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Maternal active or passive smoking causes oxidative stress in placental tissue

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Abstract

The aim of this study was to assess the influence of active and passive maternal smoking on placenta total oxidant/antioxidant status in term infants. The levels of cord blood total antioxidant capacity (TAC), total oxidant status (TOS), and oxidative stress index (OSI) were measured in samples of fetal placental tissue, cord blood, and the maternal peripheral blood serum and from 19 mothers who were active smokers, 19 who were passive smokers, and 22 who were nonsmokers (not exposed to active or passive smoking). The pregnancies were between 37 and 40 weeks' gestation, were uncomplicated, and the infants were delivered vaginally. Birth weight and head circumference in the active smokers were significantly (P < 0.001) lower than those in the controls. Placenta, cord blood, and the maternal peripheral TAC levels were significantly lower in the active smokers compared with the controls (P < 0.001), while TOS and OSI levels were significantly higher in the active and passive smokers than in the controls (P < 0.001). A positive significant correlation was found between active maternal smoking and placenta TOS and OSI levels (P < 0.016), and a significant negative correlation was found between number of cigarettes exposed to and birthweight and head circumference (P < 0.05). In conclusion, active or passive maternal smoking is associated with important alterations in oxidant and antioxidant balance in fetal placental tissue and causes potent oxidative stress.

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Abbreviations

TAC:

total antioxidant capacity

TOS:

total oxidant status

OSI:

Oxidative stress index

References

  1. Ahn MR, Kumazawa S, Hamasaka T, Bang KS, Nakayama T (2004) Antioxidant activity and constituents of propolis collected in various areas of Korea. J Agric Food Chem 52:7286–7292

    Article  PubMed  CAS  Google Scholar 

  2. Arab K, Steghens JP (2004) Serum lipid hydroperoxides measurement by an automated xylenol orange method. Anal Biochem 325:158–163

    Article  PubMed  CAS  Google Scholar 

  3. Aycicek A, Erel O, Kocyigit A (2005) Decreased total antioxidant capacity and increased oxidative stress in passive smoker infants and their mothers. Pediatr Int 47:635–639

    Article  PubMed  CAS  Google Scholar 

  4. Aycicek A, Erel O, Kocyigit A (2005) Increased oxidative stress in infants exposed to passive smoking. Eur J Pediatr 164:775–778

    Article  PubMed  CAS  Google Scholar 

  5. Aycicek A, Erel O, Kocyigit A et al (2006) Breast milk provides better antioxidant power than do formula. Nutrition 22:616–619

    Article  PubMed  CAS  Google Scholar 

  6. Aycicek A, Ipek A (2008) Maternal active or passive smoking causes oxidative stress in cord blood. Eur J Pediatr 167:81–85

    Article  PubMed  CAS  Google Scholar 

  7. Bartal M (2001) Health effects of tobacco use and exposure. Monaldi Arch Chest Dis 56:545–554

    PubMed  CAS  Google Scholar 

  8. Bolisetty S, Naidoo D, Lui K et al (2002) Postnatal changes in maternal and neonatal plasma antioxidant vitamins and the influence of smoking. Arch Dis Child Fetal Neonatal Ed 86:F36–F40

    Article  PubMed  CAS  Google Scholar 

  9. Cao G, Prior RL (1998) Comparison of different analytical methods for assessing total antioxidant capacity of human serum. Clin Chem 44:1309–1315

    PubMed  CAS  Google Scholar 

  10. Chelchowska M, Laskowska-Klita T, Leibschang J (2005) The effect of tobacco smoking during pregnancy on concentration of malondialdehyde in blood of mothers and in umbilical cord blood. Ginekol Pol 76:960–965

    PubMed  Google Scholar 

  11. Cliver SP, Goldenberg RL, Cutter GR et al (1992) The relationships among psychosocial profile, maternal size, and smoking in predicting fetal growth retardation. Obstet Gynecol 80:262–267

    PubMed  CAS  Google Scholar 

  12. Cross CE, O’Neill CA, Reznick AZ et al (1993) Cigarette smoke oxidation of human plasma constituents. Ann NY Acad Sci 686:72–89

    Article  PubMed  CAS  Google Scholar 

  13. Dewan N, Brabin B, Wood L et al (2003) The effects of smoking on birthweight-forgestational-age curves in teenage and adult primigravidae. Public Health 117:31–35

    Article  PubMed  CAS  Google Scholar 

  14. Durak I, Elgun S, Kemal Bingol N et al (2002) Effects of cigarette smoking with different tar content on erythrocyte oxidant/antioxidant status. Addict Biol 7:255–258

    Article  PubMed  CAS  Google Scholar 

  15. Erel O (2004) A novel automated direct measurement method for total antioxidant capacity using a new generation, more stable ABTS radical cation. Clin Biochem 37:277–285

    Article  PubMed  CAS  Google Scholar 

  16. Erel O (2004) A novel automated method to measure total antioxidant response against potent free radical reactions. Clin Biochem 37:112–119

    Article  PubMed  CAS  Google Scholar 

  17. Erel O (2005) A new automated colorimetric method for measuring total oxidant status. Clin Biochem 38:1103–1111

    Article  PubMed  CAS  Google Scholar 

  18. Fayol L, Gulian JM, Dalmasso C et al (2005) Antioxidant status of neonates exposed in utero to tobacco smoke. Biol Neonate 87:121–126

