The DOI matches its Crossref record; 51 of the 51 references it cites were found in a registry or an index.
Cardiac contractile dysfunction in Lep/Lep obesity is accompanied by NADPH oxidase activation, oxidative modification of sarco(endo)plasmic reticulum Ca2+-ATPase and myosin heavy chain isozyme switch
Open accessAbstract
Aims/hypothesis Obesity is an independent risk factor for heart diseases but the underlying mechanism is not clear. This study examined cardiac contraction, oxidative stress, oxidative modification of sarco(endo)plasmic reticulum Ca2+-ATPase (SERCA) and the myosin heavy chain (MHC) isoform switch in obese mice.Methods Mechanical properties were evaluated in ventricular myocytes from C57BL/6J lean and Lep/Lep obese mice (formerly known as ob/ob mice), including peak shortening (PS), time to 50 or 90% PS, time to 50 or 90% relengthening (TR50, TR90), maximal velocity of shortening/relengthening (+/-dL/dt), intracellular Ca2+ and its decay (tau). Oxidative stress, lipid peroxidation, protein damage and SERCA activity were assessed by glutathione/glutathione disulfide, malondialdehyde, protein carbonyl and 45Ca2+ uptake, respectively. NADPH oxidase was determined by immunoblotting.Results Myocytes from Lep/Lep mice displayed depressed PS and +/- dL/dt, prolonged TR50, TR90, elevated resting [Ca2+]i, prolonged tau, reduced contractile capacity at high stimulus frequencies and diminished responsiveness to extracellular Ca2+ compared with lean controls. Cardiac glutathione/glutathione disulfide was decreased whereas malondialdehyde, protein carbonyl, membrane p47(phox) and membrane gp91(phox) were increased in the Lep/Lep group. SERCA isoenzyme 2a was markedly modified by oxidation in Lep/Lep hearts and associated with decreased 45Ca2+ uptake. The MHC isozyme displayed a shift from the alpha to the beta isoform in Lep/Lep hearts. Short-term incubation of angiotensin II with myocytes mimicked the mechanical defects, SERCA oxidation and 45Ca2+ uptake seen in Lep/Lep myocytes. Incubation of the NADPH oxidase inhibitor apocynin with Lep/Lep myocytes alleviated contractile defects without reversing SERCA oxidation or activity.Conclusions/interpretation These data indicate that obesity-related cardiac defects may be related to NADPH oxidase activation, oxidative damage to SERCA and the MHC isozyme switch.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“In ob/ob mice, cardiomyocyte contractile function is reduced and is associated with reduced calcium sensitivity and altered calcium transients (88, 207).”
From Cardiac remodeling in obesity (2008) · cites this paper as [207]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Positional cloning of the mouse obese gene and its human homologue
Zhang, Y., Proenca, R., Maffei, M., Barone, M., Leopold, L., & Friedman, J. M. (1994) · Nature · doi:10.1038/372425a0 · Cited by 13,419
Increased oxidative stress in obesity and its impact on metabolic syndrome
Furukawa, S., Fujita, T., Shimabukuro, M., Iwaki, M., Yamada, Y., Nakajima, Y., Nakayama, O., Makishima, M., Matsuda, M., & Shimomura, I. (2004) · Journal of Clinical Investigation · doi:10.1172/jci21625 · Cited by 5,508
