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Role of certain saturated fatty acids in the development of oxidative stress in pregnant women with COVID-19

https://doi.org/10.36604/1998-5029-2026-100-138-144

Abstract

Introduction. As evidence on the pathogenesis of COVID-19 in pregnancy accumulates, researchers increasingly focus on the destabilization of various metabolic pathways, including lipid profile disturbances and the initiation of oxidative stress.

Aim. To comparatively analyze plasma concentrations of palmitic and stearic saturated fatty acids (SFAs) and assess their role in the development of oxidative stress in pregnant women with moderate COVID-19 during the second trimester.

Materials and methods. A case–control study included 39 women in the second trimester with confirmed moderate COVID-19 (main group) and 40 pregnant women with no history of or current SARS-CoV-2 infection (control group). The concentrations of primary (dienic conjugates) and end products (thiobarbituric acid-reactive substances, TBARS) of lipid peroxidation were studied in peripheral blood plasma using spectrophotometric methods. Enzyme-linked immunosorbent assay (ELISA) was employed to determine 8-isoprostane levels and total antioxidant capacity (TAC). Quantitative analysis of SFAs was performed by gas chromatography.

Results. The main group showed statistically significant increases in palmitic acid (1.33-fold; p < 0.001) and stearic acid (1.34-fold; p < 0.001), alongside intensified lipid peroxidation: elevated diene conjugates (1.9-fold; p < 0.001), TBARS (2-fold; p < 0.001), and 8-isoprostane (>2-fold; p < 0.001), coupled with a 1.62-fold reduction in plasma TAC (p < 0.001). Strong positive correlations were found between palmitic and stearic acid levels and both TBARS (rs = 0.72 and rs = 0.68, respectively; p < 0.001) and 8- isoprostane (rs = 0.74 and rs = 0.72, respectively; p < 0.001). Statistically significant inverse correlations were also observed between these SFAs and TAC (rs = –0.70 and rs = –0.67, respectively; p < 0.001).

Conclusion. Moderate COVID-19 during the second trimester of pregnancy is associated with a significant elevation in plasma palmitic and stearic acid concentrations. The identified correlations suggest that SFA imbalance and pro-oxidant burden form a unified pathogenetic cascade in moderate COVID-19 during mid-gestation.

About the Authors

N. A. Ishutina
Far Eastern Scientific Center of Physiology and Pathology of Respiration
Russian Federation

Nataliа A. Ishutina, PhD, D.Sc. (Biol.), Professor DVO RAS, Leading Staff Scientist of Laboratory of Mechanisms of Etiopathogenesis and Recovery Processes of the Respiratory System at Non-Specific Lung Diseases

22 Kalinina Str., Blagoveshchensk, 675000 



I. A. Andrievskaya
Far Eastern Scientific Center of Physiology and Pathology of Respiration
Russian Federation

Irina A. Andrievskaya, PhD, D.Sc. (Biol.), Professor RAS, Head of Laboratory of Mechanisms of Etiopathogenesis and Recovery Processes of the Respiratory System at Non-Specific Lung Diseases

22 Kalinina Str., Blagoveshchensk, 675000 



I. V. Dovzhikova
Far Eastern Scientific Center of Physiology and Pathology of Respiration
Russian Federation

Inna V. Dovzhikova, PhD, DSc (Biol.), Leading Staff Scientist, Laboratory of Mechanisms of Etiopathogenesis and Recovery Processes of the Respiratory System at Non-Specific Lung Diseases

22 Kalinina Str., Blagoveshchensk, 675000 



N. N. Dorofienko
Far Eastern Scientific Center of Physiology and Pathology of Respiration
Russian Federation

Nikolay N. Dorofienko, PhD (Med.), Senior Staff Scientist, Laboratory of Mechanisms of Etiopathogenesis and Recovery Processes of the Respiratory System at Non-Specific Lung Diseases

22 Kalinina Str., Blagoveshchensk, 675000 



References

1. Komilova M.O., Zufarova Sh.A., Yuldasheva A.S. [Features of the course of COVID-19 viral infection during pregnancy]. Ekonomika i sotsium 2022; 2-2(93):705–710 (in Russian).

2. Sun G., Zhang Y., Liao Q., Cheng Y. Blood test results of pregnant covid-19 patients: an updated case-control study. Front. Cell Infect. Microbiol. 2020; 10:560899. https://doi.org/10.3389/fcimb.2020.560899

3. Ma Y., Nenkov M., Chen Y., Press A.T., Kaemmerer E., Gassler N. Fatty acid metabolism and acyl-CoA synthetases in the liver-gut axis. World J. Hepatol. 2021; 13(11):1512–1533. https://doi.org/10.4254/wjh.v13.i11.1512

4. Korbecki J., Bajdak-Rusinek K. The effect of palmitic acid on inflammatory response in macrophages: an overview of molecular mechanisms. Inflamm. Res. 2019; 68(11):915–932. https://doi.org/10.1007/s00011-019-01273-5

5. Lambertucci R.H., Leandro C.G., Vinolo M.A., Nachbar R.T., Dos Reis Silveira L., Hirabara S.M., Curi R., PithonCuri T.C. The effects of palmitic acid on nitric oxide production by rat skeletal muscle: mechanism via superoxide and iNOS activation. Cell Physiol. Biochem. 2012; 30(5):1169–1180. https://doi.org/10.1159/000343307. Erratum in: Cell Physiol. Biochem. 2013; 31(1):14. PMID: 23171868.

