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Mouse Model of Surgically-induced Endometriosis by Auto-transplantation of Uterine Tissue
Published on: January 6, 2012
Investigation of endothelin-1 receptor antagonist bosentan in a rat endometriosis model
Saliha Sena Karcioglu1, Zekai Halici2, Elif Cadirci1
1Department of Pharmacology, Faculty of Medicine, Ataturk University, Erzurum, 25240, Turkey.
Abstract:
The study aimed to investigate the roles of endothelin-1 and endothelin receptors in a rat endometriosis model and to demonstrate how bosentan (BOS), an endothelin receptor blocker, could potentially serve as a novel treatment for endometriosis. Overall, 36 rats were divided into groups as follows: Group 1: Sham, Group 2: endometriosis, Group 3: Sham + BOS100 mg/kg, Group 4: endometriosis + BOS 25 mg/kg, Group 5: endometriosis + BOS 50 mg/kg, and Group 6: endometriosis + BOS 100 mg/kg. In the first laparotomy, an experimental endometriosis model was created by implanting a 0.5 × 0.5 cm2 piece of autologous endometrial tissue in Groups 2, 4, 5, and 6. After waiting for 4 weeks, a second laparotomy was performed to measure the endometriotic lesions in Groups 2, 4, 5, and 6. Following the measurements, Groups 4, 5, and 6 received oral administration of BOS at doses of 25 mg/kg, 50 mg/kg, and 100 mg/kg, respectively, for 2 weeks. Three groups received 100 mg/kg of BOS during the same time period. After the drug administration, a third laparotomy was performed, and the endometriotic lesions in Groups 2, 4, 5, and 6 were re-measured. Histopathological, immunohistochemical, biochemical, and molecular analyses of endometriotic lesion samples obtained after the experiment revealed a significant increase in the levels of TNF-α, TGF-β, MMP-9, ET-1, eNOS, VEGF, ETR-A, ETR-B, and MAPkinase in the experimental endometriosis group (Group 2). Conversely, these levels were significantly reduced in the BOS treatment groups (Groups 4, 5, and 6) in a dose-dependent manner compared to Group 2. Similarly, surface area measurements of endometriotic lesions showed a dose-dependent reduction in the BOS-treated groups (Groups 4, 5, and 6). The roles of endothelin-1 and its receptors in the pathophysiology and treatment of the endometriosis model of rats were demonstrated histopathologically, immunohistochemically, biochemically, and molecularly using BOS. This study can shed light on clinical treatment protocols for women with endometriosis.
Insights
This study shows that bosentan (BOS), an endothelin receptor blocker, effectively reduced endometriotic lesion size in a rat model. BOS treatment significantly decreased key inflammatory and growth factors, suggesting its potential as a novel endometriosis therapy.
Area of Science:
- Reproductive Endocrinology
- Pharmacology
- Oncology
Background:
- Endometriosis is a complex gynecological disorder with limited treatment options.
- Endothelin-1 (ET-1) and its receptors are implicated in endometriosis pathophysiology.
- Targeting the endothelin pathway presents a potential therapeutic strategy.
Purpose of the Study:
- To investigate the role of ET-1 and its receptors in a rat endometriosis model.
- To evaluate the efficacy of bosentan (BOS), an endothelin receptor blocker, as a novel treatment for endometriosis.
Main Methods:
- An experimental endometriosis model was established in rats.
- Rats received varying doses of BOS (25, 50, 100 mg/kg) or sham treatment.
- Lesion size, histopathology, and molecular markers (TNF-α, TGF-β, MMP-9, ET-1, eNOS, VEGF, ETR-A, ETR-B, MAPkinase) were analyzed.
Main Results:
- Endometriotic lesions showed significantly increased levels of inflammatory and angiogenic factors.
- BOS treatment dose-dependently reduced lesion size and the expression of these factors.
- ET-1 and its receptor pathways were confirmed to be involved in endometriosis progression.
Conclusions:
- Endothelin signaling plays a crucial role in endometriosis development and progression.
- Bosentan demonstrates significant therapeutic potential for endometriosis by targeting endothelin pathways.
- This research may inform future clinical treatment strategies for endometriosis.