Congenital leptin deficiency is associated with severe early-onset obesity in humans
Montague, C. T., Farooqi, I. S., Whitehead, J. P., Soos, M. A., Rau, H., Wareham, N. J., Sewter, C. P., Digby, J. E., Mohammed, S. N., Hurst, J. A., et al. (1997) · Nature · doi:10.1038/43185 · Cited by 2,936
Diabetes, Obesity, and the Brain
Schwartz, M. W., & Porte, D. (2005) · Science · doi:10.1126/science.1104344 · Cited by 841
The vascular NAD(P)H oxidases as therapeutic targets in cardiovascular diseases
Cai, H., Griendling, K. K., & Harrison, D. G. (2003) · Trends in Pharmacological Sciences · doi:10.1016/s0165-6147(03)00233-5 · Cited by 687
S-Glutathiolation by peroxynitrite activates SERCA during arterial relaxation by nitric oxide
Adachi, T. K., Weisbrod, R. M., Pimentel, D. R., Ying, J., Sharov, V. S., Schöneich, C., & Cohen, R. A. (2004) · Nature Medicine · doi:10.1038/nm1119 · Cited by 662
Stolk, J. N., Hiltermann, T. J. N., Dijkman, J. H., & Verhoeven, A. J. (1994) · American Journal of Respiratory Cell and Molecular Biology · doi:10.1165/ajrcmb.11.1.8018341 · Cited by 650
Touyz, R. M., Chen, X., Tabet, F., Yao, G., He, G., Quinn, M. T., Pagano, P. J., & Schiffrin, E. L. (2002) · Circulation Research · doi:10.1161/01.res.0000020404.01971.2f · Cited by 590
Development of insulin resistance and obesity in mice overexpressing cellular glutathione peroxidase
McClung, J. P., Roneker, C. A., Mu, W., Lisk, D. J., Langlais, P., Liu, F., & Lei, X. G. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0308096101 · Cited by 536
Oxidative stress and protein aggregation during biological aging
Squier, T. C. (2001) · Experimental Gerontology · doi:10.1016/s0531-5565(01)00139-5 · Cited by 519
Flagged first, then by citations
Cited by
Sorted by citations
Items 101–186 of 186
Thonusin, C., Nawara, W., Arinno, A., Khuanjing, T., Prathumsup, N., Ongnok, B., Chattipakorn, S. C., & Chattipakorn, N. (2023) · Journal of Pineal Research · doi:10.1111/jpi.12884 · Cited by 24
Bode, C., & Bugger, H. (2014) · Hämostaseologie · doi:10.5482/hamo-14-09-0038 · Cited by 19
Zhang, F., Lin, J. J., Tian, H. N., & Wang, J. (2023) · Experimental Physiology · doi:10.1113/ep091309 · Cited by 19
Physiological regulation of cardiac contractility by endogenous reactive oxygen species
Perjés, Á., Kubin, A., Kónyi, A., Szabados, S., Cziráki, A., Skoumal, R., Ruskoaho, H. J., & Szokodi, I. (2011) · Acta Physiologica · doi:10.1111/j.1748-1716.2011.02391.x · Cited by 19
Abnormal Ca 2+ Cycling in Failing Ventricular Myocytes: Role of NOS1-Mediated Nitroso-Redox Balance
Ziolo, M. T., & Houser, S. R. (2014) · Antioxidants and Redox Signaling · doi:10.1089/ars.2014.5873 · Cited by 18
de Oliveira-Junior, S. A., Dal‐Pai‐Silva, M., Martinez, P. F., de Campos, D. H. S., Lima‐Leopoldo, A. P., Leopoldo, A. S., do Nascimento, A. F., Okoshi, M. P., Okoshi, K., Padovani, C. R., et al. (2010) · PubMed · Cited by 18
Li, L., Hua, Y., Dong, M., Li, Q., Smith, D. T., Yuan, M., Jones, K. R., & Ren, J. T. (2012) · Obesity · doi:10.1038/oby.2012.106 · Cited by 18
Self-citationSeravalle, G., & Grassi, G. M. (2024) · Springer eBooks · doi:10.1007/978-3-031-62491-9_5 · Cited by 22
