Morphological and functional aspects of acute kidney injury after fetal programing in the offspring of diabetic rats

References

• Magaton A, Gil FZ, Casarini DE, et al. Maternal diabetes mellitus – early consequences for the offspring. Pediatr Nephrol 2007;22:37–43
   PubMedGoogle Scholar
• Rocha SO, Gomes GN, Forti AL, et al. Long-term effects of maternal diabetes on vascular reactivity and renal function in rat male offspring. Pediatr Res 2005;58:1274–9
   PubMedGoogle Scholar
• Gomes GN, Gil FZ. Prenatally programmed hypertension: role of maternal diabetes. Braz J Med Biol Res 2011;44:899–904
   PubMedGoogle Scholar
• Hokke1 SN, Armitage1 JA, Puelles VG, et al. Altered ureteric branching morphogenesis and nephron endowment in offspring of diabetic and insulin-treated pregnancy. PLoS One 2013;8:81–9
   Google Scholar
• Amri K, Freund N, Vilar J, et al. Adverse effects of hyperglycemia on kidney development in rats: in vivo and in vitro studies. Diabetes 1999;48:2240–5
   PubMed Web of Science ®Google Scholar
• Lucas SR, Costa Silva VL, Miraglia SM, Zaladek Gil F. Functional and morphometric evaluation of offspring kidney after intrauterine undernutrition. Pediatr Nephrol 1997;11:719–23
   PubMedGoogle Scholar
• Paller MS. Acute renal failure: controversies, clinical trials, and future directions. Seminar Nephrol 1998;18:482–9
   PubMedGoogle Scholar
• Gupta A, Puri V, Sharma R, Puri S. Folic acid induces acute renal failure (ARF) by enhancing renal prooxidant state. Exp Toxicol Pathol 2012;64:225–32
   PubMedGoogle Scholar
• Yan J, Li X, Su R, et al. Long-term effects of maternal diabetes on blood pressure and renal function in rat male offspring. PLoS One 2014;9:e88269
   Google Scholar
• Wichi RB, Souza SB, Casarini DE, et al. Increased blood pressure in the offspring of diabetic mothers. Am J Physiol Reg Integrat Compar Physiol 2005;288:R1129–33
   Google Scholar
• Rocco L, Gil FZ, da Fonseca Pletiskaitz TM, et al. Effect of sodium overload on renal function of offspring from diabetic mothers. Pediatr Nephrol 2008;23:2053–60
   PubMedGoogle Scholar
• Bernardis LL, Patterson BD. Correlation between ‘Lee index' and carcass fat content in weanling and adult female rats with hypothalamic lesions. J Endocrinol 1968;40:527–8
   PubMed Web of Science ®Google Scholar
• Holemans K, Gerber RT, Meurrens K, et al. Streptozotocin diabetes in the pregnant rat induces cardiovascular dysfunction in adult offspring. Diabetologia 1999;42:81–9
   PubMed Web of Science ®Google Scholar
• Joannidis M, Bonn G, Pfaller W. Lipid peroxidation – an initial event in experimental acute renal failure. Renal Physiol Biochem 1989;12:47–55
   PubMedGoogle Scholar
• Zimmermann HD, Maykemper B, Dieker P. Intra- and extrarenal vascular changes in the acute renal failure of the rat caused by high-dose folic acid injection. Virchows Archiv A Patholog Anatomy Histol 1977;376:47–73
   PubMedGoogle Scholar
• Moritz KM, Dodic M, Wintour EM. Kidney development and the fetal programming of adult disease. Bioessays 2003;25:212–20
   PubMed Web of Science ®Google Scholar
• Dickinson H, Walker DW, Wintour EM, Moritz K. Maternal dexamethasone treatment at midgestation reduces nephron number and alters renal gene expression in the fetal spiny mouse. Am J Physiol Reg Integrat Compar Physiol 2007;292:R453–61
   Google Scholar
• Urbschat A, Obermuller N, Haferkamp A. Biomarkers of kidney injury. Biomarkers 2011;16:S22–30
   PubMed Web of Science ®Google Scholar
• Dall'Ago P, Silva VO, De Angelis KL, et al. Reflex control of arterial pressure and heart rate in short-term streptozotocin diabetic rats. Brazilian journal of medical and biological research 2002;35:843–849
   PubMedGoogle Scholar
• Akiyama N, Okumura K, Watanabe Y, et al. Altered acetylcholine and norepinephrine concentrations in diabetic rat hearts. Role of parasympathetic nervous system in diabetic cardiomyopathy. Diabetes 1989;38:231–6
   PubMedGoogle Scholar
• Tomlinson KC, Gardiner SM, Hebden RA, Bennett T. Functional consequences of streptozotocin-induced diabetes mellitus, with particular reference to the cardiovascular system. Pharmacol Rev 1992;44:103–50
   PubMed Web of Science ®Google Scholar
• Eckberg DL, Harkins SW, Fritsch JM, et al. Baroreflex control of plasma norepinephrine and heart period in healthy subjects and diabetic patients. J Clin Invest 1986;78:366–74
   PubMedGoogle Scholar
• McDowell TS, Chapleau MW, Hajduczok G, Abboud FM. Baroreflex dysfunction in diabetes mellitus. I. Selective impairment of parasympathetic control of heart rate. Am J Physiol 1994;266:H235–43
   PubMed Web of Science ®Google Scholar
• McDowell TS, Hajduczok G, Abboud FM, Chapleau MW. Baroreflex dysfunction in diabetes mellitus. II. Site of baroreflex impairment in diabetic rabbits. Am J Physiol 1994;266:H244–9
   Google Scholar
• Maeda CY, Fernandes TG, Timm HB, Irigoyen MC. Autonomic dysfunction in short-term experimental diabetes. Hypertension 1995;26:1100–4
   PubMed Web of Science ®Google Scholar
• Schaan BD, Maeda CY, Timm HB, et al. Time course of changes in heart rate and blood pressure variability in streptozotocin-induced diabetic rats treated with insulin. Brazil J Med Biol Res 1997;30:1081–6
   PubMedGoogle Scholar
• Dall'Ago P, Fernandes TG, Machado UF, et al. Baroreflex and chemoreflex dysfunction in streptozotocin-diabetic rats. Brazil J Med Biol Res 1997;30:119–24
   PubMed Web of Science ®Google Scholar
• Furuland H, Linde T, Englund A, Wikstrom B. Heart rate variability is decreased in chronic kidney disease but may improve with hemoglobin normalization. J Nephrol 2008;21:45–52
   PubMed Web of Science ®Google Scholar
• Pumprla J, Howorka K, Groves D, et al. Functional assessment of heart rate variability: physiological basis and practical applications. Int J Cardiol 2002;84:1–14
   PubMed Web of Science ®Google Scholar
• Schein PS, Loftus S. Streptozotocin: depression of mouse liver pyridine nucleotides. Cancer Res 1968;28:1501–6
   PubMedGoogle Scholar