Term
Name the hypothalamic hormones |
|
Definition
•GHRH
•Somatostatin
•Thyrotropin releasing hormone (TRH)
•Corticotropin releasing hormone (CRH)
•GnRH
•Dopamine (PIH)
|
|
|
Term
|
Definition
•Found in pancreas and CNS
•Inhibits release of GH, thyrotropin, glucagon, insulin and gastrin
•Inhibits the release of gut peptides including VIP (vasoactive intestionalomas)
|
|
|
Term
Name the somatostatin analogue
Use?
ADR? |
|
Definition
Octreotide: synthetic octapeptide somatostatin analog (long duration of action)
Used in tx of:
–Acromegaly
–Carcinoid syndrome (serotonin 5-HT - biomarker)
–Gastrinoma, VIPoma
–Esophageal varices related bleeding
ADR: Gall stone formation
|
|
|
Term
GnRH analogs.
ROA & why this is important?
Uses |
|
Definition
•Pulsatile administration is used to stimulate the release of FSH and LH from the anterior pituitary - pituitary and gonadotropin stimulation in infertility
•In contrast, long term (2 to 4 weeks) administration leads to decreased FSH and LH secretion, after initially stimulation –Chemical castration: useful in hormone dependent tumors (prostrate, breast), endometriosis and fibrioids
|
|
|
Term
Name the GnRH agonist drugs
Use? |
|
Definition
GnRH agonist preparations
•Gonadorelin – short acting
•Leuprolide (CA prostate), Nafarelin, Buserelin, Goserelin – long acting
Prostate cancer & Male baldness
|
|
|
Term
Name the GnRH antagonist drugs
|
|
Definition
GnRH antagonist preparation:
•They are pure antagonists and do NOT cause initial surge of FSH and LH
•Ganirelix
•Cetrorelix
|
|
|
Term
What are the other uses of GnRH agonists? |
|
Definition
GnRH agonists are used to suppress gonadotropin
secretion (in steady dosage) in patients with:
–Prostatic carcinoma
–Endometriosis
–Precocious puberty (early puberty)
|
|
|
Term
Which 2 hormones are released from a different area? |
|
Definition
Oxytocin (uterine muscles & mammory glands)
ADH/ vasopressin (kidney)
- supraoptic & paraventricular nucleus of the hypothalamus - transported to the posterior pituitary for release |
|
|
Term
|
Definition
Somatotrophin - growth hormone
FSH - Oestrogen
LH - Progesterone |
|
|
Term
What are the drugs used as GH analogs?
Use?
ADR? |
|
Definition
•Somatropin (Humatrope)
Somatrem (Protropin)
GH deficiency, chronic renal failure, turner’s syndrome & Wasting in patients with HIV/AIDS.
A/E : includes edema (due to increase Na retention), carpal tunnel syndrome, rarely ↑ ICT
|
|
|
Term
What is Laron syndrome?
What is used to treat it?
MOA? |
|
Definition
Laron syndrome, or Laron-type dwarfism, is an autosomal recessive disorder characterized by an insensitivity to growth hormone (GH).
•IGF-1 preparation: Mecasermin
•It is recombinant IGF-1 and an effective treatment for GH insensitive patients also approved for GH deficiency.
|
|
|
Term
What are the symptoms of Acromegaly?
What is used to treat it?
MOA? |
|
Definition
acromegaly - characterised by acralenlargement and soft tissue overgrowth of the hands and feet, coarsening of facial features and thickening of the skin. •Pegvisomant – (Somavert): a new GH receptor antagonist. |
|
|
Term
Patient was given treatment for growth, resulting in dementia, tremors and lack of motor co-ordination.
What is the disorder?
What was the patient given?
|
|
Definition
Creutzfeldt-Jakob disease (CJD)
It resulted because of human cadaver GH preparations. |
|
|
Term
What is the precursor for ACTH & MSH?
What is the role of ACTH? |
|
Definition
Proopiomelanocortin (POMC)
stimulate the zona faciculata and zona reticularis to produce the cortisol and adrenal androgens. |
|
|
Term
What are the ACTH analogs?
ADR's? |
|
Definition
•Corticotropin - porcine ACTH.
•Cosyntropin - synthetic form of human ACTH.
•ADR: Acne, hirsutism**
|
|
|
Term
What is another use of Cosyntropin |
|
Definition
•Cosyntropin - is employed in diagnostic test to diagnose congenital adrenal hyperplasia.
