| 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. |  | 
        |  |