The DOI matches its Crossref record; 25 of the 25 references it cites were found in a registry or an index.
Prevention of diabetes-associated embryopathy by overexpression of the free radical scavenger copper zinc superoxide dismutase in transgenic mouse embryos
Abstract
Objectives It has recently been suggested that oxygen free radicals are involved in the high incidence of fetal dysmorphogenesis that is associated with diabetic pregnancies. The purpose of the current investigation was to study the effect of copper zinc superoxide dismutase, a free radical scavenging enzyme, on the prevention of diabetes-associated embryopathy in mice. Study design Mice used in this study were either transgenic, bearing the human copper zinc superoxide dismutase gene, or nontransgenic controls. Diabetes was generated by streptozotocin administration on days 6 and 7 of gestation. Hyperglycemia developed on day 8 and was maintained through day 10 (critical period of organogenesis). On day 10 fetuses were examined for external anomalies, and their crown-rump lengths and deoxyribonucleic acid content were determined. Results Induction of maternal diabetes produced a significant reduction in mean crown-rump length of control embryos (4.48 +/- 0.7 mm vs 3.65 +/- 0.6 mm, p = 0.0001), whereas transgenic embryos were not affected (4.72 +/- 0.6 mm vs 4.45 +/- 0.8 mm, p > 0.05). After induction of diabetes fetal loss and malformation rates were significantly higher in control embryos (6.0% vs 23.8% and 8.4% vs 16.5%, respectively). Transgenic embryos were practically unaffected by diabetes and showed fetal loss and malformation rates of 5.9% and 4.4%, respectively, after induction of diabetes. Conclusions Elevated levels of copper zinc superoxide dismutase, a key enzyme in the metabolism of free oxygen radicals, elicit a protective effect against diabetes-associated embryopathy.
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“Burton (2009) reported that in animals with genetically impaired antioxidant enzyme activity and in diabetic rats in whom ROS levels were increased, the offspring had congenital abnormalities (Hagay et al. 1995;Eriksson, 1999;Nicol et al. 2000).”
From Iron, Oxidative Stress and Health (2012) · cites this paper as Hagay et al. 1995
Citations
Cites
Superoxide dismutase: Improved assays and an assay applicable to acrylamide gels
Beauchamp, C., & Fridovich, I. (1971) · Analytical Biochemistry · doi:10.1016/0003-2697(71)90370-8 · Cited by 12,892
Pryor, W. A. (1976) · Cited by 1,876
Hunt, J. V., Dean, R. T., & Wolff, S. P. (1988) · Biochemical Journal · doi:10.1042/bj2560205 · Cited by 779
Diabetes mellitus and free radicals
Wolff, S. P. (1993) · British Medical Bulletin · doi:10.1093/oxfordjournals.bmb.a072637 · Cited by 660
Epstein, C. J., Avraham, K. B., Lovett, M., Smith, S. H., Elroy‐Stein, O., Rotman, G., Bry, C., & Groner, Y. (1987) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.84.22.8044 · Cited by 454
Self-citationOxygen Radicals, Hydrogen Peroxide, and Oxygen Toxicity
Fridovich, I. (1976) · Elsevier eBooks · doi:10.1016/b978-0-12-566501-8.50013-4 · Cited by 435
Malformations in infants of diabetic mothers
Mills, J. L. (1982) · Teratology · doi:10.1002/tera.1420250316 · Cited by 392
Eriksson, U. J., Dahlstrom, E., Larsson, K., & Hellerström, C. (1982) · Diabetes · doi:10.2337/diab.31.1.1 · Cited by 310
Self-citationEriksson, U. J., & Borg, L. A. H. (1991) · Diabetologia · doi:10.1007/bf00405004 · Cited by 252
Self-citationEriksson, U. J., & Borg, L. (1993) · Diabetes · doi:10.2337/diab.42.3.411 · Cited by 230
Self-citation
Research works printed but not linked: 1
- Eriksson, 1993, Increased superoxide dismutase (SOD) activity in embryos of transgenic mice protects from the teratogenic effects of a diabetic environment, Diabetes, 42, 85A
Cited by
Sorted by citations
Items 101–149 of 149
Vitamin E and thetreatment and prevention of diabetes: a case for a controlled clinical trial.
