Gonadal Hormones Flashcards

1
Q

Name 3 natural estrogens?

A
  • Estrone (E1)
  • Estradiol (E2)
  • Estriol (E3)
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2
Q

Where do conjugated estrogens come from?

A

• Conjugated estrogens are blended equine estrogens
either isolated from the urine of pregnant mares or
synthetically produced.

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3
Q

Name 2 synthetic estrogens?

A

Steroidal
• Ethinyl estradiol
• Mestranol (pro-drug converted to ethinyl estradiol)

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4
Q

MOA of estrogens?

A

Mechanism of action
• Estradiol bind to the estrogen receptor to form a
steroid hormone receptor complex
• Hormone-receptor complex → cell nucleus
→ changes in gene expression

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5
Q

Effects of Estrogen: Female maturation, endometrial, and Metabolic?

A

Female Maturation
• Development of female secondary sex characteristics

Endometrial
• Endometrial proliferation

Metabolic
• The effects of estrogens on selected aspects of mineral,
lipid, carbohydrate, and protein metabolism are
important for understanding their pharmacological
actions.

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6
Q

Effects of Estrogens: Bone, Lipids, and Coagulation?

A

Bone
• Decreases resorption of bone (increases mass)

Lipids
• Increase in HDL and decrease in LDL

Coagulation
• Increase hepatic production of factors 2, 7, 9 & 10 and fibrinogen
• Decreases antithrombin III activity
• Increases risk of thromboembolic events

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7
Q

Effects of Estrogen: protein synthesis, vasculature, and fluid balance? Other effects?

A

Protein Synthesis
• Increase in hepatic production of binding proteins eg, SHBG

Vasculature
• Increase production of NO
• Increase production of prostacyclin

Fluid Balance
• Na+ and H20 retention

Other Effects
• Reproductive Function
• Sexual Behavior
• GI Tract

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8
Q

PK of Estrogens?

A

Route of Delivery
• Oral, parenteral, intravaginally, or transdermal patch

Metabolism
• Conjugation by cytochrome enzymes
• Use enterohepatic circulation (metabolized in liver, excreted in bile, hydrolyzed by intestinal bacteria and reabsorbed as active drug)

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9
Q

Clinical uses of estrogens?

A

Postmenopausal Hormonal Therapy
• Decreases risk of osteoporosis (does not treat
osteoporosis)
• Reestablishes feedback on hypothalamic control of NE
secretion, leading to decreased frequency of hot flashes
• Reverses postmenopausal atrophy of the vulva, vagina,
urethra, and trigone of the bladder

Primary Hypogonadism
• Treatment begun with estrogen between ages 11-13
• Progestin added after first uterine bleeding

Treatment of Androgen-Dependent Prostate cancer

Oral Contraceptives

Menstrual Abnormalities

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10
Q

Minor AE of estrogens and Contraindications?

A
Minor
• Uterine bleeding
• Nausea
• Breast tenderness
• Melasma
• Peripheral edema

Contraindications
• Cytochrome inducers can lead to reduction in efficacy

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11
Q

Moderate to severe AE of Estrogens?

A
Moderate/Severe
• Increased risk of endometrial cancer (can be offset by combining estrogen with progestin)
• Increase in frequency of migraines
• Cholestasis and gallbladder disease
• Hypertension
• Thromboembolism
• Depression
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12
Q

Names 3 Selective Estrogen Receptor Modulators(SERMS)

A

Tamoxifen
Raloxifene
Clomiphene

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13
Q

MOA of each SERM?

A

Mechanism of Action
They bind to estrogen receptors but can act as
antagonists or agonists depending on the tissue.

Tamoxifen – Antagonist in breast tissue; agonist in nonbreast tissues (endometrium, liver, bone)

Raloxifene – Antagonist in uterus and breast tissue;
agonist in the bone (inhibits resorption)

Clomiphene – Antagonist in hypothalamus (prevents
normal feedback inhibition)

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14
Q

Clinical Use of each SERM?

A

Tamoxifen
• Prevention and treatment of hormone-responsive breast cancer

Raloxifene
• Prevention of hormone-responsive breast cancer
• Prevention and treatment of osteoporosis in postmenopausal
women

Clomiphene
• Treatment of infertility associated with anovulatory
cycles (eg, PCOS)

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15
Q

AE of Tamoxifen?

A

Tamoxifen
• Hot flashes and nausea
• Endometrial hyperplasia (increased risk of cancer)
• Thromboembolism

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16
Q

AE of Raloxifene?

A
Raloxifene
• Hot flashes and nausea
• Leg cramps
• Thromboembolism
• NO RISK of endometrial hyperplasia
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17
Q

AE of Clomiphene?

A

Clomiphene
• Hot flashes, nausea, vomiting, weight gain, breast
tenderness
• Ovarian hyper-stimulation
• Multiple simultaneous pregnancies (10%)
• Visual disturbances

18
Q

Name on Selective estrogen receptor degrader/downregulator?

A

Fulvestrant

19
Q

MOA and clinical use of SERDs?

A

Mechanism of Action
They bind to estrogen receptors and cause the receptor to be degraded and thus downregulated in all tissues

Clinical Uses
Adjuvant treatment of hormone-receptor positive
metastatic breast cancer that is resistant to first-line
antiestrogen (tamoxifen) therapy

20
Q

PK and AE of SERDS?

A

Pharmacokinetics
Given IM

Adverse Effects
• Hot flashes
• Arthralgias
• Myalgias.

