Pharmacology of Immunomodulary Drugs Flashcards

1
Q

adrenocorticosteroids

A

steroids released by the adrenal cortex
*3 main categories
1. glucocorticoids (metabolic and immune activity - cortisol)
2. mineralocorticoids (salt-retaining activity - aldosterone)
3. androgenic or estrogenic activity

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2
Q

normal glucocorticoid secretion

A

*cortisol secreted normally in low stress conditions
*stimulated by ACTH (pituitary hormone)
*highest in early morning - circadian rhythm

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3
Q

glucocorticoids - big picture - mechanism of action

A

*most effects are from ALTERING GENE EXPRESSION, leading to changes in protein synthesis
*this takes time

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4
Q

mechanism of action - glucocorticoids (detailed)

A
  1. steroid dissociated from CBG (corticosteroid-binding globulin)
  2. intracellular glucocorticoid receptors (GR) are bound to chaperone proteins (including Hsp90)
  3. binding of steroids to GR causes release of chaperone proteins
  4. steroid-GR complex dimerizes and enters nucleus
  5. steroid-GR complex binds to glucocorticoid response element (GRE) on regulatory region of the gene (repressing or stimulating that gene)
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5
Q

metabolic effects of glucocorticoids

A

*increase serum glucose levels (various ways) and increase insulin secretion
*activates lipolysis (increases insulin resistance)
*promote protein breakdown
*breaking down bones (increases risk of fractures)

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6
Q

long-term results of metabolic effects of steroids

A

*decreased muscle mass
*buffalo hump (fat at back of neck)
*moon face (facial fat)
*osteoporosis
*thinning of the skin
*hyperglycemia/worsening of diabetes

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7
Q

anti-inflammatory effects of steroids

A

*INHIBIT phospholipase A2 (decreases prostaglandins)
*DECREASE expression of COX-2 (decreases prostaglandins)

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8
Q

effects of steroids on blood cells

A

*increases neutrophil concentration in circulation (reduces other WBCs)
*reduced ability of macrophages to fxn
*reduced production of inflammatory cytokines

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9
Q

other effects of steroids

A

*neurologically (initially, insomnia and euphoria; long-term, depression)
*peptic ulcers
*increases platelets and RBCs

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10
Q

names of synthetic glucocorticoids (steroids)

A

-hyrdocortisone
-cortisone
-prednisone
-prednisolone
-methylprednisone (SOLU-MEDROL)
-triamcinolone
-betamethasone
-dexamethasone (DECADRON)

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11
Q

short-term adverse effects of synthetic steroids

A

*neuro (insomnia, behavior changes, hypomania, acute psychosis)
*increased glucose
*increased appetite
*peptic ulcers
*GI upset
*mask signs of infection

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12
Q

long-term adverse effects of synthetic steroids

A

*fat redistribution
*increased hair on face
*acne
*muscle wasting
etc

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13
Q

adrenal suppression with synthetic steroids

A

-after ~14 days, the cortisol-producing cells are suppressed
*therefore, need to give them increased steroids if in “stressful situation” (sepsis)
*need to gradually taper off therapy rather than discontinuing abruptly

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14
Q

what must you do prior to starting a pt on long-term steroids

A

RULE OUT TUBERCULOSIS

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15
Q

immunosuppressant: rituximab (rituxan)

A

*depletes CD20 B lymphocytes
*used in oncology
*ADE: rash

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16
Q

immunosuppressant: anti-TNF drugs

A
  1. humira (adalimumab)
  2. remicade (infliximab)
  3. enbrel (etanercept)
17
Q

adverse effects of anti-TNF drugs

A

*injection site/infusion rxns
*increased risk of skin cancer
*increased risk of certain infections (TB, hep B)
*heart failure
*anti-drug antibodies

18
Q

immunosuppressant: soliris (eculizumab)

A

*binds to C5
*NEED TO GIVE MENINGOCOCCAL VACCINE PRIOR TO THERAPY

19
Q

immunosuppressant: Tysabri (natalizumab)

A

*antibody against alpha-4 integrin
*PML is a rare side effect

20
Q

what histamine receptor is most involved in allergic reactions

A

H-1

21
Q

first generation H1-antagonists

A

*example = benadryl (diphenhydramine)
*allergies, OTC sleep aid, motion sickness

22
Q

second generation H1-antagonists

A

*less sedation and less anticholinergic effects than first generation
*examples = zyrtec (cetirizine), allegra (fexofenadine), and claratin (loratadine)

23
Q

adverse effects of first generation H1-antagonists

A

*sedation
*anticholinergic effects