Abstract
Purpose
Zinc restriction during fetal and postnatal development could program cardiovascular diseases in adulthood. The aim of this study was to determine the effects of zinc restriction during fetal life, lactation, and/or post-weaning growth on cardiac inflammation, apoptosis, oxidative stress, and nitric oxide system of male and female adult rats.
Methods
Wistar rats were fed a low- or a control zinc diet during pregnancy and up to weaning. Afterward, offspring were fed either a low- or a control zinc diet until 81 days of life. IL-6 and TNF-α levels, TUNEL assay, TGF-β1 expression, thiobarbituric acid-reactive substances that determine lipoperoxidation damage, NADPH oxidase-dependent superoxide anion production, antioxidant and nitric oxide synthase activity, mRNA and protein expression of endothelial nitric oxide synthase, and serine1177 phosphorylation isoform were determined in left ventricle.
Results
Zinc deficiency activated apoptotic and inflammatory processes and decreased TGF-β1 expression and nitric oxide synthase activity in cardiac tissue of both sexes. Male zinc-deficient rats showed no changes in endothelial nitric oxide synthase expression, but a lower serine1177 phosphorylation. Zinc deficiency induced an increase in antioxidant enzymes activity and no differences in lipoperoxidation products levels in males. Females were less sensitive to this deficiency exhibiting lower increase in apoptosis, lower decrease in expression of TGF-β1, and higher antioxidant and nitric oxide enzymes activities. A zinc-adequate diet during postnatal life reversed most of these mechanisms.
Conclusion
Prenatal and postnatal zinc deficiency induces alterations in cardiac apoptotic, inflammatory, oxidative, and nitric oxide pathways that could predispose the onset of cardiovascular diseases in adult life.
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References
Geelhoed JJ, Jaddoe VW (2010) Early influences on cardiovascular and renal development. Eur J Epidemiol 25:677–692. doi:10.1007/s10654-010-9510-0
Rogers LK, Velten M (2011) Maternal inflammation, growth retardation, and preterm birth: insights into adult cardiovascular disease. Life Sci 89:417–421. doi:10.1016/j.lfs.2011.07.017
Sandstead HH (1995) Is zinc deficiency a public health problem? Nutrition 11:87–92
Spann MN, Smerling J, Gustafssona H, Foss S, Altemus M, Monk C (2015) Deficient maternal zinc intake-but not folate-is associated with lower fetal heart rate variability. Early Hum Dev 91:169–172. doi:10.1016/j.earlhumdev.2015.01.007
Vallee BL, Falchuk KH (1993) The biochemical basis of zinc physiology. Physiol Rev 73:79–118
Maret W (2009) Molecular aspects of human cellular zinc homeostasis: redox control of zinc potentials and zinc signals. Biometals 22:149–157. doi:10.1007/s10534-008-9186-z
Guilbert JJ (2003) The world health report 2002—reducing risks, promoting healthy life. Educ Health (Abingdon) 16:230
Lee SR, Noh SJ, Pronto JR, Jeong YJ, Kim HK, Song IS, Xu Z, Kwon HY, Kang SC, Sohn EH, Ko KS, Rhee BD, Kim N, Han J (2015) The critical roles of zinc: beyond impact on myocardial signaling. Korean J Physiol Pharmacol 19:389–399. doi:10.4196/kjpp.2015.19.5.389
Little PJ, Bhattacharya R, Moreyra AE, Korichneva IL (2010) Zinc and cardiovascular diseases. Nutrition 26:1050–1057. doi:10.1016/j.nut.2010.03.007
Formigari A, Irato P, Santon A (2007) Zinc, antioxidant systems and metallothionein in metal mediated-apoptosis: biochemical and cytochemical aspects. Comp Biochem Physiol C Toxicol Pharmacol 146:443–459
Prasad AS (2008) Clinical, immunological, anti-inflammatory and antioxidant roles of zinc. Exp Gerontol 43:370–377
Prasad AS (2014) Zinc: an antioxidant and anti-inflammatory agent: role of zinc in degenerative disorders of aging. J Trace Elem Med Biol 28:364–371. doi:10.1016/j.jtemb.2014.07.019
Bonaventura P, Benedetti G, Albarède F, Miossec P (2015) Zinc and its role in immunity and inflammation. Autoimmun Rev 14:277–285. doi:10.1016/j.autrev.2014.11.008
