Nitrosative stress parameters as potential biomarkers in combat trauma
Abstract
As a result of severe injuries and post-traumatic stress disorder, sexual dysfunction and fertility disorders are among the complications men experience. The mechanisms of the effects of combat trauma are complex and include an imbalance of the immune system, which leads to severe inflammatory reactions and other immunomodifying effects after injury. An early r e sponse to an acute inflammatory injury, such as wound healing, is the production of nitric oxide (NO) as a result of L-arginine metabolism. NO is an important regulator of cellular functions throughout the wound healing process, stimulating fibroblasts to produce collagen, promoting matrix deposition, remodeling, and angiogenesis. However, insufficient or excessive NO synthesis negatively affects wound healing. The aim of the study was to investigate the prognostic power of arginase activity parameters and individual NO synthase isoforms as potential biomarkers of nitrosative stress in men with combat trauma. The study e x amined 68 men with combat trauma, including 42 men aged 20 – 39 years and 26 men aged 40 – 53 years. Criteria for inclusion in the control groups: 30 healthy men aged 20 – 39 years and 18 men aged 40 – 53 years with normal levels of cNOs, iNOs and arg i nase activity, somatically healthy, without sexual dysfunction. In all groups, the activity of NO synthases and arginase as markers of nitrosative stress was measured spectrophotometrically in blood serum and lymphocyte samples. The prognostic power of the parameters of cNOS, iNOS and arginase activity in the combat trauma and control groups was determined by the receiver opera t ing characteristic curve (ROC curve). Based on the ROC analysis, the threshold value of cNOS activity in blood lymphocytes was determined, which is an integral highly sensitive criterion for unfavorable prognosis in combat trauma. For men aged 20 – 39 years, this figure is ≤37.5 nmol NADPH(H + )/min. mg with a sensitivity of 61.9% and a maximum specificity of 100 . 0 %, while for the group of men aged 40 – 53 years, the cutoff value is ≤38.4 nmol NADPH(H + )/min. mg with a sensitivity of 65. 4 % and a maximum specificity. In the ROC analysis of iNOS activity in lymphocytes of men with combat trauma in relation to healthy men, an excellent model quality was obtained with the maximum area under the ROC curve for patients of both age groups. The lymphocyte arginase activity in the two age groups of men with combat trauma were characterized by the very good diagnostic accuracy of the test. Thus, the parameters of oxidative-nitrosative stress, in particular the activity of constitutive and inducible isoforms of NO synthase and arginase in blood serum and lymphocytes can be potential markers in distinguishing pathological changes in men affected by combat (bullet and shrapnel wounds). The inducible isoform of NO synthase has been shown in studies to be a highly sensitive and highly specific marker regardless of the age of men.References
Angka, L., Khan, S. T., Kilgour, M. K., Xu, R., Kennedy, M. A., & Auer, R. C. (2017). Dysfunctional natural killer cells in the aftermath of cancer surgery. International Journal of Molecular Sciences, 18(8), 1787.
Bronte, V., Serafini, P., Mazzoni, A., Segal, D. M., & Zanovello, P. (2003). L-arginine metabolism in myeloid cells controls T-lymphocyte functions. Trends in Immunology, 24(6), 301–305.
Campbell, L., Saville, C. R., Murray, P. J., Cruickshank, S. M., & Hardman, M. J. (2013). Local arginase 1 activity is required for cutaneous wound healing. Journal of Investigative Dermatology, 133(10), 2461–2470.
Canè, S., Geiger, R., & Bronte, V. (2024). The roles of arginases and arginine in immunity. Nature Reviews Immunology, 25, 266–284.
Castillo, O., Chen, I. K., Amini, E., Yafi, F. A., & Barham, D. W. (2022). Male sexual health related complications among combat veterans. Sexual Medicine Reviews, 10(4), 691–697.
Chromy, B. A., Eldridge, A., Forsberg, J. A., Brown, T. S., Kirkup, B. C., Jaing, C., Be, N. A., Elster, E., & Luciw, P. A. (2013). Wound outcome in combat injuries is associated with a unique set of protein biomarkers. Journal of Translational Medicine, 11(1), 281.
Dufour-Gaume, F., Frescaline, N., Cardona, V., & Prat, N. J. (2023). Danger signals in traumatic hemorrhagic shock and new lines for clinical applications. Frontiers in Hysiology, 13, 999011.
