Drugs For Endocrine System Flashcards

1
Q

This drug is a GnRH analogue. When________ binds the GnRH receptors in the pituitary, there is an initial release of LH and FSH; however, continued administration of leuprolide leads to the desensitization and downregulation of the GnRH receptors, thereby eventually resulting in decreased release of LH and FSH. Decreased levels of LH and FSH lead to decreased levels of estrogens and testosterone.

A

leuprolide, Other GnRH analogues include nafarelin and goserelin.

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2
Q

Bone cell that promotes bone formation

A

Osteoblast

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3
Q

Osteoporosis

A

Abnormal loss of bone with increased risk of fractures, spinal deformities, and loss of stature; remaining bone is histologically normal

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4
Q

Osteomalacia

A

A condition of abnormal mineralization of adult bone secondary to nutritional
deficiency of vitamin D or inherited defects in the formation or action of active vitamin D metabolites

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5
Q

Osteoclast

A

Bone cell that promotes bone resorption

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6
Q

A bone disorder, of unknown origin, characterized by excessive bone destruction and disorganized repair. Complications include skeletal deformity, musculoskeletal pain, kidney stones, and organ dysfunction secondary to pressure from bony overgrowth

A

Paget’s disease

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7
Q

The same as osteomalacia, but occurs in the growing skeleton

A

Rickets

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8
Q

An osteoblast-derived growth factor that stimulates osteoclast activity and osteoclast precursor differentiation

A

RANK ligand

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9
Q

Beta adrenergic antagonist

A

Propranolol

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10
Q

Other antithyroid agents

A

Potassium iodide solution
• Radioactive sodium iodide I- 131

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11
Q

Identify the sites of action of antithyroid drugs in the biochemical pathway for thyroid hormone synthesis and release.

A
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12
Q

Thyroperoxidase is important

A

Involved in three different steps in thyroid hormone synthesis
More efficient at combining DIT than MIT, thus more T4 released than T3
Very good drug target
1.
SYNTHESIS OF THYROID HORMONES
Thyroglobulin is synthesized in the thyroid epithelial cell and

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13
Q

Levothyroxine (Synthetic T4)

Mechanism of action
Adverse reactions

Drug interactions

A
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14
Q

Adverse reactions Levothyroxine (Synthetic T4)

A

Tachycardia, heat intolerance, tremors, arrhythmias

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15
Q

Levothyroxine (Synthetic T4) Drug interactions

A

Coffee, fiber, soya products, aluminum hydroxide, calcium supplements, cholestyramine, ferrous sulfate, sucralfate  Reduce absorption
Estrogens, androgens, glucocorticoids alter TBG and TOTAL T3 and T4 levels [Free form is normal]

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16
Q

Levothyroxine Mechanism of action

A

Nuclear receptor Thyroid Receptor with Retinoid X Receptor
Gene transcription Growth, development, and calorigenesis •Stable composition leads to consistent and predictable blood levels •Few allergic reactions, Once-daily dosing

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17
Q

Liothyronine (Synthetic T3)

A
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18
Q

Denosumab

A

Binds to RANKL and prevents it from stimulating osteoclast differentiation and function Mimics OPG

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19
Q

Alendronate [Bisphosphonate]

