Mitigation of endometriosis using regenerative cerium oxide nanoparticles

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This study demonstrates that cerium oxide nanoparticles mitigate endometriosis lesions in mice by decreasing oxidative stress and inhibiting angiogenesis, while also protecting oocytes from endometriosis-related damage.

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The paper investigated whether regenerative cerium oxide nanoparticles (nanoceria), which scavenge reactive free radicals, can mitigate endometriosis-related pathology. Using a mouse model, the study reported decreased oxidative stress and inhibition of angiogenesis, alongside mitigation of endometrial lesions. It also reported that nanoceria protected oocytes exposed to endometriosis-related adverse effects, assessed in part with visualization methods and including living human oocyte observations, with the major caveat that the evidence for efficacy is based on a murine model. This paper is centrally about endometriosis — it tests nanoceria for reducing oxidative stress, suppressing angiogenesis, and mitigating endometriosis lesions in mice.

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Abstract

Cerium oxide nanoparticles (nanoceria) have recently received attention from the scientific community due to their unique free radicals (specially superoxide radical and hydrogen peroxide) scavenging property in biological system, both in vitro and in vivo. It is suggested that free radicals play an important role in the pathogenesis of endometriosis. In this study we have shown that nanoceria mitigate the endometrial lesions induced in mice model by decreasing oxidative stress and inhibiting angiogenesis. Moreover, nanoceria were also observed to protect endometriosis-related adverse effects on the oocytes, which is critical for successful pregnancy. Summarizing, nanoceria have shown promising efficacy against endometriosis related pathogenesis.From the clinical editorFree radicals have been implemented in the pathogenesis of endometriosis. In a murine model the authors demonstrated successful treatment of endometriosis with nanoceria, and protection of endometriosis-related adverse effects on the oocytes, paving the way to potential clinical translational applications in the future.
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Keywords

Cerium oxide nanoparticles; Antioxidant; Endometriosis; Anti-angiogenesis; LIVING HUMAN OOCYTES; OXIDATIVE-STRESS; MEIOTIC SPINDLE; MOUSE MODEL; ANTIOXIDANT; POLSCOPE; WOMEN; CARDIOMYOPATHY; VISUALIZATION; ANGIOGENESIS; Nanoscience & Nanotechnology; Medicine, Research & Experimental

Abstract

Cerium oxide nanoparticles (nanoceria) have recently received attention from the scientific community due to their unique free radicals (specially superoxide radical and hydrogen peroxide) scavenging property in biological system, both in vitro and in vivo. It is suggested that free radicals play an important role in the pathogenesis of endometriosis. In this study we have shown that nanoceria mitigate the endometrial lesions induced in mice model by decreasing oxidative stress and inhibiting angiogenesis. Moreover, nanoceria were also observed to protect endometriosis-related adverse effects on the oocytes, which is critical for successful pregnancy. Summarizing, nanoceria have shown promising efficacy against endometriosis related pathogenesis. From the Clinical Editor: Free radicals have been implemented in the pathogenesis of endometriosis. In a murine model the authors demonstrated successful treatment of endometriosis with nanoceria, and protection of endometriosis-related adverse effects on the oocytes, paving the way to potential clinical translational applications in the future. (C) 2013 Elsevier Inc. All rights reserved. Journal Title Nanomedicine-Nanotechnology Biology and Medicine Volume 9 Issue/Number 3 Publication Date 1-1-2013 Document Type Article Language English First Page 439 Last Page 448 WOS Identifier ISSN 1549-9634 Recommended Citation "Mitigation of endometriosis using regenerative cerium oxide nanoparticles" (2013). Faculty Bibliography 2010s. 3780. https://stars.library.ucf.edu/facultybib2010/3780

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Condition tags

endometriosis

MeSH descriptors

Cerium Endometriosis Nanoparticles Animals Antigens, CD34 Antigens, CD34 Antioxidants Antioxidants Biomarkers Biomarkers Cell Line Cerium Cerium Endometriosis Endometriosis Endometrium Endometrium Endometrium Endometrium Female

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