Fomichova, O., Oliveira, P. F., & Bernardino, R. L. (2024). Exploring the interplay between inflammation and male fertility. The FEBS Journal, 2024, 17366.
Gould, A. N., & Candy, G. P. (2017). The role of L-arginine in wound healing. In: Patel, V. B., Preedy, V. R., & Rajendram, R. (Eds.). L-Arginine in clinical nutrition. Humana, Cham. Pp. 577–588.
Greiner, M., Pfeiffer, D., & Smith, R. D. (2000). Principles and practical application of the receiver-operating characteristic analysis for diagnostic tests. Preventive Veterinary Medicine, 45(1–2), 23–41.
Hassanzad, M., & Hajian-Tilaki, K. (2024). Methods of determining optimal cut-point of diagnostic biomarkers with application of clinical data in ROC analysis: An update review. BMC Medical Research Methodology, 24(1), 84.
Hierholzer, C., Harbrecht, B., Menezes, J. M., Kane, J., MacMicking, J., Nathan, C. F., Peitzman, A. H., Billiar, T. R., & Tweardy, D. J. (1998). Essential role of induced nitric oxide in the initiation of the inflammatory response after hemorrhagic shock. Journal of Experimental Medicine, 187(6), 917–928.
Katz, R. (2004). Biomarkers and surrogate markers: An FDA perspective. Neurotherapeutics, 1(2), 189–195.
Kiang, J. G. (2004). Inducible heat shock protein 70 kD and inducible nitric oxide synthase in hemorrhage/resuscitation-induced injury. Cell Research, 14, 450–459.
Kurhaluk, N., & Tkaczenko, H. (2025). L-Arginine and nitric oxide in vascular regulation – Experimental findings in the context of blood donation. Nutrients, 17(4), 665.
Lavryk, G. S., Korniychuk, O. P., Besedina, A. S., & Vorobets, Z. D. (2017). The arginase pathway of L-arginine metabolism of peripheral blood lymphocytes in patients with acne vulgaris. Regulatory Mechanisms in Biosystems, 8(4), 596–601.
Lee, C. C., Marill, K. A., Carter, W. A., & Crupi, R. S. (2001). A current concept of trauma-induced multiorgan failure. Annals of Emergency Medicine, 38(2), 170–176.
Lee, Y. T., Tan, Y. J., & Oon, C. E. (2018). Molecular targeted therapy: Treating cancer with specificity. European Journal of Pharmacology, 834, 188–196.
Lee, Y.-K., Ahn, Y., Leem, D.-H., Baek, J.-A., Ko, S.-O., & Shin, H.-K. (2010). The effect of heat shock protein 70 on inducible nitric oxide synthase during sepsis in rats. Journal of Korean Association of Oral and Maxillofacial Surgeons, 36(5), 346–352.
Li, R., Ye, J. J., Gan, L., Zhang, M., Sun, D., Li, Y., Wang, T., & Chang, P. (2023). Traumatic inflammatory response: pathophysiological role and clinical value of cytokines. European Journal of Trauma and Emergency Surgery, 50(4), 1313–1330.
Lundberg, J. O., & Weitzberg, E. (2022). Nitric oxide signaling in health and disease. Cell, 185(16), 2853–2878.
Makarov, V. V., Nehoduiko, V. V., Feskov, V. M., Petiunin, O. H., Smolianyk, K. M., & Syzyi, M. Y. (2024). Features of combat trauma pathogenesis. Emergency Medicine, 20(7), 554–562.
Marik, P. E., & Flemmer, M. (2012). The immune response to surgery and trauma: Implications for treatment. Journal of Trauma and Acute Care Surgery, 73(4), 801–808.
Morris Jr., S. M. (2012). Arginases and arginine deficiency syndromes. Current Opinion in Clinical Nutrition and Metabolic Care, 15(1), 64–70.
Musci, G., Persichini, T., Casadei, M., Mazzone, V., Venturini, G., Polticelli, F., & Colasanti, M. (2006). Nitrosative/oxidative modifications and ageing. Mechanisms of Ageing and Development, 127(6), 524–551.
Nowak, M., Wójcik, J., Logoń, K., Kaczmarek, M., Łyżwa, K., Zapała, J., & Piotrowski, P. (2023). The impact of post-traumatic stress disorder on sexual dysfunction. Psychiatria, 20(2), 100–107.