Halliwell, B. B. (2002) · PubMed · Cited by 19
Iron, Oxidative Stress and Health
Udipi, S., Ghugre, P., & Gokhale, C. (2012) · Oxidative Stress - Molecular Mechanisms and Biological Effects · doi:10.5772/34975 · Cited by 17
“diabetic rats in whom ROS levels were increased, the offspring had congenital abnormalities (Hagay et al. 1995; Eriksson, 1999; Nicol et al. 2000).”
BackgroundMéndez, J. D., & Palomar-Morales, M. (1999) · Reproductive Toxicology · doi:10.1016/s0890-6238(99)00039-8 · Cited by 17
Free radicals and antioxidants status in neonates with congenital malformation
Mishra, S., Mukhopadhyay, B., Gongopadhyay, A., Rani, A., & Gavel, R. (2015) · Journal of Indian Association of Pediatric Surgeons · doi:10.4103/0971-9261.161037 · Cited by 17
Genetic and environmental influence on diabetic rat embryopathy
Ejdesjö, A., Wentzel, P., & Eriksson, U. (2010) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00543.2010 · Cited by 15
Self-citationCan we prevent diabetic birth defects with micronutrients?
Wentzel, P. (2009) · Diabetes Obesity and Metabolism · doi:10.1111/j.1463-1326.2009.01053.x · Cited by 14
Hami, J., Vafaei‐Nezhad, S., Haghir, D., & Haghir, H. (2015) · Journal of Molecular Neuroscience · doi:10.1007/s12031-015-0661-z · Cited by 13
Genetic variations in the GLUT3 gene associated with myelomeningocele
Connealy, B. D., Northrup, H., & Au, K. S. (2014) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2014.05.013 · Cited by 13
Congenital Malformations in Experimental Diabetic Pregnancy: Aetiology and Antioxidative Treatment
Simán, M. (1997) · Upsala Journal of Medical Sciences · doi:10.3109/03009739709178933 · Cited by 12
Petty, H. R., Kindzelskii, A. L., Chaiworapongsa, T., Petty, A. R., & Romero, R. J. (2005) · The Journal of Maternal-Fetal & Neonatal Medicine · doi:10.1080/14767050500361679 · Cited by 11
Larouche, G., & Hales, B. F. (2009) · Birth Defects Research Part A Clinical and Molecular Teratology · doi:10.1002/bdra.20595 · Cited by 11
Tiboni, G. M., Bucciarelli, T., Amicarelli, F., Angelucci, S., Iammarrone, E., Bellati, U., Sacchetta, P., & Ilio, C. D. (1997) · Archives of Toxicology · doi:10.1007/s002040050466 · Cited by 11
Eriksson, U. J., & Wentzel, P. (2012) · Methods in molecular biology · doi:10.1007/978-1-61779-867-2_26 · Cited by 10
Self-citationImpact of Oxidative Stress on Development
Wells, P. G., Miller‐Pinsler, L., & Shapiro, A. M. (2014) · Oxidative stress in applied basic research and clinical practice · doi:10.1007/978-1-4939-1405-0_1 · Cited by 10
Evidence of Oxidative Stress in the Brains of Fetuses with CNS Anomalies and Islet Cell Hyperplasia
Hockett, P. K., Emery, S. C., Hansen, L. A., & Masliah, E. (2004) · Pediatric and Developmental Pathology · doi:10.1007/s10024-001-0130-2 · Cited by 10
White, V., Capobianco, E., Higa, R., Martínez, N., Sosa, M., Pustovrh, M. C., & Jawerbaum, A. (2010) · Free Radical Research · doi:10.3109/10715762.2010.512039 · Cited by 10
Wang, C., Cai, Z.-X., You, Z.-L., Guo, H.-S., Shang, D.-J., Wang, X.-L., Zhang, L., Ma, L.-J., Tan, J., Le, W.-D., et al. (2014) · Neurochemical Research · doi:10.1007/s11064-014-1392-1 · Cited by 9
Kase, B. A., Northrup, H., & Au, K. S. (2013) · American Journal of Obstetrics and Gynecology · doi:10.1016/j.ajog.2013.06.004 · Cited by 9
