Development of a subcutaneous endometriosis rat model

In: Acta Cirurgica Brasileira · 2015 · vol. 30(1) , pp. 6–12 · doi:10.1590/s0102-86502015001000002 · W2019233116
article OA: gold CC0 ⤵ 9 in-corpus citations
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AI-generated summary by claude@2026-06, 2026-06-08

This study developed a subcutaneous endometriosis rat model by autoimplanting uterine fragments, which was reproducible and suitable for evaluating drug effects like estradiol, medroxyprogesterone acetate, triptorelin pamoate, and acetylsalicylic acid.

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Abstract

PURPOSE: To present a rat model of subcutaneous endometriosis for the study of pathophysiology and the effects of drugs. METHODS: Fifty three-month-old female Wistar rats (Rattus norvergicus) were distributed into one control group and four treatment groups: estradiol (2.5; 5; 10mg/kg sc), medroxyprogesterone acetate (0.5; 2; 5mg/kg sc), triptorelin pamoate (0.18; 0.56mg/kg sc) and acetylsalicylic acid (3mg/kg per os). The animals were autoimplanted subcutaneously with 4x4-mm uterine fragments to induce endometriosis. The endometriomas were measured on days 1, 7, 14 and 21. The relative dry and wet weights of the endometrioma were used to evaluate response to the drug. Endometrial -like tissue was confirmed by histology. The greatest weight gain was observed on day 14 (relative wet weight: 29.1 ± 6.7mg%, relative dry weight: 5.3 ± 0.9mg %). Treatments were administered between day 5 and day 14. RESULTS: The relative wet weight of the hemiuterus in the 10mg/kg estradiol group differed significantly from control and the other two estradiol groups (p=0.0001). In the medroxyprogesterone acetate group the weight decreased significantly but this decrease was not dose-dependent. Weight reduction was also significant in the triptorelin pamoate and the acetylsalicylic acid groups. CONCLUSION: The model of subcutaneous endometriosis is reproducible, low-cost and easy to perform, and suitable for the study of pathophysiology and the effects of drugs.

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endometriosisendometrioma

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