21
Q

Name 3 aromatase inhibitors? MOA of each?

A

Anastrozole (non-steroidal)
Letrozole (non-steroidal)
Exemestrane (steroidal)

Mechanism of Action
Inhibit peripheral conversion of androgens to estrogen
• Anastrozole and Letrozole are competitive, reversible
inhibitors
• Exemestrane is an irreversible inhibitor

22
Q

Clinical use and AE of aromatase inhibitors?

A

Used as adjuvant chemotherapy in estrogen receptor positive breast cancer

AE
• Hot flashes 
• Nausea 
• Fatigue 
• Alopecia 
• Dermatitis
23
Q

Name Natural and Synthetic progestins(there are 6 synthetic)

A

Natural Progestins
• Progesterone

Synthetic Progestins 
• Medroxyprogesterone 
• Norgestrol 
• Norethindrone 
• Norgestimate 
• Desogestreol 
• Drospirenone
24
Q

MOA of Progestins?

A

Mechanism of action
• Progestins enter the cell and bind progesterone
receptors
• The lipid-receptor complex binds to a progesterone
response element (PRE) and activates gene expression

25
Q

Main Effect of Progestins?

A

• Decreases growth and increases vascularization of
endometrium (prevents endometrial hyperplasia)
• Thickening of cervical mucus (inhibits movement of
sperm)
• Associated with an increase in body temperature
• Maintenance of pregnancy

26
Q

PK and Metabolism of Progestins

A

Route of Delivery
• Oral, parenteral and transdermal patch
Metabolism
• Conjugation by cytochrome enzymes
• Use enterohepatic circulation (metabolized in liver,
excreted in bile, hydrolyzed by intestinal bacteria and
reabsorbed as active drug)

27
Q

Clinical use of progestins?

A
  • Oral Contraceptives
  • Endometrial Cancer
  • Abnormal Uterine Bleeding
  • Hormone Replacement Therapy
  • Infertility
  • Diagnostic test of estrogen secretion
28
Q

AE of progestins?

A
  • Uterine bleeding
  • Weight gain
  • Insulin resistance
  • Depression
  • Changes in libido
  • Headache
  • Thromboembolic events (rare)
  • Decrease HDL levels (androgenic progestins)
29
Q

Name antiprogestin, moa, clinical use, and AE?

A

Mifepristone

MOA
Competitive inhibitor at progesterone receptor

Clinical Uses
Used in combination with misoprostol as abortifacient

Adverse Effects
Vomiting, diarrhea, abdominal / pelvic pain and uterine bleeding

30
Q

Name 3 androgens?

A

Testosterone
Methyltestosterone
Danazol

31
Q

MOA of androgens?

A

Mechanism of action
• In skin, prostate seminal vesicles, and epididymis,
testosterone is converted to 5a-dihydrotestosterone
(DHT) by 5a-reductase and binds to the intracellular
androgen receptor

32
Q

Main Effects of Androgens?

A

Male Maturation
• Development of male secondary sex characteristics
• Increases lean body mass, stimulate body hair growth
and sebum secretion

Sexual function
• Increased libido

Metabolic
• Reduction of hormone binding and other carrier proteins
• Increased synthesis of clotting factors, triglyceride lipase, a1-antitrypsin, haptoglobin and sialic acid

33
Q

PK of Androgens?

A

Testosterone
• Given IM, transdermally, topically and as buccal tablets
• Metabolized before being excreted in the urine

Testosterone Derivatives
• Methyltestosterone and danazol can be given orally

34
Q

Clinical use of androgens?

A

Testosterone / Methyltestosterone
• Males with primary or secondary hypogonadism
• Chronic wasting associated with HIV or cancer
• Stimulate anabolism to promote recovery after burns or other injuries
• Increase lean body mass and endurance in athletes
(unapproved)

Danazol (also has anti-estrogen activity)
• Endometriosis
• Fibrocystic breast disease

35
Q

AE of androgens in males and females?

A

Females
• Masculinization, acne, facial hair growth, deepening of
the voice, male pattern baldness, excessive muscle
development
• Menstrual irregularities

Males
• Priapism, impotence, decreased spermatogenesis
• Gynecomastia
• Gonadal atrophy

36
Q

AE in children and generally?

A

Children
• Abnormal sexual maturation
• Growth disturbances due to premature closing of the
epiphyseal plates

General
• Increase LDL and decrease HDL
• Fluid retention → edema

37
Q

AE of androgens in athletes?

A

Athletes
• Reduction in testicular size (high doses)
• Hepatic abnormalities
• Increased aggression

38
Q

Name 3 Anti androgen drugs?

A

Androgen Receptor Antagonists
Flutamide
Spironolactone

5a-reductase Inhibitor
Finasteride

Steroid Synthesis Inhibitor
Ketoconazole

39
Q

Flutamide overview, clinical use, and AE?

A

Flutamide
Non-steroidal competitive inhibitor at androgen receptors

Clinical use: Prostate carcinoma

Adverse effects: mild gynecomastia, hot flashes,
reversible hepatotoxicity

40
Q

Spironolactone overview, clinical use, and AE?

A

Spironolactone
Mineralocorticoid receptor and androgen receptor
antagonist

Clinical use: Reduction of androgenic symptoms due to PCOS (hirsutism), aldosteronism, diuretic

Adverse effects: Gynecomastia, amenorrhea,
hyperkalemia