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Journal of Immunology Research
Volume 2016, Article ID 9151607, 9 pages
http://dx.doi.org/10.1155/2016/9151607
Research Article

Influence of the Expression of Inflammatory Markers on Kidney after Fetal Programming in an Experimental Model of Renal Failure

1Discipline of General Pathology, Institute of Biological and Natural Sciences, Federal University of Triângulo Mineiro, Uberaba, MG, Brazil
2Department of Health Sciences, Lavras Federal University, Lavras, MG, Brazil
3Discipline of Physiology, Institute of Biological and Natural Sciences, Federal University of Triângulo Mineiro, Uberaba, MG, Brazil
4Nephrology Division, Federal University of São Paulo (UNIFESP), São Paulo, SP, Brazil
5Department of Immunology, Institute of Biomedical Sciences IV, University of São Paulo (USP), São Paulo, SP, Brazil
6Department of General Pathology, Institute of Tropical Pathology and Public Health, Federal University of Goiás, Goiânia, GO, Brazil

Received 20 August 2016; Revised 25 October 2016; Accepted 8 November 2016

Academic Editor: Margarete D. Bagatini

Copyright © 2016 Carlos Donizete Pereira Júnior et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

Linked References

  1. D. J. P. Barker and C. Osmond, “Infant mortality, childhood nutrition, and ischaemic heart disease in England and Wales,” The Lancet, vol. 327, no. 8489, pp. 1077–1081, 1986. View at Publisher · View at Google Scholar · View at Scopus
  2. N. B. Ojeda, D. Grigore, and B. T. Alexander, “Intrauterine growth restriction: fetal programming of hypertension and kidney disease,” Advances in Chronic Kidney Disease, vol. 15, no. 2, pp. 101–106, 2008. View at Publisher · View at Google Scholar · View at Scopus
  3. J. Yan, X. Li, R. Su, K. Zhang, and H. Yang, “Long-term effects of maternal diabetes on blood pressure and renal function in rat male offspring,” PLoS ONE, vol. 9, no. 2, Article ID e88269, 2014. View at Publisher · View at Google Scholar · View at Scopus
  4. D. C. Damasceno, G. T. Volpato, Y. K. Sinzato et al., “Genotoxicity and fetal abnormality in streptozotocin-induced diabetic rats exposed to cigarette smoke prior to and during pregnancy,” Experimental and Clinical Endocrinology and Diabetes, vol. 119, no. 9, pp. 549–553, 2011. View at Publisher · View at Google Scholar · View at Scopus
  5. S. O. Rocha, G. N. Gomes, A. L. L. Forti et al., “Long-term effects of maternal diabetes on vascular reactivity and renal function in rat male offspring,” Pediatric Research, vol. 58, no. 6, pp. 1274–1279, 2005. View at Publisher · View at Google Scholar · View at Scopus
  6. P. H. O. Lima, Y. K. Sinzato, R. B. Gelaleti, I. M. P. Calderon, M. V. C. Rudge, and D. C. Damasceno, “Genotoxicity evaluation in severe or mild diabetic pregnancy in laboratory animals,” Experimental and Clinical Endocrinology and Diabetes, vol. 120, no. 5, pp. 303–307, 2012. View at Publisher · View at Google Scholar · View at Scopus
  7. M. S. Palier, “Acute renal failure: Controversies, clinical trials, and future directions,” Seminars in Nephrology, vol. 18, no. 5, pp. 482–489, 1998. View at Google Scholar · View at Scopus
  8. C. S. Yajnik and U. S. Deshmukh, “Fetal programming: maternal nutrition and role of one-carbon metabolism,” Reviews in Endocrine and Metabolic Disorders, vol. 13, no. 2, pp. 121–127, 2012. View at Publisher · View at Google Scholar · View at Scopus
  9. T. Radaelli, A. Varastehpour, P. Catalano, and S. Hauguel-de Mouzon, “Gestational diabetes induces placental genes for chronic stress and inflammatory pathways,” Diabetes, vol. 52, no. 12, pp. 2951–2958, 2003. View at Publisher · View at Google Scholar · View at Scopus
  10. C. F. Rueda-Clausen, P. López-Jaramillo, C. Luengas, M. del Pilar Oubiña, V. Cachofeiro, and V. Lahera, “Inflammation but not endothelial dysfunction is associated with the severity of coronary artery disease in dyslipidemic subjects,” Mediators of Inflammation, vol. 2009, Article ID 469169, 8 pages, 2009. View at Publisher · View at Google Scholar · View at Scopus
