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Exam (elaborations)

PMCOL 343 - Final Exam Latest Update

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PMCOL 343 - Final Exam Latest Update ...

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  • September 10, 2024
  • 6
  • 2024/2025
  • Exam (elaborations)
  • Questions & answers
  • PMCOL 343
  • PMCOL 343
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PMCOL 343 - Final Exam Latest
Update

Diphenoxylate - Answer Opioid that controls diarrhea (causes constipation)

Loperamide - Answer Opioid that controls diarrhea (causes constipation)

Dextromethorphan - Answer Opioid that suppresses cough by acting on nTS
(non-analgesic)

IV anesthetics - Answer Propofol, ketamine, etomidate, methohexital, thiopentone
(barbiturate)

Inhalation anaesthetics - Answer Sevoflurane, deflurane, isoflurane, N2O

For neuromuscular blockades - Answer Succinylcholine, rocuronium, atrcurium,
cisatracuriu, neostigmine

adjuvant agents for anesthesia - Answer opioids, midazolam, dexmedetomidine

Propofol - Answer GABA-A agonist. IV anasethetic with rapid onset, predictable half-life,
anti-emetic and anticonvulsant properties, no hangover. Commonly used for TIVA.

Etodimate - Answer GABA-A agonist (potentiator), IV anaesthetic

Ketamine - Answer NMDA antagonist, analgesic and anesthetic effects, increases
HR/BP, but can be used for procedural sedation

Benzodiazepines - Answer GABA-A agonist, use during operations, also anxiolytic,
sedative, anterograde amnesia, and anticonvulsant, minimal CV and rest depression,
quick onset, short half life

Flumazenil - Answer Reverses the effects of benzodiazepines

Dexmedetomidine - Answer Alpha 2 agonist, used for sedation, limited rest depression,
ut causes hypotension and brachycardia, slow onset

Cocaine - Answer Ester local anesthetic, block Na channels

Procaine - Answer Ester local anesthetic, block Na channels

Lidocaine - Answer Amide local anesthetic, block Na channels

Bupivacaine - Answer Amide local anesthetic, block Na channels, R (+) binds more
readily to cardiac Na channels and is more cardio toxic (S (-) better)

, Pegvisomant - Answer Recombinant growth hormone antagonist (for acromegaly or
gigantism)

Octreotide - Answer Somatostatin receptor agonist (to decrease growth and treat
acromegaly and gigantism)

Dexamethasone - Answer higher affinity and specificity for GC receptor (30:0), long
acting

Fludrocortisone - Answer higher affinity and specificity for MC receptor (0:250)

Hydrocortisone - Answer GC replacement therapy, does not replicate circadian rhythm
of cortisol secretion

Continuous subcutaneous hydrocortisone infusion (CSHI) - Answer GC replacement
therapy, follows more closely with cortisol physiology (slow rise in morning) but does
not have ultra radian pulsatility.

Chronocort - Answer GC replacement therapy with delayed absorption, mimics cortisol
levels most closely

Ketoconazole - Answer anti-fungal that inhibits 17alpha-hydroxylase, used to treat
Cushing's disease (decrease cortisol and DHEA) but can cause increases in
progesterone and aldosterone

Metyrapone - Answer Inhibits 11beta-hydroxylase, used to treat Cushing's Disease
(decrease cortisol, corticosterone, and aldosterone) but can cause hirsutism and
hypertension

Mifepristone - Answer GC and progesterone antagonist that binds to GC and
progesterone receptors and has much higher binding affinity. Used for patients with
ectopic ACTH secretion or adrenal carcinoma. Also a SPRM which can be used as
emergency contraception to inhibit LH surge and ovulation.

Selective GR Modulators (SGRMs) - Answer steroid or non-steroid compounds that
favour trans repressing actions of GR (rather than transactivation). Also has
anti-inflammatory effects.

Anastrozole - Answer Aromatase inhibitor; steroidal or non-steroidal, selective inhibition
of estrogen synthesis, treatment for breast cancer with no risk of uterine cancer or
venous thromboembolism

Clomiphene Citrate - Answer Selective estrogen receptor modulator, blocks ERs in
pituitary and hypothalamus (so decrease negative feedback and increase estrogen
secretion) - only useful in people with a functioning HPO axis. Stimulates ovulation due
to increase in LH.

Tamoxifen - Answer SERM, antagonistic in breast tissue, agonistic in bone, agonist in
uterus (bad), modulation of signalling proteins, and activation of apoptosis. It is a

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