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WHO monographs on selected medicinal plants - travolekar.ru

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<str<strong>on</strong>g>WHO</str<strong>on</strong>g> <str<strong>on</strong>g>m<strong>on</strong>ographs</str<strong>on</strong>g> <strong>on</strong> <strong>selected</strong> <strong>medicinal</strong> <strong>plants</strong><br />

hip or significant changes in markers of b<strong>on</strong>e turnover were seen in any of<br />

the groups (39).<br />

A 12-week randomized, double-blind, placebo-c<strong>on</strong>trolled trial was<br />

c<strong>on</strong>ducted involving 252 menopausal women aged 45–60 years. The<br />

women, who were experiencing > 35 hot flushes per week, were randomly<br />

assigned to receive either Promensil (82 mg total isoflav<strong>on</strong>es), Rimostil<br />

(57.2 mg total isoflav<strong>on</strong>es) or a placebo. The primary outcome measures<br />

were mean absolute changes for high-density lipoprotein cholesterol,<br />

se<strong>ru</strong>m osteocalcin and urinary N-telopeptide. The sec<strong>on</strong>dary outcome<br />

measures were mean changes of total cholesterol, low-density lipoprotein<br />

cholesterol, the ratio of high-density lipoprotein cholesterol to lowdensity<br />

lipoprotein cholesterol, and triglycerides. Ninety-eight per cent of<br />

the participants completed the 12-week protocol. Women who took Rimostil<br />

or Promensil had greater mean increases in high-density lipoprotein<br />

cholesterol than those who took placebo; however, this change was<br />

small (< 2 mg/dl) and was not statistically significant. There was a significant<br />

decrease in triglyceride levels am<strong>on</strong>g women who took Rimostil<br />

(14.4 mg/dl) or Promensil (10.9 mg/dl) compared to those who took the<br />

placebo. The decrease was seen primarily am<strong>on</strong>g women with elevated<br />

baseline triglyceride levels. There were no differences in mean changes of<br />

total cholesterol, low-density lipoprotein cholesterol, or the ratio of highdensity<br />

lipoprotein cholesterol to low-density lipoprotein cholesterol<br />

am<strong>on</strong>g treatment groups. There were no statistically significant differences<br />

between treatment groups for b<strong>on</strong>e turnover markers. It was c<strong>on</strong>cluded<br />

that compared with placebo, extracts c<strong>on</strong>taining isoflav<strong>on</strong>es decrease<br />

levels of triglycerides in symptomatic menopausal women;<br />

however, this effect was small (38).<br />

Treatment of prostate cancer<br />

A n<strong>on</strong>randomized, n<strong>on</strong>-blinded trial with historically matched c<strong>on</strong>trols<br />

from archival tissue assessed the effects of acute exposure to a dietary<br />

supplement of isoflav<strong>on</strong>es in men with clinically significant prostate cancer<br />

before radical prostatectomy. Thirty-eight patients were rec<strong>ru</strong>ited to<br />

the study up<strong>on</strong> diagnosis of prostate cancer. Before surgery, 20 of the men<br />

c<strong>on</strong>sumed 160 mg/day of red clover-derived dietary isoflav<strong>on</strong>es, c<strong>on</strong>taining<br />

a mixture of genistein, daidzein, form<strong>on</strong><strong>on</strong>etin and biochanin A.<br />

Se<strong>ru</strong>m prostate-specific antigen, testoster<strong>on</strong>e and biochemical factors were<br />

measured, and clinical and pathological parameters were recorded. The<br />

incidence of apoptosis in prostate tumour cells from radical prostatectomy<br />

specimens was compared between 18 treated and 18 untreated c<strong>on</strong>trol<br />

tissues. There were no significant differences between pretreatment and<br />

post-treatment se<strong>ru</strong>m prostate-specific antigen, Gleas<strong>on</strong> score, se<strong>ru</strong>m<br />

346

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