  11. J.-P. Albertini, P. Valensi, B. Lormeau et al., “Elevated concentrations of soluble E-selectin and vascular cell adhesion molecule-1 in NIDDM: effect of intensive insulin treatment,” Diabetes Care, vol. 21, no. 6, pp. 1008–1013, 1998. View at Publisher · View at Google Scholar · View at Scopus
  12. E. Leinonen, E. Hurt-Camejo, O. Wiklund, L. M. Hultén, A. Hiukka, and M.-R. Taskinen, “Insulin resistance and adiposity correlate with acute-phase reaction and soluble cell adhesion molecules in type 2 diabetes,” Atherosclerosis, vol. 166, no. 2, pp. 387–394, 2003. View at Publisher · View at Google Scholar · View at Scopus
  13. W. Wojakowski and J. Gminski, “Soluble ICAM-1, VCAM-1 and E-selectin in children from families with high risk of atherosclerosis,” International Journal of Molecular Medicine, vol. 7, no. 2, pp. 181–185, 2001. View at Google Scholar · View at Scopus
  14. F. K. Marcondes, F. J. Bianchi, and A. P. Tanno, “Determination of the estrous cycle phases of rats: some helpful considerations,” Brazilian Journal of Biology, vol. 62, no. 4, pp. 609–614, 2002. View at Publisher · View at Google Scholar · View at Scopus
  15. A. Gupta, V. Puri, R. Sharma, and S. Puri, “Folic acid induces acute renal failure (ARF) by enhancing renal prooxidant state,” Experimental and Toxicologic Pathology, vol. 64, no. 3, pp. 225–232, 2012. View at Publisher · View at Google Scholar · View at Scopus
  16. M. Correa-Costa, M. A. Landgraf, M. F. Cavanal et al., “Inflammatory milieu as an early marker of kidney injury in offspring rats from diabetic mothers,” European Journal of Pharmacology, vol. 689, no. 1–3, pp. 233–240, 2012. View at Publisher · View at Google Scholar · View at Scopus
  17. R. Muniyappa, M. Montagnani, K. K. Koh, and M. J. Quon, “Cardiovascular actions of insulin,” Endocrine Reviews, vol. 28, no. 5, pp. 463–491, 2007. View at Publisher · View at Google Scholar · View at Scopus
  18. C. M. Turner, N. Arulkumaran, M. Singer, R. J. Unwin, and F. W. Tam, “Is the inflammasome a potential therapeutic target in renal disease?” BMC Nephrology, vol. 15, no. 1, article 21, 2014. View at Publisher · View at Google Scholar · View at Scopus
  19. E. K. Grishman, P. C. White, and R. C. Savani, “Toll-like receptors, the NLRP3 inflammasome, and interleukin-1β in the development and progression of type 1 diabetes,” Pediatric Research, vol. 71, no. 6, pp. 626–632, 2012. View at Publisher · View at Google Scholar · View at Scopus
  20. B. S. Dellamea, C. B. Leitão, R. Friedman, and L. H. Canani, “Nitric oxide system and diabetic nephropathy,” Diabetology and Metabolic Syndrome, vol. 6, no. 1, article 17, 2014. View at Publisher · View at Google Scholar · View at Scopus
  21. J. Y. Youn, L. Gao, and H. Cai, “The p47 phox- and NADPH oxidase organiser 1 (NOXO1)-dependent activation of NADPH oxidase 1 (NOX1) mediates endothelial nitric oxide synthase (eNOS) uncoupling and endothelial dysfunction in a streptozotocin-induced murine model of diabetes,” Diabetologia, vol. 55, no. 7, pp. 2069–2079, 2012. View at Publisher · View at Google Scholar · View at Scopus
  22. L. J. Stallons, R. M. Whitaker, and R. G. Schnellmann, “Suppressed mitochondrial biogenesis in folic acid-induced acute kidney injury and early fibrosis,” Toxicology Letters, vol. 224, no. 3, pp. 326–332, 2014. View at Publisher · View at Google Scholar · View at Scopus
  23. S. Chen, S. W. Hong, M. C. I.-D. La Cruz, M. Isono, A. Casaretto, and F. N. Ziyadeh, “The key role of the transforming growth factor-β system in the pathogenesis of diabetic nephropathy,” Renal Failure, vol. 23, no. 3-4, pp. 471–481, 2001. View at Publisher · View at Google Scholar · View at Scopus
  24. H. S. Lee, “Mechanisms and consequences of TGF-β overexpression by podocytes in progressive podocyte disease,” Cell and Tissue Research, vol. 347, no. 1, pp. 129–140, 2012. View at Publisher · View at Google Scholar · View at Scopus
