Determination of the effects of monosodium glutamate, calcitriol and coenzyme Q substances on suppressing immune system cells

Authors

DOI:

https://doi.org/10.71336/jabs.1509

Keywords:

Immune system, immunosuppression, PBMC, Coenzyme Q, calcitriol and MSG

Abstract

The immune system is one of the most crucial systems in the human body, as it plays a vital role in destroying pathogens and foreign particles. Any disruption in immune system activity can lead to specific diseases called "opportunistic diseases," such as lupus, rheumatoid arthritis, and multiple sclerosis. In such cases, immunomodulatory agents are used. In this study, peripheral blood mononuclear cells (PBMC) from a single healthy donor were cultured and then stimulated with lipopolysaccharide (LPS), which induces the release of inflammatory cytokines, to create an experimental model similar to those used in autoimmune diseases. For this purpose, PBMC cells were isolated from donor blood and cultured. Various concentrations were applied, and LPS was induced at the determined stimulating concentration (IC50) of 20,000 ng/ml. Cytotoxicity was then determined by applying monosodium glutamate (MSG), calcitriol, and coenzyme Q at effective concentrations (IC50) determined through preliminary experiments. According to the obtained data, a 70% (p<0.001) cytotoxic effect was observed in MSG-treated cells after 24 hours. 48 hours after substance application, MSG showed a 90% (p<0.001) cytotoxic effect on cells, while coenzyme Q10 showed an 89% (p<0.01) cytotoxic effect. Calcitriol did not exhibit inhibitory properties on PBMCs. 72 hours after the substances were applied, coenzyme Q10 showed a 94% cytotoxic effect on cells. 96 hours after the substances were applied to LPS-induced PBMC cells, no difference was observed between the groups. As a result, it was found that the substances applied may have different effects depending on time, in line with the findings obtained. Considering the effects of the substances on PBMCs, it is important to investigate their effects in more detail in some disease conditions where it is desired to inhibit immune system cells, so that they can be evaluated as an option in treatment. A full understanding of the effectiveness and safety of these substances is important for individualized treatment approaches.

References

[1] Macpherson, G., & Austyn, J. (2013). Exploring Immunology: Concepts and Evidence, 5-47, USA

[2] Mantle, D., & Hargreaves, I. P. (2024). Coenzyme Q10 and Autoimmune Disorders: An Overview. International Journal of Molecular Sciences, 25(8), 4576. https://doi.org/10.3390/ijms25084576

[3] Schildberger, A., Rossmanith, E., Eichhorn, T., Strassl, K., Weber, V. (2013). Monocytes, peripheral blood mononuclear cells, and THP-1 cells exhibit different cytokine expression patterns following stimulation with lipopolysaccharide. Mediators Inflamm. 697972.

[4] Marieb, E., N., Hoehn, K. (2014). Human Anatomy & Physiology, 753-755.

[5] Stolzenberg-Solomon, RZ, Vieth, R., Azad, A., Pietinen, P., Taylor, P. R… (2006). A prospective nested case-control study of vitamin D status and pancreatic cancer risk in male smokers. Cancer Res. 66, 20, 10213‐10219.

[6] Chlebowski, RT, Johnson, KC, Kooperberg, C., Pettinger, M., Wactawski-Wende, J…(2008). Calcium plus vitamin D supplementation and the risk of breast cancer. Journal of the National Cancer Institute. 100, 22, 1581-1591.

[7] Stolzenberg-Solomon, RZ, Hayes, RB, Horst, RL, Anderson, KE, Hollis, B. W… (2009). Serum vitamin D and risk of pancreatic cancer in the prostate, lung, colorectal, and ovarian screening trial. Cancer Res. 69, 4, 1439‐1447.

[8] Martinesi, M., Treves, C., d'Albasio, G., Bagnoli, S., Bonanomi, A. B… (2008). Vitamin D Derivatives Induce Apoptosis and Downregulate ICAM-1 levels in peripheral blood mononuclear cells of inflammatory bowel disease patients. Inflamm Bowel Dis. 14(5), 597-604.

