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Protective effect of antioxidants on cardiac function in adult offspring exposed to prenatal overnutrition

Published online by Cambridge University Press:  11 March 2022

Jialing Zhang
Affiliation:
Institute of Pediatrics, Children’s Hospital of Fudan University, Shanghai, China NHC Key Laboratory of Neonatal Diseases, Fudan University, Shanghai, China
Li Cao
Affiliation:
Ultrasound Department, Obstetrics and Gynecology Hospital of Fudan University, Shanghai, China
Wenji Wang
Affiliation:
Institute of Pediatrics, Children’s Hospital of Fudan University, Shanghai, China NHC Key Laboratory of Neonatal Diseases, Fudan University, Shanghai, China
Yu Huo
Affiliation:
NHC Key Laboratory of Neonatal Diseases, Fudan University, Shanghai, China Cardiovascular Center, Children’s Hospital of Fudan University, Shanghai, China
Yuanzheng Zheng
Affiliation:
NHC Key Laboratory of Neonatal Diseases, Fudan University, Shanghai, China Cardiovascular Center, Children’s Hospital of Fudan University, Shanghai, China
Fang Wu
Affiliation:
Department of Neonatology, Shanghai General Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China
Yonghao Gui*
Affiliation:
NHC Key Laboratory of Neonatal Diseases, Fudan University, Shanghai, China Cardiovascular Center, Children’s Hospital of Fudan University, Shanghai, China
*
Address for correspondence: Yonghao Gui, NHC Key Laboratory of Neonatal Diseases, Fudan University, 399 Wanyuan Road, Minhang District, Shanghai 201102, China. Email: yh_gui@163.com

Abstract

Maternal overnutrition-induced fetal programming predisposes offspring to cardiovascular health issues throughout life. Understanding how these adverse cardiovascular effects are regulated at the maternal–fetal crosstalk will provide insight into the mechanisms of these cardiovascular diseases, which will help in further identifying potential targets for intervention. Here, we uncover a role of oxidative stress caused by prenatal overnutrition in governing cardiac damage. Mice exposed to maternal obesity showed remarkable pathological cardiomyocyte hypertrophy (p male < 0.001, Cohen’s d male = 1.77; p female < 0.001, Cohen’s d female = 1.94), increased collagen content (p male < 0.001, Cohen’s d male = 2.13; p female < 0.001, Cohen’s d female = 2.71), and increased levels of transforming growth factor β (TGF-β) (p male < 0.001, Cohen’s d male = 3.02; p female < 0.001, Cohen’s d female = 4.52), as well as left ventricular dysfunction in adulthood. To cope with increased oxidative stress in the myocardial tissue of offspring from obese mothers, we sought to decrease the effect of oxidative stress and prevent the development of these cardiovascular conditions with use of the antioxidant N-acetylcysteine during pregnancy. As predicted, after treatment with the antioxidant, there was greatly mitigated cardiomyocyte hypertrophy (p male < 0.001, Cohen’s d male = 1.31; p female < 0.001, Cohen’s d female = 0.82) and cardiac fibrosis, including decreased composition of collagen fibers (p male < 0.01, Cohen’s d male = 1.45; p female < 0.05, Cohen’s d female = 1.23) and reduced levels of TGF-β (p male < 0.05, Cohen’s d male = 1.83; p female < 0.01, Cohen’s d female = 3.81). We also observed improved left ventricle contractile function together with the alleviation of enhanced oxidative stress in the myocardial tissue of offspring. Collectively, these results established a crucial role of oxidative stress in prenatal overnutrition-associated ventricular remodeling and cardiac dysfunction. Our findings provided an important target for intervention of cardiovascular disease in overnutrition-related fetal programming.

Type
Original Article
Copyright
© The Author(s), 2022. Published by Cambridge University Press in association with International Society for Developmental Origins of Health and Disease

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Footnotes

Jialing Zhang and Li Cao are contributed equally to this work.

