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Article 2025 · 5 citations

New Potential Agent in Ovarian Ischemia Reperfusion Injury: Alpha Pinene

Gulakar, Basak, Sebin, Saime Ozbek, Laloglu, Esra, Tanyeli, Ayhan, Guler, Mustafa Can, Erbas, Elif, Can, Serpil

Abstract

Ovarian torsion causes problems such as infertility in women due to ischemia-reperfusion (I/R) injury. alpha-Pinene (AP) is a monoterpene with known anti-inflammatory, antioxidant, and antiapoptotic impacts. In the present investigation, the protective impact of AP was examined in the ovarian I/R model. 28 Wistar-Albino female rats were used in the study. TNF-alpha, IL-1 beta, IL-10, MDA, IMA, SOD, and SIRT-1 levels were determined in ovarian tissue by ELISA method. Histopathological and immunohistochemical analyses were conducted to determine Bcl-2, Caspase-3, LC3B, and NF kappa B levels in ovarian tissues. TNF-alpha, IL-1 beta, IMA, and MDA levels were reduced in the treatment groups than the I/R group dose-dependent, while IL-10, SOD, and SIRT-1 levels increased substantially. Caspase-3 immunoreactivity declined in the treatment groups while Bcl-2 levels increased. LC3B and NF kappa B levels, which rise with I/R injury, were reduced considerably in the treatment groups. In addition, hemorrhage, edema, vascular congestion, and follicular degeneration due to I/R injury decreased in the treatment groups. The present investigation shows that AP has anti-inflammatory, antiapoptotic, and autophagy inhibitory effects against I/R damage in ovarian tissues and reduces oxidative stress. The results indicate that AP may be a potential protective agent in clinical use. Further research is needed before AP can be used in the clinic.

Keywords
inflammation ovarian ischemia-reperfusion injury oxidative stress alpha-Pinene OXIDATIVE STRESS ISCHEMIA/REPERFUSION INJURY APOPTOSIS EXPRESSION DETORSION TORSION IMPACT
WoS Categories
Biochemistry & Molecular Biology Toxicology
Sustainable Development Goals
Citation
Journal
JOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGY
Year
2025
Volume
39
Issue
6
ISSN
1095-6670
eISSN
1099-0461
DOI
10.1002/jbt.70318
WoS UID
WOS:001497169700001
Open via DOI