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Effectiveness of Gamma Oryzanol on prevention of surgical induced endometriosis development in rat model

Infertility is believed to be triggered by endometriosis whose pathophysiology and the etiology is still unknown. Certain genes play pivotal roles in pathogenesis of endometriosis. Natural products and plants are used as important sources for production of new drugs. The current study assesses the e...

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Autores principales: Eisalou, Mohammad Yari, Farahpour, Mohammad Reza
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857219/
https://www.ncbi.nlm.nih.gov/pubmed/35181729
http://dx.doi.org/10.1038/s41598-022-06883-4
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author Eisalou, Mohammad Yari
Farahpour, Mohammad Reza
author_facet Eisalou, Mohammad Yari
Farahpour, Mohammad Reza
author_sort Eisalou, Mohammad Yari
collection PubMed
description Infertility is believed to be triggered by endometriosis whose pathophysiology and the etiology is still unknown. Certain genes play pivotal roles in pathogenesis of endometriosis. Natural products and plants are used as important sources for production of new drugs. The current study assesses the effects of gamma-oryzanol (GO) in a rat model with surgically induced endometriosis. The experimental endometriosis was induced in 24 wistar rats, and the animals were subsequently subdivided into endometriosis-sole (endom group), 3000 and 6000 µg/kg GO (GO-3000 and GO-6000) and Vit C groups. The protein levels of estrogen receptor-alpha (ER-α), Steroidogenic factor 1 (SF1), Sirtuin 1 (SIRT1), heme oxygenase 1 (HO1), light chain 3 (LC3B) and Beclin1 (BECN1) were assessed. TUNEL staining was used for detecting the apoptosis rate. The results revealed that protein levels of SF1, HO1, and total LC3B significantly (P < 0.05) decreased in GO-6000-treated groups compared to endom group. Moreover, the protein level of BECN1 and SIRT-1 significantly (P < 0.05) increased in GO-6000-treated groups compared to endom group. GO treatment did not imply any significant difference (P > 0.05) concerning the protein levels of ER-α. The TUNEL staining results showed higher TUNEL-positive cells reactions in the rats treated with GO-6000 and Vit C. Thus, GO is involved in improving condition rats involved with endometriosis through modulation in the protein levels of some molecules and also induction of apoptosis.
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spelling pubmed-88572192022-02-22 Effectiveness of Gamma Oryzanol on prevention of surgical induced endometriosis development in rat model Eisalou, Mohammad Yari Farahpour, Mohammad Reza Sci Rep Article Infertility is believed to be triggered by endometriosis whose pathophysiology and the etiology is still unknown. Certain genes play pivotal roles in pathogenesis of endometriosis. Natural products and plants are used as important sources for production of new drugs. The current study assesses the effects of gamma-oryzanol (GO) in a rat model with surgically induced endometriosis. The experimental endometriosis was induced in 24 wistar rats, and the animals were subsequently subdivided into endometriosis-sole (endom group), 3000 and 6000 µg/kg GO (GO-3000 and GO-6000) and Vit C groups. The protein levels of estrogen receptor-alpha (ER-α), Steroidogenic factor 1 (SF1), Sirtuin 1 (SIRT1), heme oxygenase 1 (HO1), light chain 3 (LC3B) and Beclin1 (BECN1) were assessed. TUNEL staining was used for detecting the apoptosis rate. The results revealed that protein levels of SF1, HO1, and total LC3B significantly (P < 0.05) decreased in GO-6000-treated groups compared to endom group. Moreover, the protein level of BECN1 and SIRT-1 significantly (P < 0.05) increased in GO-6000-treated groups compared to endom group. GO treatment did not imply any significant difference (P > 0.05) concerning the protein levels of ER-α. The TUNEL staining results showed higher TUNEL-positive cells reactions in the rats treated with GO-6000 and Vit C. Thus, GO is involved in improving condition rats involved with endometriosis through modulation in the protein levels of some molecules and also induction of apoptosis. Nature Publishing Group UK 2022-02-18 /pmc/articles/PMC8857219/ /pubmed/35181729 http://dx.doi.org/10.1038/s41598-022-06883-4 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Eisalou, Mohammad Yari
Farahpour, Mohammad Reza
Effectiveness of Gamma Oryzanol on prevention of surgical induced endometriosis development in rat model
title Effectiveness of Gamma Oryzanol on prevention of surgical induced endometriosis development in rat model
title_full Effectiveness of Gamma Oryzanol on prevention of surgical induced endometriosis development in rat model
title_fullStr Effectiveness of Gamma Oryzanol on prevention of surgical induced endometriosis development in rat model
title_full_unstemmed Effectiveness of Gamma Oryzanol on prevention of surgical induced endometriosis development in rat model
title_short Effectiveness of Gamma Oryzanol on prevention of surgical induced endometriosis development in rat model
title_sort effectiveness of gamma oryzanol on prevention of surgical induced endometriosis development in rat model
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8857219/
https://www.ncbi.nlm.nih.gov/pubmed/35181729
http://dx.doi.org/10.1038/s41598-022-06883-4
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