Onufrovych, O. K., Fafula, R. V., Vorobets, M. Z., Besedina, A. S., Melnyk, O. V., Vorobets, D. Z., & Vorobets, Z. D. (2024). Parameters of oxidative, nitrasive and anti-oxidative status in men with erectile dysfunction due to combat trauma. Regulatory Mechanisms in Biosystems, 15(1), 97–101.
Pedrazini, M. C., Martinez, E. F., dos Santos, V. A. B., & Groppo, F. C. (2024). L-arginine: Its role in human physiology, in some diseases and mainly in viral multiplication as a narrative literature review. Future Journal of Pharmaceutical Sciences, 10(1), 99.
Qualls, J. E., Subramanian, C., Rafi, W., Smith, A. M., Balouzian, L., DeFreitas, A. A., & Murray, P. J. (2012). Sustained generation of nitric oxide and control of mycobacterial infection requires argininosuccinate synthase 1. Cell Host and Microbe, 12(3), 313–323.
Racké, K., & Warnken, M. (2010). L-arginine metabolic pathways. The Open Nitric Oxide Journal, 2, 9–19.
Reznikov, A. G. (2023). Stress-induced disorders of reproductive functions. Fiziologichnyi Zhurnal, 69(6), 97–107.
Satriano, J. (2004). Arginine pathways and the inflammatory response: Interregulation of nitric oxide and polyamines. Amino Acids, 26, 321–329.
Sharma, J. N., Al-Omran, A., & Parvathy, S. S. (2007). Role of nitric oxide in inflammatory diseases. Inflammopharmacology, 15, 252–259.
Stasyuk, N., Gayda, G., Yepremian, H., Stepien, A., & Gonchar, M. (2017). Fluorometric enzymatic assay of L-arginine. Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 170, 184–190.
Sverdlov, A. L., Ngo, D. T., Chan, W. P., Chirkov, Y. Y., & Horowitz, J. D. (2014). Aging of the nitric oxide system: Are we as old as our NO? Journal of the American Heart Association, 3(4), e000973.
Swets, J. A. (1988). Measuring the accuracy of diagnostic systems. Science, 240(4857), 1285–1293.
Thomas, D. D., Ridnour, L. A., Isenberg, J. S., Flores-Santana, W., Switzer, C. H., Donzelli, S., Hussain, P., Vecoli, C., Paolocci, N., Ambs, S., Colton, C. A., Harris, C. C., Roberts, D. D., & Wink, D. A. (2008). The chemical biology of nitric oxide: Implications in cellular signaling. Free Radical Biology and Medicine, 45(1), 18–31.
Thompson, K. B., Krispinsky, L. T., & Stark, R. J. (2019). Late immune consequences of combat trauma: A review of trauma-related immune dysfunction and potential therapies. Military Medical Research, 6, 11.
Toma, C., De Cillà, S., Palumbo, A., Garhwal, D. P., & Grossini, E. (2021). Oxidative and nitrosative stress in age-related macular degeneration: A review of their role in different stages of disease. Antioxidants, 10(5), 653.
Tsikas, D., & Wu, G. (2015). Homoarginine, arginine, and relatives: Analysis, metabolism, transport, physiology, and pathology. Amino Acids, 47, 1697–1702.
Vorobets, M. Z., Vorobets, D. Z., Chaplyk, V. V., Onufrovych, O. K., Besedina, A. S., Fafula, R. V., Vorobets, Z. D., & Chemerys, O. M. (2024). The diagnostic value of the NO-synthase, Ca2+- and Na+-dependent ATP-hydrolase systems and the therapeutic potential of NO-stimulators in erectile dysfunction of men injured as a result of combat operations (combat trauma). Regulatory Mechanisms in Biosystems, 15(4), 760–766.
Wink, D. A., Hines, H. B., Cheng, R. Y., Switzer, C. H., Flores-Santana, W., Vitek, M., Ridnour, L. A., & Colton, C. A. (2011). Nitric oxide and redox mechanisms in the immune response. Journal of Leukocyte Biology, 89(6), 873–891.
Authors retain copyright and grant the journal right of first publication with the work simultaneously licensed under a Creative Commons «Attribution» 4.0 License that allows others to share the work with an acknowledgement of the work's authorship and initial publication in this journal.


