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Estrogens and progestins are endogenous hormones that produce numerous physiological actions. In women, these include developmental effects, neuroendocrine actions involved in the control of ovulation, the cyclical preparation of the reproductive tract for fertilization and implantation, and major actions on mineral, carbohydrate, protein, and lipid metabolism. Estrogens also have important actions in males, including effects on bone, spermatogenesis, and behavior. Well-characterized receptors for each hormone mediate biological actions in both the unliganded and the liganded states.
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The most common uses of estrogens and progestins are for contraception and menopausal hormone therapy (MHT) in women, but the specific compounds and dosages used in these two settings differ substantially. Antiestrogens are used in the treatment of hormone-responsive breast cancer and infertility. Selective estrogen receptor modulators (SERMs) that display tissue-selective agonist or antagonist activities are useful to prevent breast cancer and osteoporosis. The main use of antiprogestins has been for medical abortion.
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A number of naturally occurring and synthetic environmental chemicals mimic, antagonize, or otherwise affect the actions of estrogens in experimental test systems. The precise effect of these agents on humans is unknown but is an area of active investigation.
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Abbreviations
AF: activation function
CHD: coronary heart disease
COMT: catechol-O-methyl transferase
DES: diethylstilbestrol
ER: estrogen receptor
ERα: estrogen receptor α
ERβ: estrogen receptor β
ERE: estrogen response element
ERT: estrogen replacement therapy
FP: PGF2α receptor
FSH: follicle-stimulating hormone
GABA: γ-aminobutyric acid
GnRH: gonadotropin-releasing hormone
GPCR: G protein–coupled receptor
hCG: human chorionic gonadotropin
HDL: high-density lipoprotein
HERS: Heart and Estrogen/Progestin Replacement Study
HRT: hormone replacement therapy
HSP: heat shock protein
IGF: insulinlike growth factor
IU: intrauterine
IUD: intrauterine device
IUI: intrauterine insemination
IUS: intrauterine system
LDL: low-density lipoprotein
LH: luteinizing hormone
LNg: levonorgestrol, as in LNg-IUS
LNg14 or 20: LNg, 14 or 20 µg/24h
LPA: lipoprotein A
MHT: menopausal hormone therapy
MPA: medroxyprogesterone acetate
MWS: Million Women Study
NcoR: nuclear hormone receptor corepressor
NE: norepinephrine
OHSS: ovarian hyperstimulation syndrome
PAI-1: plasminogen activator inhibitor 1
PCOS: polycystic ovary syndrome
PG: prostaglandin
PID: pelvic inflammatory disease
PR: progesterone receptor
PRE: progesterone response element
PRM: progesterone receptor modulator
ROS: reactive oxygen species
SERM: selective estrogen receptor modulator
SHBG: sex hormone–binding globulin
SRC-1: steroid-receptor coactivator 1
WHI: Women’s Health Initiative
WHIMS: Women’s Health Initiative Memory Study
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Chemistry and Synthesis
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Many steroidal and nonsteroidal compounds, some of which are shown in Table 44–1 and Figure 44–1, possess estrogenic activity. Estrogens interact with two receptors of the nuclear receptor superfamily, termed ERα and ERβ. The most potent naturally occurring estrogen in humans, for both ERα- and ERβ-mediated actions, is 17β-estradiol, followed by estrone and estriol. Each contains a phenolic A ring with a hydroxyl group at carbon 3 and a β-OH or ketone in position 17 of ring ...