    Article  PubMed  CAS  Google Scholar 

  19. Harma M, Harma M, Erel O (2003) Increased oxidative stress in patients with hydatidiform mole. Swiss Med Wkly 133:563–566

    PubMed  CAS  Google Scholar 

  20. Harma M, Harma M, Erel O (2005) Oxidative stress in women with preeclampsia. Am J Obstet Gynecol 192:656–657

    Article  PubMed  Google Scholar 

  21. Hellerstedt WL, Himes JH, Story M et al (1997) The effects of cigarette smoking and gestational weight change on birth outcomes in obese and normal-weight women. Am J Public Health 87:591–596

    Article  PubMed  CAS  Google Scholar 

  22. Hu ML, Louie S, Cross CE et al (1993) Antioxidant protection against hyochlorous acid in human plasma. J Lab Clin Med 121:257–262

    PubMed  CAS  Google Scholar 

  23. Karcaaltincaba D, Kandemir O, Yalvac S et al (2009) Cigarette smoking and pregnancy: results of a survey at a Turkish women’s hospital in 1,020 patients. J Obstet Gynaecol 29:480–486

    Article  PubMed  CAS  Google Scholar 

  24. Kim DH, Suh YS, Mun KC (2004) Tissue levels of malondialdehyde after passive smoke exposure of rats for a 24-week period. Nicotine Tob Res 6:1039–1042

    Article  PubMed  CAS  Google Scholar 

  25. Kondo T, Tagami S, Yoshioka A et al (1994) Current smoking of elderly men reduces antioxidants in alveolar macrophages. Am J Respir Crit Care Med 149:178–182

    PubMed  CAS  Google Scholar 

  26. Liu X, Lu J, Liu S (1999) Synergistic induction of hydroxyl radical-induced DNA singlestrand breaks by chromium (VI) compound and cigarette smoke solution. Mutat Res 440:109–117

    PubMed  CAS  Google Scholar 

  27. Martinez FD, Wright AL, Taussig LM (1994) The effect of paternal smoking on the birthweight of newborns whose mothers did not smoke. Group Health Medical Associates. Am J Public Health 84:1489–1491

    Article  PubMed  CAS  Google Scholar 

  28. Polidori MC, Mecocci P, Stahl W et al (2003) Cigarette smoking cessation increases plasma levels of several antioxidant micronutrients and improves resistance towards oxidative challenge. Br J Nutr 90:147–150

    Article  PubMed  CAS  Google Scholar 

  29. Rabus M, Demirbağ R, Sezen Y et al (2008) Plasma and tissue oxidative stress index in patients with rheumatic and degenerative heart valve disease. Türk Kardiyol Dern Ars 36:536–540

    PubMed  Google Scholar 

  30. Rahman I, MacNee W (1996) Oxidant/antioxidant imbalance in smokers and chronic obstructive pulmonary disease. Thorax 51:348–350

    Article  PubMed  CAS  Google Scholar 

  31. Reeves S, Bernstein I (2008) Effects of maternal tobacco-smoke exposure on fetal growth and neonatal size. Expert Rev Obstet Gynecol 3:719–730

    Article  PubMed  Google Scholar 

  32. Roberts VH, Smith J, McLea SA et al (2009) Effect of increasing maternal body mass index on oxidative and nitrative stress in the human placenta. Placenta 2:169–175

    Article  Google Scholar 

  33. Rogers JM (2009) Tobacco and pregnancy. Reprod Toxicol 28:152–160

    Article  PubMed  CAS  Google Scholar 

  34. Shepard MJ, Bakketeig LS, Jacobsen G et al (1996) Maternal body mass, proportional weight gain, and fetal growth in parous women. Paediatr Perinat Epidemiol 10:207–219

    Article  PubMed  CAS  Google Scholar 

  35. Varvarigou AA, Fouzas S, Beratis NG (2010) Effect of prenatal tobacco smoke exposure on fetal growth potential. J Perinat Med (in press)

  36. Yoshie Y, Ohshima H (1997) Synergistic induction of DNA strand breakage by cigarette tar and nitric oxide. Carcinogenesis 18:1359–1366

    Article  PubMed  CAS  Google Scholar 

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Acknowledgements

We are most grateful to the technical staff of the Laboratory and Delivery Unit at Sanliurfa Women's Hospital and Harran University Medical Faculty Research Hospital Biochemistry Department for their assistance in conducting this study.

Declaration of competing ınterests

We wish to disclose a competing interest(s) such as those defined above or others that may be perceived to influence the results and discussion reported in this paper.

Institutional competing ınterests

We aware that our academic institution or employment has not a financial interest in or a financial conflict with the subject matter or materials discussed in this manuscript.

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Correspondence to Ali Aycicek.

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Aycicek, A., Varma, M., Ahmet, K. et al. Maternal active or passive smoking causes oxidative stress in placental tissue. Eur J Pediatr 170, 645–651 (2011). https://doi.org/10.1007/s00431-010-1338-9

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  • DOI: https://doi.org/10.1007/s00431-010-1338-9

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