[9] Osuch, D., Opala, D., Staszczyk, I., Drabik, A., Szczotka, D., Szemplińska, A., … Anderska, A. (2024). The role of vitamin D in selected autoimmune diseases - review. Quality in Sport, 20, 54077. https://doi.org/10.12775/QS.2024.20.54077

[10] Gutierrez-Mariscal, F.M., Arenas-de Larriva, AP, Limia-Perez, L., Romero-Cabrera, J.L., Yubero-Serrano, EM, & López-Miranda, J. (2020). Coenzyme Q10 Supplementation for the Reduction of Oxidative Stress: Clinical Implications in the Treatment of Chronic Diseases. International journal of molecular sciences, 21(21), 7870.

[11] Quiles, J. L., Farquharson, A. J., Ram, M. C. (2003). Coenzyme Q differentially modulates phospholipid hydroperoxide glutathione peroxidase gene expression and free radicals production in malignant and non-malignant prostate cells. Biofactors. 18, 1-4, 265‐270.

[12] Jovic, ZK, Veselinovic, M., Milovanovic, M., Krankenhaus, M., Sarac, M. (2009). Monosodium glutamate induces apoptosis in naive and memory human B cells. Bratisl Lek Listy 110, 10, 636-640.

[13] Falalyeyeva, TM, Leschenko, IV, Beregova, TV, Lazarenko, LM, Savchuk, OM (2017). Probiotic strains of lactobacilli and bifidobacteria alter pro- and anti-inflammatory cytokines production in rats with monosodium glutamate-induced obesity. Fiziol Zh. 63, 1, 17-25.

[14] Castrogiovanni, D., Gaillard, R., C., Giovambattista, A., Spinedi, E. (2008). Neuroendocrine, Metabolic, and Immune Functions during the Acute Phase Response of Inflammatory Stress in Monosodium Glutamate-Damaged, Hyperadipose Male Rat. Neuroendocrinology. 88, 227-234.

[15] Das D, Banerjee A, Manna K, Sarkar D, Shil A, Sikdar Ne E Bhakta M, Mukherjee S, Maji BK (2023). Quercetin counteracts monosodium glutamate to mitigate immunosuppression in the thymus and spleen via redox-guided cellular signaling. Phytomedicine. 2024 Apr;126:155226. doi: 10.1016/j.phymed.2023.155226. Epub 2023 Nov 29. PMID: 38387276.

[16] Verhoeckx K, Cotter P, López-Expósito I, Kleiveland C, Lea T, Mackie A, Requena T, Swiatecka D, Wichers H. (0215). The impact of food bioactives on health: in vitro and ex vivo models. Book. library.oapen.org https://link.springer.com/book/10.1007/978-3-319-16104-4

[17] Nair, R., Maseeh, A. (2012). Vitamin D: The “sunshine” vitamin. J Pharmacol Pharmacother. 3, 2, 118‐126 .

[18] Stio, M., Martinesi, M., Bruni, S., Treves, C., Bagnoli, S... (2006). Interaction among vitamin D 3 analogue KH 1060, TNF-α, and vitamin D receptor protein in peripheral blood mononuclear cells of inflammatory bowel disease patients. Int Immunopharmacol. 6, 7, 1083-1092.

[19] Saracligil, B., Ozturk, B., Unlu, A., Abusoglu,S., Tekin, G. (2017). The effect of vitamin D on MCF-7 breast cancer cell metabolism. Bratisl Med J. 118, 2, 101-106.

[20] Pavlovic, Voja, Sokolovic, D., Jevtovic-stoimenov, T. (2007). Effect of monosodium glutamate on oxidative stress and apoptosis in rat thymus. Effect of monosodium glutamate on oxidative stress and apoptosis in rat thymus. Mol Cell Biochem. 303(1-2), 161‐166.

[21] Gollapudi, S., Gupta, S. (2016). Reversal of oxidative stress-induced apoptosis in T and B lymphocytes by Coenzyme Q10 (CoQ10). 5, 2, 41-47.

Determination of the effects of monosodium glutamate, calcitriol and coenzyme Q substances on suppressing immune system cells

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Published

2025-09-29

How to Cite

Sabah , M. S., Turgut Coşan, D., Calis , İ. U., & Mutlu, F. (2025). Determination of the effects of monosodium glutamate, calcitriol and coenzyme Q substances on suppressing immune system cells. Journal of Applied Biological Sciences, 19(3), 232–236. https://doi.org/10.71336/jabs.1509

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