Messeder, D. J., Camacho-Pereira, J., & Galina, A. (2012) · The International Journal of Biochemistry & Cell Biology · doi:10.1016/j.biocel.2012.02.002 · Cited by 17
Myocardial Insulin Resistance: An Overview of Its Causes, Effects, and Potential Therapy
Toit, E. F. D., & Donner, D. G. (2012) · InTech eBooks · doi:10.5772/50619 · Cited by 18
de Andrade, D. C., de Oliveira, G. P., Menezes, L. D. S., Nascimento, A. L. R., de Carvalho, S. N., Stumbo, A. C., Thole, A. A., Garcia‐Souza, É. P., Moura, A. S., de Carvalho, L., et al. (2019) · Nutrition Metabolism and Cardiovascular Diseases · doi:10.1016/j.numecd.2019.09.001 · Cited by 17
Hitsumoto, T. (2015) · Journal of Nippon Medical School · doi:10.1272/jnms.82.274 · Cited by 16
Chromium supplement inhibits skeletal muscle atrophy in hindlimb-suspended mice
Dong, F., Hua, Y., Zhao, P., Ren, J. T., Du, ., & Sreejayan, N. (2008) · The Journal of Nutritional Biochemistry · doi:10.1016/j.jnutbio.2008.09.006 · Cited by 16
Self-citationYuan, F., Lei, Y., Wang, Q., Esberg, L. B., Huang, Z., Scott, G. I., Li, X., & Ren, J. T. (2014) · Toxicology Letters · doi:10.1016/j.toxlet.2014.12.018 · Cited by 15
Self-citationHitsumoto, T., & Shirai, K. (2015) · Diabetes Metabolic Syndrome and Obesity · doi:10.2147/dmso.s80907 · Cited by 13
Ren, J. T. (2007) · Obesity · doi:10.1038/oby.2007.350 · Cited by 13
Self-citationden Bergh, A. V., Vangheluwe, P., Vanderper, A., Carmeliet, P., Wuytack, F., Janssens, S. P., Flameng, W. J., Holvoet, P., & Herijgers, P. (2009) · European Journal of Heart Failure · doi:10.1093/eurjhf/hfp156 · Cited by 12
Fu, M., Bombardier, É., Gamu, D., & Tupling, A. R. (2020) · Biochemical Journal · doi:10.1042/bcj20200346 · Cited by 11
Hitsumoto, T. (2018) · Cardiology Research · doi:10.14740/cr733w · Cited by 11
Hitsumoto, T. (2017) · Cardiology Research · doi:10.14740/cr545w · Cited by 10
Pathogenesis and therapy of autoimmunity-induced dilated cardiomyopathy
Zhao, P. (2009) · Frontiers in bioscience · doi:10.2741/3334 · Cited by 10
Hitsumoto, T. (2018) · Cardiology Research · doi:10.14740/cr713w · Cited by 9
Diabetes disturbs functional adaptation of the remote myocardium after ischemia/reperfusion
Funk, F., Kronenbitter, A. V., Isić, M., Flocke, V., Gorreßen, S., Semmler, D., Brinkmann, M., Beck, K., Steinhoff, O., Srivastava, T., et al. (2022) · Journal of Molecular and Cellular Cardiology · doi:10.1016/j.yjmcc.2022.09.002 · Cited by 9
Knebel, B., Fahlbusch, P., Poschmann, G., Dille, M. A., Wahlers, N., Stühler, K., Hartwig, S., Lehr, S., Schiller, M., Jacob, S., et al. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20102559 · Cited by 9
CYP2E1 overexpression inhibits microsomal Ca2+-ATPase activity in HepG2 cells
Caro, A. A., Evans, K. L., & Cederbaum, A. I. (2008) · Toxicology · doi:10.1016/j.tox.2008.10.020 · Cited by 9
Liu, Y., Huang, H., Xia, W., Tang, Y., Yuan, M., Tang, Q., & Huang, C. (2011) · Biomedicine & Aging Pathology · doi:10.1016/j.biomag.2010.08.001 · Cited by 8
Boldt, K., Rios, J. L., Joumaa, V., & Herzog, W. (2020) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2020-0275 · Cited by 8
Wei, J. J., Tu, F., Dong, F., Deng, Q., Abudureyimu, M., Yu, W., Cai, G., Pei, J., Pei, Z., & Ren, J. T. (2022) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2022.130281 · Cited by 8