•To diagnose adrenal insufficiency in a test that measures cortisol before and after cosyntropin injection
|
|
|
Term
Name the gonadotropins
Action |
|
Definition
FSH -
Females - Folicle stimulation & release of oestrogen
Males - Spermatogenesis
LH -
Females - stimulates ovulation
Males - testosterone release |
|
|
Term
Name the Gonadotropin analogues
Uses? |
|
Definition
•Urofollitropin / Follitropin is a FSH agonist.
•Menotropins contains FSH and LH.
•Human Chorionic Gonadotropin is a LH agonist
–Used to treat un-descended testis – aka criptorchism (if no anatomical blockade)
Uses:
•To induce ovulation
•Infertility in men and women
|
|
|
Term
Prolactin Release Inhibitory Hormone
AKA?
Use?
If there is a Defect what happens?
How is this treated? |
|
Definition
Dopamine which inhibits the release of prolactin
Hyperprolactinemia, galactorrhea & infertility - treat with D2 agonist - Bromocriptine or CABERGOLINE |
|
|
Term
What is used in the treatment of preterm labour
MOA? |
|
Definition
ATOSIBAN - oxytocin antagonist
- during late pregnancy the uterus becomes very sensitive to oxytocin due to an up-regulation of receptors, this causes the uterine muscle to contract, which is not beneficial in pre term labour, thus an oxytocin antagonist is given.
Can also give - B2 agonist, Ca channel blocker |
|
|
Term
What is used to induce labour?
What are other uses of this analog?
What are the ADR's
When is it contraindicated? |
|
Definition
•Synthetic oxytocin used to induce uterine contractions during labor.
•It is also used to prevent postpartum uterine hemorrhage. (DOC: ergots**)
•A nasal preparation is available for milk let down reflex in nursing mothers.
•ADR's - Seizures, hypotension and hyponatremia are usual adverse effects.
•It is contraindicated in fetal distress, cephalopelvic disproportion
|
|
|
Term
What is the DOC for post partum hemmorhage?
MOA?
What can also be used? |
|
Definition
Ergonovine - Given IM in Postpartum hemorrhage and Placental retention
MOA: Acts through Alpha or serotonin receptors
Oxytocin agonist
|
|
|
Term
When is ADH or Vasopressin released?
Where does it act? |
|
Definition
In response to a low ECF volume, i.e Hypotension, hypovolemia, hyperosmolarity
V1 - Blood vessels - Vasoconstriction
V2 - Collecting duct - Fluid retention
Both leading to an increased BP |
|
|
Term
|
Definition
****Diabetes insipidus (neurogenic)
Nocturia
Bleeding oesophageal varices
Haemophilia A (increases factor VIII)
vonWillbrand’s disease (increases vW factor)
|
|
|
Term
Name the natural oestrogen's |
|
Definition
Estradiol,
Estrone
Estriol.
|
|
|
Term
Name the synthetic steroidal estrogens |
|
Definition
Ethinyl Estradiol,
Mestranol.
|
|
|
Term
Name the synthetic non steroidal estrogens |
|
Definition
Diethylstilbestrol,
Dienestrol |
|
|
Term
What are the Uses of Oestrogen's? |
|
Definition
•Hypogonadism in girls.
•Hormonal replacement therapy
•Contraception
•Osteoporosis
•Prostate carcinoma
•Turner's syndrome (Gonadal dysgenesis).
|
|
|
Term
What are the ADR's associated with Oestrogen? |
|
Definition
↑ risk of myocardial infarction, stroke,
gall stones and pulmonary embolism - due to the increase in factor II, VII, IX, X, fibrinogen and ↓ anti-thrombin
Mastalgia (pain in breast)
↑ the risk of endometrial and breast cancer.
|
|
|
Term
What is a specific use of diethylstilbestrol (DES).
What is a specific ADR of DES?
|
|
Definition
DES is still one of the most commonly used agents for the hormonal treatment of advanced prostate cancer - via negative feedback decreasing LH levels
DES during breast feeding increase vaginal adenocarcinoma in female offspring.
|
|
|
Term
Estrogen antagonist
Drug?
Use?
MOA? |
|
Definition
Clomiphene
Used as ovulation inducing drug for patients who have cycles where oocyte is not released
Acts as a competitive inhibitor at estrogen receptor - It decrease the negative feedback of estrogen on hypothalamus / pituitary and increase FSH / LH secretion.
