Original Article

Nicotinamide Riboside Preserves Ovarian Injury in Experimental Sepsis Model in Rats

Volume 55 · Issue 2 · January 2023 Publish Date: June 1, 2023
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Jale Selli
Department of Histology and Embryology, Alanya Alaaddin Keykubat University Faculty of Medicine, Antalya, Turkey
Dilek Vural Keles
Department of Nursing, Kırklareli University Faculty of Health Sciences, Kırklareli, Turkey
Osman Nuri Keles
Department of Histology and Embryology, Atatürk University Faculty of Medicine, Erzurum, Turkey
Muhammet Celik
Department of Medical Biochemistry, Atatürk University Faculty of Medicine, Erzurum, Turkey
Zeliha Yetim
Department of Histology and Embryology, University of Health Science Hamidiye International Faculty of Medicine, İstanbul, Turkey
Selli, J., Vural Keles, D., Keles, O. N., Celik, M., & Yetim, Z. (2023). Nicotinamide Riboside Preserves Ovarian Injury in Experimental Sepsis Model in Rats. The Eurasian Journal of Medicine, 55(2), 128–134. https://doi.org/10.5152/eurasianjmed.2023.22255
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Abstract

Objective: The aim of the study is to investigate the protective effects of nicotinamide riboside on oxidative stress in an experimental sepsis model created by cecal ligation and puncture.

Materials and Methods: Rats were divided into 3 groups randomly: sham-operated (control) group, sep- sis group, and nicotinamide riboside-treated group. Sepsis model-induced cecal ligation and puncture was applied to sepsis group rats. Animals in the nicotinamide riboside-treated group were administered nicotin- amide riboside intraperitoneally (500 mg/kg). Tissue specimens from rats were biochemically calculated for their activities of catalase, superoxide dismutase, glutathione peroxidase, myeloperoxidase, and malondialde- hyde levels. Ovarian tissues of all rats were histopathologically evaluated.

Results: Catalase, superoxide dismutase, and glutathione peroxidase activities were lower in the sepsis group compared to the sham-operated (control) group. Superoxide dismutase activity was significantly higher in the nicotinamide riboside-treated group than in control and sepsis group (P < .05). Myeloperoxidase activi- ties and mean malondialdehyde concentration of ovarian tissue were lower in nicotinamide riboside-treated group than in sepsis group (P < .05). The light microscopic assessment revealed that ovarian tissue was protected, and inflammation and interstitial edema decreased in nicotinamide riboside-treated group. The follicular damage findings were notably decreased in nicotinamide riboside-treated group in comparison to sepsis group (P<0.05).

Conclusion: Our findings indicated that nicotinamide riboside diminished ovarian injury in sepsis via inhibiting tissue infiltration and increasing endogenous antioxidant capacity. Nicotinamide riboside administration may represent a new treatment approach for the prevention of sepsis-induced ovarian injury.

Cite this article as: Selli J, Vural Keles D, Nuri Keles ON, Celik M, Yetim Z. Nicotinamide riboside preserves ovarian injury in an experimental sepsis model in rats. Eurasian J Med. 2023;55(2), 128-134.

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Published In
Journal The Eurasian Journal of Medicine
Volume / Issue Volume 55 · Issue 2 · January 2023
Pages 128-134
History
Published Online June 1, 2023
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Affiliations
Jale Selli
Department of Histology and Embryology, Alanya Alaaddin Keykubat University Faculty of Medicine, Antalya, Turkey
Dilek Vural Keles
Department of Nursing, Kırklareli University Faculty of Health Sciences, Kırklareli, Turkey
Osman Nuri Keles
Department of Histology and Embryology, Atatürk University Faculty of Medicine, Erzurum, Turkey
Muhammet Celik
Department of Medical Biochemistry, Atatürk University Faculty of Medicine, Erzurum, Turkey
Zeliha Yetim
Department of Histology and Embryology, University of Health Science Hamidiye International Faculty of Medicine, İstanbul, Turkey
Cite this Article
Selli, J., Vural Keles, D., Keles, O. N., Celik, M., & Yetim, Z. (2023). Nicotinamide Riboside Preserves Ovarian Injury in Experimental Sepsis Model in Rats. The Eurasian Journal of Medicine, 55(2), 128–134. https://doi.org/10.5152/eurasianjmed.2023.22255
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