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Genistein Affects Estrogen Receptor Alpha (ER-α)/Estrogen Receptor Beta (ER-β) Ratio, and Nuclear Factor-Kappa Beta (NF-κβ) in Mice Model of Endometriosis.
- Source :
- Bahrain Medical Bulletin; Sep2021, Vol. 43 Issue 3, p601-608, 8p
- Publication Year :
- 2021
-
Abstract
- Background: Currently, treatment of endometriosis remains expensive. One of low-cost treatments for this disease is genistein. This study aimed to assess the effect of genistein on Estrogen Receptor Alpha (ER-α) and Estrogen Receptor Beta (ER-β) ratio and Nuclear Factor-Kappa Beta (NF-κβ) in mice model of endometriosis remain unclear. Methods: This study is experimental using post-test research design. Twenty-four female mice (Mus musculus) model of endometriosis were fed genistein. The mice were divided into four groups with various doses of genistein, i.e., 1,30 mg/mice/day (group P1); 1,95 mg/mice/day (group P2); 2,60 mg/mice/day (P3), and; 3,25 mg/mouse/day (group P4). We fed the mouse using a sonde for 14 days. On the fifth day, the mice were sacrificed and dissected to take the peritoneal tissue. The tissue was coloured using Immunohistochemistry staining (IH) and microscopically assessed at 400x magnification calculated at 1000 cells in order to observe the expression of RE-α, RE-β, and NFkB. Results: Genistein at various doses had a significant effect on the RE-α / RE-β ratio. The higher the genistein dose given, the lower the RE-α / RE-β ratio. In addition, genistein dose of 3.25 mg / day significantly reduced NFkB expression. Conclusions: Genistein in various doses have been shown to significantly influence the RE-α / RE-β ratio. In other words, the higher the dose of genistein given will decrease the RE-α / RE-β ratio. [ABSTRACT FROM AUTHOR]
- Subjects :
- ANIMAL disease models
LABORATORY mice
ESTROGEN receptors
GENISTEIN
ENDOMETRIOSIS
Subjects
Details
- Language :
- English
- ISSN :
- 10128298
- Volume :
- 43
- Issue :
- 3
- Database :
- Complementary Index
- Journal :
- Bahrain Medical Bulletin
- Publication Type :
- Academic Journal
- Accession number :
- 152964962