A/E– multiple pregnancy and ovarian enlargement.
|
|
|
Term
|
Definition
•First generation: Norethindrone, Ethynodiol diacetate.
•Second generation: Levonorgestrel, Norgestrel.
•Third generation: Desogestrel, Norgestimate.
•Fourth generation:Drospirenone.
|
|
|
Term
What are the clinical uses of the progestins?
ADR's? |
|
Definition
-HRT - to counteract the endometrial hyperplasia seen with Oestrogen
-Contraception
•Breakthrough bleeding,
Hirsuitism and acne (androgenic)
•Abnormal lipid and glucose levels.
|
|
|
Term
Antiprogestin
Drug?
MOA?
Use? |
|
Definition
Mifepristone:
•It is a progesterone receptor antagonist. It is also a glucocorticoid receptor antagonist.
•If mifepristone is taken shortly after intercourse, it prevents pregnancy.
•Mifepristone (in combination with miopristol) widely used to terminate early pregnancy.
|
|
|
Term
Oral contraceptives
Types?
MOA? |
|
Definition
1.Estrogen and Progestin
2.Progestin Only
These exert the contraceptive effect mainly
through selective inhibition of gonadotropin
release from the pituitary, especially
midcycle LH surge (which initiates ovulation)
|
|
|
Term
Name the constituents of Oral contraceptives |
|
Definition
•Estrogen:
Ethinly estradiol (EE),
Mestranol
•Progesterone:
Norethindrone,
Norgestrel,
Levonorgestrel,
Desogestrel,
Drospirenone
|
|
|
Term
What is the difference between Monophasic, triphasic & diphasic hormoal contraceptives |
|
Definition
Biphasic - contains the same amount of progesterone & estrogen throughout the cycle
Triphasic & Diphasic - contain a variable amount of Estrogen & Progesterone over the cycle |
|
|
Term
What are the Postcoital contraceptives? |
|
Definition
•Oral levonorgestrel: within 120 hours for best results.
•Estrogens & Progestins : It is started within 72 hrs for best results.
•Mifepristone is effective as postcoital contraception along with misopristol (PGE1) .
|
|
|
Term
Where is testosterone produced? |
|
Definition
95% in the Leydig cells of the testies
5% in the adrenal gland |
|
|
Term
|
Definition
Synthetic Androgens : It is a weak androgen, derivative of testosterone which has anti-estrogenic activity.
•Primarily used in endometriosis and fibrocystic breast disease.
•It is also used in the treatment of hereditary angioedema (↑C-1 esterase inhibitor).
|
|
|
Term
Testosterone
ROA
Specific Drugs and their ROA |
|
Definition
•It is given i.m or transdermally to avoid extensive hepatic metabolism.
•Testosterone cypionate is available for intramuscular administration.
•Methyltestosterone is active orally and resistant to hepatic metabolism, but can result in hepatoxicity.
|
|
|
Term
Name the progesterone only mini pills
ROA?
duration of action?
Use? |
|
Definition
•Norethindrone (Nor-QD): oral admin.
•Levonorgesterol: implanted under the skin - effective for 5 years
•Medroxyprogesterone depot injection - 3 months
Suited for smoker, breast feeding and estrogen intolerance |
|
|
Term
Name the synthetic androgens
Clinical use?
ADR?
Contraindications? |
|
Definition
Oxandrolone
Nandrolone
Clinical uses :
Hypogonadism, Endometriosis, Anemia, Osteoporosis, Aging. Illicit use in athletics**
Adverse effects :
Hirsutism, acne, deepening of voice.
Cholestatic jaundice.
Contraindications: Pregnancy & Prostate cancer.
|
|
|
Term
Finasteride
MOA?
Use?
ADR? |
|
Definition
•Orally active and inhibits 5-α-reductase -II enzyme which converts testosterone to dihydrotestosterone - producing a reduction of dihydrotestosterone in prostate and skin.
•It is approved for treatment of benign hypertrophy of prostate.
Loss of labido, erectile dysfuncion
|
|
|
Term
|
Definition
Androgen blocker
Ca of prostate |
|
|
Term
What is the best combination therapy used in BPH?
Why? |
|
Definition
Alpha 1 blocker & 5-alpha reductase inhibitror
-it reduces all the symptoms i.e urinary retention, urinary insufficiency etc. |
|
|