ATI RN
Cardiovascular Pharmacology Drug Class Questions
Question 1 of 5
Which competitive neuromuscular blocking agent could be used in patients with renal failure?
Correct Answer: A
Rationale: The correct answer is A: Atracurium. Atracurium is preferred in patients with renal failure because it is metabolized by Hoffman elimination independent of renal or hepatic function. Succinylcholine (B) is not recommended in renal failure due to prolonged paralysis. Pipecuronium (C) and Doxacurium (D) are primarily eliminated by renal excretion, making them unsuitable for patients with renal failure.
Question 2 of 5
Beta-blocking drugs-induced chronically lower blood pressure may be associated with theirs effects on:
Correct Answer: D
Rationale: The correct answer is D: All of the above. Beta-blocking drugs lower blood pressure by affecting multiple systems. 1. The heart: Beta blockers reduce heart rate and contractility, leading to decreased cardiac output. 2. The blood vessels: Beta blockers cause vasodilation, reducing peripheral resistance. 3. The renin-angiotensin system: Beta blockers can inhibit renin release, decreasing angiotensin II levels and reducing vasoconstriction. Therefore, the effects of beta blockers on the heart, blood vessels, and renin-angiotensin system collectively result in chronically lower blood pressure. Choices A, B, and C are incorrect because beta blockers impact all these systems, not just one.
Question 3 of 5
Which of the following benzodiazepines is used mainly for hypnosis?
Correct Answer: C
Rationale: The correct answer is C: Flurazepam. Flurazepam is a benzodiazepine commonly used for its sedative-hypnotic properties, making it ideal for treating insomnia and inducing sleep. Clonazepam (A) is mainly used for seizure disorders and panic disorder. Lorazepam (B) is primarily used for anxiety and agitation. Midazolam (D) is commonly used for sedation before medical procedures. Therefore, Flurazepam is the most appropriate choice for hypnosis among the options provided.
Question 4 of 5
Indicate the antiseizure drug, which is a sulfonamide derivative, blocking Na+ channels and having additional ability to inhibit T-type Ca2+ channels:
Correct Answer: B
Rationale: The correct answer is B: Zonisamide. Zonisamide is a sulfonamide derivative that blocks Na+ channels and also inhibits T-type Ca2+ channels. This dual mechanism of action helps in controlling seizures. Tiagabine (A) inhibits GABA reuptake, Ethosuximide (C) blocks T-type Ca2+ channels only, and Primidone (D) is metabolized into phenobarbital, which enhances GABAergic activity.
Question 5 of 5
Which of the following mediators is found mainly in long descending pathways from the midbrain to the dorsal horn?
Correct Answer: B
Rationale: The correct answer is B: Dynorphin. Dynorphin is mainly found in long descending pathways from the midbrain to the dorsal horn. It acts as an endogenous opioid peptide that modulates pain perception. Prostaglandin E, Enkephalin, and Glutamate are not primarily found in these pathways. Prostaglandin E is involved in inflammation and fever, Enkephalin acts as an endogenous opioid peptide in pain modulation, and Glutamate is a major excitatory neurotransmitter in the central nervous system. Thus, B is the correct choice based on its specific localization in the described pathways.