Research Article

Antioxidative Effects of Boron Minerals in LPS-Induced Psoriasis Model

Volume: 53 Number: 2 June 5, 2026
EN TR

Antioxidative Effects of Boron Minerals in LPS-Induced Psoriasis Model

Abstract

Objectives: Psoriasis is a chronic inflammatory skin disorder that substantially affects patients’ quality of life. Oxidative stress arises when there is a disruption in the balance between reactive oxygen species (ROS) and the body's antioxidant defense mechanisms, significantly contributing to its pathophysiology. This study aimed to investigate the effects of various boron compounds—borax, colemanite, boric acid, and ulexite—on oxidative stress markers in an LPS-induced psoriasis-like cell culture model using HaCaT keratinocytes. Methods: HaCaT cells were stimulated with LPS to induce a psoriasis-mimicking inflammatory response. Subsequently, cells were treated with different boron compounds. To evaluate antioxidant activity and lipid peroxidation, oxidative stress markers such as superoxide dismutase (SOD), glutathione peroxidase (GPx), and malondialdehyde (MDA) were examined. Results: Boron compounds modulated oxidative stress parameters by enhancing SOD and GPx activities and reducing lipid peroxidation, as reflected by decreased MDA levels. Among the tested agents, colemanite and ulexite exhibited the strongest antioxidant activities, likely attributable to their distinct mineral compositions. Conclusion: Findings suggest that boron compounds hold therapeutic potential for reducing oxidative stress in psoriasis-like conditions. Further research is needed to clarify the underlying molecular mechanisms and to refine boron-based therapeutic applications.

Keywords

Ethical Statement

Ethical approval was not required for this study as it involved only cell culture experiments.

References

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Details

Primary Language

English

Subjects

Health Care Administration, Medical Education, Health Services and Systems (Other)

Journal Section

Research Article

Authors

Sibel Göçmen This is me
Türkiye

Publication Date

June 5, 2026

Submission Date

January 30, 2026

Acceptance Date

April 1, 2026

Published in Issue

Year 2026 Volume: 53 Number: 2

APA
Er Urgancı, B., Çakal, S., Doğan, C., Göçmen, S., & Şimşek, D. S. (2026). Antioxidative Effects of Boron Minerals in LPS-Induced Psoriasis Model. Dicle Medical Journal, 53(2), 343-350. https://doi.org/10.5798/dicletip.1964432
AMA
1.Er Urgancı B, Çakal S, Doğan C, Göçmen S, Şimşek DS. Antioxidative Effects of Boron Minerals in LPS-Induced Psoriasis Model. Dicle Medical Journal. 2026;53(2):343-350. doi:10.5798/dicletip.1964432
Chicago
Er Urgancı, Buket, Sacide Çakal, Cihangir Doğan, Sibel Göçmen, and Doç.dr Selda Şimşek. 2026. “Antioxidative Effects of Boron Minerals in LPS-Induced Psoriasis Model”. Dicle Medical Journal 53 (2): 343-50. https://doi.org/10.5798/dicletip.1964432.
EndNote
Er Urgancı B, Çakal S, Doğan C, Göçmen S, Şimşek DS (June 1, 2026) Antioxidative Effects of Boron Minerals in LPS-Induced Psoriasis Model. Dicle Medical Journal 53 2 343–350.
IEEE
[1]B. Er Urgancı, S. Çakal, C. Doğan, S. Göçmen, and D. S. Şimşek, “Antioxidative Effects of Boron Minerals in LPS-Induced Psoriasis Model”, Dicle Medical Journal, vol. 53, no. 2, pp. 343–350, June 2026, doi: 10.5798/dicletip.1964432.
ISNAD
Er Urgancı, Buket - Çakal, Sacide - Doğan, Cihangir - Göçmen, Sibel - Şimşek, Doç.dr Selda. “Antioxidative Effects of Boron Minerals in LPS-Induced Psoriasis Model”. Dicle Medical Journal 53/2 (June 1, 2026): 343-350. https://doi.org/10.5798/dicletip.1964432.
JAMA
1.Er Urgancı B, Çakal S, Doğan C, Göçmen S, Şimşek DS. Antioxidative Effects of Boron Minerals in LPS-Induced Psoriasis Model. Dicle Medical Journal. 2026;53:343–350.
MLA
Er Urgancı, Buket, et al. “Antioxidative Effects of Boron Minerals in LPS-Induced Psoriasis Model”. Dicle Medical Journal, vol. 53, no. 2, June 2026, pp. 343-50, doi:10.5798/dicletip.1964432.
Vancouver
1.Buket Er Urgancı, Sacide Çakal, Cihangir Doğan, Sibel Göçmen, Doç.dr Selda Şimşek. Antioxidative Effects of Boron Minerals in LPS-Induced Psoriasis Model. Dicle Medical Journal. 2026 Jun. 1;53(2):343-50. doi:10.5798/dicletip.1964432