Diosmin Mitigates Cyclophosphamide Induced Premature Ovarian Insufficiency in Rat Model

The current study was designed to investigate the protective role of diosmin against cyclophosphamide-induced premature ovarian insufficiency (POI). Female Swiss albino rats received a single intraperitoneal dose of cyclophosphamide (200 mg/kg) followed by 8 mg/kg/day for the next 15 consecutive day...

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Main Authors: Noha M. Abogresha, Sally S. Mohammed, Marwa M. Hosny, Hoda Y. Abdallah, Ahmed M. Gadallah, Sahar M. Greish
Format: Article
Language:English
Published: MDPI AG 2021-03-01
Series:International Journal of Molecular Sciences
Subjects:
Online Access:https://www.mdpi.com/1422-0067/22/6/3044
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author Noha M. Abogresha
Sally S. Mohammed
Marwa M. Hosny
Hoda Y. Abdallah
Ahmed M. Gadallah
Sahar M. Greish
author_facet Noha M. Abogresha
Sally S. Mohammed
Marwa M. Hosny
Hoda Y. Abdallah
Ahmed M. Gadallah
Sahar M. Greish
author_sort Noha M. Abogresha
collection DOAJ
description The current study was designed to investigate the protective role of diosmin against cyclophosphamide-induced premature ovarian insufficiency (POI). Female Swiss albino rats received a single intraperitoneal dose of cyclophosphamide (200 mg/kg) followed by 8 mg/kg/day for the next 15 consecutive days either alone or in combination with oral diosmin at 50 or 100 mg/kg. Histopathological examination of ovarian tissues, hormonal assays for follicle stimulating hormone (FSH), estradiol (E2), and anti-Mullerian hormone (AMH), assessment of the oxidative stress status, as well as measurement of the relative expression of miRNA-145 and its target genes [vascular endothelial growth factor B <i>(VEGF-B)</i> and regulator of cell cycle (<i>RGC32</i>)] were performed. Diosmin treatment ameliorated the levels of E2, AMH, and oxidative stress markers. Additionally, both low and high diosmin doses significantly reduced the histopathological alterations and nearly preserved the normal ovarian reserve. MiRNA-145 expression was upregulated after treatment with diosmin high dose. miRNA-145 target genes were over-expressed after both low and high diosmin administration. Based on our findings, diosmin has a dose-dependent protective effect against cyclophosphamide-induced ovarian toxicity in rats.
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spelling doaj.art-c4cd50db5c6049fca5ae634f73a5c86b2023-11-21T10:47:13ZengMDPI AGInternational Journal of Molecular Sciences1661-65961422-00672021-03-01226304410.3390/ijms22063044Diosmin Mitigates Cyclophosphamide Induced Premature Ovarian Insufficiency in Rat ModelNoha M. Abogresha0Sally S. Mohammed1Marwa M. Hosny2Hoda Y. Abdallah3Ahmed M. Gadallah4Sahar M. Greish5Physiology Department, Faculty of Medicine, Suez Canal University, Ismailia 41522, EgyptHistology and Cell Biology Department, Faculty of Medicine, Suez Canal University, Ismailia 41522, EgyptMedical Biochemistry and Molecular Biology Department, Faculty of Medicine, Suez Canal University, Ismailia 41522, EgyptDepartment of Histology and Cell Biology (Genetics Unit), Faculty of Medicine, Suez Canal University, Ismailia 41522, EgyptObstetrics and Gynecology Department, Faculty of Medicine, Suez Canal University, Ismailia 41522, EgyptPhysiology Department, Faculty of Medicine, Suez Canal University, Ismailia 41522, EgyptThe current study was designed to investigate the protective role of diosmin against cyclophosphamide-induced premature ovarian insufficiency (POI). Female Swiss albino rats received a single intraperitoneal dose of cyclophosphamide (200 mg/kg) followed by 8 mg/kg/day for the next 15 consecutive days either alone or in combination with oral diosmin at 50 or 100 mg/kg. Histopathological examination of ovarian tissues, hormonal assays for follicle stimulating hormone (FSH), estradiol (E2), and anti-Mullerian hormone (AMH), assessment of the oxidative stress status, as well as measurement of the relative expression of miRNA-145 and its target genes [vascular endothelial growth factor B <i>(VEGF-B)</i> and regulator of cell cycle (<i>RGC32</i>)] were performed. Diosmin treatment ameliorated the levels of E2, AMH, and oxidative stress markers. Additionally, both low and high diosmin doses significantly reduced the histopathological alterations and nearly preserved the normal ovarian reserve. MiRNA-145 expression was upregulated after treatment with diosmin high dose. miRNA-145 target genes were over-expressed after both low and high diosmin administration. Based on our findings, diosmin has a dose-dependent protective effect against cyclophosphamide-induced ovarian toxicity in rats.https://www.mdpi.com/1422-0067/22/6/3044premature ovarian insufficiencymiRNA-145oxidative stress
spellingShingle Noha M. Abogresha
Sally S. Mohammed
Marwa M. Hosny
Hoda Y. Abdallah
Ahmed M. Gadallah
Sahar M. Greish
Diosmin Mitigates Cyclophosphamide Induced Premature Ovarian Insufficiency in Rat Model
International Journal of Molecular Sciences
premature ovarian insufficiency
miRNA-145
oxidative stress
title Diosmin Mitigates Cyclophosphamide Induced Premature Ovarian Insufficiency in Rat Model
title_full Diosmin Mitigates Cyclophosphamide Induced Premature Ovarian Insufficiency in Rat Model
title_fullStr Diosmin Mitigates Cyclophosphamide Induced Premature Ovarian Insufficiency in Rat Model
title_full_unstemmed Diosmin Mitigates Cyclophosphamide Induced Premature Ovarian Insufficiency in Rat Model
title_short Diosmin Mitigates Cyclophosphamide Induced Premature Ovarian Insufficiency in Rat Model
title_sort diosmin mitigates cyclophosphamide induced premature ovarian insufficiency in rat model
topic premature ovarian insufficiency
miRNA-145
oxidative stress
url https://www.mdpi.com/1422-0067/22/6/3044
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