Fetal growth restriction and markers for mitochondrial dysfunction


Cite item

Full Text

Open Access Open Access
Restricted Access Access granted
Restricted Access Subscription or Fee Access

Abstract

Objective. To comparatively analyze the content of mitochondrial components in the placenta and whole blood of women with physiological and fetal growth restriction-complicated pregnancy. Subjects and methods. Examinations were made in 32 women (10 patients with physiological pregnancy and 12 patients with diagnosed fetal growth restriction) starting at 24 weeks’ gestation. The levels of OPA1, DRP1, VDAC1, TFAM, and hOGG1 proteins were estimated using chemiluminescence western blotting. The blood levels of mitochondrial DNA copy number were determined by real-time PCR. Results. There was an increased hOGG1 protein content without changes in the levels of mitochondrial fusion and fragmentation factors in the placental tissue of the examined groups. There was a significant reduction in mitochondrial DNA abundance at 25, 29, and 37 weeks’ gestation in the blood of patients with fetal growth restriction compared to the similar weeks of physiological pregnancy. Conclusion. There are pronounced manifestations of oxidative stress in fetal growth restriction-complicated pregnancy. The reduction in the maternal blood mitochondrial DNA abundance in fetal growth restriction may be suggestive of obvious mitochondrial dysfunction in the placenta and be used as a prognostic marker for this pathology

Full Text

Restricted Access

About the authors

Polina A. Vishnyakova

National Medical Research Center of Obstetrics, Gynecology, and Perinatology named after Academician V.I. Kulakov, Ministry of Health of Russia

Email: p_vishnyakova@oparina4.ru
PhD, Researcher, Laboratory of mitochondrial medicine

Iuliia A. Sukhanova

National Medical Research Center of Obstetrics, Gynecology, and Perinatology named after Academician V.I. Kulakov, Ministry of Health of Russia

Email: suhanova_julia@hotmail.com
Researcher, Laboratory of mitochondrial medicine

Asmik G. Mikaelyan

National Medical Research Center of Obstetrics, Gynecology, and Perinatology named after Academician V.I. Kulakov, Ministry of Health of Russia

Email: mikaelyan_asmik@bk.ru
Graduate student, Department of pregnancy loss prevention and therapy

Yulia S. Bulatova

National Medical Research Center of Obstetrics, Gynecology, and Perinatology named after Academician V.I. Kulakov, Ministry of Health of Russia

Email: yu.bulatova@mail.ru
Graduate student, Department of pregnancy loss prevention and therapy

Sofia V. Pyataeva

National Medical Research Center of Obstetrics, Gynecology, and Perinatology named after Academician V.I. Kulakov, Ministry of Health of Russia

Email: biosonya@gmail.com
PhD, Researcher, Laboratory of mitochondrial medicine

Ivan S. Balashov

National Medical Research Center of Obstetrics, Gynecology, and Perinatology named after Academician V.I. Kulakov, Ministry of Health of Russia

Email: i_balashov@oparina4.ru
Expert, the Bioinformatics research group

Pavel I. Borovikov

National Medical Research Center of Obstetrics, Gynecology, and Perinatology named after Academician V.I. Kulakov, Ministry of Health of Russia

Email: p_borovikov@oparina4.ru
Head of the Bioinformatics research group

Nana K. Tetruashvili

National Medical Research Center of Obstetrics, Gynecology, and Perinatology named after Academician V.I. Kulakov, Ministry of Health of Russia

Email: tetrauly@mail.ru
M.D., PhD, Head of the Department of pregnancy loss prevention and therapy

Mikhail Y. Vyssokikh

National Medical Research Center of Obstetrics, Gynecology, and Perinatology named after Academician V.I. Kulakov, Ministry of Health of Russia

Email: m_vysokikh@oparina4.ru
PhD, Head of the Mitochondrial medicine research group

References

  1. Romo A., Carceller R., Tobajas J. Intrauterine growth retardation (IUGR): epidemiology and etiology. Pediatr. Endocrinol. Rev. 2009; 6(Suppl. 3): 332-6.
  2. Lawn J.E., Cousens S., Zupan J.; Lancet Neonatal Survival Steering Team. 4 million neonatal deaths: When? Where? Why? Lancet. 2005; 365(9462): 891-900.
  3. Kaufmann P., Black S., Huppertz B. Endovascular trophoblast invasion: implications for the pрthogenesis of intrauterine growth retardation and preeclampsia. Biol. Reprod. 2003; 69(1): 1-7.
  4. Duhig K., Chappell L.C., Shennan A.H. Oxidative stress in pregnancy and reproduction. Obstet. Med. 2016; 9(3): 113-6.
  5. Biri A., Bozkurt N., Turp A., Kavutcu M., Himmetoglu Ö., Durak I. Role of oxidative stress in intrauterine growth restriction. Gynecol. Obstet. Invest. 2007; 64(4): 187-92.
  6. Karacay Ö., Sepici-Dincel A., Karcaaltincaba D., Sahin D., Yalvaç S., Akyol M. et al. A quantitative evaluation of total antioxidant status and oxidative stress markers in preeclampsia and gestational diabetic patients in 24-36 weeks of gestation. Diabetes Res. Clin. Pract. 2010; 89(3): 231-8.
  7. Korshunov S.S., Skulachev V.P., Starkov A.A. High protonic potential actuates a mechanism of production of reactive oxygen species in mitochondria. FEBS Lett. 1997; 416(1): 15-8.
  8. Мартусевич А.К., Карузин К.А. Окислительный стресс и его роль в формировании дизадаптации и патологии. Биорадикалы и антиоксиданты. 2015; 2(2): 5-18.
  9. Lee H.C., Wei Y.H. Mitochondrial biogenesis and mitochondrial DNA maintenance of mammalian cells under oxidative stress. Int. J. Biochem. Cell Biol. 2005; 37(4): 822-34.
  10. Shadel G.S. Expression and maintenance of mitochondrial DNA: new insights into human disease pathology. Am. J. Pathol. 2008; 172(6): 1445-56.
  11. Tan D., Goerlitz D.S., Dumitrescu R.G., Han D., Seillier-Moiseiwitsch F., Spernak S.M. et al. Associations between cigarette smoking and mitochondrial DNA abnormalities in buccal cells. Carcinogenesis. 2008; 29(6): 1170-7.
  12. Holland O., Nitert M.D., Gallo L.A., Vejzovic M., Fisher J.J., Perkins A.V. Placental mitochondrial function and structure in gestational disorders. Placenta. 2017; 54: 2-9.
  13. Williams M.A., Sanchez S.E., Ananth C.V., Hevner K., Qiu C., Enquobahrie D.A. Maternal blood mitochondrial DNA copy number and placental abruption risk : results from a preliminary study. Int. J. Mol. Epidemiol. Genet. 2013; 4(2): 120-7.

Supplementary files

Supplementary Files
Action
1. JATS XML

This website uses cookies

You consent to our cookies if you continue to use our website.

About Cookies