Lab 2 -- Neuro Flashcards

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1
Q

Nociception

A
  • noxious stimulus giving rise to pain perception
  • stimulus activates nociceptors
  • thermal, mechanical, chemical
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2
Q

Analgesics

A
  • APAP
  • local anaesthetics
  • NSAIDs
  • Opioids
  • stops the sense of pain without the loss of consciousness
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3
Q

Analgesic sites of action

A
  • brain
  • dorsal horn
  • nerve conduction
  • site of injury
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4
Q

Opioid + alpha2- agonist site of action

A
  • brain
  • dorsal horn
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5
Q

Local anesthetics Site of action

A
  • dorsal horn
  • peripheral nerve
  • site of injury
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6
Q

Anti-inflammatory site of action

A
  • site of injury
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7
Q

Opioids

A
  • interact with opioid receptors in the CNS and GI tract
  • mimics the endogenous neurotransmitter – opiopeptins
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8
Q

Natural opiate drugs

A
  • morphine
  • codeine
  • thebaine
  • papaverine
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9
Q

endogenous peptides

Natural Opiopeptins

A
  • endorphins
  • enkephalins
  • dynorphins
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10
Q

Synthetics and smi-synthetic Opioid drugs

A
  • diamorphine
  • methadone
  • oxycodone
  • hydrocodone
  • fentanyl
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11
Q

Opioid common structure

A
  • phenanthrene ring
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12
Q

Opioid receptors

A
  • located on cell membranes
  • Mu, Kappa, Delta
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13
Q

Mu receptor

A
  • binding site of endorphine and enkephalin (endorphine with greater affinity)
  • binding site of morphine
  • causes: analgesia, respiratory depression, physical
    dependence, euphoria
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14
Q

Delta receptors

A
  • site for endorphin and enkephalin (greater affinity for enkephalin)
  • causes: spinal analgesia, modulation of the mu
    receptor
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15
Q

Kappa receptors

A
  • dynorphin is the endogenous ligand
  • causes: spinal analgesia, miosis, sedation
  • females more responsive than males
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16
Q

Full agonist opioid drugs

A
  • morphine
  • meperidine
  • methadone
  • codeine
  • fentanyl
  • diamorphine
17
Q

Antagonist Opioid drugs

A

Naloxone
naltrexone

18
Q

Partial agonist opioid drugs

A
  • pentazocine
  • nalbuphine
  • buprenorphine
  • butorphanol
19
Q

Dose response curve

A
  • provide relationship of dose of the drug to its pharmacological effects
20
Q

Threshold dose

A
  • lowest concentration of a dose that can be detected
21
Q

maximum dose

A
  • dose that which even if we increase the dose, the response will no longer increase
22
Q

EC50 or ED50

A
  • dose at which 50% of the maximum response is acheived
23
Q

Opioid MOA

A
  • open K+ channel (K outflow = hyperpolarize)
  • inhibit opening of voltage-gated Ca channel (decrease NT release)
24
Q

Opioid CNS effects

A
  • Analgesia, euphoria, sedation
  • Respiratory depression, cough suppression
  • Truncal rigidity
  • Nausea, vomiting
  • Miosis (Constricted pupils)
25
Q

Opioid GI effects

A
  • Decreased GI motility
  • Constriction of biliary smooth muscle
26
Q

Tolerance

A
  • Decrease in pharmacologic response following
    repeated or prolonged drug administration.
27
Q

Dependence

A
  • Physical dependence is associated with withdrawal
    symptoms
  • Psychological dependence is associated with craving
28
Q

Naloxone

antagonist

A
  • Affinity for all three opioid receptors
    – Main clinical use to treat respiratory depression
    caused by opioid overdose
  • Precipitates withdrawal symptoms in addicts
29
Q

Naltrexone

A
  • longer half-life than naloxone
30
Q

Tail flick test

A
  • baseline is measured and compared to after drug administration to observe effectivenees of analgesia
31
Q

Animal hazards

A
  • Allergy
  • Zoonoses (disease transmittion)
  • animal bites