A comparative analysis of biochemical markers of systemic inflammation in experimental models of acute and chronic organ damage in laboratory animals

Authors

DOI:

https://doi.org/10.15587/2519-8025.2026.356223

Keywords:

systemic inflammation, oxidative stress, inflammatory markers, experimental nephropathies, toxic hepatitis, adrenaline-induced myocarditis, UV erythema

Abstract

Aim. The aim of the study was to determine and comparatively analyse the specified markers in models of acute and chronic inflammation of various localisation and genesis in laboratory animals.

Materials and Methods. The study was conducted using models, such as adrenal myocarditis, tetrachloromethane hepatitis, UV erythema, folacin-induced nephropathy, and doxorubicin nephropathy.

Results. The content of total protein, C-reactive protein, creatinine, urea, TBA-AP, as well as the activity of cytolysis enzymes ALT and AST in nephropathy models were determined. The results of experimental studies showed the heterogeneity of marker changes depending on the selected model. In the UV erythema model, the diameter of erythema, CRP, and ALT significantly increased, while the content of TBA-AP decreased against the background of experimental pathology. In tetrachloromethane hepatitis, there was an increase in the liver mass coefficient, CRP content, TBA-AP, ALT and AST activity, and a decrease in total protein. Adrenaline myocarditis was accompanied by an increase in cardiac mass index, CRP, TBA-AP and AST activity. In both models of nephropathy (folic acid and doxorubicin), the kidney mass index increased; creatinine and urea levels rose, while total protein levels decreased; CRP levels increased in the model of nephropathy caused by folic acid and doxorubicin, while TBA-AP levels and ALT and AST activity increased significantly.

Conclusions. The experimental data obtained indicate a pronounced activation of systemic inflammation and oxidative stress in all model pathologies, but the degree and spectrum of changes in markers differ depending on the aetiological factor and organotropism of the pathologic process

