Regression of experimental endometriotic implants in a rat model with the angiotensin II receptor blocker losartan
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Losartan treatment in a rat model reduced endometriotic implant size and decreased plasma levels of VEGF, TNF-α, PTX-3, and CRP.
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Abstract
AIM: Endometriosis is a common disease in women of reproductive age, and many different treatments have been developed, although none has provided a cure. In this study, the efficacy of losartan, an angiotensin II type 1 receptor blocker and an antiangiogenic and anti-inflammatory agent, on regression of experimental endometriotic implants in a rat model was investigated. METHODS: Peritoneal endometriosis was surgically induced in 16 mature female Sprague-Dawley rats. The peritoneal endometriotic implant was confirmed after 28 days, and the animals were divided randomly into two groups. The control group (n = 8) was given 4 mL/day tap water by oral gavage, and the losartan group (n = 8) was given 20 mg/kg per day losartan p.o. We compared endometriotic implant size, extent and severity of adhesion, as well as plasma and peritoneal lavage fluid cytokine levels including vascular endothelial growth factor (VEGF) and tumor necrosis factor (TNF)-α, plasma inflammatory factor pentraxin-3 (PTX-3) and C-reactive protein (CRP) between the treatment groups. RESULTS: Mean surface endometriotic area, histological score of implants, adhesion formation, plasma VEGF, TNF, PTX-3 and CRP levels were significantly lower in the losartan group compared with control (P < 0.05). Furthermore, the peritoneal VEGF level was lower in the losartan group than in the control group (P 0.05). CONCLUSION: Losartan suppressed the implant surface area of experimental endometriosis in rats and reduced the levels of plasma VEGF, TNF-α, PTX-3 and CRP.
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References (42)
- Angiogenic Factors in Endometriosis via openalex
- Anti-angiogenic treatment strategies for the therapy of endometriosis via openalex
- Apoptosis and endometriosis via openalex
- Clinical Presentation and Diagnosis of Endometriosis via openalex
- Combined blockade of angiotensin II type 1 receptor and activation of peroxisome proliferator-activated receptor- by telmisartan effectively inhibits vascularization and growth of murine endometriosis-like lesions via openalex
- Comparison of aromatase inhibitor (letrozole) and immunomodulators (infliximab and etanercept) on the regression of endometriotic implants in a rat model via openalex
- Effect of GnRH analogues on apoptosis and release of interleukin-1 and vascular endothelial growth factor in endometrial cell cultures from patients with endometriosis via openalex
- Effect of Peroxisome Proliferator—Activated Receptor-γ Agonist Rosiglitazone on the Induction of Endometriosis in an Experimental Rat Model via openalex
- Effect of the immunomodulator leflunomide on the induction of endometriosis in an experimental rat model via openalex
- ENDOMETRIOSIS via openalex
- ENDOMETRIOSIS via openalex
- Endometriosis: current concepts and therapy via openalex
- Endometriosis: hormone regulation and clinical consequences of chemotaxis and apoptosis via openalex
- Extracts from "Clinical Evidence": Endometriosis via openalex
- High-dose atorvastatin causes regression of endometriotic implants: a rat model via openalex
- Immunology and Endometriosis via openalex
- Leflunomide—an Immunomodulator—Induces Regression of Endometrial Explants in a Rat Model of Endometriosis via openalex
- Morphometric study of the stromal vascularization in peritoneal endometriosis via openalex
- Peritoneal endometriosis is an inflammatory disease via openalex
- Peritoneal endometriosis is an inflammatory disease via openalex
- Peroxisome proliferator‐activated receptor‐gamma agonist rosiglitazone reduces the size of experimental endometriosis in the rat model via openalex
- Peroxisome proliferator-activated receptor-γ ligand reduced tumor necrosis factor-α-induced interleukin-8 production and growth in endometriotic stromal cells via openalex
- The relationship between microvessel density, proliferative activity and expression of vascular endothelial growth factor-A and its receptors in eutopic endometrium and endometriotic lesions via openalex
- W1971586374 via openalex
- W2116073327 via openalex
- W2140246703 via openalex
- W2142285406 via openalex
- W2146493861 via openalex
- W2169471480 via openalex
- W1502305149 via openalex
- W2040564940 via openalex
- W7073664733 via openalex
- W2041563335 via openalex
- W2042498523 via openalex
- W2059612167 via openalex
- W2014091868 via openalex
- W2068951648 via openalex
- W2012546272 via openalex
- W2095019266 via openalex
- W2098736824 via openalex
- W2104354342 via openalex
- W2004591427 via openalex
Cited by (5)
- The Promises of Natural Killer Cell Therapy in Endometriosis 2022
- The protective effects of Azilsartan against hypoxia in endometrial stromal cells: an implication in endometriosis 2022
- Does endometriosis increase susceptibility to COVID-19 infections? A case–control study in women of reproductive age 2021
- Analysis of key candidate genes and pathways of endometriosis pathophysiology by a genomics-bioinformatics approach 2019
- Combination therapy with telmisartan and parecoxib induces regression of endometriotic lesions 2017
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- last seen: 2026-08-25T06:10:03.373225+00:00
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- last seen: 2026-06-10T17:14:06.276822+00:00
- pubmed
- last seen: 2026-05-13T22:18:15.805398+00:00
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