Self-citationZhang, R.-H., Guo, H., Kandadi, M. R., Wang, X., & Ren, J. T. (2012) · Experimental Diabetes Research · doi:10.1155/2012/829758 · Cited by 10
Self-citationAfanasiev, S. A., Kondratieva, D. S., Rebrova, Т. Y., Batalov, R. E., & Popov, S. V. (2015) · Journal of Diabetes Research · doi:10.1155/2016/2548689 · Cited by 7
Boldt, K., MacDonald, G. Z., Joumaa, V., & Herzog, W. (2020) · Applied Physiology, Nutrition, and Metabolism · doi:10.1139/apnm-2019-0726 · Cited by 7
Gómez-Viquez, N. L., Balderas‐Villalobos, J., Bello-Sánchez, M. D., Mayorga-Luna, M., Mailloux‐Salinas, P., García‐Castañeda, M., Pérez, E. B. R., Mártinez-Ávila, M. A., Camacho, L., Bravo, G., et al. (2021) · Archives of Physiology and Biochemistry · doi:10.1080/13813455.2021.1895224 · Cited by 7
Liu, Y., Huang, H., Xia, W., Tang, Y., Yuan, M., Tang, Q., & Huang, C. (2010) · Biomedicine & Pharmacotherapy · doi:10.1016/j.biopha.2010.08.007 · Cited by 7
RetractedCardiometabolic Phenotype in HFpEF: Insights from Murine Models
Ogurtsova, E., Arefieva, T. I., Filatova, A. Y., Radyukhina, N. V., & Ovchinnikov, A. G. (2025) · Biomedicines · doi:10.3390/biomedicines13030744 · Cited by 6
Kang, K., Ko, J.-Y., Lee, H., Shin, S. Y., Lee, W. S., Hong, J., Kim, S., Lee, S., & Oak, M. (2022) · Journal of Korean Medical Science · doi:10.3346/jkms.2022.37.e55 · Cited by 6
Kita, T., Sato, S., Yamasaki, S., Ueno, Y., Kimura, G., Ketema, R. M., Kawahara, T., Kurasaki, M., & Saito, T. (2019) · International Journal of Food Sciences and Nutrition · doi:10.1080/09637486.2019.1576598 · Cited by 6
Clinical impact of skin autofluorescence on high-sensitivity troponin T in hypertensive patients
Hitsumoto, T. (2017) · Clinical Hypertension · doi:10.1186/s40885-017-0076-y · Cited by 5
Reduction of oxidative stress improves insulin signaling in cardiac tissue of obese mice
Rodrigues, M. S., Pieri, B. L. D. S., Silveira, G. D. B., Zaccaron, R. P., Venturini, L. M., Comin, V. H., Luiz, K. D., & Silveira, P. C. L. (2020) · Einstein (São Paulo) · doi:10.31744/einstein_journal/2020ao5022 · Cited by 5
Effects of obesity on the cardiac proteome
Vileigas, D. F., & Cicogna, A. C. (2020) · Endocrine and Metabolic Science · doi:10.1016/j.endmts.2020.100076 · Cited by 5
Hitsumoto, T. (2017) · Cardiology Research · doi:10.14740/cr632w · Cited by 5
Jung, S., Ahn, N., Park, J.-S., & Kim, K. (2018) · Exercise Science · doi:10.15857/ksep.2018.27.2.126 · Cited by 4
Liu, Y., Shi, H., Li, C., Zhuang, H., Li, Y., He, X., Jiang, Y., Jin, Z., Guo, Z., Ong, S., et al. (2026) · Cardiovascular Diabetology · doi:10.1186/s12933-026-03125-z · Cited by 3
Li, Q., Fang, C. X., Nunn, J. M., Zhang, J., LaCour, K. H., & Ren, J. T. (2006) · Life Sciences · doi:10.1016/j.lfs.2006.08.038 · Cited by 3
Self-citationClinical Impact of Hemorheology on Subclinical Myocardial Injury in Patients with Hypertension
Hitsumoto, T. (2018) · Journal of Clinical Medicine Research · doi:10.14740/jocmr3652 · Cited by 3
Kubasik-Juraniec, J., & Knap, N. (2009) · PubMed · Cited by 2
Ultrastructural response of arcuate nucleus neurons to fasting in aged rats.
