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Fitoestrogeni

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Fitoestrogeni Estrogen Receptor Estrogen Receptors Estrogen Receptors ER-a Uterus, testis, pituitary, ovary, epididymis, and adrenal gland. ER-b (Kuiper et al. 1996 ... – PowerPoint PPT presentation

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Title: Fitoestrogeni


1
Fitoestrogeni
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ER in cell cycle progression
Myc
ER
Cdc25A
CyclinE Cdk2
CyclinD1 Cdk4
E2F
Rb
DNA pol a Cyclins E,A B-Myb
G1
S
5
Estrogen Receptor
6
Estrogen Receptors
http//www.bio.cmu.edu/Courses/BiochemMols/ER/ERc
hime
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Estrogen Receptors
  • ER-a
  • Uterus, testis, pituitary, ovary, epididymis, and
    adrenal gland.
  • ER-b (Kuiper et al. 1996)
  • brain, kidney, prostrate, ovary, lung, bladder,
    intestine, and epididymis.
  • 88 identity with rat ER-b 47 identity with
    human ER-a
  • Membrane localized ER (Pietras and Szego, 1997)
  • ERa and b differ in C-terminal ligand binding
    domains and N-terminal transactivation domains.
    Highest homology in DNA binding domain.

8
Estradiol
Growth factors
MAPK
P
P
P
P
P
DBD
AF-2
AF-1
AH
9
Regulation of ER activity by coactivators and
corepressors
10
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Estrogen Signaling
Hall et al. 2001. J. Biol. Chem., 276 36869-36872
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ER effects on different cell types
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Estrogen has multiple effects
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Antiestrogens can stop harmful effects of estrogen
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Ligand Induces a Conformational Change in the
LBD that Repositions helix 12
No Ligand
Agonist
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NR Antagonists Alter the Position of Helix 12
Agonist (ER)
Antagonist (ER)
No Ligand
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SERMs
(Selective Estrogen Receptor Modulators)
18
Phytoestrogens
Aherne and OBrien, 2002. Nutrition 1875-81.
19
Phytoestrogens
Benassayag, et al., 2002. J. Chromatogr.B
777233-248.
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Comparison of binding affinities and
transactivation of estrogen and phytoestrogens
Belcher Zsarnovszky, 2001. J. Pharmacol. Exp.
Therap. 299408-414
21
Dietary Sources of Phytoestrogens
22
Pytoestrogens in humans
  • Fitoestrogeni hanno una attivita piu debole di
    quella degli estrogeni circolanti (17-b-estradiol
    or estrone).
  • Fitoestrogeni possono legarsi alla sex steroid
    binding protein (SBP) e a-feroprotein (AFP) e
    circolare.
  • Fitoestrogeni sono coniugati nel fegato (da
    sulfotransferasi and UDP-glucoronyosyl
    transferasi), circolano nel plasma ed escreti
    nelle urine.
  • Livelli di Fitoestrogeni sono piu alti nei
    fluidi dei dotti prostatici e mammari di quelli
    del plasma.
  • Le urine dei vegetariani possono contenere 1000
    volte piu Fitoestrogeni che estrogeni totali.
  • Fitoestrogeni hanno effetti inibitori a 0.5-50mM
    che sono livelli simili alle urine.

23
Fitoestrogeni (PEs) della Soia
  • Genistein, daidzein, coumesterol, and equol si
    legano e transattivano ER a and b (0.1-10mM)
  • Genistetin ha una affinita piu alta per ERb.
  • Soia PEs influenzano la progressione del ciclo
    cellulare, crescita e differenziamento. Hanno
    attivita antiossidanti.

24
Red wine phytoestrogensResveratrol, quercetin,
and anthocyanins
  • Antioxidant, anti-apoptosis,
    anti-inflammatory, anti-cancer, and
    anti-invasive.
  • Reduces Cu-induced LDL oxidation by binding to
    LDL via a glycosidic ether bond. Increases HDL
    cholesterol. Inhibits platelet activation.
  • Ameliorates neuronal damage due to ethanol
    consumption. Probably via antioxidant effect.
    Minimizes effects of NOS activity by ehtanol.
    Inhibits ethanol-induced arachidonic acid release
    and cycloxygenase activity.
  • Anti-ageing role?
  • inhibitory effects on cancer initiation,
    growth promotion progression and angiogenesis in
    model systems.
  • The anti-proliferative activity of resveratrol
    is mediated by p38-MAPKs via p53 mediated
    inhibition. Resveratrol may inhibit apoptosis
    induced by oxidized lipoproteins through
    inhibition of NF-kB and AP-1 pathways.
  • Resveratrol inhibits protein kinase C, Akt,
    and FAK activities in ER a () breast cancer
    cells.

25
Genistein
Genistein  446-72-0
Genistein  446-72-0
Genistein  446-72-0
Synonyms 4',5,7-Trihydroxyisoflavone
Synonyms 4',5,7-Trihydroxyisoflavone
Synonyms 4',5,7-Trihydroxyisoflavone
4',5,7-Trihydroxyisoflavone
  • Both estrogenic and anti-estrogenic effects
  • Inhibitor of tyrosine kinases
  • 20-fold higher binding affinity for ER-b than
    ER-a (Makela et al. 1999)

26
Phytoestrogens in Human Health
  • Cancer preventive
  • Post-menopausal supplement
  • Prevention of osteoporosis
  • Cardiovascular health
  • Fertility
  • Breast enhancement

References Kurzer, 2003. J. Nutr. 133
1983S-1986S. Benassayag, et al., 2002. J.
Chromatogr.B 777233-248.
27
Cancer preventive
  • Benefits to human breast and uterine cancer
    controversial.
  • Genistein can be carcinogenic in uterine cancer
    at neonatal exposure.
  • Cancer protective in animal studies, especially
    when exposed during breast development.
  • Isoflavonoids and lignans stimulate proliferation
    of ER breast cancer cells.
  • Inhibit cell growth at high concentrations and in
    ERa (-) breast cancer cells.
  • Therefore, ER b may have cancer protective
    effect.
  • Anti-angiogenic effects of genistein, daidzein,
    and biochanin A may contribute to antitumor
    activity.
  • Anti-oxidants in vitro and in vivo.

28
Post-menopausal therapy
  • In 2002, the Womens Health Initiative (WHI)
    trial of estrogen/progestin therapy was halted
    midtrial due to high incidence of breast cancer
    and cardiovascular disease.
  • Consumption of 30mg/d soy isoflavones may reduce
    hot flashes by 30-50.

29
Prevention of osteoporosis
  • Isoflavone intake increases bone mineral density.
  • Can be useful in preventing post-menopausal
    osteoporosis.
  • Diets rich in phytoestrogens can protect
    long-term bone loss (Setchell Lydeking-Olsen,
    2003. Am. J. Clin. Nutr. 78593S-609S) .

30
Cardiovascular health
  • Average intake of 47g/day soy protein results in
    9 decrease in total cholesterol,13 decrease in
    LDL cholesterol, and a trend towards HDL
    cholesterol.
  • Flavanoids decrease platelet aggregation.
  • Genistein-induced inhibition of growth factor
    activity can interfere with platelet and thrombin
    action.

31
Effects on fertility (premenopausal)
  • Interferes with menstrual cycle (delay)
  • Reduced LH and FSH and progesterone.
  • Male rodents exposed to PEs in early life
    impaired semen quality, congenital malformations,
    testicular cancer
  • (coumesterol, delay in mating)
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