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

A

t

22
Q

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

A

t

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
Q

therapeutic doses of trimethoprim are very specific to ____

A

bacterial folate metabolsim

26
Q

how does bacterial resistance to trimethoprim occur?

A

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
Q

on its own, trimethoprim is ____ (bacteriostatic or bactericidal), and when combined with a sulfonamide it is ____

A

bacteriostatic; bactericidal

28
Q

ciprofloxacin is an example of a ____ type antibiotic

A

fluoroquinolone

29
Q

____(enzyme) is important for keeping the bacterial DNA from getting tangled during replication

A

DNA gyrase

30
Q

DNA gyrase is a bacteria specific form of _____ enzymes

A

topoisomerase

31
Q

topoisomerase enzymes function by ___

A

cutting DNA starnds to keep them in order

32
Q

the nicks in a DNA strand made by topoisomerase enzymes are _____ for the DNA replication process to continue

A

reattached

33
Q

fluoroquinolnes act by inhibiting bacterial ____ enzyme

A

DNA gyrase

34
Q

MOA of fluoroquinolnes

A

inhibit bacterial DNA gyrase, which prevents the rejoining of the DNA strands

35
Q

are fluoroquinolones bactericidal or bacteriostatic at high concentrations?

A

bactericidal

36
Q

in general, fluoroquinolones are ___ spectrum

A

broad

37
Q

t/f there is significant resistance to fluoroquinolones, especially cipro

A

t

38
Q

what are the resistance mechanisms to fluoroquinolones?

A

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
Q

Rifamin bind to bacterial ____ enzyme

A

RNA polymerase

40
Q

RNA polymerase is involved in bacterial DNA ____ and the making of _____

A

transcription; mRNA

41
Q

MOA of Rifampin

A

binds to RNA polymerase–DNA strand complex and prevents the elongation of the grwoing mRNA strand, stopping transcription and leads to death

42
Q

rifampin is a ____spectrum

A

broad

43
Q

t/f Rifampim is only used if bacteria shows sensitivity to it, because of resistance

A

t

44
Q

when Rifampin is used, it is usually combined with something else (t/f)

A

t

45
Q

Rifampin is used in the treatment of ____ in some cases

A

tuberculosis

46
Q

Rifampin may induce ___ enzymes in humans

A

CYP450

47
Q

rifampin has been shown to reduce circulating hormones levels of ___

A

oral contraceptives