Author Biographies

Igor Seniuk, National University of Pharmacy

PhD, Associate Professor

Department of Biological Chemistry and Microbiology

Liubov Galuzinska, National University of Pharmacy

PhD, Associate Professor

Department of Biological Chemistry and Microbiology

Nataliia Polovko, National University of Pharmacy

Doctor of Pharmaceutical Sciences, Professor

Department of Pharmaceutical Technology of Drugs

Anatolii Loshakov, Kyiv Vitamin Plant

Electronic Equipment Technician/Operator

Kateryna Strelchenko, School Gravity LLC

PhD, Associate Professor, Director

References

  1. Caragea, D. C., Boldeanu, L., Assani, M.-Z., Caragea, M.-E., Stroe-Ionescu, A.-Ștefania, Popa, R. et al. (2025). Assessment of AOPP, TBARS, and Inflammatory Status in Diabetic Nephropathy and Hemodialyzed Patients. International Journal of Molecular Sciences, 26 (21), 10670. https://doi.org/10.3390/ijms262110670
  2. Dopierała, M., Nitz, N., Król, O., Wasicka-Przewoźna, K., Schwermer, K., Pawlaczyk, K. (2025). New and Emerging Biomarkers in Chronic Kidney Disease. Biomedicines, 13 (6), 1423. https://doi.org/10.3390/biomedicines13061423
  3. Dang, P., Li, B., Li, Y. (2024). Prognostic potential of inflammatory markers in chronic kidney disease patients combined with acute myocardial infarction. Frontiers in Cardiovascular Medicine, 11. https://doi.org/10.3389/fcvm.2024.1430215
  4. Li, C., Chen, X., Zha, W., Fang, S., Shen, J., Li, L. et al. (2025). Impact of gut microbiota in chronic kidney disease: natural polyphenols as beneficial regulators. Renal Failure, 47 (1). https://doi.org/10.1080/0886022x.2025.2506810
  5. Quetglas-Llabrés, M. M., Díaz-López, A., Bouzas, C., Monserrat-Mesquida, M., Salas-Salvadó, J., Ruiz-Canela, M. et al. (2025). Association Between Oxidative–Inflammation Biomarkers and Incident Chronic Kidney Disease in People with High Cardiovascular Risk: A Nested Case–Control Study. Antioxidants, 14 (8), 975. https://doi.org/10.3390/antiox14080975
  6. Gao, W., Wang, X., Zou, Y., Wang, S., Dou, J., Qian, S. (2025). Progress in the application of novel inflammatory indicators in chronic kidney disease. Frontiers in Medicine, 12. https://doi.org/10.3389/fmed.2025.1500166
  7. Hanusrichterova, J., Baranovicova, E., Barosova, R., Kolomaznik, M., Mikolka, P., Kosutova, P. et al. (2025). Metabolic profiling in experimental guinea pig models of bacterial and allergic inflammation. Metabolomics, 21 (2). https://doi.org/10.1007/
  8. s11306-025-02239-x
  9. Assani, M.-Z., Novac, M. B., Dijmărescu, A. L., Stroe-Ionescu, A.-Ștefania, Boldeanu, M. V., Siloși, I., Boldeanu, L. (2025). Intersecting Pathways of Inflammation, Oxidative Stress, and Atherogenesis in the Evaluation of CKD: Emerging Biomarkers PCSK9, EPHX2, AOPPs, and TBARSs. Life, 15 (8), 1287. https://doi.org/10.3390/life15081287
  10. He, P., Zhang, J., Tian, N., Deng, Y., Zhou, M., Tang, C., Ma, Y., Zhang, M. (2025). The relationship between C-reactive protein to lymphocyte ratio and the prevalence of chronic kidney disease in US adults: a cross-sectional study. Frontiers in Endocrinology, 15. https://doi.org/10.3389/fendo.2024.1469750
  11. Zhang, H., Qi, X., Yang, L., Xia, P., Ling, J., Zheng, X. et al. (2025). Advances in anthocyanin nanoparticle delivery systems in anti-inflammatory therapies. Pharmacological Research, 222, 108038. https://doi.org/10.1016/j.phrs.2025.108038
  12. Fotouh, A., Elbarbary, N. K., Momenah, M. A., Khormi, M. A., Mohamed, W. H., Sherkawy, H. S. et al. (2025). Hepatoprotective effects of mesenchymal stem cells in carbon tetrachloride–induced liver toxicity in rats: restoration of liver parameters and histopathological evaluation. American Journal of Veterinary Research, 1–10. https://doi.org/10.2460/ajvr.25.03.0074
  13. El-Marasy, S. A., El Awdan, S. A., Hassan, A., Abdallah, H. M. I. (2020). Cardioprotective effect of thymol against adrenaline-induced myocardial injury in rats. Heliyon, 6 (7), e04431. https://doi.org/10.1016/j.heliyon.2020.e04431
  14. Yan, L. (2021). Folic acid‐induced animal model of kidney disease. Animal Models and Experimental Medicine, 4 (4), 329–342. https://doi.org/10.1002/ame2.12194
  15. Hu, H., Xie, C., Weng, Z., Yu, P., Wang, Y., Shan, L. (2022). Dexrazoxane Alleviated Doxorubicin-Induced Nephropathy in Rats. Pharmacology, 107 (3-4), 206–215. https://doi.org/10.1159/000521220
  16. Myronchenko, S., Naumova, O., Zvyagintseva, T. (2016). Тhe impact of ultraviolet irradiation on morpho-functional state of skin in guinea pigs. Georgian Med News, 95–100.
  17. Кононський, О. І. (2002). Органічна хімія. Київ: Вища школа, 246
  18. Roberts, W. L., Moulton, L., Law, T. C., Farrow, G., Cooper-Anderson, M., Savory, J., Rifai, N. (2001). Evaluation of Nine Automated High-Sensitivity C-Reactive Protein Methods: Implications for Clinical and Epidemiological Applications. Part 2. Clinical Chemistry, 47 (3), 418–425. https://doi.org/10.1093/clinchem/47.3.418
  19. Reitman, S., Frankel, S. (1957). A Colorimetric Method for the Determination of Serum Glutamic Oxalacetic and Glutamic Pyruvic Transaminases. American Journal of Clinical Pathology, 28 (1), 56–63. https://doi.org/10.1093/ajcp/28.1.56
  20. Draper, H. H., Hadley, M. (1990). Malondialdehyde determination as index of lipid Peroxidation. Oxygen Radicals in Biological Systems Part B: Oxygen Radicals and Antioxidants, 421–431. https://doi.org/10.1016/0076-6879(90)86135-i
  21. Schumann, G., Bonora, R., Ceriotti, F., Férard, G., Ferrero, C. A., Franck, P. F. H. et al. (2002). IFCC Primary Reference Procedures for the Measurement of Catalytic Activity Concentrations of Enzymes at 37°C. Part 5. Reference Procedure for the Measurement of Catalytic Concentration of Aspartate Aminotransferase. Clinical Chemistry and Laboratory Medicine, 40 (7). https://doi.org/10.1515/cclm.2002.125
  22. Скляров, О. Я. (Ред.) (2023). Практикум з біологічної хімії. Львів: ЛНМУ, 120–122.
  23. Tang, X., Wu, J., Zhang, H., Zhong, L., Su, R., Ma, M. et al. (2025). UVB radiation and amphibian resilience: Analyzing skin color, immune suppression and oxidative stress in Rana kukunoris from different elevations. Ecotoxicology and Environmental Safety, 294, 118075. https://doi.org/10.1016/j.ecoenv.2025.118075
  24. Fotouh, A., Elbarbary, N. K., Momenah, M. A., Khormi, M. A., Mohamed, W. H., Sherkawy, H. S. et al. (2025). Hepatoprotective effects of mesenchymal stem cells in carbon tetrachloride–induced liver toxicity in rats: restoration of liver parameters and histopathological evaluation. American Journal of Veterinary Research, 1–10. https://doi.org/10.2460/ajvr.25.03.0074
  25. Zhu, Z., Zhang, M., Wang, Z., Jiang, C., Huang, C., Cheng, H. et al. (2023). Chronic β-adrenergic stress contributes to cardiomyopathy in rodents with collagen-induced arthritis. Acta Pharmacologica Sinica, 44 (10), 1989–2003. https://doi.org/10.1038/
  26. s41401-023-01099-2
  27. Liu, T., Li, M. (2025). Therapeutic potential of common Phytoestrogens found in traditional Chinese medicine in chronic kidney diseases. Frontiers in Pharmacology, 16. https://doi.org/10.3389/fphar.2025.1599097
  28. Akwari, A., George, E., Obia, U., Nyirenda, M., Mbuki, R., Nkanu, E. E. (2025). Doxorubicin Induced Hepatotoxicity, Apoptosis and Renal Dysfunction: Role of Hesperidin in Potentiation or Attenuation in Male Wistar Rats. British Journal of Healthcare & Medical Research, 12 (1), 347–353. https://doi.org/10.14738/bjhr.1201.18159

Published

2026-03-31

How to Cite

Seniuk, I., Galuzinska, L., Polovko, N., Loshakov, A., & Strelchenko, K. (2026). A comparative analysis of biochemical markers of systemic inflammation in experimental models of acute and chronic organ damage in laboratory animals. ScienceRise: Biological Science, (1 (45), 12–18. https://doi.org/10.15587/2519-8025.2026.356223

Issue

Section

Biological research