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Original Articles

Effects of gestational thiamine-deprivation and/or exposure to ethanol on crucial offspring rat brain enzyme activities

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Pages 2458-2466 | Received 18 Jan 2019, Accepted 11 Sep 2019, Published online: 25 Sep 2019

References

  • Ornoy A, Ergaz Z. Alcohol abuse in pregnant women: effects on the fetus and newborn, mode of action and maternal treatment. Int J Environ Res Public Health. 2010;7(2):364–379
  • Olney JW, Wozniak DF, Farber NB, et al. The enigma of fetal alcohol neurotoxicity. Ann Med. 2002;34(2):109–119.
  • Fukui Y, Sakata-Haga H. Intrauterine environment–genome interaction and children’s development (1): ethanol: a teratogen in developing brain. J Toxicol Sci. 2009;34(Suppl. 2):SP273–SP278.
  • Gil-Mohapel J, Titterness AK, Patten AR, et al. Prenatal ethanol exposure differentially affects hippocampal neurogenesis in the adolescent and aged brain. Neuroscience. 2014;273:174–188.
  • Hamilton DA, Akers KG, Rice JP, et al. Prenatal exposure to moderate levels of ethanol alters social behavior in adult rats: relationship to structural plasticity and immediate early gene expression in frontal cortex. Behav Brain Res. 2010;207(2):290–304.
  • Sutherland RJ, McDonald RJ, Savage DD. Prenatal exposure to moderate levels of ethanol can have long-lasting effects on learning and memory in adult offspring. Psychobiology. 2000;28:532–539.
  • Shea KM, Hewitt AJ, Olmstead MC, et al. Maternal ethanol consumption by pregnant guinea pigs causes neurobehavioral deficits and increases ethanol preference in offspring. Behav Pharmacol. 2012;23(1):105–112.
  • Nio E, Kogure K, Yae T, et al. The effects of maternal ethanol exposure on neurotransmission and second messenger systems: a quantitative autoradiographic study in the rat brain. Brain Res Dev Brain Res. 1991;62(1):51–60.
  • Sanjeeva Reddy TS, Ramakrishnan CV. Effects of maternal thiamine deficiency on the lipid composition of rat whole brain, gray matter and white matter. Neurochem Int. 1982;4(6):495–499.
  • Rawat AK. Developmental changes in the brain levels of neurotransmitters as influenced by maternal ethanol consumption in the rat. J Neurochem. 1977;28(6):1175–1182.
  • Stolakis V, Liapi C, Zarros A, et al. Exposure to ethanol during neurodevelopment modifies crucial offspring rat brain enzyme activities in a region-specific manner. Metab Brain Dis. 2015;30(6):1467–1477.
  • Ponnappa BC, Rubin E. Modeling alcohol’s effects on organs in animal models. Alcohol Res Health. 2000;24(2):93–104.
  • Bâ A. Alcohol and B1 vitamin deficiency-related stillbirths. J Matern Fetal Neonatal Med. 2009;22(5):452–457.
  • Matsuda T, Cooper JR. Thiamine as an integral component of brain synaptosomal membranes. Proc Natl Acad Sci USA. 1981;78(9):5886–5889.
  • Hirsch JA, Parrott J. New considerations on the neuromodulatory role of thiamine. Pharmacology. 2012;89(1–2):111–116.
  • Martin PR, Levin S, Impeduglia G, et al. Thiamine deficiency in utero alters response to ethanol in adulthood. Psychopharmacology (Berl). 1989;97(2):253–256.
  • Ferreira-Vieira TH, de Freitas-Silva DM, Ribeiro AF, et al. Perinatal thiamine restriction affects central GABA and glutamate concentrations and motor behavior of adult rat offspring. Neurosci Lett. 2016;617:182–187.
  • Nardone R, Höller Y, Storti M, et al. Thiamine deficiency induced neurochemical, neuroanatomical, and neuropsychological alterations: a reappraisal. ScientificWorldJournal. 2013;2013:309143.
  • Oliveira FA, Galan DT, Ribeiro AM, et al. Thiamine deficiency during pregnancy leads to cerebellar neuronal death in rat offspring: role of voltage-dependent K+ channels. Brain Res. 2007;1134(1):79–86.
  • Bâ A, N’Douba V, D’Almeida MA, et al. Effects of maternal thiamine deficiencies on the pyramidal and granule cells of the hippocampus of rat pups. Acta Neurobiol Exp (Wars). 2005;65(4):387–398.
  • Bâ A. Functional vulnerability of developing central nervous system to maternal thiamine deficiencies in the rat. Dev Psychobiol. 2005;47(4):408–414.
  • Fournier H, Butterworth RF. Effects of thiamine deficiency on thiamine-dependent enzymes in regions of the brain of pregnant rats and their offspring. Metab Brain Dis. 1990;5(2):77–84.
  • Plaitakis A, Hwang EC, Woert MH, et al. Effect of thiamin deficiency on brain neurotransmitter systems. Ann N Y Acad Sci. 1982;378:367–381.