Mariani E, Cattini L, Neri S, Malavolta M, Mocchegiani E, Ravaglia G, Facchini A (2006) Simultaneous evaluation of circulating chemokine and cytokine profiles in elderly subjects by multiplex technology: relationship with zinc status. Biogerontology 7:449–459
Förstermann U, Sessa WC (2012) Nitric oxide synthases: regulation and function. Eur Heart J 33:829–837. doi:10.1093/eurheartj/ehr304
Liu Y, Feng Q (2012) NOing the heart: role of nitric oxide synthase-3 in heart development. Differentiation 84:54–61. doi:10.1016/j.diff.2012.04.004
Tomat A, Elesgaray R, Zago V, Fasoli H, Fellet A, Balaszczuk AM, Schreier L, Costa MA, Arranz C (2010) Exposure to zinc deficiency in fetal and postnatal life determines nitric oxide system activity and arterial blood pressure levels in adult rats. Br J Nutr 3:382–389. doi:10.1017/S0007114510000759
Tomat AL, Costa MA, Girgulsky LC, Veiras L, Weisstaub AR, Inserra F, Balaszczuk AM, Arranz CT (2007) Zinc deficiency during growth: influence on renal function and morphology. Life Sci 80:1292–1302
Tomat AL, Inserra F, Veiras L, Vallone MC, Balaszczuk AM, Costa MA, Arranz C (2008) Moderate zinc restriction during fetal and postnatal growth of rats: effects on adult arterial blood pressure and kidney. Am J Physiol Regul Integr Comp Physiol 295:543–549. doi:10.1152/ajpregu.00050.2008
Tomat AL, Weisstaub AR, Jauregui A, Pineiro A, Balaszczuk AM, Costa MA, Arranz CT (2005) Moderate zinc deficiency influences arterial blood pressure and vascular nitric oxide pathway in growing rats. Pediatr Res 58:672–676
Tomat AL, Juriol LV, Gobetto MN, Veiras LC, Mendes Garrido Abregú F, Zilberman J, Fasoli H, Elesgaray R, Costa MA, Arranz CT (2013) Morphological and functional effects on cardiac tissue induced by moderate zinc deficiency during prenatal and postnatal life in male and female rats. Am J Physiol Heart Circ Physiol 305:H1574–H1583. doi:10.1152/ajpheart.00578.2013
Kuwahara F, Kai H, Tokuda K, Kai M, Takeshita A, Egashira K, Imaizumi T (2002) Transforming growth factor-beta function blocking prevents myocardial fibrosis and diastolic dysfunction in pressure-overloaded rats. Circulation 106:130–135
Villar AV, Garcia R, Llano M, Cobo M, Merino D, Lantero A, Tramullas M, Hurlé JM, Hurlé MA, Nistal JF (2013) BAMBI (BMP and activin membrane-bound inhibitor) protects the murine heart from pressure-overload biomechanical stress by restraining TGF-beta signaling. Biochim Biophys Acta 2:323–335
Dabek J, Kułach A, Monastyrska-Cup B, Gasior Z (2006) Transforming growth factor beta and cardiovascular diseases: the other facet of the ‘protective cytokine’. Pharmacol Rep 58:799–805
Engelmann GL, Boehm KD, Birchenall-Roberts MC, Ruscetti FW (1992) Transforming growth factor-beta 1 in heart development. Mech Dev 38:85–97
Mercado-Pimentel ME, Runyan RB (2007) Multiple transforming growth factor-beta isoforms and receptors function during epithelial mesenchymal cell transformation in the embryonic heart. Cells Tissues Organs 185:146–156
Lamouille S, Xu J, Derynck R (2014) Molecular mechanisms of epithelial-mesenchymal transition. Nat Rev Mol Cell Biol 15:178–196
Ramos-Mondragón R, Galindo CA, Avila G (2008) Role of TGF-β on cardiac structural and electrical remodeling. Vasc Health Risk Manag 4:1289–1300
Leask A (2015) Getting to the heart of the matter: new insights into cardiac fibrosis. Circ Res 116(7):1269–1276
Dropmann A, Dediulia T, Breitkopf-Heinlein K, Korhonen H, Janicot M, Weber SN, Thomas M, Piiper A, Bertran E, Fabregat I, Abshagen K, Hess J, Angel P, Coulouarn C, Dooley S, Meindl-Beinker NM (2016) TGF-β1 and TGF-β2 abundance in liver diseases of mice and men. Oncotarget 7(15):19499–19518
Reeves PG, Nielsen FH, Fahey GC Jr (1993) AIN-93 purified diets for laboratory rodents: final report of the American Institute of Nutrition ad hoc writing committee on the reformulation of the AIN-76A rodent diet. J Nutr 123:1939–1951