References

Yu, Y, Arah, OA, Liew, Z, et al. Maternal diabetes during pregnancy and early onset of cardiovascular disease in offspring: population based cohort study with 40 years of follow-up. BMJ. 2019; 367, l6398.CrossRefGoogle ScholarPubMed
Razaz, N, Villamor, E, Muraca, GM, Bonamy, AE, Cnattingius, S. Maternal obesity and risk of cardiovascular diseases in offspring: a population-based cohort and sibling-controlled study. Lancet Diabetes Endocrinol. 2020; 8(7), 572581.CrossRefGoogle ScholarPubMed
Fox, R, Kitt, J, Leeson, P, Aye, CYL, Lewandowski, AJ. Preeclampsia: risk factors, diagnosis, management, and the cardiovascular impact on the offspring. J Clin Med. 2019; 8(10), 1625.CrossRefGoogle ScholarPubMed
Gaillard, R. Maternal obesity during pregnancy and cardiovascular development and disease in the offspring. Eur J Epidemiol. 2015; 30(11), 11411152.CrossRefGoogle ScholarPubMed
Ingul, CB, Loras, L, Tegnander, E, Eik-Nes, SH, Brantberg, A. Maternal obesity affects fetal myocardial function as early as in the first trimester. Ultrasound Obstet Gynecol. 2016; 47(4), 433442.CrossRefGoogle Scholar
Bayoumy, S, Habib, M, Abdelmageed, R. Impact of maternal diabetes and obesity on fetal cardiac functions. Egypt Heart J. 2020; 72(1), 46.CrossRefGoogle ScholarPubMed
Zhang, J, Cao, L, Tan, Y, Zheng, Y, Gui, Y. N-acetylcysteine protects neonatal mice from ventricular hypertrophy induced by maternal obesity in a sex-specific manner. Biomed Pharmacother. 2021; 133(8), 110989.CrossRefGoogle Scholar
Gluckman, PD, Hanson, MA, Buklijas, T. A conceptual framework for the developmental origins of health and disease. J Dev Orig Health Dis. 2010; 1(1), 618.CrossRefGoogle ScholarPubMed
Buffington, SA, Di Prisco, GV, Auchtung, TA, Ajami, NJ, Petrosino, JF, Costa-Mattioli, M. Microbial reconstitution reverses maternal diet-induced social and synaptic deficits in offspring. Cell. 2016; 165(7), 17621775.CrossRefGoogle ScholarPubMed
Johns, EC, Denison, FC, Norman, JE, Reynolds, RM. Gestational diabetes mellitus: mechanisms, treatment, and complications. Trends Endocrinol Metab. 2018; 29(11), 743754.CrossRefGoogle ScholarPubMed
Chiswick, C, Reynolds, RM, Denison, F, et al. Effect of metformin on maternal and fetal outcomes in obese pregnant women (EMPOWaR): a randomised, double-blind, placebo-controlled trial. Lancet Diabetes Endocrinol. 2015; 3(10), 778786.CrossRefGoogle ScholarPubMed
Fernandez-Twinn, DS, Hjort, L, Novakovic, B, Ozanne, SE, Saffery, R. Intrauterine programming of obesity and type 2 diabetes. Diabetologia. 2019; 62(10), 17891801.CrossRefGoogle ScholarPubMed
Tan, BL, Norhaizan, ME, Liew, WP. Nutrients and oxidative stress: friend or foe? Oxid Med Cell Longev. 2018; 2018, 9719584.CrossRefGoogle ScholarPubMed
Biobaku, F, Ghanim, H, Batra, M, Dandona, P. Macronutrient-mediated inflammation and oxidative stress: relevance to insulin resistance, obesity, and atherogenesis. J Clin Endocrinol Metab. 2019; 104(12), 61186128.CrossRefGoogle ScholarPubMed
Litzenburger, T, Huber, EK, Dinger, K, et al. Maternal high-fat diet induces long-term obesity with sex-dependent metabolic programming of adipocyte differentiation, hypertrophy and dysfunction in the offspring. Clin Sci (Lond). 2020; 134(7), 921939.CrossRefGoogle ScholarPubMed
