Which of the following structures was most likely the site of action of the botulinum toxin injected into the extrinsic ocular muscles of the 22-year-old man with strabismus?

Questions 229

ATI RN

ATI RN Test Bank

Central Nervous System Stimulants and Related Drugs NCLEX Questions Quizlet Questions

Question 1 of 5

Which of the following structures was most likely the site of action of the botulinum toxin injected into the extrinsic ocular muscles of the 22-year-old man with strabismus?

Correct Answer: B

Rationale: Botulinum toxin primarily acts at somatic nerve terminals by blocking the release of acetylcholine, leading to muscle paralysis. In the context of strabismus treatment, the toxin targets the nerve terminals supplying the extrinsic ocular muscles, specifically affecting neuromuscular transmission at the neuromuscular junction. This action results in localized muscle weakness and temporary paralysis, aiding in the correction of strabismus.

Question 2 of 5

Which of the following muscle relaxants was most likely given to a patient who exhibited transient muscle fasciculations followed by generalized paralysis within 1 minute of administration?

Correct Answer: B

Rationale: In this scenario, the correct answer is B) Succinylcholine. Succinylcholine is a depolarizing neuromuscular blocker that acts quickly by initially causing muscle fasciculations before inducing paralysis. This rapid onset of action is due to its ability to bind to the acetylcholine receptor, leading to sustained depolarization of the motor endplate. Option A) Cisatracurium is a non-depolarizing neuromuscular blocker that does not cause fasciculations or rapid onset paralysis like succinylcholine. Option C) Dantrolene is a skeletal muscle relaxant used to treat malignant hyperthermia and spasticity but does not cause the described rapid onset of paralysis. Option D) Vecuronium is a non-depolarizing neuromuscular blocker that also does not exhibit the rapid onset of action seen with succinylcholine. Educationally, understanding the mechanisms of action of different muscle relaxants is crucial for healthcare providers, especially in anesthesia and critical care settings. Recognizing the unique characteristics of each drug can help in selecting the most appropriate agent for specific clinical scenarios, optimizing patient care, and avoiding adverse events.

Question 3 of 5

A 34-year-old woman suffering from hemifacial spasms started treatment with botulinum toxin injected directly into the abnormally contracting muscles. Which of the following molecular actions most likely mediated the therapeutic effect of the drug in the patient's disorder?

Correct Answer: D

Rationale: The correct answer is D. Botulinum toxin works by inhibiting the release of acetylcholine from cholinergic terminals, leading to muscle paralysis and relaxation. This action prevents the excessive muscle contractions seen in hemifacial spasms. Inhibition of acetylcholine exocytosis from cholinergic terminals is the mechanism behind the therapeutic effect of botulinum toxin in this case.

Question 4 of 5

Which of the following drugs would be most appropriate for this patient?

Correct Answer: B

Rationale: Baclofen is a muscle relaxant commonly used to treat muscle spasms, making it the most appropriate choice for a patient with muscle spasms. Phenobarbital is an antiseizure medication and would not be indicated for this patient. Tubocurarine and succinylcholine are neuromuscular blocking agents used during surgery, but baclofen would be more appropriate for muscle spasms outside of surgical settings. Chlorpromazine is an antipsychotic medication and would not be indicated for muscle spasms.

Question 5 of 5

Which of the following drugs did the patient most likely take?

Correct Answer: A

Rationale: In this scenario, the correct answer is A) Valproic acid. Valproic acid is a central nervous system stimulant commonly prescribed for seizure disorders such as epilepsy. It works by increasing the levels of a neurotransmitter called gamma-aminobutyric acid (GABA) in the brain, which helps to reduce seizure activity. Carbamazepine (option B) is also an antiepileptic drug, but it works by a different mechanism compared to valproic acid. Carbamazepine primarily acts by blocking sodium channels in the brain to prevent abnormal electrical activity that can lead to seizures. Lamotrigine (option C) is another antiepileptic medication that works by inhibiting the release of glutamate, an excitatory neurotransmitter in the brain. It is not a central nervous system stimulant like valproic acid. Ethosuximide (option D) is used to treat absence (petit mal) seizures and works by reducing the abnormal electrical activity in the brain associated with this specific type of seizure. It is not a central nervous system stimulant like valproic acid. In an educational context, understanding the mechanisms of action of different antiepileptic drugs is crucial for healthcare professionals to make informed decisions regarding the selection of appropriate medications for patients with seizure disorders. This knowledge helps optimize patient care and outcomes by tailoring treatment to individual needs based on the underlying pathology and desired therapeutic effects.

Access More Questions!

ATI RN Basic


$89/ 30 days

ATI RN Premium


$150/ 90 days

Similar Questions