The effect of pre-eclampsia-like syndrome induced by L-NAME on learning and memory and hippocampal glucocorticoid receptor expression: A rat model

References

• Magee LA, Pels A, Helewa M, et al. Diagnosis, evaluation, and management of the hypertensive disorders of pregnancy: executive summary. J Obstet Gynaecol Can 2014;36:416–41.
   PubMedGoogle Scholar
• Boger RH, Diemert A, Schwedhelm E, et al. The role of nitric oxide synthase inhibition by asymmetric dimethylarginine in the pathophysiology of preeclampsia. Gynecol Obstet Invest 2010;69:1–13.
   PubMed Web of Science ®Google Scholar
• Pereza N, Peterlin B, Volk M, et al. A critical update on endothelial nitric oxide synthase gene variations in women with idiopathic recurrent spontaneous abortion: genetic association study, systematic review and meta-analyses. Mol Hum Reprod 2015;21:466–78.
   PubMed Web of Science ®Google Scholar
• Yallampalli C, Garfield RE. Inhibition of nitric oxide synthesis in rats during pregnancy produces signs similar to those of preeclampsia. Am J Obstet Gynecol 1993;169:1316–20.
   PubMed Web of Science ®Google Scholar
• Baylis C, Mitruka B, Deng A. Chronic blockade of nitric oxide synthesis in the rat produces systemic hypertension and glomerular damage. J Clin Invest 1992;90:278–81.
   PubMed Web of Science ®Google Scholar
• Molnar M, Suto T, Toth T, et al. Prolonged blockade of nitric oxide synthesis in gravid rats produces sustained hypertension, proteinuria, thrombocytopenia, and intrauterine growth retardation. Am J Obstet Gynecol 1994;170:1458–66.
   PubMed Web of Science ®Google Scholar
• Salas SP, Altermatt F, Campos M, et al. Effects of long-term nitric oxide synthesis inhibition on plasma volume expansion and fetal growth in the pregnant rat. Hypertension 1995;26:1019–23.
   PubMed Web of Science ®Google Scholar
• Helmbrecht GD, Farhat MY, Lochbaum L, et al. L-arginine reverses the adverse pregnancy changes induced by nitric oxide synthase inhibition in the rat. Am J Obstet Gynecol 1996;175:800–5.
   PubMed Web of Science ®Google Scholar
• Ortiz-Mantilla S, Choudhury N, Leevers H, et al. Understanding language and cognitive deficits in very low birth weight children. Dev Psychobiol 2008;50:107–26.
   PubMed Web of Science ®Google Scholar
• Sluncheva B, Vakrilova L, Emilova Z, et al. Prevention of brain hemorrhage in infants with low and extremely low birth weight and infants treated with surfactants. Late observation. Akush Ginekol (Sofiia) 2006;45:34–8.
   PubMedGoogle Scholar
• Elgen I, Sommerfelt K, Ellertsen B. Cognitive performance in a low birth weight cohort at 5 and 11 years of age. Pediatr Neurol 2003;29:111–6.
   PubMed Web of Science ®Google Scholar
• Rickards AL, Kelly EA, Doyle LW, et al. Cognition, academic progress, behavior and self-concept at 14 years of very low birth weight children. J Dev Behav Pediatr 2001;22:11–8.
   PubMed Web of Science ®Google Scholar
• Wu CS, Sun Y, Vestergaard M, et al. Preeclampsia and risk for epilepsy in offspring. Pediatrics 2008;122:1072–8.
   PubMed Web of Science ®Google Scholar
• Liu X, Zhao W, Liu H, et al. Developmental and functional brain impairment in offspring from preeclampsia-like rats. Mol Neurobiol 2016;53:1009–19.
   PubMed Web of Science ®Google Scholar
• Morris RG, Garrud P, Rawlins JN, et al. Place navigation impaired in rats with hippocampal lesions. Nature 1982;297:681–3.
   PubMed Web of Science ®Google Scholar
• D’Hooge R, De Deyn PP. Applications of the Morris water maze in the study of learning and memory. Brain Res Brain Res Rev 2001;36:60–90.
   PubMed Web of Science ®Google Scholar
• Hogg K, Blair JD, McFadden DE, et al. Early onset pre-eclampsia is associated with altered DNA methylation of cortisol-signalling and steroidogenic genes in the placenta. PLoS One 2013;8:e62969.
   PubMed Web of Science ®Google Scholar
• Aufdenblatten M, Baumann M, Raio L, et al. Prematurity is related to high placental cortisol in preeclampsia. Pediatr Res 2009;65:198–202.
   PubMed Web of Science ®Google Scholar
• Vianna P, Bauer ME, Dornfeld D, et al. Distress conditions during pregnancy may lead to pre-eclampsia by increasing cortisol levels and altering lymphocyte sensitivity to glucocorticoids. Med Hypotheses 2011;77:188–91.
   PubMed Web of Science ®Google Scholar
• Palma-Gudiel H, Cordova-Palomera A, Leza JC, et al. Glucocorticoid receptor gene (NR3C1) methylation processes as mediators of early adversity in stress-related disorders causality: a critical review. Neurosci Biobehav Rev 2015;55:520–35.
