The phenothiazines have a variety of actions at different receptor types. However, they do not appear to interact with receptors for

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Pharmacology CNS Drugs Quizlet Questions

Question 1 of 5

The phenothiazines have a variety of actions at different receptor types. However, they do not appear to interact with receptors for

Correct Answer: C

Rationale: In pharmacology, understanding the specific receptor interactions of different drug classes is crucial for effective patient care. In the case of phenothiazines, they are known to interact with various receptor types, but they do not interact with nicotine receptors (Option C). This is because phenothiazines primarily act on dopamine (Option A), histamine (Option B), and norepinephrine (Option D) receptors. The correct answer, Option C (Nicotine), is based on the pharmacological profile of phenothiazines, which do not exhibit any significant affinity for nicotine receptors. This distinction is important as it helps in understanding the specific mechanism of action of phenothiazines and their therapeutic effects. Options A, B, and D are incorrect because phenothiazines are known to interact with dopamine, histamine, and norepinephrine receptors, respectively. Understanding these interactions is essential in clinical practice when using phenothiazines to treat various conditions such as schizophrenia, bipolar disorder, and nausea. Educationally, this question serves to reinforce the knowledge of pharmacological interactions of CNS drugs, highlighting the specificity of drug-receptor interactions. It emphasizes the importance of understanding the pharmacodynamics of medications to make informed clinical decisions and ensure safe and effective patient care.

Question 2 of 5

A 24-year-old man with a history of partial seizures has been treated with standard anticonvulsants for several years. He is currently taking valproic acid, which is not fully effective, and his neurologist prescribes a new drug. Unfortunately, the patient develops toxic epidermal necrolysis. The new drug prescribed was

Correct Answer: C

Rationale: The correct answer is C) Lamotrigine. Lamotrigine is a commonly used anticonvulsant that has shown efficacy in treating partial seizures. It is known to have a lower risk of causing severe skin reactions compared to other anticonvulsants like carbamazepine or phenytoin. Felbamate (A) is associated with a higher risk of causing serious adverse effects, including aplastic anemia and hepatic failure, but not specifically toxic epidermal necrolysis. Gabapentin (B) and Tiagabine (D) are anticonvulsants used to treat seizures but are not typically associated with causing toxic epidermal necrolysis. Educationally, understanding the side effect profiles of different anticonvulsants is crucial for healthcare providers when selecting appropriate medications for patients with seizure disorders. Lamotrigine's lower risk of causing severe skin reactions makes it a favorable choice for individuals who may be predisposed to such reactions, as seen in the case of the patient developing toxic epidermal necrolysis.

Question 3 of 5

The brief duration of action of an ultra-short-acting barbiturate is due to

Correct Answer: D

Rationale: The correct answer is D) Rapid rate of redistribution from the brain due to its high liposolubility. Ultra-short-acting barbiturates, like thiopental, have a high lipid solubility which allows them to quickly enter the brain and induce anesthesia. However, their rapid redistribution from the brain to other tissues with lower blood flow results in their short duration of action. Option A is incorrect because a slow rate of metabolism in the liver would actually prolong the duration of action by allowing more of the drug to remain active in the body for a longer period of time. Option B is incorrect because low lipid solubility would limit the drug's ability to cross the blood-brain barrier and exert its pharmacological effects in the brain, thus not explaining the brief duration of action. Option C is incorrect because a high degree of binding to plasma proteins would affect the distribution of the drug in the bloodstream but not specifically account for the rapid clearance from the brain. Educationally, understanding the pharmacokinetic properties of drugs, such as lipid solubility and distribution, is crucial in pharmacology. This knowledge helps healthcare professionals predict the onset, duration, and intensity of drug effects, enabling them to make informed decisions regarding drug therapy and patient care.

Question 4 of 5

An overdose victim presents to the emergency department with an elevated heart rate, decreased blood pressure, dilated pupils, and lethargy, upon arrival to the ICU, she has a generalized tonic-clonic seizure that is treated with IV diazepam and fosphenytoin. Which of the following is the most likely intoxicant?

Correct Answer: A

Rationale: In this scenario, the correct answer is A) Amitriptyline. Amitriptyline is a tricyclic antidepressant that can cause anticholinergic effects, including tachycardia, hypotension, dilated pupils, and central nervous system depression leading to lethargy and seizures. The administration of IV diazepam and fosphenytoin to treat the seizure further supports this as they are commonly used in tricyclic antidepressant overdose. Option B) Methanol typically presents with metabolic acidosis and visual disturbances rather than the symptoms described in the case. Option C) Acetaminophen overdose is associated with liver toxicity and not the constellation of symptoms presented. Option D) Oxycodone overdose would more likely present with respiratory depression and pinpoint pupils, which are not seen in this case. Understanding the signs and symptoms of different drug overdoses is crucial for healthcare professionals to provide appropriate and timely interventions. Recognizing the specific manifestations of various intoxicants can guide treatment decisions and improve patient outcomes. By linking theoretical knowledge with practical application in clinical scenarios, learners can enhance their diagnostic skills and decision-making abilities in real-world healthcare settings.

Question 5 of 5

Phenytoin is effective for the treatment of all of the following types of seizures except

Correct Answer: D

Rationale: Phenytoin is a widely used antiepileptic drug that is effective for treating generalized tonic-clonic, simple partial, and complex partial seizures. However, it is not effective in treating absence seizures. The correct answer is D) Absence because phenytoin works by blocking voltage-gated sodium channels, which helps control the rapid firing of neurons seen in tonic-clonic and partial seizures. Absence seizures involve a different mechanism, primarily involving thalamic T-type calcium channels, which phenytoin does not effectively target. Generalized tonic-clonic, simple partial, and complex partial seizures are types of seizures where phenytoin's mechanism of action is beneficial, making them responsive to this medication. Understanding the specific mechanisms of action of different antiepileptic drugs is crucial in selecting the appropriate treatment for different types of seizures, as not all medications are effective for all seizure types. This knowledge helps healthcare providers tailor treatment plans to individual patients, optimizing seizure control and minimizing side effects.

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