Pharmacy Foundations Flashcards

1
Q

What are the two subtypes of the peripheral nervous system?

A

Somatic (Voluntary) and Autonomic (Involuntary)

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2
Q

What type of neurotransmitter does the somatic nervous system send? What receptor does it act on?

A

Acetylcholine, Nicotinic receptors

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3
Q

What are the two divisions of the autonomic nervous system?

A

Parasympathetic and sympathetic

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4
Q

What physiological responses occur when the parasympathetic system is activated?

A

Rest and Digest (SLUDD):

Salivation, Lacrimation, Urination, Diarrhea/Defecation, Digestion

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5
Q

What physiological response occurs when the sympathetic system is activated

A

Fight of Flight:

Increased HR, BP, pupil dilation, glucose dilation, bronchodilation.

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6
Q

What neurotransmitters are used and what receptors are acted on in the parasympathetic system?

A

Acetylcholine acts on the nicotinic receptor to release more acetylcholine to activate the muscarinic receptor.

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7
Q

What neurotransmitters are used and what receptors are acted on in the sympathetic system?

A

Acetylcholine act on the nicotinic receptor to release norepinephrine and epinephrine on to the adrenergic receptors (Alpha-1, Beta-1, and Beta-2 receptors)

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8
Q

Activation of the Alpha-1 Receptors result in what physiologic response?

A

Smooth muscle (including blood vessel) constriction/ Vasoconstriction

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9
Q

Beta-1 activation results in what physiological response?

A

Increased heart rate, contraction and cardiac output

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10
Q

Beta-2 activation results in what physiologic response?

A

Bronchodilation

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11
Q

What neurotransmitters do monoamine oxidase inhibitors break down?

A

Dopamine, norepinephrine, serotonin, tyramine

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12
Q

About how long should the wash out period be between use of an MAO inhibitor and a drug that increases neurotransmitters (i.e. SSRI)?

A

~14 days

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13
Q

What is pharmacodynamics?

A

The effect or change that a drug has on some type of organism (i.e. bacteria, human). “What the drug does to the body”

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14
Q

What is pharmacokinetics?

A

The effect the body has on the drug: ADME; “What the body does to the drug”

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15
Q

What is ADME?

A

Absorption
Distribution
Metabolism
Excretion

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16
Q

How can we increase the serum concentration of penicillin to allow it to cross the BBB?

A

Providing Probenecid will block the renal excretion of penicillin.

17
Q

How do you treat salicylate (Aspirin) overdoses?

A

Give IV Sodium Bicarbonate to alkalinize the urine. This causes salicylate to become ionized.

18
Q

What is phase I metabolism?

A

Chemical reactions that change the parent molecule into a metabolite. Mostly oxidation reactions but can be hydrolysis or reduction reactions. This step primarily inactivates the compound.

19
Q

What is phase II metabolism?

A

Phase II metabolism are conjugation reactions that may increase water solubility to help facilitate excretion. (i.e. glucuronidation)

20
Q

What are the 6 main CYP 450 enzymes that metabolize most drugs?

A
CYP 2C8/9, 
3A4, 
2E1, 
2D6, 
1A2
21
Q

What drugs are strong (big) inducers?

A
PS CORPS:
Phenytoin
Smoking
Carbamazepine (also an autoinducer)
Oxcarbazepine (and eslicarbazepine)
Rifampin (and rifabutin, rifapentine)
Phenobarbital
St. John's Wort
22
Q

What drugs are known to be big (strong) inhibitors?

A
G <3 Pacman
Grapefruit
Protease Inhibitors
Azole Antifungals 
Cyclosporine/Cimetidine/Cobicistat
Macrolides
Amiodarone (and dronedarone)
Non-DHP CCB (Diltiazem and verapamil)
23
Q

How long does it take for the full effect of induction to be seen? How long could it take for the effects of induction to disappear?

A

Up to 4 weeks as additional enzyme production must be built up; it may take 2-4 weeks for the induction effects to disappear completely based on the enzyme’s half life (degradation)

24
Q

What is the purpose of the P-glycoprotein pump?

A

They act as efflux pumps to pump out foreign substances out of the body and into the gut for excretion.

25
Q

What is enterohepatic recycling?

A

Already metabolized drugs that is reabsorbed from the gut, enter the portal vein and travel back to liver. Results in increased duration of action of many drugs.