Toblli JE, Cao G, Rivas C, Giani JF, Dominici FP (2016) Intravenous iron sucrose reverses anemia-induced cardiac remodeling, prevents myocardial fibrosis, and improves cardiac function by attenuating oxidative/nitrosative stress and inflammation. Int J Cardiol 212:84–91
Romero M, Caniffi C, Bouchet G, Costa MA, Elesgaray R, Arranz C, Tomat AL (2015) Chronic treatment with atrial natriuretic peptide in spontaneously hypertensive rats: beneficial renal effects and sex differences. PLoS ONE 10(3):e0120362. doi:10.1371/journal.pone.0120362
Buege JA, Aust SD (1978) Microsomal lipid peroxidation. Methods Enzymol 52:302–310
Tietze F (1959) Enzymic method for quantitative determination of nanogram amounts of total and oxidized glutathione: applications to mammalian blood and other tissues. Anal Biochem 27:502–522
Misra HP, Fridovich I (1972) The role of superoxide anion in the autoxidation of epinephrine and a simple assay for superoxide dismutase. J Bio Chem 247:3170–3175
Maehly AC, Chance B (1954) The assay of catalases and peroxidases. Methods Biochem Anal 1:357–424
Flohé L, Gunzler A (1984) Assays of glutathione peroxidase. Methods Enzymol 105:114–121
Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein–dye binding. Anal Biochem 72:248–254
Wang HJ, Pan YX, Wang WZ, Zucker IH, Wang W (2009) NADPH oxidase-derived reactive oxygen species in skeletal muscle modulates the exercise pressor reflex. J Appl Physiol 107(2):450–459
Litterio MC, Vazquez Prieto MA, Adamo AM, Elesgaray R, Oteiza PI, Galleano M, Fraga CG (2105) (-)-Epicatechin reduces blood pressure increase in high-fructose-fed rats: effects on the determinants of nitric oxide bioavailability. J Nutr Biochem 26(7):745–751
Tomat AL, Veiras LC, Aguirre S, Fasoli H, Elesgaray R, Caniffi C, Costa MA, Arranz CT (2013) Mild zinc deficiency in male and female rats: early postnatal alterations in renal nitric oxide system and morphology. Nutrition 29:568–573. doi:10.1016/j.nut.2012.09.008
Qian J, Fulton D (2013) Post-translational regulation of endothelial nitric oxide synthase in vascular endothelium. Front Physiol 13(4):347
Intapad S, Ojeda NB, Dasinger JH, Alexander BT (2014) Sex differences in the developmental origins of cardiovascular disease. Physiology (Bethesda) 29:122–132. doi:10.1152/physiol.00045.2013
Ojeda NB, Grigore D, Yanes LL, Iliescu R, Robertson EB, Zhang H, Alexander BT (2007) Testosterone contributes to marked elevations in mean arterial pressure in adult male intrauterine growth restricted offspring. Am J Physiol Regul Integr Comp Physiol 292:R758–R763
Lopez V, Keen CL, Lanoue L (2008) Prenatal zinc deficiency: influence on heart morphology and distribution of key heart proteins in a rat model. Biol Trace Elem Res 122:238–255. doi:10.1007/s12011-007-8079-2
Pelzer T, Schumann M, Neumann M, deJager T, Stimpel M, Serfling E, Neyses L (2000) 17beta-estradiol prevents programmed cell death in cardiac myocytes. Biochem Biophys Res Commun 268:192–200
Metcalfe PD, Meldrum KK (2006) Sex differences and the role of sex steroids in renal injury. J Urol 176:15–21
McCarthy TL, Centrella M (2015) Androgen receptor activation integrates complex transcriptional effects in osteoblasts, involving the growth factors TGF-β and IGF-I, and transcription factor C/EBPδ. Gene 573:129–140. doi:10.1016/j.gene.2015.07.037
Shankar AH, Prasad AS (1998) Zinc and immune function: the biological basis of altered resistance to infection. Am J Clin Nutr 68:447S–463S
Maret W, Sandstead HH (2006) Zinc requirements and the risks and benefits of zinc supplementation. J Trace Elem Med Biol 20:3–18
Zhang Y, Tocchetti CG, Krieg T, Moens AL (2012) Oxidative and nitrosative stress in the maintenance of myocardial function. Free Radic Biol Med 53:1531–1540. doi:10.1016/j.freeradbiomed.2012.07.010
Ayala A, Muñoz MF, Argüelles S (2014) Lipid peroxidation: production, metabolism, and signaling mechanisms of malondialdehyde and 4-hydroxy-2-nonenal. Oxid Med Cell Longev. doi:10.1155/2014/360438
