The effects of Sutaehwan-Gami on menopausal symptoms induced by ovariectomy in rats
<p>Abstract</p> <p>Background</p> <p>This study was undertaken to evaluate the beneficial effects of a modified prescription of Sutaehwan named Sutaehwan-Gami (SG), created by adding <it>Rhizoma dioscoreae</it> and <it>Carthami semen</it> to Suta...
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Format: | Book |
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BMC,
2012-11-01T00:00:00Z.
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Summary: | <p>Abstract</p> <p>Background</p> <p>This study was undertaken to evaluate the beneficial effects of a modified prescription of Sutaehwan named Sutaehwan-Gami (SG), created by adding <it>Rhizoma dioscoreae</it> and <it>Carthami semen</it> to Sutaehwan, on menopausal symptoms.</p> <p>Methods</p> <p>To evaluate the estrogenic effect of SG, we first examined estrogen receptor (ER) activation by SG treatment in breast adenocarcinoma cells and confirmed the estrogenic effect of SG <it>in vivo</it> ovariectomized rats. The animals were randomized into four groups: Sham operated group (Sham), saline treated ovariectomized group (OVX), SG treated group (SG) and raloxifene treated group (RLX). Animals were provided with SG at a dose of 500 mg/kg bw/day and RLX at a dose of 5.4 mg/kg bw/day with standard rat pellets for 3 months.</p> <p>Results</p> <p>SG significantly increased ERα phosphorylation, and its downstream effectors, extracellular signal-regulated kinase (ERK) and protein kinase B (Akt) phosphorylation in breast adenocarcinoma cells. Treatment with SG reversed ovariectomy-induced uterine weight reduction and weight gain. Decreases in the levels of GOT and GPT were observed in the SG group. The significantly reduced E<sub>2</sub>β level in OVX rats was raised by treatment with SG. Moreover, SG significantly increased the phosphorylation levels of ERK and Akt in the uterus.</p> <p>Conclusion</p> <p>Taken together, these data indicate that SG has phytoestrogen-like properties through ERK and Akt activation, implying that it could be protective and beneficial for the management of menopausal symptoms.</p> |
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Item Description: | 10.1186/1472-6882-12-227 1472-6882 |