  25. S. M. Ka, Y. C. Yeh, X. R. Huang et al., “Kidney-targeting Smad7 gene transfer inhibits renal TGF-β/MAD homologue (SMAD) and nuclear factor κb (NF-κB) signalling pathways, and improves diabetic nephropathy in mice,” Diabetologia, vol. 55, no. 2, pp. 509–519, 2012. View at Publisher · View at Google Scholar · View at Scopus
  26. F. N. Ziyadeh, “Mediators of diabetic renal disease: the case for TGF-β as the major mediator,” Journal of the American Society of Nephrology, vol. 15, no. 1, supplement, pp. S55–S57, 2004. View at Publisher · View at Google Scholar · View at Scopus
  27. B. Wan, L. Hao, Y. Qiu et al., “Blocking tumor necrosis factor-α inhibits folic acid-induced acute renal failure,” Experimental and Molecular Pathology, vol. 81, no. 3, pp. 211–216, 2006. View at Publisher · View at Google Scholar · View at Scopus
  28. G. Gao, B. Zhang, G. Ramesh et al., “TNF-α mediates increased susceptibility to ischemic AKI in diabetes,” American Journal of Physiology—Renal Physiology, vol. 304, no. 5, pp. F515–F521, 2013. View at Publisher · View at Google Scholar · View at Scopus
  29. K. L. Ma, Y. Zhang, J. Liu et al., “Establishment of an inflamed animal model of diabetic nephropathy,” International Journal of Biological Sciences, vol. 10, no. 2, pp. 149–159, 2014. View at Publisher · View at Google Scholar · View at Scopus
  30. J. M. Walsh, C. A. McGowan, J. A. Byrne, A. Rath, and F. M. McAuliffe, “The association between TNF-α and insulin resistance in euglycemic women,” Cytokine, vol. 64, no. 1, pp. 208–212, 2013. View at Publisher · View at Google Scholar · View at Scopus
  31. H.-T. Yuan, X.-Z. Li, J. E. Pitera, D. A. Long, and A. S. Woolf, “Peritubular capillary loss after mouse acute nephrotoxicity correlates with down-regulation of vascular endothelial growth factor-A and hypoxia-inducible factor-1 α,” American Journal of Pathology, vol. 163, no. 6, pp. 2289–2301, 2003. View at Publisher · View at Google Scholar · View at Scopus
  32. M. Mironidou-Tzouveleki, S. Tsartsalis, and C. Tomos, “Vascular endothelial growth factor (VEGF) in the pathogenesis of diabetic nephropathy of type 1 diabetes mellitus,” Current Drug Targets, vol. 12, no. 1, pp. 107–114, 2011. View at Publisher · View at Google Scholar · View at Scopus
  33. S. Chen and F. N. Ziyadeh, “Vascular endothelial growth factor and diabetic nephropathy,” Current Diabetes Reports, vol. 8, no. 6, pp. 470–476, 2008. View at Publisher · View at Google Scholar · View at Scopus
  34. K. S. Yang, J. H. Lim, T. W. Kim et al., “Vascular endothelial growth factor-receptor 1 inhibition aggravates diabetic nephropathy through eNOS signaling pathway in db/db mice,” PLoS ONE, vol. 9, no. 4, Article ID e94540, 2014. View at Publisher · View at Google Scholar · View at Scopus
  35. D. J. P. Barker, T. Forsén, A. Uutela, C. Osmond, and J. G. Eriksson, “Size at birth and resilience to effects of poor living conditions in adult life: longitudinal study,” British Medical Journal, vol. 323, no. 7324, pp. 1273–1276, 2001. View at Publisher · View at Google Scholar · View at Scopus
  36. J. W. Rich-Edwards, M. J. Stampfer, J. E. Manson et al., “Birth weight and risk of cardiovascular disease in a cohort of women followed up since 1976,” British Medical Journal, vol. 315, no. 7105, pp. 396–400, 1997. View at Publisher · View at Google Scholar · View at Scopus
  37. G. M. Weisz and W. R. Albury, “More on fetal programming of adult metabolic disorders in holocaust survivors,” The Israel Medical Association Journal, vol. 18, no. 5, pp. 250–251, 2016. View at Google Scholar
  38. G. M. Weisz and W. R. Albury, “Osteoporosis in survivors of early life starvation,” Australian Journal of Primary Health, vol. 19, no. 1, pp. 3–6, 2013. View at Publisher · View at Google Scholar · View at Scopus
  39. L. Keinan-Boker, H. Shasha-Lavsky, S. Eilat-Zanani, A. Edri-Shur, and S. M. Shasha, “Chronic health conditions in Jewish Holocaust survivors born during world war II,” Israel Medical Association Journal, vol. 17, no. 4, pp. 206–212, 2015. View at Google Scholar · View at Scopus