Colchicine

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Pharmacology CNS Drugs Classification Questions

Question 1 of 5

Colchicine

Correct Answer: A

Rationale: Colchicine is used for the treatment and prevention of acute gouty arthritis. This is the correct answer because colchicine works by decreasing the inflammatory response to uric acid crystals in the joints, thereby reducing the pain and swelling associated with acute gout attacks. It does not cause cellular proliferation (option B), act as an effective analgesic in osteoarthritis (option C), or enhance uric acid excretion (option D). Educationally, understanding the correct use of colchicine is important for healthcare professionals, especially those involved in treating patients with gout. By knowing that colchicine is specifically indicated for gouty arthritis, medical professionals can appropriately prescribe this medication and inform patients about its intended purpose and potential side effects. Understanding the mechanism of action of colchicine can also help healthcare providers explain to patients how this medication works to alleviate their symptoms.

Question 2 of 5

The difference between autonomic and somatic nerves are all except

Correct Answer: D

Rationale: The correct answer is D) None of the above. The key difference between autonomic and somatic nerves lies in their functions and control of different types of muscles. In somatic nerves, which control skeletal muscles, there is a single motor neuron that extends from the central nervous system to the muscle, resulting in voluntary control of movement. These nerves are myelinated, allowing for faster conduction of impulses. On the other hand, autonomic nerves control involuntary actions of smooth muscles, cardiac muscles, and glands. They consist of two neurons: a preganglionic neuron that synapses with a postganglionic neuron in an autonomic ganglion. Postganglionic autonomic nerves are unmyelinated, which contributes to slower conduction. Option A is incorrect because autonomic nerves do contain peripheral ganglia, unlike somatic nerves. Option B is incorrect as it incorrectly compares the myelination of motor nerves to skeletal muscles with postganglionic autonomic nerves. Option C is incorrect because the presynaptic transmitter can be the same or different in both somatic and autonomic nerves, depending on the specific neurotransmitter involved. Understanding these differences is crucial in pharmacology as drugs targeting the CNS can have varying effects on autonomic and somatic functions based on their mechanisms of action. This knowledge is essential for healthcare professionals to make informed decisions when prescribing medications that affect the central nervous system.

Question 3 of 5

Which of the following is both alpha and beta blocker?

Correct Answer: C

Rationale: In pharmacology, understanding the classification of drugs is crucial for safe and effective patient care. In this question, the correct answer is C) Labetalol. Labetalol is a unique medication that acts as both an alpha and beta blocker. This dual action makes it effective in managing conditions such as hypertension by blocking both alpha and beta receptors, resulting in vasodilation and decreased heart rate. Option A) Propranolol is a non-selective beta blocker, meaning it primarily acts on beta receptors only, not alpha receptors. Option B) Esmolol is a selective beta-1 blocker, targeting specific beta receptors but not alpha receptors. Option D) Metoprolol is also a selective beta-1 blocker, similar to esmolol, and does not have alpha-blocking properties like labetalol. Educationally, this question highlights the importance of understanding the specific pharmacological properties of drugs within the CNS drug classification. By knowing the differences between alpha and beta blockers, healthcare professionals can make informed decisions when selecting the most appropriate medication for each patient based on their condition and individual needs.

Question 4 of 5

The barbiturate of choice for induction of anaesthesia is

Correct Answer: A

Rationale: The correct answer is A) Pentothal. Pentothal, also known as thiopental, is the barbiturate of choice for induction of anesthesia due to its rapid onset of action and short duration. It produces anesthesia quickly, making it ideal for procedures requiring rapid induction and short duration of action. B) Thiamylal is another barbiturate used for induction of anesthesia, but Pentothal is preferred due to its faster onset and shorter duration. C) Methohexital is also a barbiturate used for anesthesia, but again, Pentothal is preferred for its superior induction characteristics. D) Etomidate is a non-barbiturate drug used for anesthesia induction in certain situations, but it is not a barbiturate like Pentothal. In an educational context, understanding the specific characteristics of different drugs used for anesthesia induction is crucial for healthcare professionals, especially anesthesiologists and nurses working in operating rooms. Knowing which drug is best suited for different scenarios ensures patient safety and optimal outcomes during surgical procedures. Understanding the pharmacology of CNS drugs, including barbiturates, is essential for providing safe and effective anesthesia care.

Question 5 of 5

Which of the following benzodiazepines has the shortest half-life?

Correct Answer: D

Rationale: In pharmacology, understanding the pharmacokinetics of drugs is crucial to their clinical use. The correct answer is D) Midazolam, which has the shortest half-life among the listed benzodiazepines. Midazolam is a short-acting benzodiazepine commonly used for sedation, anesthesia induction, and brief procedures due to its rapid onset and short duration of action. Its short half-life allows for precise control over the sedative effects and facilitates quick recovery post-procedure. Option A) Alprazolam is a medium-acting benzodiazepine commonly prescribed for anxiety disorders, and it has a longer half-life compared to midazolam. Option B) Oxazepam is a long-acting benzodiazepine used for alcohol withdrawal and anxiety disorders, thus having a longer half-life than midazolam. Option C) Clonazepam is an intermediate-acting benzodiazepine prescribed for seizure disorders and panic attacks, also with a longer half-life than midazolam. Understanding the differences in half-lives among benzodiazepines is essential for healthcare professionals to make informed decisions regarding drug selection based on the desired clinical effects and duration of action. This knowledge helps in optimizing patient care, minimizing side effects, and preventing drug interactions.

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