Kubasik-Juraniec, J., Zauszkiewicz–Pawlak, A., Kotlarz, G., Woźniak, M., & Knap, N. (2009) · PubMed · Cited by 2
Nitroso-Redox Crosstalk in Diabetic Cardiomyopathy
González, D. R., Treuer, A. V., & Novoa, U. (2016) · InTech eBooks · doi:10.5772/63668 · Cited by 1
Exercise Empowerment: A Multifaceted Anatomy in Managing Diabetic Myocardial Disorder
Chen, C., Xu, L., Wang, K., & Wang, T. (2025) · Journal of Cardiovascular Translational Research · doi:10.1007/s12265-025-10630-1 · Cited by 1
Carvajal, K., Arias‐Chávez, D. J., Mailloux‐Salinas, P., Bravo, G., & Gómez-Viquez, N. L. (2026) · Handbook of experimental pharmacology · doi:10.1007/164_2026_794 · Cited by 1
Oxidative stress: a key contributor to diabetic
Singal, P. K. (2010) · Cited by 1
(2008) · Current topics in membranes · doi:10.1016/s1063-5823(08)00206-8 · Cited by 1
Vigna, C. (2008) · UWSpace (University of Waterloo) · Cited by 1
Lima‐Leopoldo, A. P. (2010) · doi:10.5016/dt000614088 · Cited by 1
Reactive Oxygen Species and Cardiovascular Diseases
Engrcia, V., de Abreu, L. C., Ferreira, C., & Saldiv, P. H. N. (2012) · InTech eBooks · doi:10.5772/32706
Hegab, Z. (2012) · Research Explorer (The University of Manchester)
UNIVERSIDADE ESTADUAL PAULISTA "JÚLIO DE MESQUITA FILHO" FACULDADE DE MEDICINA
de Deus, A. F. (2015)
INFLUÊNCIA DA OXIDAÇÃO DE GLICOSE SOBRE A FUNÇÃO MIOCÁRDICA DE RATOS OBESOS
Filho, J. D. M. (2010)
Zhang, R.-H., Guo, H., Kandadi, M. R., Wang, X., & Ren, J. T. (2012)
Self-citationSabry, M. (2014) · International Journal of Biochemistry Research & Review · doi:10.9734/ijbcrr/2014/6009
Organ Protection from Oxidative Stress : a Role of Oxidative Stress in Heart Failure
Kinoshita, H. (2011) · THE JOURNAL OF JAPAN SOCIETY FOR CLINICAL ANESTHESIA · doi:10.2199/jjsca.31.116
Glucose Uptake and Its Consequence on Cardiomyocyte Function
Bertrand, L., Horman, S., & Beauloye, C. (2014) · Elsevier eBooks · doi:10.1016/b978-0-12-800093-9.00012-0 · Cited by 1
Fuel Metabolism Plasticity in Pathological Cardiac Hypertrophy and Failure
Kolwicz, S. C., & Tian, R. (2014) · Springer eBooks · doi:10.1007/978-1-4939-1227-8_11
DIABETES AND OBESITY: EVIDENCE FOR A CARDIOMYOPATHY
Ashrafi, R. (2016) · University of Liverpool · doi:10.17638/03003030
da Silva, V. L., Cicogna, A. C., Lima‐Leopoldo, A. P., & Soares, A. L. D. S. (2015)
Donner, D. G. (2015) · Griffith Research Online · doi:10.13140/rg.2.1.1191.1761
Kim, K., Ahn, N.-Y., & Kim, S. (2017) · The Official Journal of the Korean Academy of Kinesiology · doi:10.15758/jkak.2017.19.3.71
Cardiotoxicidad del estado de tolerancia a la glucosa alterada
Sommese, L. M. (2018) · doi:10.35537/10915/66305
Autophagy: A New Therapeutic Target
Ceylan, A. F. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-805253-2.00022-5
Impact of Skin Autofluorescence on High Sensitivity Troponin T in Japanese Patients with Obesity
Hitsumoto, T. (2017) · Enliven Clinical Cardiology and Research · doi:10.18650/2375-7310.411004
Influência do tempo de exposição à obesidade sobre a função cardíaca de ratos
Leopoldo, A. S. (2010) · doi:10.5016/dt000612860
Suzuki, N., Hitomi, Y., Tsuji, Y., Sakai, Y., Nishimura, M., Hashimoto, T., & Kobayashi, H. (2019) · Renal Replacement Therapy · doi:10.1186/s41100-019-0202-2
Network-Centric Identification of Disease Co-Occurrences: A Systems Biology Approach
Sahrawat, T. R., & Talwar, D. (2020) · Sumerianz Journal of Medical and Healthcare · doi:10.47752/sjmh.311.103.110 · Cited by 1