6. Sacks D., Baxter B., Campbell B.C.V., Carpenter J.S., Cognard C., Dippel D., Eesa M., Fischer U., Hausegger K., Hirsch J.A., Shazam Hussain M., Jansen O., Jayaraman M.V., Khalessi A.A., Kluck B.W., Lavine S., Meyers P.M., Ramee S., Rüfenacht D.A., Schirmer C.M., Vorwerk D. Multisociety consensus quality improvement revised consensus statement for endovascular therapy of acute ischemic stroke. Int. J. Stroke. 2018; 6:612–632. https://doi.org/10.1177/1747493018778713

7. Yang C., Lim W., Bazer F.W., Song G. Oleic acid stimulation of motility of human extravillous trophoblast cells is mediated by stearoyl-CoA desaturase-1 activity. Mol. Hum. Reprod. 2017; 23(11):755–770. https://doi.org/10.1093/molehr/gax051

8. Bicanin Ilic M., Nikolic Turnic T., Ilic I., Nikolov A., Mujkovic S., Rakic D., Jovic N., Arsenijevic N., Mitrovic S., Spasojevic M., Savic J., Mihajlovic K., Jeremic N., Joksimovic Jovic J., Pindovic B., Balovic G., Dimitrijevic A. SARSCoV-2 infection and its association with maternal and fetal redox status and outcomes: a prospective clinical study. J. Clin. Med. 2025; 14(5):1555. https://doi.org/10.3390/jcm14051555

9. Ishutina N.A., Andrievskaya I.A., Krivoschekova N.A. [Characterization of lipid peroxidation processes and antioxidant defense in parturients with COVID-19]. Bûlleten' fiziologii i patologii dyhaniâ = Bulletin Physiology and Pathology of Respiration 2024; 91:84–89 (in Russian). https://doi.org/10.36604/1998-5029-2024-91-84-89

10. Nobrega G.M., McColl E.R., Antolini-Tavares A., Souza R.T., Cecatti J.G., Costa M.L., Mysorekar I.U. Placentas from SARS-CoV-2 infection during pregnancy exhibit foci of oxidative stress and DNA damage. Am. J. Reprod. Immunol. 2025; 93(1):e70034. https://doi.org/10.1111/aji.70034

11. Orel N.M. [Biochemistry of membranes: method allowance]: Minsk: Belorusskiy gosudarstvennyy universitet; 2010 (in Russian).

12. Gavrilov V.G., Gavrilova A.R., Mazhul L.M. [Analiz methods for determining lipid peroxidation products in the blood serum test with thiobarbituric acid]. Voprosy medicinskoy chimii = Biochemistry (Moscow) Supplement Series B: Biomedical Chemistry 1987; 33(1):118–122 (in Russian).

13. Folch J., Lees M., Sloane Stanley G.H. A simple method for the isolation and purification of total lipides from animal tissues. J. Biol. Chem. 1957; 226(1):497‒509. PMID: 13428781

14. Carreau J.P., Dubacq J.P. Adaptation of a macro-scale method to the micro-scale for fatty acid methyl transesterification of biological lipid extracts. J. Chromatogr. A. 1978; 151(3):384‒390. https://doi.org/10.1016/S00219673(00)88356-9

15. Ceja-Galicia Z.A., Cespedes-Acuña C.L.A., El-Hafidi M. Protection strategies against palmitic acid-induced lipotoxicity in metabolic syndrome and related diseases. Int. J. Mol. Sci. 2025; 26(2):788. https://doi.org/10.3390/ijms26020788

16. Montuschi P., Corradi M., Ciabattoni G., Nightingale J., Kharitonov S.A., Barnes P.J. Increased 8-isoprostane, a marker of oxidative stress, in exhaled condensate of asthma patients. Am. J. Respir. Crit. Care Med. 1999; 160(1): 216– 220. https://doi.org/10.1164/ajrccm.160.1.9809140

17. Kuang H., Sun X., Liu Y., Tang M., Wei Y., Shi Y., Li R., Xiao G., Kang J., Wang F., Peng J., Xu H., Zhou F. Palmitic acid-induced ferroptosis via CD36 activates ER stress to break calcium-iron balance in colon cancer cells. FEBS J. 2023; 290(14):3664–3687. https://doi.org/10.1111/febs.16772

18. Chong M.F., Hodson L., Bickerton A.S., Roberts R., Neville M., Karpe F., Frayn K.N., Fielding BA. Parallel activation of de novo lipogenesis and stearoyl-CoA desaturase activity after 3 d of high-carbohydrate feeding. Am. J. Clin. Nutr. 2008; 87(4):817–823. https://doi.org/10.1093/ajcn/87.4.817

19. Gomes K.P., Korodimas J., Liu E., Patel N., Yang X., Goruk S., Munhoz J., Field C.J., Gibson SB. Saturated fatty acids induce lipotoxicity in lymphatic endothelial cells contributing to secondary lymphedema development. EMBO Mol. Med. 2025; 17(9):2384–2408. https://doi.org/10.1038/s44321-025-00286-4


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For citations:


Ishutina N.A., Andrievskaya I.A., Dovzhikova I.V., Dorofienko N.N. Role of certain saturated fatty acids in the development of oxidative stress in pregnant women with COVID-19. Bulletin Physiology and Pathology of Respiration. 2026;(100):138-144. (In Russ.) https://doi.org/10.36604/1998-5029-2026-100-138-144

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ISSN 1998-5029 (Print)