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Nsg 552 Psychopharmacology (Exams 1–3) At Wilkes University Exam Newest Updated Exam 2026 – 2027 Solved Questions & Answers Verified 100% Graded A+ (Latest Version)

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Nsg 552 Psychopharmacology (Exams 1–3) At Wilkes University Exam Newest Updated Exam 2026 – 2027 Solved Questions & Answers Verified 100% Graded A+ (Latest Version)

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NSG 552 PSYCHOPHARMACOLOGY (EXAMS 1–3) AT WILKES UNIVERSITY

EXAM NEWEST UPDATED EXAM 2026 – 2027 SOLVED QUESTIONS &

ANSWERS VERIFIED 100% GRADED A+ (LATEST VERSION)




1. Which dopamine pathway is hyperactive in schizophrenia and is most directly

associated with positive symptoms such as hallucinations and delusions?

A. Mesocortical pathway

B. Nigrostriatal pathway

C. Mesolimbic pathway

D. Tuberoinfundibular pathway

Answer: C

Rationale: The mesolimbic pathway (ventral tegmental area to nucleus accumbens) is

hyperactive in schizophrenia and produces positive symptoms. The mesocortical

pathway is hypoactive and associated with negative/cognitive symptoms.


2. Which serotonin receptor subtype is the primary target for atypical antipsychotic

efficacy and is also responsible for the hallucinogenic effects of psychedelics

when agonized?

A. 5-HT1A

B. 5-HT2A

, Page 2 of 120


C. 5-HT2C

D. 5-HT3

Answer: B

Rationale: 5-HT2A antagonism is crucial for atypical antipsychotic efficacy, reducing

positive symptoms and improving negative symptoms. When agonized, 5-HT2A

produces hallucinogenic effects.


3. Decreased activity of the locus coeruleus and reduced norepinephrine

transmission would most likely produce which symptom cluster?

A. Psychomotor agitation and anxiety

B. Anhedonia and decreased motivation

C. Impaired attention, psychomotor retardation, and decreased arousal

D. Hypervigilance and panic attacks

Answer: C

Rationale: The locus coeruleus is the primary source of CNS norepinephrine, regulating

arousal, attention, and vigilance. Decreased activity produces hypoarousal, impaired

concentration, and psychomotor slowing.


4. Which GABA-A receptor alpha subunit is primarily responsible for the sedative-

hypnotic and amnestic effects of benzodiazepines?

A. α2 subunit

B. α3 subunit

C. α1 subunit

D. α5 subunit

Answer: C

, Page 3 of 120


Rationale: GABA-A receptors containing the α1 subunit mediate the sedative-hypnotic

and amnestic effects of benzodiazepines. The α2 and α3 subunits are more associated

with anxiolysis and muscle relaxation.


5. During synaptic transmission, which sequence correctly describes the process

at a chemical synapse?

A. Action potential → neurotransmitter release → receptor binding → postsynaptic

potential

B. Neurotransmitter release → action potential → receptor binding → reuptake

C. Receptor binding → action potential → neurotransmitter release → degradation

D. Action potential → receptor binding → neurotransmitter release → reuptake

Answer: A

Rationale: An action potential arrives at the presynaptic terminal, neurotransmitters

are released into the synaptic cleft, they bind to postsynaptic receptors, and this

generates a postsynaptic potential.


6. Which neurotransmitter is the primary excitatory neurotransmitter in the central

nervous system?

A. GABA

B. Glutamate

C. Dopamine

D. Serotonin

Answer: B

Rationale: Glutamate is the primary excitatory neurotransmitter in the CNS. GABA is

the primary inhibitory neurotransmitter; dopamine and serotonin are modulatory.

, Page 4 of 120


7. Which neurotransmitter is primarily implicated in the rewarding effects of drugs

of abuse and is a major target for addiction pharmacotherapy?

A. Serotonin

B. Norepinephrine

C. Dopamine

D. Acetylcholine

Answer: C

Rationale: The mesolimbic dopamine pathway is the primary neural substrate for

reward, and most addictive substances increase dopamine in the nucleus accumbens.


8. Which enzyme system is primarily responsible for the metabolism of most

psychotropic medications?

A. Monoamine oxidase (MAO)

B. Cytochrome P450 (CYP450)

C. Acetylcholinesterase

D. Catechol-O-methyltransferase (COMT)

Answer: B

Rationale: The CYP450 system, particularly in the liver, is responsible for the oxidative

metabolism of most psychotropic medications, making it a major site of drug

interactions.


9. Which statement best describes the effect of a CYP450 enzyme inhibitor on

serum drug levels?

A. It decreases serum levels of drugs that are substrates of that enzyme.

B. It increases serum levels of drugs that are substrates of that enzyme.

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