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Updated: Aug 5, 2026

Mouse Model of Surgically-induced Endometriosis by Auto-transplantation of Uterine Tissue
Published on: January 6, 2012
Effects of lactoferrin and progesterone on the endometriotic lesion in a female rat model
İrem Şenyuva1, Duygu Baki Acar2, Hasan Hüseyin Demirel Bayat3
1Department of Obstetrics and Gynecology, Faculty of Medicine, Uşak University, Uşak 64200, Turkey.
Background:
Lactoferrin (LF), a multifunctional glycoprotein of the transferrin family, exhibits anti-inflammatory and immunomodulatory properties. Endometriosis is an estrogen-dependent chronic inflammatory disease commonly treated with progesterone therapy; however, progesterone receptor (PGR) resistance in endometriotic lesions has increased interest in immunomodulatory approaches.
Objective:
To evaluate the effects of LF alone and combined with progesterone on endometriotic lesions in a rat model.
Methods:
An endometriosis model was induced in female Wistar Albino rats. Rats with confirmed endometriotic lesions were randomly divided into 4 equal groups and received the following oral treatments: Control (0.5% carboxymethylcellulose), bovine LF (bLF) (100 mg/kg/d), progesterone (0.3 mg/kg/day), combination therapy (bLF [100 mg/kg/d] + progesterone [0.3 mg/kg/d]). After treatment, the rats were euthanized, histopathological and biochemically anayses were done.
Results:
No statistically significant differences were observed in volume and adhesion scores of endometriotic lesions before and after treatment (P = 0.653, P = 0.413, P = 0.890, respectively). However, PGR and inflammatory cytocine levels were decreased in all treatment groups (P = 0.001). Although serum progesterone levels did not differ between groups (P = 0.06), serum LF levels were lower in the progesterone-only group (P = 0.001). Total antioxidant status (TAS) and Plasma total oxidant status (TOS) showed no significant differences among groups (P = 0.623 and P = 0.318, respectively).
Conclusion:
LF, alone or combined with progesterone, reduced inflammatory cytokine levels associated with endometriosis-related pain, suggesting potential therapeutic value. Further studies are needed to clarify its role in progesterone resistance and the clinical management of endometriosis.

