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Content of bone morphogenetic proteins in blood plasma of rats with metabolic syndrome during mandibular defect restoration

https://doi.org/10.20538/1682-0363-2026-2-65-72

Abstract

The aim was to study the concentration of bone morphogenetic proteins-2 (BMP) and -7 in the blood plasma of rats with metabolic syndrome during reparative osteogenesis in mandibular defect.
Materials and methods. The experiments were carried out on male Wistar rats, which were divided into 4 groups: 1) naïve; 2) control (with mandibular defect); 3) metabolic syndrome; 4) experimental (with metabolic syndrome and mandibular defect). Metabolic syndrome was simulated by replacing standard feed with a high-fat and highcarbohydrate diet. The development of metabolic syndrome was confirmed by changes in body weight, glucose and triacylglycerides concentrations in blood plasma. The mandibular defect was formed in rats according to the method proposed by Grigoryan et al. The content of BMP-2 and BMP-7 in blood plasma was determined by the enzyme-linked immunoassay on days 7, 14, 21, and 28 after the surgery. We calculated the median and the interquartile range Me [Q1; Q3] and applied the Mann – Whitney U-test and the Bonferroni correction. Differences in indicators were considered significant at p < 0.025.
Results. A significant increase in the content of the studied proteins in the blood plasma was determined in the group metabolic syndrome compared to the naïve group. BMP-2 and BMP-7 concentration in rats of the control group was higher throughout the experiment compared to the naïve group (p < 0.025). In the experimental group, a decrease in the concentration of BMP-2 (on days 7, 14, and 28) and BMP-7 (on days 7–28) was found compared to the control group (p < 0.025). An increase in the concentration of BMP-2 and BMP-7 was detected in the experimental group compared to the metabolic syndrome group (p < 0.025) on day 7 and on days 7–14, respectively.
Conclusion. A significant decrease in BMP-2 and BMP-7 concentration in the blood plasma was found in rats with metabolic syndrome during mandibular reparative osteogenesis compared to animals without metabolic disorders.

About the Authors

M. V. Makarova
Kursk State Medical University (KSMU)
Russian Federation

 3 Karl Marx St., 305041 Kursk, Russian Federation 



V. N. Tsygan
Kirov Military Medical Academy
Russian Federation

6g Academician Lebedev St., 194044 Saint-Petersburg, Russian Federation 



Yu. D. Lyashev
Kursk State Medical University (KSMU)
Russian Federation

3 Karl Marx St., 305041 Kursk, Russian Federation 



A. Ye. Brusentsova
Kursk State Medical University (KSMU)
Russian Federation

3 Karl Marx St., 305041 Kursk, Russian Federation 



References

1. Ahmad P., Della Bella E., Stoddart M.J. Applications of Bone Morphogenetic Proteins in Dentistry: A Bibliometric Analysis. BioMed Res. Int. 2020;2020:5971268. DOI: 10.1155/2020/5971268.

2. Lukača N., Katavića V., Novakc S., Šućura A., Filipovića M., Kalajzić I. et al. What do we know about bone morphogenetic proteins and osteochondroprogenitors in inflammatory conditions? Bone. 2020;137:115403. DOI: 10.1016/j.bone.2020.115403.

3. Carreira A.C., Alves G.G., Zambuzzi W.F., Sogayar M.C.,Granjeiro J.M. Bone morphogenetic proteins: structure, biological function and therapeutic applications. Archives of Biochemistry and Biophysics. 2014;561:64–73. DOI: 10.1016/j.abb.2014.07.011.

4. Stokovic N., Ivanjko N., Maticic D., Luyten F.P., Vukicevic S. Bone morphogenetic proteins, carriers, and animal models in the development of novel done regenerative therapies. Materials. 2021;14(13):3513. DOI: 10.3390/ma14133513.

5. Takematsu E., Murphy M., Hou S., Steininger H., Alam A., Ambrosi T.H. et al. Optimizing delivery of therapeutic growth factors for bone and cartilage regeneration. Gels. 2023;9(5):377. DOI: 10.3390/gels9050377.

6. Janbozorgi M., Hosseinzadeh M., Taheri A., Ghafaripur S. Impact of aerobic exercise on expression of OPN and OPG genes and bmal1 protein in the done tissue of diabetic rats during two phases of light and dark circadian rhythm. Research Results in Biomedicine. 2024;10(4):520–531. DOI: 10.18413/2658-6533-2024-10-4-0-3.

7. Nadezhdina N.A., Gudyrev O.S., Nadezhdin S.V., Danilenko L.M., Dolzhikov A.A., Kremleva K.K. et al. Epoetin-alfa-induced osteogenesis in the bone organoid model. Research Results in Pharmacology. 2024;10(4):29–41. DOI: 10.18413/rrpharmacology.10.517.

8. Kotb E., El Mancy I.M., Mohamed I.G.R., Ayoub H.S.A., Rashed A.M., El-Nasser W.S. et al. Relation between erythropoietin resistance and metabolic syndrome in hemodialysis patients: A multicentric propensity score matched analysis. Journal of Investigative Medicine. 2023;71(7):753–759. DOI: 10.1177/10815589231171405.

9. Rodríguez-Merchán E.C. A Review of Recent Developments in the Molecular Mechanisms of Bone Healing. International Journal of Molecular Science. 2021;22(2):767. DOI: 10.3390/ijms22020767.

10. Макарова М.В., Ляшев Ю.Д., Солин А.В., Сериков В.С., Клевцов С.А. Особенности репаративного остеогенеза при дефектах нижней челюсти крыс с экспериментальным метаболическим синдромом. Бюллетень экспериментальной биологии и медицины. 2025;179(6):762–767. DOI: 10.47056/0365-9615-2025-179-6-762-767.

