Which one of the following CNS receptors is directly coupled to an ion channel so that the effects of its activation do not involve second messenger systems?

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ATI Intro to Pharmacology Quizlet Questions

Question 1 of 4

Which one of the following CNS receptors is directly coupled to an ion channel so that the effects of its activation do not involve second messenger systems?

Correct Answer: A

Rationale: Nicotinic acetylcholine (N ACh) receptors are ligand-gated ion channels, directly opening to allow sodium and potassium flux upon acetylcholine binding, producing rapid effects without second messengers—key in neuromuscular transmission. Alpha-adrenergic (a NE) receptors couple to G-proteins, using second messengers like IP3 or cAMP. D2A dopamine receptors inhibit adenylate cyclase via Gi proteins, involving cAMP. Mu opioid receptors (µ) also use Gi proteins, reducing cAMP and opening potassium channels indirectly. 5HT2 serotonin receptors activate phospholipase C, generating IP3. The nicotinic receptor's direct ion channel linkage distinguishes it, enabling fast synaptic responses without the delay of intracellular signaling cascades.

Question 2 of 4

A patient was prescribed sertraline (Zoloft) for the treatment of depression and anxiety. The patient's spouse calls the clinic and reports the patient is increasingly moody and seems 'disconnected with life.' What is the best response by the nurse?

Correct Answer: B

Rationale: Sertraline carries a suicide risk warning, especially early on. Moodiness and disconnection suggest potential ideation, requiring urgent clinic assessment for safety. Diphenhydramine masks symptoms. Holding medication risks withdrawal. Doubling the dose could worsen effects. B ensures immediate evaluation, making it the best response.

Question 3 of 4

The nurse administers atenolol (Tenormin) to a client with hypertension. Which finding would prompt the nurse to hold the dose and notify the physician?

Correct Answer: B

Rationale: Atenolol, a beta-blocker, lowers blood pressure and heart rate by blocking sympathetic stimulation. A heart rate of 52 bpm is bradycardic (below 60 bpm), a threshold for holding beta-blockers due to risk of inadequate perfusion, especially in hypertension where cardiac output matters. Holding and notifying the physician prevents harm, allowing reassessment. BP of 130/80 is controlled, not urgent. Respiratory rate of 18 and temperature of 98.6°F are normal. Atenolol's selectivity for beta-1 receptors makes bradycardia a key adverse effect, requiring vigilance. This action aligns with nursing protocols for beta-blockers, prioritizing cardiovascular stability, making B the finding warranting immediate intervention.

Question 4 of 4

The following drugs commonly cause hepatotoxicity:

Correct Answer: A

Rationale: Paracetamol overdose can cause severe hepatotoxicity due to the accumulation of toxic metabolites.

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