Pharm 1 Flashcards

1
Q

Mechanism of local anesthetics

A

Blocks voltage gated sodium channels in neurons that transmit pain

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2
Q

Mechanism of benzodiazepines

A

Binds to GABA A receptor and induces its ability to open chloride channel and causes hyperpolarization

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3
Q

What things use tyrosine kinase receptors

A

Insulin

GROWTH FACTORS: EGFR, platelet derived growth factor (PDGF), Nerve growth factor receptor

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4
Q

Examples of things that use cytokines receptors and describe mechanism of these receptors

A

Growth Hormones, prolactin, EPO, Interferons
These receptors do not have any intrinsic kinase activity as seen with tyrosine kinase receptors but have the JAK kinase which can phosphorylate each other and the STAT receptor. When STAT binds, JAK phosphorylates STAT which dimerizes and migrates to the nucleus and regulates transcription

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5
Q

Mechanism of vinca alkaloids

A

Anti cancer drug that prevents the formation for microtubules by binding to tubulin

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6
Q

What phase in the cell cycle are cells arrested at when you use vinca alkaloids

A

Metaphase

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7
Q

What do you give a patient who is taking cyclophosphamides to present hemorrhagic cystitis?

A

Mensa

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8
Q

Why would you give someone mannitol?

A

It is a diuretic so it is used to reduce cerebral edema

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9
Q

What drug(s) would you use to treat hyperlipidemia

A

Cholestyramine, colestipal and colesevelam; they prevent the reabsorption of bile acid

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10
Q

_____________ chelates heavy metal

A

Dimercopral

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11
Q

Phenoxybenzamine

A

Irreversible α adrenoreceptor blocker

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12
Q

Albumin is a slightly ___________ plasma protein so __________ drugs will behind to it

A

Basic; acidic

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13
Q

Penetration of the blood brain barrier depends on __________________ transport

A

Transcellular

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14
Q

_________ undergoes Phase 2 then Phase 1 reactions in its metabolism

A

Isoniazid

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15
Q

Phase 1 reactions occur in the _________ and usually converts the drug into a _______ form

A

SER; polar
Mostly catalyzed by P450 system
Oxidation, reduction, decarboxylation, deamination and hydrolytic reaction

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16
Q

Phase 2 mainly occurs in the ___________ and conjugation reactions that form a covalent bond between the drug and ______________ (list all of them)

A

Cytosol

Glucoronate, glutathione, acetate, amino acids, sulfate

17
Q

Drugs that induced cytochrome P450

A

Rifampin, phenobarbital, carbamazepine

18
Q

Drugs that inhibit cytochrome P450:

A

Ketoconazole, cimetidine, amiodarone, erythromycin, chloramphenicol, and grapefruit juice

19
Q

__________ inhibits P-glycoproteins

A

Macrolide antibiotics

20
Q

Acetominophen is metabolized by ______

A

CYP2E1

21
Q

Indirect antagonism mechanism

A

Antagonist does not bind to the receptor but instead to an intermediate macromolecule in the pathway that links the receptor to the physiological effect
Ex. Drug inhibits PKA which block the effects the β adrenoreceptor agonist

22
Q

Physiological antagonism

A

One against opposes another agonist but through DIFFERENT receptors

23
Q

Chemical antagonism

A

A drug that reacts with an agonist to form a product that cannot activate a receptor
Ex. Protamine (positively charged) binds to heparin (negatively charged) to counteract the effects of heparin

24
Q

Therapeutic window

A

Dosage range between the minimum effective therapeutic concentration and the minimum toxic concentration

25
Q

Therapeutic index

A

TD50/ED50
OR
LD50/ED50

26
Q

Drugs that follow zero order kinetics

A

Aspirin in high doses, Ethanol, and Phenytoin (anti-epileptic drug)