Abstract
Fetus and neonate growth retardation is one of the main characteristics of fetal alcohol syndrome (FAS) disorders. Ethanol can be transferred to the fetus through the placenta and to newborns through suckling. This study was designed to investigate the effects of consuming different doses of ethanol during lactation on enzymatic and tissue changes and growth indices in suckling rat pups. Forty-five lactating Wistar rats with nine lactating pups each were randomly allocated to three treatment groups. The two treatment groups received 2 and 4 % v/v ethanol, while the third group was the control on distilled water for 24 days. On day 25 after birth, 30 newborn rats were randomly selected from each group and serum activity of liver enzyme markers, lactate dehydrogenase, blood urea nitrogen, creatinine, and creatine phosphokinase enzymes was measured. Pathological examinations were performed on brain, liver, and kidney tissues. The obtained data was analyzed using one-way analysis of variance (ANOVA) and Dunnett’s tests. Enzymatic activity of lactate dehydrogenase and creatinine was significantly (p < 0.05) higher in the rats that received alcohol as compared to the control. In histopathological examinations, different injuries were observed in kidney, liver, and brain tissues of suckling pups exposed to 4 % v/v ethanol. Consumption of alcohol in the lactating rats can cause irreparable effects on the suckling neonate.
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References
Agarwal DP (2001) Genetic polymorphisms of alcohol metabolizing enzymes. Pathol Biol 49(9):703–9
Aros S, Mills JL, Iniguez G, Avila A, Conley MR, Troendle J et al (2011) Effects of prenatal ethanol exposure on postnatal growth and the insulin-like growth factor axis. Horm Res Paediatr 75(3):166–173
Azara CR, Maia IC, Rangel CN, Silva-Neto MA, Serpa RF, De Jesus EF et al (2008) Ethanol intake during lactation alters milk nutrient composition and growth and mineral status of rat pups. Biol Res 41(3):317–330
Azorin I, Portoles M, Marin P, Lazaro-Dieguez F, Megias L, Egea G et al (2004) Prenatal ethanol exposure alters the cytoskeleton and induces glycoprotein micro heterogeneity in rat newborn hepatocytes. Alcohol Alcohol 39(3):203–212
Bolkent S, Arda-Pirincci P, Bolkent S, Yanardag R, Tunali S, Yildirim S (2006) Influence of zinc sulfate intake on acute ethanol-induced liver injury in rats. World J Gastroenterol 12(27):4345–4351
Brzoska MM, Moniuszko-Jakoniuk J, Piłat-Marcinkiewicz B, Sawicki B (2003) Liver and kidney function and histology in rats exposed to cadmium and ethanol. Alcohol Alcohol 38(1):2–10
Daunais JB, Davenport AT, Helms CM, Gonzales SW, Hemby SE, Friedman DP, Farro JP, Baker EJ, Grant KA (2014) Monkey alcohol tissue research resource: banking tissues for alcohol research. Alcohol Clin Exp Res 38(7):1973–81
Dufour DR (2008) Liver disease. In: Burtis CA, Ashwood ER, Bruns DE, Sawyer BG (eds) Tietz fundamentals of clinical chemistry, 6th edn. W.B. Saunders, St. Louis, pp 675–695
Fiuza TS, Morais JOR (2005) Immuno histochemical evaluation of the postnatal effects of acute exposure to ethanol on the kinetics of granule-cell migration in rat cerebellum. Braz J Morphol Sci 22(1):19–24
Gemma S, Vichi S, Testai E (2006) Individual susceptibility and alcohol effects: biochemical and genetic aspects. Ann Ist Super Sanita 42(1):8–16
Gitto E, Marseglia L, Manti S, D’Angelo G, Barberi I, Salpietro C, Reiter RJ (2013) Protective role of melatonin in neonatal diseases. Oxidative Med Cell Longev 2013:980374. doi:10.1155/2013/980374
Gramenzi A, Caputo F, Biselli M, Kuria F, Loggi E, Andreone P et al (2006) Review article: alcoholic liver disease—pathophysiological aspects and risk factors. Aliment Pharmacol Ther 24(8):1151–1161
Gray SP, Cullen-McEwen LA, Bertram JF, Moritz KM (2012) Mechanism of alcohol-induced impairment in renal development: could it be reduced by retinoic acid? Clin Exp Pharmacol Physiol 39(9):807–813
