Which of the following drugs would most likely be effective to decrease the patient's spontaneous breathing?

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Central Nervous System Stimulants and Related Drugs NCLEX Style Questions Questions

Question 1 of 5

Which of the following drugs would most likely be effective to decrease the patient's spontaneous breathing?

Correct Answer: B

Rationale: Vecuronium is a skeletal muscle relaxant that acts as a non-depolarizing neuromuscular blocker, making it effective in decreasing spontaneous breathing by causing muscle relaxation. Diazepam, Botulinum toxin, Dantrolene, and Baclofen do not directly target skeletal muscle function in the same way as Vecuronium. Diazepam is a benzodiazepine, Botulinum toxin is used for muscle spasms, Dantrolene is a muscle relaxant used for malignant hyperthermia, and Baclofen is a muscle relaxant used for spasticity. Therefore, Vecuronium is the most appropriate choice in this scenario.

Question 2 of 5

Acute opium poisoning is treated by intravenous administration of

Correct Answer: A

Rationale: Naloxone is an opioid antagonist that rapidly reverses respiratory depression in opioid overdose.

Question 3 of 5

Corticosteroids are used in treatment of the following conditions EXCEPT:

Correct Answer: A

Rationale: Corticosteroids treat anaphylaxis (choice A), transplantation (choice B), and osteoarthritis (choice C) via anti-inflammatory effects. Hypertension (choice D) is a side effect, not an indication, making it the exception. This clarifies therapeutic scope.

Question 4 of 5

Benzodiazepines produce their actions on CNS by:

Correct Answer: B

Rationale: Benzodiazepines (e.g., diazepam, lorazepam) are CNS depressants used for anxiety, seizures, and insomnia. They exert effects by binding to a specific allosteric site on the GABAa receptor, enhancing GABA's inhibitory action. GABA, the primary inhibitory neurotransmitter, opens chloride (Cl⁻) channels, hyperpolarizing neurons and reducing excitability. Benzodiazepines increase the frequency of channel opening, potentiating this effect, leading to sedation and anxiolysis. Blocking Cl⁻ channels (choice A) would oppose inhibition, contrary to their purpose. Acting as direct agonists (choice C) is incorrect—they don't activate the receptor alone but amplify GABA's action. Antagonizing GABAb receptors (choice D) is irrelevant, as benzodiazepines target GABAa specifically. This potentiation mechanism underlies their therapeutic utility and risks like tolerance. Understanding this is key to distinguishing benzodiazepines from other CNS drugs and managing their clinical use effectively.

Question 5 of 5

Which of the following are NOT correctly paired?

Correct Answer: D

Rationale: Buspirone (choice A), Alprazolam (choice B), and Baclofen (choice C) are correctly paired (anxiolytic, some antidepressant effect, less sedative muscle relaxant). Oxazepam (choice D), a benzodiazepine, isn't a TCA, making it the incorrect pair. This tests drug classification.

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