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Nagelhout Pharmacology 2 Exam 2 Questions and Answers GRADED A+

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MOA: interference with synthesis of transmitter: cholinergic and adrenergic agents - ANSWER-sympatholytic cholinergic: choline acetyl transferase inhibitors adrenergic: a-methyl tyrosine MOA: metabolic transformation by same pathway as precursor: adrenergic agents - ANSWER-sympatholytic adrenergic: methyldopa MOA: blockade of transport system at nerve terminal membrane: cholinergic and adrenergic agents - ANSWER-sympathomimetic cholinergic: hemicholinium adrenergic: cocaine* MOA: blockade of transport system of storage vesicle: cholinergic and adrenergic agents - ANSWER-sympatholytic cholineric: vesamicol adrenergic: reserpine MOA: promotion of exocytosis or displacement of transmitter from axonal terminal: cholinergic and adrenergic agents - ANSWER-sympathomimetic cholinergic: latrotoxins adrenergic: amphetamine, tyramine MOA: prevention of release of transmitter: cholinergic and adrenergic agents: - ANSWER-sympatholytic cholinergic: botulinim toxin adrenergic: clonidine, precedex MOA: mimicry of transmitter at post junctional sites: cholinergic and adrenergic agents - ANSWER-sympathomimetic cholinergic: Methacoline Adrenergic: nicotine, phenylephrine, dobutamine,

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Nagelhout Pharm 1- Exam 3 With Correct
Answers

General Cardiac Effects of Opiates - ANSWER-Little to no effect
Minimal bradycardia
Effects more pronounced in shock or ambulating patients

Groups of Endogenous Opioid Peptides (5) - ANSWER-1. Enkephalins
a. Leu-enkephalin
b. Met-enkephalin
2. β -Endorphin
3. Dynorphins
a. Dynorphin
b. α-Neoendorphin
4. Endomorphin 1 and Endomorphin 2
5. Nociceptin

Precursor to Enkephalins - ANSWER-Proenkephalin A

Precursor to β-Endophins - ANSWER-Pro-opiomelanocortin (Pro-OMC)

Precursor to Dynorphins - ANSWER-Prodynorphin

Precursor to Endomorpins 1 & 2 - ANSWER-Unknown

Precursor to Nociceptin - ANSWER-Pronociceptin

Location of endogenous opioid peptides - ANSWER-Brain & Spinal cord
(second highest concentration in GI)

Analgesic mechanism of action of opioids - ANSWER-Actives opioid receptors on pre-
synaptic "pain pathway" nerve → prevents release of substance P (or
bradykinin/acetylcholine) to post-synaptic nerve

Analgesic mechanism of action of endogenous endorphins - ANSWER-Endorphins
released from pre-synaptic "pain relieving" nerve → pre-synaptic "pain producing nerve"
→ prevents release of substance P (or bradykinin/acetylcholine) to post-synaptic nerve

3 classes of opiate receptors - ANSWER-1. Mu µ
2. Kappa κ
3. Delta δ

Mu receptors effects (11) - ANSWER-1. Analgesia (supraspinal and spinal) (Mu-1 in
animals)
2. Euphoria & sedation

, 3. Physical dependence
4. Depression of respirations (Mu-2 in animals)
5. Miosis
6. Constipation
7. Urinary retention
8. Bradycardia
9. Pruritus
10. Skeletal rigidity
11. Biliary spasm

Kappa receptor effects (6) - ANSWER-1. Analgesia (spinal & supraspinal)
2. DYSPHORIA
3. Sedation
4. Low abuse potential
5. Miosis
6. ANTI-SHIVERING

Delta receptor effects (5) - ANSWER-(AUGMENTS MU & KAPPA EFFECTS)
1. Analgesia (supraspinal and spinal)
2. Physical dependence
3. Respiratory depression
4. Minimal constipation
5. Urinary retention

Mu receptor Agonists (3) - ANSWER-1. Endorphins
2. Morphine
3. Synthetic opioids

Kappa receptor Agonists (1) - ANSWER-Dynorphins

Delta receptor Agonists (1) - ANSWER-Enkephalins

Antagonists for all classes of opioid receptors (3) - ANSWER-1. Naloxone
2. Naltrexone (oral)
3. Nalmefene (long-lasting)

The amount of analgesia is directly proportional to...(2) - ANSWER-the amount of
respiratory depression
the amount of physical dependence

Full agonist - ANSWER-Has 100% efficacy

Partial Agonist (Agonist/Antagonist) - ANSWER-Does not have 100% efficacy
Agonist: some analgesia if given alone
Antagonist: Will reverse a full agonist if given simultaneously; suboptimal response even
at high doses
R195,97
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