080/01926230600798583 · Cited by 15

Mitochondria-Enriched Extracellular Vesicles (EVs) for Cardiac Bioenergetics Restoration: A Scoping Review of Preclinical Mechanisms and Source-Specific Strategies

Shahannaz, D. C., Sugiura, T., & Yoshida, T. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms262211052 · Cited by 17

Effect of Chrysin on Gentamicin-induced Nephrotoxicity in Laboratory Animals

Bodhank, S. L., Mukherjee-Kandhare, A. A., & Kandhare, A. D. (2016) · Pharmacologia · doi:10.5567/pharmacologia.2016.296.307 · Cited by 14

Endothelium-Derived Factors Influence Differentiation of Fat-Derived Stromal Cells Post-Exercise in Subjects with Prediabetes

Kundu, N., Domingues, C. C., Nylén, E., Paal, E. E., Kokkinos, P. F., & Sen, S. (2019) · Metabolic Syndrome and Related Disorders · doi:10.1089/met.2018.0121 · Cited by 14

Effects of Alternanthera sessilis Red leaf extracts on hydrogen peroxide-induced oxidative stress in HepG2 cells and identification of phytochemicals using HPLC-QToF-MS/MS

Hazli, U. H. A. M., Hwong, C. S., Aziz, A. A., Junit, S. M., Leong, K. H., & Kong, K. W. (2022) · South African Journal of Botany · doi:10.1016/j.sajb.2022.04.056 · Cited by 14

Extract of a polyherbal formulation ameliorates experimental nonalcoholic steatohepatitis

Azeemuddin, M. M., Rafiq, M., Anturlikar, S. D., Kumar, L. M. S., Patki, P. S., Babu, U. V., & Ramakrishnan, S. (2015) · Journal of Traditional and Complementary Medicine · doi:10.1016/j.jtcme.2014.12.002 · Cited by 13

Dietary coenzyme Q10 does not protect against cigarette smoke-augmented atherosclerosis in apoE-deficient mice

Gairola, C. G., Howatt, D. A., & Daugherty, A. (2010) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2010.02.035 · Cited by 13

Cardiac mitochondrial function and tissue remodelling are improved by a non-antihypertensive dose of enalapril in spontaneously hypertensive rats

Piotrkowski, B., Koch, O. R., de Cavanagh, E. M. V., & Fraga, C. G. (2009) · Free Radical Research · doi:10.1080/10715760902801517 · Cited by 13

Vitamin E Ameliorates the Decremental Effect of Paraquat on Cardiomyocyte Contractility in Rats

Fahim, M. A., Howarth, F. C., Nemmar, A., Qureshi, M. A., Shafiullah, M., Jayaprakash, P., & Hasan, M. Y. (2013) · PLoS ONE · doi:10.1371/journal.pone.0057651 · Cited by 13

A shortcut to mitochondrial signaling and pathology: A commentary on “Nonenzymatic formation of succinate in mitochondria under oxidative stress”

Brookes, P. S., Freeman, R. S., & Barone, M. C. (2006) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2006.03.019 · Cited by 13

Novel membrane-localizing TEMPO derivatives for measurement of cellular oxidative stress at the cell membrane

Ban, S., Nakagawa, H., Suzuki, T., & Miyata, N. (2006) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2006.11.040 · Cited by 13

Reproducibility of NIRS-derived mitochondrial oxidative capacity in highly active older adults

Fennell, C. R. J., Mauger, A. R., & Hopker, J. (2023) · Experimental Gerontology · doi:10.1016/j.exger.2023.112156 · Cited by 14

Rotenone Stereospecifically Increases (S)-2-Hydroxyglutarate in SH-SY5Y Neuronal Cells

Worth, A. J., Gillespie, K. P., Mesaros, C., Guo, L., Basu, S. S., Snyder, N. W., & Blair, I. A. (2015) · Chemical Research in Toxicology · doi:10.1021/tx500535c · Cited by 12

Mechanisms of Nanoparticle Toxicity

Singh, A. K. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-801406-6.00007-8 · Cited by 12

P‐cresyl sulfate causes mitochondrial hyperfusion in H9C2 cardiomyoblasts

Huang, T., Yip, H., Sun, C., Chen, Y., Yang, C., & Lee, F. (2020) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.15303 · Cited by 12

Estrogen: A Mitochrondrial Energizer That Keeps on Going

Burris, T. P., & Krishnan, V. (2005) · Molecular Pharmacology · doi:10.1124/mol.105.017335 · Cited by 12

Molecular characterization of two Chinese pedigrees with maternally inherited hypertension

Ding, Y., Yu, J., Guo, Q., Gao, B., & Huang, J. (2021) · The Journal of Gene Medicine · doi:10.1002/jgm.3328 · Cited by 11

Chronic GPER activation prevents ischemia/reperfusion injury in ovariectomized rats

Ibañez, A. M., Arbeláez, L. F. G., Pardo, A. C., Mosca, S. M., Lofeudo, J. M., Rueda, J. O. V., Aiello, E. A., & Giusti, V. C. D. (2021) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2021.130060 · Cited by 11

Aldosterone Suppresses Endothelial Mitochondria through Mineralocorticoid Receptor/Mitochondrial Reactive Oxygen Species Pathway

Peng, S., Tsai, C., Wu, X.-M., Huang, H.-H., Chen, Z., Lee, B., Chang, Y., Pan, C., Wu, V., Chou, C., et al. (2022) · Biomedicines · doi:10.3390/biomedicines10051119 · Cited by 11

A deeper insight on the radical scavenger activity of two simple coumarins toward OOH radical

Marino, T., Russo, N., & Galano, A. (2015) · Computational and Theoretical Chemistry · doi:10.1016/j.comptc.2015.12.010 · Cited by 10

Green extraction of healthy and additive free mitochondria with a conventional centrifuge

Lin, Y., Chen, S.-T., Chang, J., Teoh, R.-J., Liu, C., & Wang, G. (2019) · Lab on a Chip · doi:10.1039/c9lc00633h · Cited by 10

Association between yoga, physiologic and psychologic health: A cross sectional study

Forseth, B. M., Polfuss, M. L., Brondino, M. J., Lawlor, M. W., Beatka, M. J., Prom, M. J., Eells, J. T., & Lyons, J. (2021) · Complementary Therapies in Clinical Practice · doi:10.1016/j.ctcp.2021.101350 · Cited by 11

Atorvastatin protects the proliferative ability of human umbilical vein endothelial cells inhibited by angiotensin II by changing mitochondrial energy metabolism

Chang, Y., Li, Y., Ye, N., Guo, X., Zhao, L., Sun, G., & Sun, Y. (2017) · International Journal of Molecular Medicine · doi:10.3892/ijmm.2017.3200 · Cited by 10

Virus-Mimicking Liposomal System Based on Dendritic Lipopeptides for Efficient Prevention Ischemia/Reperfusion Injury in the Mouse Liver

Zhuang, R., Chen, M., Zhou, Y., Cheng, W., Zhang, T., Ni, Y., Guo, C., Tu, J., & Jiang, L. (2021) · ACS Macro Letters · doi:10.1021/acsmacrolett.0c00743 · Cited by 10

The mitochondrial multi-omic response to exercise training across tissuesPreprint

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Inhibition of sphingomyelin synthase 2 relieves hypoxia-induced cardiomyocyte injury by reinforcing Nrf2/ARE activation via modulation of GSK-3β

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