Phytoestrogens and Brain Health
Phytoestrogens are a diverse group of naturally occurring polyphenolic compounds that structurally resemble mammalian estrogens although they are distributed in plants.1 Due to their structural similarities, phytoestrogens can bind to mammalian estrogen receptors (ERs); some of them have a binding p...
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Published in | Micronutrients and Brain Health pp. 45 - 62 |
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Format | Book Chapter |
Language | English |
Published |
United Kingdom
CRC Press
2010
Taylor & Francis Group |
Subjects | |
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Abstract | Phytoestrogens are a diverse group of naturally occurring polyphenolic compounds that structurally resemble mammalian estrogens although they are distributed in plants.1 Due to their structural
similarities, phytoestrogens can bind to mammalian estrogen receptors (ERs); some of them have
a binding preference to ERβ, but, overall, they have weaker binding afnities when compared with
the female endogenous estrogen 17β-estradiol. In the mammalian system, through their interactions
with ERs, phytoestrogens can moderately interfere with the endogenous estrogen-responsive signaling and result in either estrogenic or antiestrogenic bioactivities, depending on the status of the
endogenous estrogens and the distribution of two ER subtypes, ERα and ERβ.2,3Three major subclasses of phytoestrogens have been identied and chemically dened as isoavones, lignans, and coumestans (see Table 3.1).1 Isoavones are predominantly enriched in red clover and legumes, such as soybeans; lignans are largely distributed in oilseeds, such as axseeds; and
coumestans are widely distributed in plant sprouts, such as red clover sprouts and alfalfa sprouts.
Mature red clover leaf is the known richest source of total isoavones, mainly biochanin A and
formononetin, along with lesser amounts of genistein and daidzein. Biochanin A and formononetin
are O-methylated precursor molecules of genistein and daidzein, respectively, and are enzymatically converted to genistein and daidzein once ingested in mammalians.4 Soy is the richest source of
genistein, rich in daidzein, and the known exclusive source of glycitein. Besides red clover and soy,
kudzu root is another major botanical source for isoavones, serving as the richest source of daidzein among all plants.5 Flaxseed provides the richest dietary source of lignans, with a large amount
of secoisolariciresinol and a lesser amount of matairesinol.6 Once ingested, these plant lignans are
enzymatically converted to mammalian lignans-secoisolariciresinol to enterodiol, and matairesinol to enterolactone. Coumestrol is a major coumestan, with a structure quite different from that
of isoavones while highly estrogenic due to the presence of two phenol groups at both ends, which3.1 Phytoestrogens and Human Health ...23
3.2 Human Studies of Phytoestrogens on Brain Health ...27
3.3 Standardization of Human Studies on Phytoestrogens... 323.3.1 Phytoestrogen Composition ... 33
3.3.2 Study Population ...34 |
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AbstractList | Phytoestrogens are a diverse group of naturally occurring polyphenolic compounds that structurally resemble mammalian estrogens although they are distributed in plants.1 Due to their structural
similarities, phytoestrogens can bind to mammalian estrogen receptors (ERs); some of them have
a binding preference to ERβ, but, overall, they have weaker binding afnities when compared with
the female endogenous estrogen 17β-estradiol. In the mammalian system, through their interactions
with ERs, phytoestrogens can moderately interfere with the endogenous estrogen-responsive signaling and result in either estrogenic or antiestrogenic bioactivities, depending on the status of the
endogenous estrogens and the distribution of two ER subtypes, ERα and ERβ.2,3Three major subclasses of phytoestrogens have been identied and chemically dened as isoavones, lignans, and coumestans (see Table 3.1).1 Isoavones are predominantly enriched in red clover and legumes, such as soybeans; lignans are largely distributed in oilseeds, such as axseeds; and
coumestans are widely distributed in plant sprouts, such as red clover sprouts and alfalfa sprouts.
Mature red clover leaf is the known richest source of total isoavones, mainly biochanin A and
formononetin, along with lesser amounts of genistein and daidzein. Biochanin A and formononetin
are O-methylated precursor molecules of genistein and daidzein, respectively, and are enzymatically converted to genistein and daidzein once ingested in mammalians.4 Soy is the richest source of
genistein, rich in daidzein, and the known exclusive source of glycitein. Besides red clover and soy,
kudzu root is another major botanical source for isoavones, serving as the richest source of daidzein among all plants.5 Flaxseed provides the richest dietary source of lignans, with a large amount
of secoisolariciresinol and a lesser amount of matairesinol.6 Once ingested, these plant lignans are
enzymatically converted to mammalian lignans-secoisolariciresinol to enterodiol, and matairesinol to enterolactone. Coumestrol is a major coumestan, with a structure quite different from that
of isoavones while highly estrogenic due to the presence of two phenol groups at both ends, which3.1 Phytoestrogens and Human Health ...23
3.2 Human Studies of Phytoestrogens on Brain Health ...27
3.3 Standardization of Human Studies on Phytoestrogens... 323.3.1 Phytoestrogen Composition ... 33
3.3.2 Study Population ...34 |
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Keywords | Bone Mineral Density High Soy Diet Soy Product Tr Ac Ye Ar Red Clover Er Ba Non-equol Producers Total Isoavones Ar Bo Mammalian Estrogens Lo Ca Soy Isoavones Equol Producers Soy Foods Es tA Ly Ci Op Au |
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SubjectTerms | Cellular biology Dietetics & nutrition Neurosciences |
Title | Phytoestrogens and Brain Health |
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