# Therapeutic potential of casticin in alleviating ovarian torsion/detorsion-induced ovarian and lung injuries

**Authors:** Ersen Eraslan, Ayhan Tanyeli̇, Mustafa Can Güler, Fazile Nur Eki̇nci̇ Akdemi̇r, Ömer Topdaği, Şahin Yazici, Derya Güzel Erdoğan, Esra Çinar Tanriverdi̇, Selim Çomakli

PMC · DOI: 10.22038/ijbms.2025.85990.18572 · 2025-01-01

## TL;DR

This study shows that casticin can reduce ovarian and lung damage caused by ovarian torsion in rats, suggesting it may be a promising treatment for this gynecological emergency.

## Contribution

The study demonstrates casticin's novel therapeutic potential in mitigating ovarian torsion/detorsion-induced injuries.

## Key findings

- Casticin reduced oxidative stress and inflammation markers in ovarian and lung tissues.
- Casticin improved antioxidant defense in tissues affected by torsion/detorsion.
- Casticin administration attenuated tissue damage in a rat model of ovarian torsion.

## Abstract

Ovarian torsion is a critical gynecological emergency caused by the twisting of the ovary around its supporting structures, resulting in compromised blood flow and potential ovarian damage. Ovarian torsion/detorsion (T/D) can lead to severe complications, including infertility, if not promptly addressed. This study aimed to investigate the therapeutic effects of casticin (CAST) on ovarian and lung tissue injuries induced by a bilateral ovarian T/D model in rats.

Experimental animals were randomly allocated into groups of sham, T/D, CAST 5 mg/kg, and CAST 10 mg/kg. Ovarian and lung tissues were subjected to biochemical, histopathological, and immunohistochemical analyses.

In the T/D group, markers of oxidative stress and inflammation, including myeloperoxidase (MPO) activity, malondialdehyde (MDA), oxidative stress index (OSI), tumor necrosis factor-alpha (TNF-α), and 8-hydroxy-2’ deoxyguanosine (8-OHdG), were significantly elevated (P<0.05). Conversely, superoxide dismutase (SOD) activity and total antioxidant status (TAS) levels were notably decreased (P<0.05). CAST administration significantly attenuated tissue damage by reducing oxidative stress and inflammatory markers while enhancing antioxidant defense (P<0.05).

CAST demonstrated a therapeutic effect against ovarian and lung tissue damage induced by T/D, suggesting that it may serve as a potential therapeutic agent for treating ovarian T/D-related injuries. These findings underscore the potential of CAST in clinical settings, particularly as a novel intervention to mitigate complications associated with I/R injuries in gynecological emergencies.

## Linked entities

- **Chemicals:** casticin (PubChem CID 5315263), malondialdehyde (PubChem CID 10964), 8-hydroxy-2’ deoxyguanosine (PubChem CID 135406132)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Genes:** Mpo (myeloperoxidase) [NCBI Gene 303413], Tnf (tumor necrosis factor) [NCBI Gene 24835] {aka RATTNF, TNF-alpha, Tnfa}
- **Diseases:** gynecological emergencies (MESH:D005831), inflammation (MESH:D007249), I/R injuries (MESH:C580424), tissue damage (MESH:D017695), ovarian and lung injuries (MESH:D010049), Ovarian torsion (MESH:D000082843), infertility (MESH:D007246)
- **Chemicals:** T (MESH:D014316), MDA (MESH:D008315), CAST (MESH:C054133), 8-OHdG (MESH:D000080242)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Figures

8 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12203820/full.md

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Source: https://tomesphere.com/paper/PMC12203820