Chrysin attenuates testosterone-induced benign prostate hyperplasia in rats

Shoieb, Sherif M.; Ahmed Esmat; Khalifa, Amani E.; Abdel-Naim, Ashraf B.;

Abstract


Benign prostate hyperplasia (BPH) is a common age-related health problem affecting almost 3 out of 4 men in their sixties. Chrysin is a dietary phytoestrogen found naturally in bee propolis and various plant extracts. It possesses antioxidant, anti-inflammatory and anti-proliferative properties. The current study was conducted to explore the role chrysin plays in protection against testosterone-induced BPH in rats. On grounds of a preliminary experiment, a dose of chrysin (50 mg/kg) was chosen for further investigation. Testosterone significantly depleted glutathione, suppressed superoxide dismutase and catalase activities, and elevated lipid peroxidation. Moreover, it markedly scaled down the level of cleaved caspase-3 enzyme, reduced Bax/Bcl-2 ratio and mRNA expression of p53 and p21; conversely, protein expression of proliferating cell nuclear antigen was enhanced. Chrysin alleviated testosterone-induced oxidative stress and restored cleaved caspase-3 level, Bax/Bcl-2 ratio and mRNA expression of p53 and p21 to almost control levels. Chrysin prevented the increase in binding activity of nuclear factor kappa B (NF-κB) p65 subunit, mRNA expression of insulin-like growth factor 1 (IGF-1) and insulin-like growth factor 1 receptor (IGF-1R). These data highlight the protective role of chrysin against experimentally-induced BPH. This is attributed - at least partly - to its antioxidant, antiproliferative and proapoptotic properties.


Other data

Title Chrysin attenuates testosterone-induced benign prostate hyperplasia in rats
Authors Shoieb, Sherif M.; Ahmed Esmat ; Khalifa, Amani E.; Abdel-Naim, Ashraf B.
Keywords BPH | Chrysin | Prostate | Rats | Testosterone
Issue Date 1-Jan-2018
Publisher PERGAMON-ELSEVIER SCIENCE LTD
Journal Food and Chemical Toxicology 
Volume 111
Start page 650
End page 659
ISSN 02786915
DOI 10.1016/j.fct.2017.12.017
PubMed ID 29247772
Scopus ID 2-s2.0-85038120363
Web of science ID WOS:000423248100059

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Citations 13 in pubmed
Citations 37 in scopus


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