11. Липатов В.А., Крюков А.А., Северинов Д.А., Саакян А.Р. Этические и правовые аспекты проведения экспериментальных биомедицинских исследований in vivo. Часть I. Российский медико-биологический вестник им. акад. И.П. Павлова. 2019;27(1):80–92. DOI: 10.23888/PAVLOVJ201927180-92.

12. Липатов В.А., Крюков А.А., Северинов Д.А., Саакян А.Р. Этические и правовые аспекты проведения экспериментальных биомедицинских исследований in vivo. Часть II. Российский медико-биологический вестник им. акад. И.П. Павлова. 2019;27(2):245–257. DOI: 10.23888/PAVLOVJ2019272245-257.

13. Бирулина Ю.Г., Иванов В.В., Буйко Е.Е., Быков В.В., Смаглий Л.В., Носарев А.М. и др. Экспериментальная модель метаболического синдрома у крыс на основе высокожировой и высокоуглеводной диеты диеты. Бюллетень сибирской медицины. 2020;19(4):14–20. DOI: 10.20538/1682-0363-2020-4-14-20.

14. Wong S.K., Chin K.Y., Suhaimi F.H., Ahmad F., Ima-Nirvana S. The effects of a modified high-carbohydrate high-fat diet on metabolic syndrome parameters in male rats. Experimental and Clinical Endocrinology and Diabetes. 2018;126(3):205–212. DOI: 10.1055s-0043-109352.

15. Григорьян А.С., Орлов А.А., Сабурина И.Н., Зурина И.М., Сысоев С.Д. Динамика остеогенетического процесса, вызванного инокуляцией аутологичных стромальных клеток, выделенных из жировой ткани крысы (экспериментально-морфологическое исследование). Патологическая физиология и экспериментальная терапия. 2015;59(2):4–11.

16. Воронкова О.В., Бирулина Ю.Г., Иванов В.В., Буйко Е.Е., Есимова И.Е., Григорьева А.В. и др. Особенности цитограммы и цитокинового профиля жидкости бронхоальвеолярного лаважа при экспериментальном метаболическом синдроме. Бюллетень сибирской медицины. 2022;21(4):29–36. DOI: 10.20538/1682-0363-2022-4-29-36.

17. Rossi J.L.S., Barbalho S.M., de Araujo R.R., Bechara M.D., Sloan K.P., Sloan L.A. Metabolic syndrome and cardiovascular diseases: Going beyond traditional risk factors. Diabetes Metabolism Research and Reviews. 2022;38(3):e3502. DOI: 10.1002/dmrr.3502.

18. Li. M., Willey J. The interplay between inflammation and thrombosis in COVID-19: Mechanisms, therapeutic strategies, and challenges. Thrombosis Update. 2022;8:100117. DOI: 10.1016/j.tru.2022.100117.

19. Wang M., Qiu Y., Gao L., Qi F., Bi L. The impact of IGF-1 on alveolar bone remodeling and BMP-2 expression in orthodontic tooth movement in diabetic rats. Advances in Clinical and Experimental Medicine. 2023;32(3):349–356. DOI: 10.17219/acem/153956.

20. Nett P.C., Ortmann J., Celeiro J., Haas E., Hofmann-Lehmann R., Tornillo L. et al. Transcriptional regulation of vascular bone morphogenetic protein by endothelin receptors in early autoimmune diabetes mellitus. Life Science. 2006;78(19):2213–2218. DOI: 10.1016/j.lfs.2005.09.026.

21. Cai B., Du J. Role of bone morphogenetic protein-4 in gestational diabetes mellitus-related hypertension. Experimental and Therapeutic Medicine. 2021;22(1):762. DOI: 10.3892/etm.2021.10194.

22. Carreira A.C.O., Zambuzzi W.F., Rossi M.C., Filho R.A., Sogayar M.C., Granjeiro J.M. Bone morphogenetic proteins: promising molecules for bone healing, bioengineering, and regenerative medicine. Vitamins and Hormones. 2015;99:293–322. DOI: 10.1016/bs.vh.2015.06.002.

23. Ishida K., Haudenschild D.R. Interactions between FGF21 and BMP-2 in osteogenesis. Biochemical and Biophysical Research Communications. 2013;432(4):677–682. DOI: 10.1016/j.bbrc.2013.02.019.

24. Zhou X., Chen J., Sun X., Wang F., Wang Y., Zhang Z. et al. Spatiotemporal regulation of angiogenesis/osteogenesis emulating natural bone healing cascade for vascularized bone formation. Journal of Nanobiotechnology. 2021;19(1):420. DOI: 10.1186/s12951-021-01173-z.

25. Ding T., Kang W., Li J., Yu L., Ge S. An in situ tissue engineering scaffold with growth factors combining angiogenesis and osteoimmunomodulatory functions for advanced periodontal bone regeneration. Journal of Nanobiotechnology. 2021;19(1):247. DOI: 10.1186/s12951-021-00992-4.


Review

For citations:


Makarova M.V., Tsygan V.N., Lyashev Yu.D., Brusentsova A.Ye. Content of bone morphogenetic proteins in blood plasma of rats with metabolic syndrome during mandibular defect restoration. Bulletin of Siberian Medicine. 2026;25(2):65-72. https://doi.org/10.20538/1682-0363-2026-2-65-72

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ISSN 1682-0363 (Print)
ISSN 1819-3684 (Online)