Szabo G, Bala S (2010) Alcoholic liver disease and the gut-liver axis. World J Gastroenterol 16(11):1321–1329
Irwin MR, Olmstead R, Valladares EM, Breen EC, Ehlers CL (2010) In response to: etanercept for sleep in patients with alcohol use disorder—mechanisms need to be elucidated. Biol Psychiatry 67(1):e3
Kervern M, Dubois C, Naassila M, Daoust M, Pierrefiche O (2009) Perinatal alcohol exposure in rat induces long-term depression of respiration after episodic hypoxia. Am J Respir Crit Care Med 179(7):608–614
Lamb EJ, Price CP (2008) Creatinine, urea and uric acid. In: Burtis CA, Ashwood ER, Bruns DE, Sawyer BG (eds) Tietz fundamentals of clinical chemistry, 6th edn. W.B. Saunders, St. Louis, pp 363–366
Manzo-Avalos S, Saavedra-Molina A (2010) Cellular and mitochondrial effects of alcohol consumption. Int J Environ Res Public Health 7(12):4281–4304
Namjoo AR, Soroori S, Farid M, Nourani H (2012) An unusual squamous cell carcinoma in a sheep: a case report. Comp Clin Pathol 21:1383–1386
Namjoo AR, Nasri H, Talebi-Juneghani A, Baradaran A, Rafieian-Kopaei M (2013) Safety profile of Carthamus tinctorius L. in lactation: brain, renal and hepatotoxicity. Pak J Med Sci 29(1):378–383
Ojeda ML, Vazquez B, Nogales F, Murillo ML, Carreras O (2009) Ethanol consumption by Wistar rat dams affects selenium bioavailability and antioxidant balance in their progeny. Int J Environ Res Public Health 6(8):2139–2149
Oyama LM, Couto RC, Couto GE, Damaso AR, Oller do Nascimento CM (2000) Ethanol intake during lactation. II. Effects on pups’ liver and brain metabolism. Alcohol 21(3):201–6
Panteghini M, Bais R (2008) Enzymes. In: Burtis CA, Ashwood ER, Bruns DE, Sawyer BG (eds) Tietz fundamentals of clinical chemistry, 6th edn. W.B. Saunders, St. Louis, pp 317–336
Pisani LP, Oller do Nascimento CM, Bueno AA, Biz C, Albuquerque KT, Ribeiro EB et al (2008) Hydrogenated fat diet intake during pregnancy and lactation modifies the PAI-1 gene expression in white adipose tissue of offspring in adult life. Lipids Health Dis 7:13
Porter W (2008) Clinical toxicology. In: Burtis CA, Ashwood ER, Bruns DE, Sawyer BG (eds) Tietz fundamentals of clinical chemistry, 6th edn. W.B. Saunders, St. Louis, pp 563–569
Pueta M, Abate P, Haymal OB, Spear NE, Molina JC (2008) Ethanol exposure during late gestation and nursing in the rat: effects upon maternal care, ethanol metabolism and infantile milk intake. Pharmacol Biochem Behav 91(1):21–31
Saito M (2013) Involvement of sphingolipids in ethanol neurotoxicity in the developing brain. Brain Sci 3(2):670–703
Sharpe PC (2001) Biochemical detection and monitoring of alcohol abuse and abstinence. Ann Clin Biochem 38(6):652–664
Singh M, Gupta S, Pandey R, Aggarwal HK, Aggarwal SK (2014) Oxidative stress and chronic alcohol liver disease: the current perspectives. IAJPR 4(3):1428–1446
Subramanian MG (1995) Effects of chronic alcohol administration on lactational performance in the rat. Alcohol 12(2):137–143
Tavares do Carmo MG, Nascimento CM O, Martin A, Herrera E (1999) Ethanol intake during lactation impairs milk production in rats and affects growth and metabolism of suckling pups. Alcohol 18(1):71–6
Woolfrey KM, Hunt PS, Burk JA (2005) Post natal ethanol exposure disrupts signal detection in adult rats. Neurotoxicol Teratol 27(6):815–823
Young C, Olney JW (2006) Neuroapoptosis in the infant mouse brain triggered by a transient small increase in blood alcohol concentration. Neurobiol Dis 22(3):548–554
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This study was performed in accordance with the Guide for the Care and Use of Laboratory Animals of the Islamic Azad University of Shahrekord, Iran.
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Abbasi, M., Namjoo, A. & Khamesipour, F. Ethanol effects on histobiochemical parameters of suckling pups borned from alcoholic rat mothers. Comp Clin Pathol 25, 833–839 (2016). https://doi.org/10.1007/s00580-016-2270-9
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DOI: https://doi.org/10.1007/s00580-016-2270-9