Dt. Zava et al., ESTROGEN AND PROGESTIN BIOACTIVITY OF FOODS, HERBS, AND SPICES, Proceedings of the Society for Experimental Biology and Medicine, 217(3), 1998, pp. 369-378
In this study we report on the content and bioactivity of plant (phyto
) estrogens and progestins in various foods, herbs, and spices, before
and after human consumption. Over 150 herbs traditionally used by her
balists for treating a variety of health problems were extracted and t
ested for their relative capacity to compete with estradiol and proges
terone binding to intracellular receptors for progesterone (PR) and es
tradiol (ER) in intact human breast cancer cells. The six highest ER-b
inding herbs that are commonly consumed were soy, licorice, red clover
, thyme, tumeric, hops, and verbena. The six highest PR-binding herbs
and spices commonly consumed were oregano, verbena, tumeric, thyme, re
d clover and damiana. Some of the herbs and spices found to contain hi
gh phytoestrogens and phytoprogestins were further tested for bioactiv
ity based on their ability to regulate cell growth rate in ER (+) and
ER (-) breast cancer cell lines and to induce or inhibit the synthesis
of alkaline phosphatase, an end product of progesterone action, in PR
(+) cells, In general, we found that PR-binding herbal extracts were
agonists, much like estradiol, whereas PR-binding extracts, were neutr
al or antagonists. The bioavailability of phytoestrogens and phytoprog
estins in vivo were studied by quantitating the PR-binding and PR-bind
ing capacity of saliva following consumption of soy milk, exogenous pr
ogesterone, medroxyprogesterone acetate, or wild mexican yam products
containing diosgenin. Soy milk caused a dramatic increase in saliva PR
-binding components without a concommitant rise in estradiol. Consumpt
ion of PR-binding herbs increased the progestin activity of saliva, bu
t there were marked differences in bioactivity. In summary, we have de
monstrated that many of the commonly consumed foods, herbs, and spices
contain phytoestrogens and phytoprogestins that act as agonists and a
ntagonists in vivo.