Boldt, K., Mattiello, S. M., Joumaa, V., Turnbull, J., Fedak, P. W. M., & Herzog, W. (2021) · Physical Activity and Nutrition · doi:10.20463/pan.2021.0009
Ajayi, G. O., Obi, E. U., Elegbeleye, E. N., Obayemi, P. T., & Edamisan, O. M. (2020) · Sumerianz Journal of Medical and Healthcare · doi:10.47752/sjmh.311.93.102
(2007) · Current Opinion in Endocrinology Diabetes and Obesity · doi:10.1097/med.0b013e32802e6d87
(2007) · Current Opinion in Endocrinology Diabetes and Obesity · doi:10.1097/med.0b013e3282c3a898
Current literature in diabetes
(2006) · Diabetes/Metabolism Research and Reviews · doi:10.1002/dmrr.720
(2006) · Current Opinion in Endocrinology & Diabetes · doi:10.1097/01.med.0000244230.06529.0f
Heller, K., Flocke, V., Straub, T., Ding, Z., Srivastava, T., Nowak, M. K., Funk, F., Levkau, B., Schmitt, J. P., Grandoch, M., et al. (2024) · npj Imaging · doi:10.1038/s44303-024-00044-0
NADPH oxidase, obesity, and metabolic syndrome: Therapeutic opportunity
Tikhonova, I. V., & Safronova, V. G. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-27370-4.00024-x
Obesity-Associated Cardiac Fibrosis: Mechanisms and Emerging Therapeutic Targets
Zhou, D., Tan, Y., Zhao, J., Wang, S., Wang, Z., Bai, M., Niu, X., & Zhang, Z. (2026) · Vascular Health and Risk Management · doi:10.2147/vhrm.s567568
Almohya, S. M., & Alqahtani, N. S. (2026) · Journal of the Renin-Angiotensin-Aldosterone System · doi:10.1177/14703203261431906
Lacôte, M. (2018) · theses.fr (ABES) · doi:10.70675/bc9b8426z5718z40e1zadc2zaa52fb20a6fd
Leptin and cardiovascular health
Pereira, S. X. E. R. L. (2026) · Endocrinology · doi:10.1210/endocr/bqag050
Vigna, C., Fu, M., Humaid, A., & Tupling, A. R. (2026) · Free Radical Research · doi:10.1080/10715762.2026.2727872
Metadata
- Authors
- Li, S.-Y., Yang, X., Ceylan-Isik, A. F., Du, M., Sreejayan, N., & Ren, J.
- Affiliations
- University of Wyoming (US)
- Corresponding author
- Ren, J.
- Venue
- Diabetologia
- Published
- 2006-04-13
- Volume
- 49
- Issue
- 6
- Pages
- 1434-1446
- ISSN
- 0012-186X (ISSN-L)
- 1432-0428
- OpenAlex
- W2149180473
- Cited by
- 187
- References
- 51
- Citations by year
- 2026: 6 · 2025: 4 · 2024: 4 · 2023: 3 · 2022: 8 · 2021: 6 · 2020: 10 · 2019: 8 · 2018: 11 · 2017: 10 · 2016: 7 · 2015: 12 · 2014: 10 · 2013: 10 · 2012: 16
- FWCI
- 10.19
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Diabetologia (publishedVersion)
- PubMed (publishedVersion)
- Funders
- American Diabetes Association (7-00-RA-21)
- American Heart Association (0355521Z)
- Ohio State University
- Montana State University
- National Institutes of Health
- National Institute on Aging (R03AG021324, AG-21324, R03 AG21324, 1R03 AG21324-01, R03 AG21324-01, 1 R03 AG21324)
- Topics
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiovascular Function and Risk Factors
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac electrophysiology and arrhythmias
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiomyopathy and Myosin Studies
- Keywords
- cardiac contractile dysfunction, obesity, ob/ob mice, NADPH oxidase, oxidative stress, angiotensin II, apocynin, oxidative modification, ventricular myocytes, lipid peroxidation, protein carbonylation, glutathione, p47phox
- MeSH terms
- Calcium-Transporting ATPases, Animals, Endoplasmic Reticulum, Enzyme Activation, Glutathione, Homozygote, Male, Mice, Inbred C57BL, Mice, Obese, Myocardial Contraction, Sarcoplasmic Reticulum, Cell Culture Techniques, NADPH Oxidases, Glutathione Disulfide, Calcium Signaling, Leptin, Muscle Cells, Mice
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review