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Female Sex Hormonal Steroids Overall Organization of the Topic  Structure and nomenclature - Estradiol, estrone, estriol, and progesterone  Biosynthesis.

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Presentation on theme: "Female Sex Hormonal Steroids Overall Organization of the Topic  Structure and nomenclature - Estradiol, estrone, estriol, and progesterone  Biosynthesis."— Presentation transcript:

1 Female Sex Hormonal Steroids Overall Organization of the Topic  Structure and nomenclature - Estradiol, estrone, estriol, and progesterone  Biosynthesis and metabolism of estradiol and progesterone  Synthetic estrogens - Schuler’s hypothesis  Estrogen antagonists - clomiphene and tamoxifen  Synthetic progestins  Progesterone antagonists

2 Female Sex Hormonal Steroids Estradiol Estrone Estriol Intramuscular (100%) intramuscular (33%) oral (1.6%) (estr-1,3,5-triene-3,17  -diol) (3-hydroxy-estr-1,3,5-triene-17-one) Natural Estrogens Progesterone (Pregn-4-ene-3,20-dione) Natural Progestin (?????)

3 Female Sex Steroids Physiological Activity of Natural Estrogens Reproduction and development of female sex organs Growth of secondary sex characteristics (male + female) Role in ovulation and pregnancy Role in bone density modulation (male + female) Role in mineral, carbohydrate, protein and lipid metabolism Physiological Activity of Progesterone Maintenance of Pregnancy Inhibition of follicular maturation and ovulation Prevention of spontaneous uterine contractions

4 Female Sex Steroids Concerns about carcinogenic actions of Estrogens/Progestins Early studies … tumors of breast, uterus, testis, bone, kidney … ‘Unopposed’ estrogen … especially higher risk Estrogen – progestin combination … standard practice now In a WHI study … increased total risk of breast cancer by 24% Carcinogenic actions due to trophic effects (cell proliferation effects) Alternate theory … conversion to quinones  ROS  DNA damage

5 Female Sex Steroids Therapeutic Uses Combination oral contraceptives (block ovulation) Menopausal Hormone Therapy (MHT) (secondary effects of decreased hormones … hot flashes, bone loss …) Estrogen/Progestin – dependent cancers (antagonism of ER and PR) Abortifacients (induction of uterine contractions) Other uses

6 Biosynthesis and Metabolism of Estradiol and Progesterone cholesterol pregnenolone testosterone estradiol estriol Conjugation to glucuronides, sulfates, etc…. 6a-hydroxy metabolite 20  /  -hydroxy metabolite 5  -metabolite estrone progesterone

7 Synthetic Estrogenic Estradiol look-alikes ….. agonists

8 Synthetic Estrogenic Ethinyl-estradiol R = H Diethylstilbestrol Mestranol R = CH 3 Chlorotrianisene Dienestrol Diethyl-Stilbestrols (DES)

9 Synthetic Estrogenic Schuler’s Hypothesis for Synthetic Estrogens

10 Synthetic Estrogenic

11 Estrogen Antagonists Chlorotrianisene (estrogenic ) Triphenylethylene Derivatives – Inverse Agonists

12 Selective Estrogen Receptor Modulators (SERM) – Tissue specific activity …. Estrogenic for bone growth; anti- estrogenic for uterine endometrial growth – Single Receptor  Single Response …. May not be valid!

13 Derivatize ring D Typical Progesterone Agonists 17  -hydroxy progesterone caproate Medroxyprogesterone acetate Megestrol acetate Chlormadinone acetate Progesterone Derivatize rings A & D

14 Testosterone Derivatives Unusual Progesterone Agonists Ethisterone Dimethisterone Norethisterone Norethindrone Norgestimate Norgestrel 19-Nor-testosterone Derivatives

15 Progesterone Antagonist Mifepristone (RU-486) (not the ‘morning-after pill’) Onapristone


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