Reevaluation of Antioxidative Strategies for Birth Defect Prevention in Diabetic Pregnancies
Zhao, Z. (2016) · Journal of Biomolecular Research & Therapeutics · doi:10.4172/2167-7956.1000145 · Cited by 8
Prevention of Teratogenesis in Pregnancies of Obese Rats by Vitamin E Supplementation
Alcalá, M., Bolado‐García, V. E., Sánchez‐Vera, I., Clapés, S., Dası́, F., Sáez, G. T., Carrera, E., Álvarez-Gallego, F., Loeken, M. R., & Viana, M. (2021) · Antioxidants · doi:10.3390/antiox10081173 · Cited by 8
Hunter, S. K., Wang, Y., Weiner, C. P., & Niebyl, J. R. (1997) · American Journal of Obstetrics and Gynecology · doi:10.1016/s0002-9378(97)70262-x · Cited by 8
Modulation of PGE2generation in the diabetic embryo: effect of nitric oxide and superoxide dismutase
Jawerbaum, A., Sinner, D. I., White, V., Pustovrh, M. C., Capobianco, E., Gimeno, M. A. F., & Gonzalez, E. T. (2001) · Prostaglandins Leukotrienes and Essential Fatty Acids · doi:10.1054/plef.2001.0251 · Cited by 8
Moraes-Souza, R. Q., Reinaque, A. P. B., Soares, T. S., Silva, A. L. T., Giunchetti, R. C., Takano, M. A. S., Akamatsu, M. A., Kubrusly, F. S., Macarini, F. L. D. S., Raw, I., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0172525 · Cited by 6
Cormier, C., Au, K. S., & Northrup, H. (2010) · Reproductive Sciences · doi:10.1177/1933719110388293 · Cited by 6
Offspring of Diabetic Pregnancy
Persson, B., Eriksson, U. J., & Hanson, U. (2005) · KARGER eBooks · doi:10.1159/000087430 · Cited by 6
Self-citationDiabetes Mellitus in Pregnancy
Homko, C. J., HAGAY, Z. J., & Reece, E. A. (2007) · Wiley eBooks · doi:10.1002/9780470753293.ch41 · Cited by 5
Self-citationJung, J. H., & Loeken, M. R. (2021) · Antioxidants · doi:10.3390/antiox10081156 · Cited by 4
Oxidative Stress, Antioxidative Defence and Outcome of Gestation in Experimental Diabetic Pregnancy
Cederberg, J. (2001) · Uppsala University Publications (Uppsala University) · Cited by 4
The Role of Biotransformation in Developmental Toxicity
Wells, P. G., & Winn, L. M. (2015) · Elsevier eBooks · doi:10.1016/b978-0-12-801238-3.02170-x · Cited by 3
Heme oxygenase‐1 promoter polymorphisms and risk of spina bifida
Fujioka, K., Yang, W., Wallenstein, M. B., Zhao, H. F., Wong, R. J., Stevenson, D. K., & Shaw, G. M. (2015) · Birth Defects Research Part A Clinical and Molecular Teratology · doi:10.1002/bdra.23343 · Cited by 3
The Role of Biotransformation in Developmental Toxicity
Wells, P. G., & Winn, L. M. (2010) · Elsevier eBooks · doi:10.1016/b978-0-08-046884-6.01510-4 · Cited by 3
Zinc in relation to type 1 and type 2 diabetes: An overview
Singh, U. (2014) · Journal of Applied and Natural Science · doi:10.31018/jans.v6i2.551 · Cited by 2
Wang, S., Liu, G. C., Wintergerst, K. A., & Cai, L. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-801585-8.00014-2 · Cited by 2
Kachi, T., Tanaka, D., Watanabe, S., Suzuki, R., & Tonosaki, Y. (2004) · Anatomical Science International · doi:10.1111/j.1447-073x.2004.00070.x · Cited by 2
Sharifi, F., Shajari, Z., & Feizy, A. A. (2021) · Research Square · doi:10.21203/rs.3.rs-502882/v1 · Cited by 2
[Observation on non-invasive electrode pulse electric stimulation for treatment of Bell's palsy].
