Epinephrine produces all of the following effects EXCEPT:

Questions 52

ATI RN

ATI RN Test Bank

Cardiovascular Drugs Pharmacology NCLEX Questions Questions

Question 1 of 5

Epinephrine produces all of the following effects EXCEPT:

Correct Answer: A

Rationale: In this scenario, the correct answer is A) Decrease in oxygen consumption. Epinephrine is a sympathomimetic drug that acts on adrenergic receptors. It primarily stimulates beta-adrenergic receptors, leading to various physiological effects. Epinephrine causes bronchodilation (B) by activating beta2-adrenergic receptors in the lungs, improving airflow in conditions like asthma. It also causes hyperglycemia (C) by stimulating glycogenolysis and gluconeogenesis in the liver, increasing blood glucose levels. Mydriasis (D) occurs due to the activation of alpha1-adrenergic receptors in the iris radial muscle, causing pupil dilation. The decrease in oxygen consumption (option A) is not a typical effect of epinephrine. In fact, epinephrine can increase oxygen consumption due to its stimulatory effects on the cardiovascular system, leading to increased heart rate and contractility. In an educational context, understanding the effects of epinephrine is crucial for healthcare professionals, especially in emergency situations like anaphylaxis or cardiac arrest where epinephrine is commonly used. Knowing the pharmacological actions of epinephrine helps in safe and effective administration based on the desired outcomes.

Question 2 of 5

Which of the following agents blocks the chloride channel directly?

Correct Answer: D

Rationale: In the context of cardiovascular pharmacology, the correct answer is D) Picrotoxin because it is a GABA receptor antagonist that directly blocks the chloride channel. This mechanism of action leads to an excitatory effect on the central nervous system. A) Secobarbital is a barbiturate that acts as a positive allosteric modulator of the GABA-A receptor, enhancing the inhibitory effects of GABA, but it does not directly block the chloride channel. B) Flumazenil is a benzodiazepine receptor antagonist used for benzodiazepine overdose to reverse sedative effects by competitively binding to benzodiazepine receptors, not chloride channels. C) Zaleplon is a non-benzodiazepine sedative-hypnotic agent that acts on the GABA-A receptor complex but does not directly block the chloride channel. Understanding the mechanisms of action of different drugs is crucial in pharmacology as it helps healthcare professionals make informed decisions about drug selection, dosing, and potential interactions. Knowing how specific drugs interact with receptors and channels allows for the safe and effective use of medications in patient care.

Question 3 of 5

The drug of choice in the treatment of myoclonic seizures is:

Correct Answer: A

Rationale: In the treatment of myoclonic seizures, the drug of choice is Valproate (Option A). Valproate is an antiepileptic medication that has been found to be effective in managing myoclonic seizures due to its broad-spectrum anticonvulsant properties. Valproate works by increasing the levels of gamma-aminobutyric acid (GABA), an inhibitory neurotransmitter in the brain, which helps to reduce abnormal electrical activity that triggers seizures. Phenobarbital (Option B) is a barbiturate that is more commonly used in the treatment of generalized tonic-clonic seizures and partial seizures. While it may have some efficacy in myoclonic seizures, Valproate is generally preferred due to its better side effect profile and effectiveness. Phenytoin (Option C) is another antiepileptic drug that is more commonly used for partial seizures and tonic-clonic seizures. It is not the drug of choice for myoclonic seizures because it may exacerbate myoclonic activity in some cases. Felbamate (Option D) is not typically used as a first-line treatment for myoclonic seizures due to its potential for serious side effects, such as aplastic anemia and hepatic failure. It is usually reserved for refractory cases when other treatments have failed. In an educational context, understanding the appropriate pharmacological management of different types of seizures is crucial for healthcare professionals, especially those working in neurology or emergency settings. Knowing the specific indications and contraindications of various antiepileptic drugs can help optimize patient care and improve outcomes for individuals with epilepsy or seizure disorders.

Question 4 of 5

Second-order pain is:

Correct Answer: B

Rationale: In the context of pharmacology, understanding pain pathways and types of pain is crucial for effective pain management using cardiovascular drugs. Second-order pain, as indicated by option B, is described as dull, burning pain. This type of pain is often associated with C-fibers, which are unmyelinated and slower in transmission compared to A-delta fibers. Dull, burning pain is typically less localized and can be more diffuse compared to sharp, well-localized pain, which is associated with A-delta fibers. Additionally, second-order pain is not effectively reduced by non-narcotic analgesics, as these drugs are more suited for milder, acute pain rather than the persistent, burning nature of second-order pain. Understanding the characteristics of different types of pain is essential for selecting appropriate pharmacological interventions for pain management in cardiovascular patients, ensuring optimal patient care and outcomes.

Question 5 of 5

Indicate the drug, which decreases the craving for alcohol or blunts pleasurable “high” that comes with renewed drinking:

Correct Answer: C

Rationale: In the context of pharmacology and substance use disorders, the correct answer is C) Naltrexone. Naltrexone is an opioid receptor antagonist that works by reducing the rewarding effects of alcohol, thereby decreasing the craving for alcohol and blunting the pleasurable "high" associated with drinking. It is commonly used as part of a comprehensive treatment plan for alcohol dependence. A) Disulfiram is a medication that works by causing unpleasant effects (such as nausea, vomiting, and headache) when alcohol is consumed, acting as a deterrent to drinking rather than reducing cravings. B) Amphetamine is a central nervous system stimulant and is not used specifically to decrease alcohol cravings or the pleasurable effects of alcohol. D) Diazepam is a benzodiazepine used primarily for its anxiolytic properties and is not indicated for reducing alcohol cravings or the rewarding effects of alcohol. Educationally, understanding the mechanisms of action of different drugs used in the treatment of substance use disorders is crucial for healthcare professionals, especially in pharmacology and addiction medicine. By knowing how each medication works, healthcare providers can make informed decisions about the most appropriate treatment options for their patients, leading to better outcomes in managing substance use disorders.

Access More Questions!

ATI RN Basic


$89/ 30 days

ATI RN Premium


$150/ 90 days

Similar Questions