   PubMed Web of Science ®Google Scholar
• Lu NZ, Wardell SE, Burnstein KL, et al. International Union of Pharmacology. LXV. The pharmacology and classification of the nuclear receptor superfamily: glucocorticoid, mineralocorticoid, progesterone, and androgen receptors. Pharmacol Rev 2006;58:782–97.
   Google Scholar
• Zou Y, Zuo Q, Huang S, et al. Resveratrol inhibits trophoblast apoptosis through oxidative stress in preeclampsia-model rats. Molecules 2014;19:20570–9.
   PubMed Web of Science ®Google Scholar
• Tian M, Zhang Y, Liu Z, et al. The PD-1/PD-L1 inhibitory pathway is altered in pre-eclampsia and regulates T cell responses in pre-eclamptic rats. Sci Rep 2016;6:27683.
   PubMed Web of Science ®Google Scholar
• Teng RJ, Wu TJ, Sharma R, et al. Early neonatal hypotension in premature infants born to preeclamptic mothers. J Perinatol 2006;26:471–5.
   PubMed Web of Science ®Google Scholar
• Moonen RM, Huizing MJ, Cavallaro G, et al. Plasma levels of dimethylarginines in preterm very low birth weight neonates: its relation with perinatal factors and short-term outcome. Int J Mol Sci 2015;16:19–39.
   Web of Science ®Google Scholar
• DJ Barker,Osmond C. Low birth weight and hypertension. BMJ 1988;297:134–5.
   PubMed Web of Science ®Google Scholar
• Barker DJ, Osmond C, Golding J, et al. Growth in utero, blood pressure in childhood and adult life, and mortality from cardiovascular disease. BMJ 1989;298:564–7.
   PubMed Web of Science ®Google Scholar
• Mathew V, Ayyar SV. Developmental origins of adult diseases. Indian J Endocrinol Metab 2012;16:532–41.
   PubMedGoogle Scholar
• Grantham-McGregor SM, Lira PI, Ashworth A, et al. The development of low birth weight term infants and the effects of the environment in northeast Brazil. J Pediatr 1998;132:661–6.
   PubMed Web of Science ®Google Scholar
• Vieau D, Sebaai N, Leonhardt M, et al. HPA axis programming by maternal undernutrition in the male rat offspring. Psychoneuroendocrinology 2007;32 Suppl 1:S16–20.
   PubMed Web of Science ®Google Scholar
• Haas DM, Dantzer J, Lehmann AS, et al. The impact of glucocorticoid polymorphisms on markers of neonatal respiratory disease after antenatal betamethasone administration. Am J Obstet Gynecol 2013;208:215.e211–6.
   PubMed Web of Science ®Google Scholar
• Xiong F, Zhang L. Role of the hypothalamic-pituitary-adrenal axis in developmental programming of health and disease. Front Neuroendocrinol 2013;34:27–46.
   PubMed Web of Science ®Google Scholar
• Chen YF, Li YF, Chen X, et al. Neuropsychiatric disorders and cognitive dysfunction in patients with Cushing’s disease. Chin Med J (Engl) 2013;126:3156–60.
   PubMed Web of Science ®Google Scholar
• Starkman MN, Giordani B, Berent S, et al. Elevated cortisol levels in Cushing’s disease are associated with cognitive decrements. Psychosom Med 2001;63:985–93.
   PubMed Web of Science ®Google Scholar
• Forget H, Lacroix A, Cohen H. Persistent cognitive impairment following surgical treatment of Cushing’s syndrome. Psychoneuroendocrinology 2002;27:367–83.
   PubMed Web of Science ®Google Scholar
• Grillon C, Smith K, Haynos A, et al. Deficits in hippocampus-mediated Pavlovian conditioning in endogenous hypercortisolism. Biol Psychiatry 2004;56:837–43.
   PubMed Web of Science ®Google Scholar
• Kim JJ, Yoon KS. Stress: metaplastic effects in the hippocampus. Trends Neurosci 1998;21:505–9.
   PubMed Web of Science ®Google Scholar
• Donley MP, Schulkin J, Rosen JB. Glucocorticoid receptor antagonism in the basolateral amygdala and ventral hippocampus interferes with long-term memory of contextual fear. Behav Brain Res 2005;164:197–205.
   PubMed Web of Science ®Google Scholar
• Roozendaal B, McReynolds JR, McGaugh JL. The basolateral amygdala interacts with the medial prefrontal cortex in regulating glucocorticoid effects on working memory impairment. J Neurosci 2004;24:1385–92.
   PubMed Web of Science ®Google Scholar
• Lupien SJ, Buss C, Schramek TE, et al. Hormetic influence of glucocorticoids on human memory. Nonlinearity Biol Toxicol Med 2005;3:23–56.
   PubMedGoogle Scholar
• Conrad CD. The relationship between acute glucocorticoid levels and hippocampal function depends upon task aversiveness and memory processing stage. Nonlinearity Biol Toxicol Med 2005;3:57–78.
   PubMedGoogle Scholar
• Smith SM, Vale WW. The role of the hypothalamic-pituitary-adrenal axis in neuroendocrine responses to stress. Dialogues Clin Neurosci 2006;8:383–95.
   PubMedGoogle Scholar