  • Liapi C, Feskou I, Zarros A, et al. Effects of gestational and lactational choline deprivation on brain antioxidant status, acetylcholinesterase, (Na+,K+)- and Mg2+-ATPase activities in offspring rats. Clin Chem Lab Med. 2007;45(5):651–656.
  • Tsakiris S. Effects of l-phenylalanine on acetylcholinesterase and Na+,K+-ATPase activities in adult and aged rat brain. Mech Ageing Dev. 2001;122(5):491–501.
  • Lowry OH, Rosebrough NJ, Farr AL, et al. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951;193(1):265–275.
  • Koromilas C, Liapi C, Zarros A, et al. Inhibition of Na+,K+-ATPase in the hypothalamus, pons and cerebellum of the offspring rat due to experimentally-induced maternal hypothyroidism. J Matern Fetal Neonatal Med. 2015;28(12):1438–1444.
  • Ellman GL, Courtney KD, Andres Jr V, et al. A new and rapid colorimetric determination of acetylcholinesterase activity. Biochem Pharmacol. 1961;7:88–95
  • Bowler K, Tirri R. The temperature characteristics of synaptic membrane ATPases from immature and adult rat brain. J Neurochem. 1974;23(3):611–613.
  • Bâ A. Effects of thiamine deficiency on food intake and body weight increment in adult female and growing rats. Behav Pharmacol. 2012;23(5–6):575–581.
  • Zarros A, Liapi C, Al-Humadi H, et al. Experimentally-induced Wernicke’s encephalopathy modifies crucial rat brain parameters: the importance of Na+,K+-ATPase and a potentially neuroprotective role for antioxidant supplementation. Metab Brain Dis. 2013;28(3):387–396.
  • Alspach JD, Ingraham LL. Inhibition of acetylcholinesterase by thiamine. A structure–function study. J Med Chem. 1977;20(1):161–164.
  • Kulkarni AB, Gaitonde BB. Effects of early thiamin deficiency and subsequent rehabilitation on the cholinergic system in developing rat brain. J Nutr Sci Vitaminol (Tokyo). 1983;29(2):217–225.
  • Kojima H, Mineta-Kitajima R, Saitoh-Harada N, et al. Prenatal ethanol exposure affects the activity and mRNA expression of neuronal membrane enzymes in rat offspring. Life Sci. 1994;55(18):1433–1442.
  • Ledig M, Tholey G, Kopp P, et al. An experimental study of fetal alcohol syndrome in the rat: biochemical modifications in brain and liver. Alcohol Alcohol. 1989;24(3):231–240.
  • Rudeen PK, Guerri C. The effects of alcohol exposure in utero on acetylcholinesterase, Na/K-ATPase and Ca-ATPase activities in six regions of rat brain. Alcohol Alcohol. 1985;20(4):417–425.
  • Marques A, Guerri C. Effects of ethanol on rat brain (Na + K)ATPase from native and delipidized synaptic membranes. Biochem Pharmacol. 1988;37(4):601–606.
  • Aloia RC, Paxton J, Daviau JS, et al. Effect of chronic alcohol consumption on rat brain microsome lipid composition, membrane fluidity and Na+–K+-ATPase activity. Life Sci. 1985;36(10):1003–1017.
  • Druse MJ, Kelly GM. Maternal ethanol consumption: effect on (Na+–K+)-ATPase in rat offspring. Alcohol. 1985;2(5):667–670.
  • Ledig M, Kopp P, Mandel P. Effect of ethanol on adenosine triphosphatase and enolase activities in rat brain and in cultured nerve cells. Neurochem Res. 1985;10(9):1311–1324.
  • Moloney B, Leonard BE. Pre-natal and post-natal effects of alcohol in the rat: II. Changes in gamma-aminobutyric acid concentration and adenosine triphosphatase activity in the brain. Alcohol Alcohol. 1984;19(2):137–140.
  • Kalant H, Rangaraj N. Interaction of catecholamines and ethanol on the kinetics of rat brain (Na++K+)-ATPase. Eur J Pharmacol. 1981;70(2):157–166.
  • Syapin PJ, Alkana RL. Ethanol-induced inhibition of mouse brain adenosine triphosphatase activities: lack of interaction with norepinephrine in vitro. Alcohol Clin Exp Res. 1986;10(6):635–640.
  • Rangaraj N, Kalant H. Acute and chronic catecholamine-ethanol interactions on rat brain (Na++K+)-ATPase. Pharmacol Biochem Behav. 1980;13(Suppl. 1):183–189.
  • Mousseau DD, Rao VL, Butterworth RF. Na+,K+-ATPase activity is selectively increased in thalamus in thiamine deficiency prior to the appearance of neurological symptoms. Eur J Pharmacol. 1996;300(3):191–196.
  • Matsuda T, Iwata H. Decrease of high affinity ouabain binding in rat cerebellum and hypothalamus by thiamin deficiency. Brain Res. 1987;437(2):375–378.
  • Meyer EM, Cooper JR. Correlations between Na+,K+-ATPase activity and acetylcholine release in rat cortical synaptosomes. J Neurochem. 1981;36(2):467–475.
  • Johnson JH, Crider BP. Increases in Na+,K+-ATPase activity of erythrocytes and skeletal muscle after chronic ethanol consumption: evidence for reduced efficiency of the enzyme. Proc Natl Acad Sci USA. 1989;86(20):7857–7860.

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