Powell, TL, Barner, K, Madi, L, et al. Sex-specific responses in placental fatty acid oxidation, esterification and transfer capacity to maternal obesity. Biochim Biophys Acta Mol Cell Biol Lipids. 2021; 1866(3), 158861.CrossRefGoogle ScholarPubMed
Heslehurst, N, Vieira, R, Akhter, Z, et al. The association between maternal body mass index and child obesity: a systematic review and meta-analysis. PLoS Med. 2019; 16(6), e1002817.CrossRefGoogle ScholarPubMed
Freitas, R, Vasques, ACJ, Ribeiro, FB, et al. Maternal and paternal obesity are associated with offspring obestatin levels in the Nutritionistsʼ Health Study. Nutrition. 2021; 83, 111067.CrossRefGoogle ScholarPubMed
Persson, M, Razaz, N, Edstedt Bonamy, AK, Villamor, E, Cnattingius, S. Maternal overweight and obesity and risk of congenital heart defects. J Am Coll Cardiol. 2019; 73(1), 4453.CrossRefGoogle ScholarPubMed
Eitmann, S, Nemeth, D, Hegyi, P, et al. Maternal overnutrition impairs offspring’s insulin sensitivity: a systematic review and meta-analysis. Matern Child Nutr. 2020; 16(4), e13031.CrossRefGoogle ScholarPubMed
Han, L, Ren, C, Li, L, et al. Embryonic defects induced by maternal obesity in mice derive from Stella insufficiency in oocytes. Nat Genet. 2018; 50(3), 432442.CrossRefGoogle ScholarPubMed
Azad, MB, Archibald, A, Tomczyk, MM, et al. Nonnutritive sweetener consumption during pregnancy, adiposity, and adipocyte differentiation in offspring: evidence from humans, mice, and cells. Int J Obes (Lond). 2020; 44(10), 21372148.CrossRefGoogle ScholarPubMed
Siddeek, B, Mauduit, C, Chehade, H, et al. Long-term impact of maternal high-fat diet on offspring cardiac health: role of micro-RNA biogenesis. Cell Death Discov. 2019; 5(1), 71.CrossRefGoogle ScholarPubMed
Blackmore, HL, Niu, Y, Fernandez-Twinn, DS, Tarry-Adkins, JL, Giussani, DA, Ozanne, SE. Maternal diet-induced obesity programs cardiovascular dysfunction in adult male mouse offspring independent of current body weight. Endocrinology. 2014; 155(10), 39703980.CrossRefGoogle ScholarPubMed
Xue, Q, Chen, F, Zhang, H, et al. Maternal high-fat diet alters angiotensin II receptors and causes changes in fetal and neonatal ratsdagger. Biol Reprod. 2019; 100(5), 11931203.CrossRefGoogle ScholarPubMed
Lockhart, M, Wirrig, E, Phelps, A, Wessels, A. Extracellular matrix and heart development. Birth Defects Res A Clin Mol Teratol. 2011; 91(6), 535550.CrossRefGoogle ScholarPubMed
Khalil, H, Kanisicak, O, Prasad, V, et al. Fibroblast-specific TGF-beta-Smad2/3 signaling underlies cardiac fibrosis. J Clin Invest. 2017; 127(10), 37703783.CrossRefGoogle ScholarPubMed
Maity, S, Muhamed, J, Sarikhani, M, et al. Sirtuin 6 deficiency transcriptionally up-regulates TGF-beta signaling and induces fibrosis in mice. J Biol Chem. 2020; 295(2), 415434.CrossRefGoogle ScholarPubMed
Miller, TA, Dodson, RB, Mankouski, A, et al. Impact of diet on the persistence of early vascular remodeling and stiffening induced by intrauterine growth restriction and a maternal high-fat diet. Am J Physiol Heart Circ Physiol. 2019; 317(2), H424H433.CrossRefGoogle Scholar
Wang, Q, Zhu, C, Sun, M, et al. Maternal obesity impairs fetal cardiomyocyte contractile function in sheep. FASEB J. 2019; 33(2), 25872598.CrossRefGoogle ScholarPubMed
