clinical pharmacology and drug action bds2 Flashcards

1
Q

what is a drug

A

a chemical substance other than food that when administered to a living organism produces a biological effect on the structure or function of the body

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2
Q

what are medicinal drugs

A

substances intended for the use of diagnosis, prevention and treatment of disease

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3
Q

what are non medicinal drugs also referred to as

A

recreational

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4
Q

what are non medicinal drugs

A

illegal substances such as cannabis, heroin and cocaine, as well as legal substances such as caffeine, nicotine and alcohol

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5
Q

what are the three classifications for drug effects

A

therapeutic
side
adverse

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6
Q

what is included under the therapeutic effects of drugs

A

intended/desired outcomes of drug administration
seen as beneficial

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7
Q

what are the features of drug side effects

A

these are unintended effects that are known and predictable
they are usually harmful or negative but can occasionally be beneficial
they do not hinder the primary effect of the drug

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8
Q

what are the features of adverse drug effects

A

these are undesirable and unpredictable
usually more severe and harmful compared to side effects and can hinder the treatment or cause complications

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9
Q

what are the main drug types used in dentistry

A

local anaesthetics
antimicrobials
anxiolytics
analgesics

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10
Q

brief description of LA in dentistry

A

lidocaine and articaine
used for pain prevention during procedures

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11
Q

brief description of antimicrobials in dentistry

A

treat and prevent infections
eg penicillin and fluconazole

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12
Q

brief description of anxiolytics in dentistry

A

reduce anxiety
diazepam and midazolam

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13
Q

describe analgesics in dentistry

A

paracetamol and ibuprofen, reduces post operative pain

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14
Q

what is pharmacodynamics

A

the effects of the drug on the body and mechanism of action
basically looking at what the drug does to the body

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15
Q

what is pharmacokinetics

A

term to describe the four stages of absorption, distribution, metabolism and excretion of drugs
basically looking at what the body does to the drug

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16
Q

what are the four stages to pharmacokinetics

A

absorption
distribution
metabolism
excretion

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17
Q

what can drugs do

A
  • simulate normal body communications
  • interrupt normal body communications
  • act on non host organisms to aid body defences
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18
Q

what are the two methods of host communication

A

hormone messages which deliver general information to all tissues
neural messages which deliver targeted information to specific tissues

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19
Q

effect of thyroid hormone

A

regulate metabolism and growth

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20
Q

effect of insulin and glucagon

A

regulate blood sugar levels

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21
Q

effect of adrenal gland hormones

A

regulate stress response, blood pressure, immune system and other essential functions

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22
Q

effect of sex hormones

A

puberty, pregnancy, menstruation, sperm production, sex drive

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23
Q

why can high doses of one hormone mimic the effects of another

A

because the structure of different hormones can be very similar

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24
Q

effects of hyperthyroidism

A

rapid metabolism
high pulse rate
sweating and heat intolerance
anxiety and agitation
weight loss

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25
effects of hypothyroidism
cold intolerance coarse skin memory loss slow pulse low metabolism
26
do drugs treating hypo/hyperthyroidism affect the thyroid gland
no
27
function of the autonomic nervous system
regulate involuntary body processes eg heart rate, digestion and breathing
28
what are the two components of the autonomic nervous system
sympathetic and parasympathetic
29
how does the sympathetic nervous system control heart rate
adrenergic stimulation to speed up the heart via beta adrenergic receptors
30
how does the parasympathetic nervous system control heart rate
slows the heart via cholinergic receptors
31
what are autonomic drugs
drugs that enhance or inhibit the function of the parasympathetic nervous system and parasympathetic nervous system
32
what are some examples of autonomic drugs
adrenaline atenolol pilocarpine atropine
33
which autonomic drug is a beta agonist
adrenaline
34
which autonomic drug is a beta blocker
atenolol
35
which autonomic drug is a cholingeric agonist
pilocarpine
36
which autonomic drug is a cholinergic blocker
atropine
37
topical administration
drug applied to the tissue where it acts
38
drug applied to the whole organism
systemic administration
39
drug administered by injection
parenteral administration
40
drug applied to skin for absorption
transdermal administration
41
drug injected into the tissues of the skin
subcutaneous administration
42
drug injected into muscle
intramuscular administration
43
drug injected into vein
intravenous administration
44
drug applied to the mucosa for adsorption
transmucosal administration
45
what are the four main modes of action of drugs
activation or blocking of receptors activating or blocking enzyme function opening or blocking ion channels facilitation or blocking transport systems
46
what can receptors be coupled to
ion channels g proteins enzymes gene transcription
47
describe the interaction between receptors and ion channels
agonist stimulates the receptor G protein interacts directly with and changes the open probability of the ion channel
48
describe the relationship between receptors and enzymes
agonist stimulates the receptor and the G protein activates or inhibits the enzyme that gives rise to second messengers
49
what is efficacy
how effective the drug is at producing a response from the receptor
50
how is drug efficacy determined
affinity and occupancy
51
what is drug affinity
how avidly the drug binds to the receptor
52
what is drug occupancy
how much time the drug spends on the receptor
53
what is the measure of drug affinity
Kd (dissociation constant)
54
describe Kd values in relation to affinity
low dissociation constant value means there is a high number of receptors occupied at a low drug concentration meaning there is high affinity high dissociation constant shows that drugs and receptors are more weakly attracted to each other as there are less receptors occupied at the same drug concentration inversely proportional values (low Kd means high affinity)
55
what is an agonist
a drug that binds to the receptors and initiates the same action that would be produced by the substance be it a hormone or a neurotransmitter which would normally bind to the receptor
56
what is a partial agonsit
this binds to the receptor but only partially to activate the receptor. there is less efficacy in comparison to an agonist meaning it produces less than the maximal effect increased partial agonist concentration will improve efficacy for some but not for others
57
what is the difference between agonists and partial agonists
if the drug is an agonist, it binds to the receptor and causes 100% effect. if it is partial, it binds but only partially activates it, so the signal is less than 100%
58
what is an antagonist
drug that binds to but does not activate the receptor, therefore blocking the response
59
describe competitive antagonists
these bind to the same site on the receptor as an agonist therefore blocking the agonists action
60
describe non competitive antagonists
bind to a different site on the receptor from the agonist, called an allosteric site, which prevents activation of the receptor
61
describe reversible antagonists
these bind non covalently and can be displaced. antagonist effects can be reduced by increases the concentration of the agonist such as atenolol
62
describe irreversible antagonists
these bind to tightly to the receptor that it cannot be displaced, therefore this reduces the available receptors for the agonist. the antagnostic effect is insurmountable at any concentration of the agonist
63
how can drugs change enzyme action
by inhibition. the competitive substrate antagonism means the drug competes with the substrate to bind to the enzyme non competitive substrate inhibition means the drug binds to different sites from the substrate, causing a conformational change in enzyme structure which in turn prevents substrate interaction
64
how can the ion channels be affected
cell electrical activity or ion influx
65
which two factors affect drug efficacy
occupancy and affinity