A

Inhibition of osteoclast mediated bone resorption

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20
Q

Raloxifene

A

Estrogen agonist effect in bone + antagonist in breast and
endometrium

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21
Q

Cinacalcet uses

A

Hyperparathyroidism

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22
Q

Activates calcium sensing receptor

A

Cinacalcet

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23
Q

Osteoporosis in postmenopausal women drug to give

A

Raloxifene

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24
Q

Raloxifene A/E

A

Hot flashes, thromboembolism

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25
Hypocalcemia A/E
Cinacalcet
26
Osteoporosis use drug
Denosumab
27
Denosumab A/E
Osteonecrosis of the jaw, risk of infection
28
Esophageal irritation, osteonecrosis of the jaw A/E
Alendronate [Bisphosphonate]
29
Inhibition of osteoclast mediated bone resorption
Alendronate [Bisphosphonate]
30
Give what drug for Osteoporosis, Paget’s disease
Alendronate [Bisphosphonate]
31
What drug is use with Hyperparathyroidism
Cinacalcet
32
Mecasermin
Growth failure in children with severe IGF-1 deficiency unresponsive to growth hormone administration
33
Patients with acromegaly
Lanreotide Octreotide
34
Desmopressin
Diabetes insipidus, children with nocturnal enuresis, hemorrhagic conditions
35
prostate and breast cancer, endometriosis, uterine fibroids, precocious puberty name that drug
Leuprolide
36
Acromegaly in patients who are resistant to somatostatin analogs
Pegvisomant
37
Advanced prostate cancer name that drug
Ganirelix
38
Mecasermin
Growth failure in children with severe IGF-1 deficiency unresponsive to growth hormone administration
39
Diagnostic test for adrenal insufficiency name that drug
Cosyntropin
40
The main adverse effect is hypoglycemia indicated for the treatment of growth failure in children with severe IGF-1 deficiency. recombinant form of human IGF-1
Mecasermin
41
used to treat patients with acromegaly. it has a much longer half-life of about 80 minutes. administered subcutaneously every 8 hours, and its adverse effects include nausea, vomiting, abdominal cramps, steatorrhea (excessive fat in the feces), and gallstones.
octreotide- Somatostatin (growth hormone–inhibiting hormone
42
These drugs are particularly useful in the treatment of persons with elevated growth hormone and prolactin secretion.
In patients with acromegaly, the use of cabergoline
43
pegylated analog of growth hormone that acts as a growth hormone receptor antagonist in target organs and normalizes serum IGF-1 concentrations in 97% of persons with acromegaly
Pegvisomant Growth Hormone Receptor Antagonist
44
The drug appears to have a good safety profile, but it may elevate serum levels of liver enzymes, which should be monitored
Pegvisomant
45
A large number of gonadotropin preparations are available for the treatment of infertility and hypogonadism in men and women
menotropins
46
Gonadotropin-Releasing Hormone Agonists name them. A/E
goserelin, histrelin, leuprolide, nafarelin, and triptorelin Hot flashes
47
Ganirelix, cetrorelix, and degarelix are synthetic peptides that act as___________ All of the agents are absolutely contraindicated during pregnancy. adverse effects of these agents are ________and _________.
Ganirelix, cetrorelix, and degarelix are synthetic peptides that act as competitive antagonists at GnRH receptors in the pituitary gland hypersensitivity allergic reactions, including anaphylaxis
48
Both the idiopathic and secondary forms of hyperprolactinemia can be treated with a
dopamine agonist such as cabergoline or bromocriptine
49
_________and________ are both ergot alkaloid derivatives
Bromocriptine and cabergoline are both ergot alkaloid derivatives
50
_____________selectively activates dopamine D2 receptors in the pituitary gland and suppresses the secretion of prolactin.
Cabergoline
51
The drug has an elimination half-life of about 65 hours and a long duration of action. The most common adverse effects of________ are nausea, headache, and dizziness
cabergoline
52
Synthetic oxytocin (P itocin ) usage
The drug is given to induce contractions during labor, to prevent postpartum uterine hemorrhage, and to stimulate milk let-down in nursing mothers.
53
A deficiency of pituitary vasopressin secretion leads to diabetes insipidus, a condition characterized by excessive water excretion (polyuria) and increased water intake (polydipsia). Diabetes insipidus is usually treated with________
desmopressin
54
Desmopressin solutions are available for injection and as a nasal spray that is used to prevent____. Desmopressin overdose can result in dilutional________.
nocturnal urine production and enuresis in patients with diabetes insipidus. Hyponatremia
55
selective antagonist at V2 receptors. It is indicated for the treatment of euvolemic and hypervolemic hyponatremia in hospitalized patients. Treatment of SIADH
Tolvaptan
56
Which drug is used to reduce the secretion of gonadotropins and gonadal steroids in children with precocious puberty? (A) cabergoline (B) menotropins (C) leuprolide (D) gonadorelin (E) octreotide
C
57
Which drug for treating acromegaly acts by blocking receptors for growth hormone? (A) pegvisomant (B) somatropin (C) octreotide (D) leuprolide (E) cabergoline
A
58
By which mechanism does cabergoline relieve symptoms of hyperprolactinemia in persons with a prolactin-secreting pituitary adenoma? (A) blocks prolactin receptors (B) blocks receptors for prolactin-releasing hormone (C) exerts a cytotoxic effect on pituitary adenoma cells (D) activates receptors for prolactin-inhibiting hormone (E) stimulates the breakdown of prolactin
A
59
Octreotide is correctly described by which of the following statements? (A) It is identical to naturally occurring somatostatin. (B) It is used to treat growth hormone deficiency. (C) It is administered orally. (D) It is a more potent inhibitor of growth hormone secretion than is somatostatin.
D
60
Which sequence of gonadotropin preparations is used to induce ovulation? (A) choriogonadotropin alfa then lutropin alfa (B) follitropin alfa then lutropin alfa (C) choriogonadotropin alfa then follitropin beta (D) chorionic gonadotropin (hCG) then lutropin alfa (E) follitropin alfa then follitropin beta
B
61
Calcitonin therapeutic Uses:
Hypercalcemia Paget’s disease of bone Malignancy Osteoporosis Limited efficacy
62
Calcitonin adverse effects:
Nausea Flushing of face and hands Nasal irritation Injection site inflammation
63
parafollicular (C) cells of thyroid gland Inhibits osteoclastic activity Decreases calcium reabsorption by kidney
CALCITONIN