Protein Synthesis Inhibitors Flashcards

1
Q

Amino glycosides

  • how do you know if drug is this category
  • mechanism
  • special
  • Side effects
A
  • mycins (gentamicin)(Amikacin)
  • bind to 30S ribosome subunit, bactericidal
  • -block initiation
  • -block translation+cause premature termination
  • -mess with proofreading activity
  • Postantibiotic effect-due to bad proteins in drugs-bacteria is still killed after medicine cleared from body
  • All are neprhotixic if used over 5 days, elderly, renal insufficient (usually reversible effects), Some are ototoxic (with long use/eldery)-iether auditory or vestribbular-but reversible
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2
Q

Amino glycosides

-names (6) + damage

A
Streptomycin-vestibular
Tobramycin/gentamycin-bad neprho and vestibular
Amikacin-Auditory
Neomycin-bad neprho, auditory
Kanamycin-auditory
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3
Q

Most nephrotoxic aminoglycosides

A

Tobramycin, Gentamcyin, neomycin

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4
Q

Streptomycin

  • mech
  • cllnical use
  • toxicity
A
  • Aminoglycoside
  • 2nd line for Tb used in combo with other agents to prevent resistance (INH and Rifampin)
  • vesitublar toxic
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5
Q

Tobramycin and Gentamicin

  • mech
  • clnical use
  • toxicity
A

Amino glycoside

Gm- severe infection (sepsis/penumonia), resistance prevented by B-lactam, topical (wounds/burns/lesion), gentamicin much cheaper

very nephrotoxic
gentamicin is vestibular toxic

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6
Q

Amikacin

  • mech
  • clnical use
  • toxicity
A

Aminglycoside

kanamycin derivative-less toxic, when bak resistance to other aminoglyocsides

Auditory tox

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7
Q

Neomycin and Kanamycin

  • mech
  • clnical use
  • toxicity
A

Aminoglyoside

-Topical use only, Infected surfaces (skin/eyes/joints/plueral cavity/abscessed cavities), neomycinpolymycin-bactiracin combo=neosporin or neocin (eyes)

Neomycin is nephro, kana and neo are auditory too

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8
Q

Amino glycoside general use

Tetracycline general use

Macrolide

A

ONLY GRAM NEGATIVE (bactericidal)

Gm+ and - and protozoa (bacteriostatic)

bacteriostatic (but cidal at high concentrations) vs aerobic gm + and some gm-

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9
Q

Tetracyclines

  • how do you know if drug is this category
  • mechanism
  • difference between drugs/absorption
  • Side effects
A

-cycline

Binds to 30S ribosome suunbit, prevents tRNA from binding to A site blocking peptide elongation

Differences between are pharmokinetics (duration of action), food impairs absorption (except doxy), alkaline pH pairs absorption, and Multivalent free cations turn off drug (Ca, Mg, Fe, Al)

NVD (stops with eating), forming bone (tooth) discoloration), forming bone deformity and growth inhibition, impair liver function, kidney excretion (except doxy)=accumulation at impairment, photosensitivity

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10
Q

1st tetracycline category

-uses

A

oral/short (6-8hrs)-cholotetracycline, oxytetracycline, tetracycline

Rickettsiae (1st line) mycoplasma pneumonia, clap (2nd line)-UTI stuff, some spirochetes, combos for (H. pylori ulcers, plague, tularemia, brucellosis), protozoa

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11
Q

2nd tetracycline category

-uses

A

oral/intermediate (12hrs)-demelocycline and metacycline

Rickettsiae (1st line) mycoplasma pneumonia, clap (2nd line)-UTI stuff, some spirochetes, combos for (H. pylori ulcers, plague, tularemia, brucellosis), protozoa

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12
Q

3rd tetracycline category

  • uses
  • special
A

oral/ (doxy can be IV)-16-18 hrs (long)…absorption not impacted by food

Rickettsiae (1st line) mycoplasma pneumonia, clap (2nd line)-UTI stuff, some spirochetes, combos for (H. pylori ulcers, plague, tularemia, brucellosis), protozoa

Doxy has no kidney tox or photosensitivity

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13
Q

4th tetracycline category

-uses

A

IV only, 36 hours active

brad spectrum uses vs tetracycline resistant strains-MDR strains…skin infections, intraabdomianal infections, pneumonia

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14
Q

protein synthesis inhibitors (major classes)

A

Aminoglycosides-mycins

Tetracylcines-cylcines

Marcolides-also mycins………but Omycins (cept neomycin)

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15
Q

Macrolide
mech
side fx
use

A

bind reversibly to 50s ribosome and inhibit translocation step of protein synthesis=bacteriostatic (but @ high concentrations bactericidal)

not many-GI NVD/aneoreixa, acute choleststatic hepatitis @ hypersensitive reaction

bacteriostatic vs aerobic gm+ and some gm -

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16
Q

Macrolide examples (4) and times

A

eryhomycin (1.5 hrs), clarithomycin (6hrs) and azithromycin (Z pak) 3 days, and telithromycin (10 hours)

17
Q

Erythromycin

A

1.5hrs

use if allergic to penicillin for staph,

1st line for corynebacteria (diphtheria), chlamydia (resp, neonatal, ocular) or community acquired pneumonia

otitis media, strep, Cap, pertussis, diphtheria

least GI effect of macrolide family

18
Q

Clarithormycin

A

6 hours

use if allergic to penicillin for staph,

1st line for corynebacteria (diphtheria), chlamydia (resp, neonatal, ocular) or community acquired pneumonia

otitis media, strep, Cap, pertussis, diphtheria

least GI effect of macrolide family

19
Q

Azithromycin

A

3 days

use if allergic to penicillin for staph,

1st line for corynebacteria (diphtheria), chlamydia (resp, neonatal, ocular) or community acquired pneumonia

otitis media, strep, Cap, pertussis, diphtheria

20
Q

Telithromycin

A

10 hours

used against macrolide resistant bacteria

only respoitroy tract infections including community pneumonia, sinusitis, strep

21
Q

Other protein synthesis inhibitors
-group + most popular of group+use (general)

what in common

A

Lincosamide:Clindamycin (all gm+)

Streptogramin:Quinupristin-daflospristin (systemic staph infection or VRE E. faecium, MSSA)

Oxazolidinone:Linezolid (MDR Gm+ including MRSA, VRE, streptococci)

50s inhibitors

22
Q

Lincosamide

  • mech
  • other name
  • clincial
A

Clindamycin
50s inhibitor
-gm+ (aerobic/anerobic)
-skin and soft tissue infections by strep/staph (incdling MRSA)

23
Q

Streptogramins

  • mech
  • other name
  • clincial
A
Quinpristin-daflospristin
50s inhibitor
-IV only
-systemic infections by staph or VRE E. faecium (not faecallis)
-not MRSA (but MSSA okay)
24
Q

Oxazolidinones

  • mech
  • other name
  • clincial
A

Linezolid

50s inhibitor

MDR Gram + bacteria, MRSA, VRE, streptococci
-wonder drug-save for really bad