Guo, Q., Yan, J.-Z., Yan, W.-S., & Xiao, M.-Z. (2006) · PubMed · Cited by 2
Postimplantation diabetic embryopathy
Eriksson, U. J., & Wentzel, P. (2018) · CRC Press eBooks · doi:10.1201/9781315382104-41 · Cited by 1
Self-citationEffects of Pregnancy on Metabolism
Diamond, M. P., & Rossi, G. (2001) · Comprehensive physiology · doi:10.1002/cphy.cp070231 · Cited by 1
Fetal Outcome in Experimental Diabetic Pregnancy
Zabihi, S. (2008) · Uppsala University Publications (Uppsala University) · Cited by 1
A History of Diabetes in Pregnancy
Kalter, H. (2011) · Springer eBooks · doi:10.1007/978-94-007-1557-8 · Cited by 3
Pregestational Diabetes and Congenital Heart Defects: Role of Reactive Oxygen Species
Moazzen, H. (2014) · Scholarship@Western (Western University)
Machado, A. F. A., Scott, W. J., & Collins, M. D. (2003) · Springer eBooks · doi:10.1007/0-306-48412-9_20
Gutierrez, J. C. (2009) · VTechWorks (Virginia Tech)
Biochemistry status of glycosylated hemoglobin and lipid profile in gestational diabetes patients.
Kedari, G. S. R. (2010) · Recent Research in Science and Technology
Post-implantation diabetic embryopathy
Eriksson, U. J., & Wentzel, P. (2008) · Series in maternal-fetal medicine · doi:10.3109/9781439802007.024
Self-citationMaternal and Fetal Conditions With Consequences for the Fetal Brain
du Plessis, A. J., & Volpe, J. J. (2024) · Elsevier eBooks · doi:10.1016/b978-0-443-10513-5.00011-5
The Role of Biotransformation in Developmental Toxicity
Wells, P. G., & Winn, L. M. (2024) · Elsevier eBooks · doi:10.1016/b978-0-323-95488-4.00155-8
Embryonic Gene Alterations in rats Caused by Exposure to Diabetes and/or Obesity
Ehtesham, E. (2012) · University Library of Skövde (University of Skövde)
Metadata
- Authors
- Hagay, Z. J., Weiss, Y., Zusman, I., Peled-Kamar, M., Reece, E. A., Eriksson, U. J., & Groner, Y.
- Affiliations
- Kaplan Medical Center (IL)
- Weizmann Institute of Science (IL)
- Hebrew University of Jerusalem (IL)
- Temple University (US)
- Uppsala University (SE)
- Corresponding author
- Hagay, Zion J.
- ORCID
- Groner, Yoram
- Venue
- American Journal of Obstetrics and Gynecology
- Publisher
- Elsevier BV
- Published
- 1995-10
- Volume
- 173
- Issue
- 4
- Pages
- 1036-1041
- ISSN
- 0002-9378 (ISSN-L)
- OpenAlex
- W2050726467
- Cited by
- 149
- References
- 25
- Citations by year
- 2024: 2 · 2023: 1 · 2021: 3 · 2020: 1 · 2019: 1 · 2018: 1 · 2017: 2 · 2016: 7 · 2015: 9 · 2014: 9 · 2013: 5 · 2012: 10
- FWCI
- 10.69
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- American Journal of Obstetrics and Gynecology (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Obstetrics and Gynecology › Gestational Diabetes Research and Management
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Birth, Development, and Health
- Health Sciences › Nursing › Nutrition and Dietetics › Trace Elements in Health
- Keywords
- copper-zinc superoxide dismutase, oxygen free radicals, transgenic embryos, maternal diabetes, streptozotocin-induced diabetes, fetal death, crown-rump length, organogenesis, antioxidant defense
- MeSH terms
- Congenital Abnormalities, Analysis of Variance, Animals, Diabetes Mellitus, Experimental, Embryo, Mammalian, Female, Humans, Mice, Transgenic, Pregnancy, Pregnancy in Diabetics, Superoxide Dismutase, Gene Expression, Chi-Square Distribution, Odds Ratio, Free Radical Scavengers, Mice
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