Part 4: DNA/RNA Synthesis Inhibitors Flashcards

1
Q

how is metronidazole activated?

A

inactive when circulating in our bodies, but activates when taken up by anaerobic microbes

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2
Q

why is metronidazole only active when inside microbes?

A

the microbes have enzymes and cofactors that are required for anaerobic metabolism and these same pathways activate the drug by reduction

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3
Q

metronidazole has active ___ metabolites once activated by microbes

A

cytotoxic

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4
Q

MOA of metronidazole active metabolites

A

bind to DNA, which inhibits replication and DNA damage and fragmentation, leading to death

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5
Q

is metronidazole bacteristatic or bactericidal?

A

bactericidal

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6
Q

why is metronidazole only used to treat specific infections?

A

b/c it specifically targets anaerobes

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7
Q

t/f anaerobe resistance is less common for metronidazole than for other antibiotics

A

true

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8
Q

how does a bacteria get resistance to metronidazole?

A

mutations in bacterial enzymes that would be responsible for the activation of metronidazole

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9
Q

give an example of an infection that metronidazole could be used for

A

bacterial vaginosis

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10
Q

t/f bacteria can make their own folic acid

A

t

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11
Q

folic acid or folate is a key molecule in the making of ____ for DNA synthesis

A

nucleotides

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12
Q

what 2 enzymes are critical to bacterial folic acid synthesis?

A

dihydropteroate and dihydrofolate reductase

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13
Q

without dihydropteroate and dihydrofolate reductase, bacteria cannot make new ____ and will die

A

DNA

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14
Q

give an example of a sulphonamide antibiots

A

sulphamethoxazole

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15
Q

sulfonamides are competitive inhibitors of the _____ enzyme in bacteria

A

dihydropteroate

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16
Q

why do sulfonamides not impact human cells?

A

we do not have the dihydrpteroate enzyme

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17
Q

MOA of sulfonamides

A

structurally similar to PABA, impairs bacteria dihydropteroate synthase which blocks folic acid production, so not enough nucleotides can be made to effectively replicate DNA

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18
Q

are sulfonamides bactericidal or bacteriostatic? ?

A

bacteriostatic

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19
Q

enzyme inhibition by sulphonamides is ___ (reversible or irreversible)

A

reversible

20
Q

how can bacteria become resistant to sulphonamides?

A

learn to make more PABA to out-compete drug

21
Q

t/f resistance to sulfa drugs has become so common that they are typically not given as monotherapies

22
Q

t/f allergies to sulfa drugs are common and are typically characterized by itchy rashes and hives

23
Q

trimethoprim is a competitive inhibitor of the ____ enzyme

A

dihydrofolate reductase

24
Q

what is a disadvantage of trimethoprim inhibiting dihydrofolate reductase? why is this not too big of a deal?

A

humans also have this enzyme ; the drug has much higher affinity for the bacterial enzyme

25
therapeutic doses of trimethoprim are very specific to ____
bacterial folate metabolsim
26
how does bacterial resistance to trimethoprim occur?
bacteria increases the capacity of their metabolic pathway and increasing expression of dihydrofolate reductase, or they can make mutations in the enzyme that limit drug binding, and lastly, efflux pumps
27
on its own, trimethoprim is ____ (bacteriostatic or bactericidal), and when combined with a sulfonamide it is ____
bacteriostatic; bactericidal
28
ciprofloxacin is an example of a ____ type antibiotic
fluoroquinolone
29
____(enzyme) is important for keeping the bacterial DNA from getting tangled during replication
DNA gyrase
30
DNA gyrase is a bacteria specific form of _____ enzymes
topoisomerase
31
topoisomerase enzymes function by ___
cutting DNA starnds to keep them in order
32
the nicks in a DNA strand made by topoisomerase enzymes are _____ for the DNA replication process to continue
reattached
33
fluoroquinolnes act by inhibiting bacterial ____ enzyme
DNA gyrase
34
MOA of fluoroquinolnes
inhibit bacterial DNA gyrase, which prevents the rejoining of the DNA strands
35
are fluoroquinolones bactericidal or bacteriostatic at high concentrations?
bactericidal
36
in general, fluoroquinolones are ___ spectrum
broad
37
t/f there is significant resistance to fluoroquinolones, especially cipro
t
38
what are the resistance mechanisms to fluoroquinolones?
primary way is the exclusion of the drug from the cell by reduced entry of by efflux pumps; some strains may have mutations in DNA gyrase
39
Rifamin bind to bacterial ____ enzyme
RNA polymerase
40
RNA polymerase is involved in bacterial DNA ____ and the making of _____
transcription; mRNA
41
MOA of Rifampin
binds to RNA polymerase--DNA strand complex and prevents the elongation of the grwoing mRNA strand, stopping transcription and leads to death
42
rifampin is a ____spectrum
broad
43
t/f Rifampim is only used if bacteria shows sensitivity to it, because of resistance
t
44
when Rifampin is used, it is usually combined with something else (t/f)
t
45
Rifampin is used in the treatment of ____ in some cases
tuberculosis
46
Rifampin may induce ___ enzymes in humans
CYP450
47
rifampin has been shown to reduce circulating hormones levels of ___
oral contraceptives