ATI RN
Peripheral Nervous System Drugs Questions
Question 1 of 5
If farmers exposed to 'insecticides' ('irreversible' cholinesterase inhibitors) are given medical kits that contain atropine. Which one of the following effects of the cholinesterase inhibitor will NOT be blocked by the atropine?
Correct Answer: D
Rationale: The correct answer is D) Skeletal muscle overstimulation, eventually leading to skeletal muscle paralysis. Rationale: Atropine is a muscarinic antagonist that blocks the action of acetylcholine on muscarinic receptors in the peripheral nervous system. In this case, atropine would block the effects of excessive acetylcholine due to cholinesterase inhibition by insecticides. A) Bronchoconstriction/bronchospasm is caused by excessive cholinergic stimulation and can be blocked by atropine. B) Increased bladder/urinary tract activity is mediated by cholinergic receptors and can be blocked by atropine. C) Increased bowel motility (diarrhea) is also a result of cholinergic overactivity, which can be reversed by atropine. Educational context: Understanding the pharmacological actions of atropine and cholinesterase inhibitors is crucial in managing cases of insecticide poisoning. Atropine is used as an antidote to counteract the effects of cholinesterase inhibitors by blocking the excessive stimulation of muscarinic receptors. This knowledge is essential for healthcare professionals, especially those working in emergency medicine or toxicology, to effectively treat and manage patients exposed to cholinesterase inhibitors.
Question 2 of 5
Verapamil is a drug used for treating hypertension. It should be used with caution with other drugs that can depress heart rate or contractility. Which drug, if given with verapamil, might therefore cause the greatest risk of depressing heart rate, contractile force or impulse conduction?
Correct Answer: C
Rationale: Verapamil is a calcium channel blocker that works by relaxing blood vessels and slowing the heart rate, making it effective in treating hypertension. When combined with other drugs that can also depress heart rate or contractility, there is a risk of additive effects leading to severe cardiovascular depression. The correct answer is C) Propranolol. Propranolol is a beta-blocker that slows heart rate, reduces the force of heart contractions, and blocks the impulse conduction through the AV node. When taken with verapamil, which also affects heart rate and contractility, the combined effect can lead to excessive depression of these functions, potentially causing bradycardia, reduced cardiac output, and even heart block. A) Albuterol is a beta-2 adrenergic agonist that actually increases heart rate and contractility, so it would not pose as much risk when combined with verapamil. B) Scopolamine is an anticholinergic drug that primarily affects the parasympathetic nervous system and would not have a significant impact on heart rate or contractility when combined with verapamil. D) Isoproterenol is a non-selective beta-adrenergic agonist that increases heart rate and contractility, so it would not pose as much risk for depressing these functions when used with verapamil. Understanding the potential interactions between drugs targeting the cardiovascular system is crucial in clinical practice to prevent adverse effects and ensure patient safety. Healthcare professionals need to be aware of these interactions to make informed decisions when prescribing medications to patients with cardiovascular conditions.
Question 3 of 5
Which of the following descriptions best fits the drug phenylephrine?
Correct Answer: B
Rationale: The correct answer is B) Stimulates α-adrenergic receptors, causing useful mucous membrane decongestion, or overall vasoconstriction and a rise of blood pressure. Phenylephrine is a sympathomimetic drug that primarily acts by stimulating α-adrenergic receptors, leading to vasoconstriction. This vasoconstriction effect is useful in conditions such as nasal congestion, where it can reduce swelling in mucous membranes and improve breathing. The rise in blood pressure is also a known effect of phenylephrine due to its vasoconstrictive properties. Option A is incorrect because phenylephrine does not block muscarinic receptors; instead, it primarily acts on adrenergic receptors. Option C is also incorrect as phenylephrine does not block β-adrenergic receptors. Option D is incorrect as phenylephrine is not typically used for managing hypertension due to its potential to raise blood pressure. Educationally, understanding the mechanism of action of drugs like phenylephrine is crucial for healthcare professionals to make informed decisions when prescribing medications. Knowledge of how phenylephrine works on adrenergic receptors helps in understanding its clinical uses and potential side effects, thereby improving patient care and safety.
Question 4 of 5
X is drug that contains a mixture of amphetamines. It is used for managing Attention-Deficit/Hyperactivity disorder (ADHD). The drug causes autonomic effects that can be fatal if an overdose is taken. How does X work in the body?
Correct Answer: D
Rationale: The correct answer is D) Releases neuronal noradrenaline, causing excessive sympathetic effects, e.g., severe rises of blood pressure. This drug, containing a mixture of amphetamines, works by increasing the release of neurotransmitters such as noradrenaline from nerve terminals. This leads to heightened sympathetic nervous system activity, resulting in effects like increased heart rate, elevated blood pressure, and dilated airways. In the context of managing ADHD, these effects can help improve focus and attention. Option A is incorrect because blocking muscarinic receptors would not lead to the described effects; instead, it would cause symptoms opposite to those of atropine poisoning. Option B is incorrect as blocking B-2 receptors would not explain the autonomic effects described. Option C is incorrect as inhibiting MAO would not cause the observed sympathetic responses. Educationally, understanding how drugs like these work in the body is crucial for healthcare professionals to make informed decisions when prescribing, monitoring, and managing patients on such medications. It highlights the importance of pharmacological knowledge in assessing potential side effects and adverse reactions that may occur with drug therapy.
Question 5 of 5
The autonomic nervous system is also known as
Correct Answer: D
Rationale: The correct answer is D) All of the above. The autonomic nervous system is also known as the visceral nervous system, the vegetative nervous system, and the involuntary nervous system. The term "visceral" refers to the internal organs controlled by the autonomic nervous system, highlighting its role in regulating bodily functions such as digestion and heart rate. "Vegetative" emphasizes the automatic, unconscious nature of the system's control over essential bodily processes. "Involuntary" reflects the fact that these functions occur without conscious effort or control. Option A) Visceral alone does not encompass the full scope of the autonomic nervous system's functions and control over both visceral and involuntary processes. Option B) Vegetative is a more limited term that does not capture the entirety of the autonomic system's functions. Option C) Involuntary nervous system is accurate but incomplete, as it does not highlight the autonomic system's specific role in regulating visceral functions. Understanding these terms is crucial in grasping the complexity and importance of the autonomic nervous system in maintaining homeostasis and responding to internal and external stimuli. By choosing option D), students demonstrate a comprehensive understanding of the various names used to describe this essential regulatory system in the body.