Langley-Evans SC, Sculley DV (2005) Programming of hepatic antioxidant capacity and oxidative injury in the ageing rat. Mech Ageing Dev 126:804–812
Strehlow K, Rotter S, Wassmann S, Adam O, Grohe C, Laufs K, Bohm M, Nickenig G (2003) Modulation of antioxidant enzyme expression and function by estrogen. Circ Res 93:170–177
Siti HN, Kamisah Y, Kamsiah J (2015) The role of oxidative stress, antioxidants and vascular inflammation in cardiovascular disease (a review). Vasc Pharmacol 71:40–56. doi:10.1016/j.vph.2015.03.005
Truong-Tran AQ, Carter J, Ruffin RE, Zalewski PD (2001) The role of zinc in caspase activation and apoptotic cell death. Biometals 14:315–330
Truong-Tran AQ, Ho LH, Chai F, Zalewski PD (2000) Cellular zinc fluxes and the regulation of apoptosis/gene-directed cell death. J Nutr 130:1459S–1466S
Yousef MI, El-Hendy HA, El-Demerdash FM, Elagamy EI (2002) Dietary zinc deficiency induced-changes in the activity of enzymes and the levels of free radicals, lipids and protein electrophoretic behavior in growing rats. Toxicology 175:223–234
Davidson SM, Duchen MR (2006) Effects of NO on mitochondrial function in cardiomyocytes: pathophysiological relevance. Cardiovasc Res 71:10–21
Massion PB, Feron O, Dessy C, Balligand JL (2003) Nitric oxide and cardiac function: ten years after, and continuing. Circ Res 93:388–398
Zaobornyj T, Ghafourifar P (2012) Strategic localization of heart mitochondrial NOS: a review of the evidence. Am J Physiol Heart Circ Physiol 303:H1283–H1293. doi:10.1152/ajpheart.00674.2011
Rastaldo R, Pagliaro P, Cappello S, Penna C, Mancardi D, Westerhof N, Losano G (2007) Nitric oxide and cardiac function. Life Sci 81:779–793
Vanhoutte PM, Zhao Y, Xu A, Leung SW (2016) Thirty years of saying NO: sources, fate, actions, and misfortunes of the endothelium-derived vasodilator mediator. Circ Res 119(2):375–396
Rafikov R, Fonseca FV, Kumar S, Pardo D, Darragh C, Elms S, Fulton D, Black SM (2011) eNOS activation and NO function: structural motifs responsible for the posttranslational control of endothelial nitric oxide synthase activity. J Endocrinol 210:271–284
Nuedling S, Kahlert S, Loebbert K, Doevendans PA, Meyer R, Vetter H, Grohé C (1999) 17 beta-estradiol stimulates expression of endothelial and inducible NO synthase in rat myocardium in vitro and in-vivo. Cardiovasc Res 43:666–674
Acknowledgements
We thank Daniela Cardelli Alcalde, Franco Brunello, Julieta Gondolesi, Agustina Castañon, Hector Fasoli, and Gabriela Noceti for technical assistance and Ana Borthwick for proofreading and language assistance. This study was supported by University of Buenos Aires: 2013/2015: 20020120200056; 2014/2017: 20020130100026BA. Consejo Nacional de Investigaciones Científicas y Técnicas (CONICET): 2011–2015; PIP-11220080101121; PIP-11220110100581.
Author contributions
MNG, FMGA, MED, GP, and LVJ involved in animal care and diet preparation. JET studied the immunohistochemistry of pro-inflammatory cytokines. FMGA, MED, and LVJ were responsible for the determination of cardiac oxidative stress. RE, MNG, FMGA, and LVJ assessed the cardiac NOS activity. MNG, ALT, and LVJ involved in cardiac eNOS mRNA expression by RT-qPCR. LVJ, GP, and AC studied cardiac eNOS, p-eNOS (Ser 1177), and TGF-β1 protein expression by Western blot analysis. LVJ, OP, and LG performed TUNEL assay. MNG, FMGA, LVJ, and ALT involved in NADPH oxidase-dependent superoxide anion production. CTA, RE, and ALT were responsible for experimental design, scientific and technical supervision, and analysis of results. LVJ, ALT, RE, and CTA drafted the manuscript.
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Juriol, L.V., Gobetto, M.N., Mendes Garrido Abregú, F. et al. Cardiac changes in apoptosis, inflammation, oxidative stress, and nitric oxide system induced by prenatal and postnatal zinc deficiency in male and female rats. Eur J Nutr 57, 569–583 (2018). https://doi.org/10.1007/s00394-016-1343-5
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DOI: https://doi.org/10.1007/s00394-016-1343-5