Loche, E, Blackmore, HL, Carpenter, AA, et al. Maternal diet-induced obesity programmes cardiac dysfunction in male mice independently of post-weaning diet. Cardiovasc Res. 2018; 114(10), 13721384.CrossRefGoogle ScholarPubMed
Ahmed, A, Liang, M, Chi, L, et al. Maternal obesity persistently alters cardiac progenitor gene expression and programs adult-onset heart disease susceptibility. Mol Metab. 2021; 43(2), 101116.CrossRefGoogle ScholarPubMed
Porrello, ER, Mahmoud, AI, Simpson, E, et al. Regulation of neonatal and adult mammalian heart regeneration by the miR-15 family. Proc Natl Acad Sci USA. 2013; 110(1), 187192.CrossRefGoogle ScholarPubMed
Porrello, ER, Mahmoud, AI, Simpson, E, et al. Transient regenerative potential of the neonatal mouse heart. Science. 2011; 331(6020), 10781080.CrossRefGoogle ScholarPubMed
Haubner, BJ, Schneider, J, Schweigmann, U, et al. Functional recovery of a human neonatal heart after severe myocardial infarction. Circ Res. 2016; 118(2), 216221.CrossRefGoogle ScholarPubMed
Castellan, RF, Vitiello, M, Vidmar, M, et al. miR-96 and miR-183 differentially regulate neonatal and adult postinfarct neovascularization. JCI Insight. 2020; 5(14), e134888.CrossRefGoogle ScholarPubMed
Norris, RA, Borg, TK, Butcher, JT, Baudino, TA, Banerjee, I, Markwald, RR. Neonatal and adult cardiovascular pathophysiological remodeling and repair: developmental role of periostin. Ann N Y Acad Sci. 2008; 1123(1), 3040.CrossRefGoogle ScholarPubMed
Zhao, GJ, Zhao, CL, Ouyang, S, et al. Ca(2+)-dependent NOX5 (NADPH Oxidase 5) exaggerates cardiac hypertrophy through reactive oxygen species production. Hypertension. 2020; 76(3), 827838.CrossRefGoogle ScholarPubMed
Bugger, H, Pfeil, K. Mitochondrial ROS in myocardial ischemia reperfusion and remodeling. Biochim Biophys Acta Mol Basis Dis. 2020; 1866(7), 165768.CrossRefGoogle ScholarPubMed
Liang, J, Wu, M, Chen, C, Mai, M, Huang, J, Zhu, P. Roles of reactive oxygen species in cardiac differentiation, reprogramming, and regenerative therapies. Oxid Med Cell Longev. 2020; 2020, 2102841.CrossRefGoogle ScholarPubMed
Nicholas, LM, Ozanne, SE. Early life programming in mice by maternal overnutrition: mechanistic insights and interventional approaches. Philos Trans R Soc Lond B Biol Sci. 2019; 374(1770), 20180116.CrossRefGoogle ScholarPubMed
Vaughan, OR, Rosario, FJ, Powell, TL, Jansson, T. Normalisation of circulating adiponectin levels in obese pregnant mice prevents cardiac dysfunction in adult offspring. Int J Obes (Lond). 2020; 44(2), 488499.CrossRefGoogle ScholarPubMed
Shankar, K, Harrell, A, Liu, X, Gilchrist, JM, Ronis, MJ, Badger, TM. Maternal obesity at conception programs obesity in the offspring. Am J Physiol Regul Integr Comp Physiol. 2008; 294(2), R528538.CrossRefGoogle ScholarPubMed
Monks, J, Orlicky, DJ, Stefanski, AL, et al. Maternal obesity during lactation may protect offspring from high fat diet-induced metabolic dysfunction. Nutr Diabetes. 2018; 8(1), 18.CrossRefGoogle ScholarPubMed
Oben, JA, Mouralidarane, A, Samuelsson, AM, et al. Maternal obesity during pregnancy and lactation programs the development of offspring non-alcoholic fatty liver disease in mice. J Hepatol. 2010; 52(6), 913920.CrossRefGoogle ScholarPubMed
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