Neurotransmitters – Dopamine MCQs With Answer
Understanding neurotransmitters—especially dopamine—is essential for B. Pharm students preparing for pharmacology and therapeutics. This concise, exam-focused set covers dopamine biosynthesis, storage, release, receptors (D1–D5), signal transduction, reuptake and metabolism by MAO and COMT, and clinical implications in Parkinson’s disease, schizophrenia, addiction, and endocrine disorders. You will also review dopaminergic pharmacotherapy, including levodopa, dopamine agonists, antipsychotics, MAO-B inhibitors, DAT modulators, and adverse effects. The MCQs emphasize mechanistic detail, receptor pharmacology, drug interactions, and diagnostic approaches relevant to pharmacy practice. Answers reinforce learning and application to patient care. Now let’s test your knowledge with 30 MCQs on this topic.
Q1. Which enzyme catalyzes the rate-limiting step in dopamine biosynthesis?
- Tyrosine hydroxylase
- L-DOPA decarboxylase
- Monoamine oxidase
- Catechol-O-methyltransferase
Correct Answer: Tyrosine hydroxylase
Q2. The immediate precursor of dopamine in the biosynthetic pathway is:
- Tyrosine
- L-DOPA
- Norepinephrine
- Homovanillic acid
Correct Answer: L-DOPA
Q3. Which cofactor is essential for tyrosine hydroxylase activity?
- Tetrahydrobiopterin (BH4)
- Vitamin B12
- Biotin
- Folate
Correct Answer: Tetrahydrobiopterin (BH4)
Q4. Dopamine is metabolized primarily by which two enzymes?
- MAO and COMT
- Acetylcholinesterase and MAO
- Monoamine oxidase and acetaldehyde dehydrogenase
- COMT and alcohol dehydrogenase
Correct Answer: MAO and COMT
Q5. Which dopamine receptor family is primarily coupled to Gs proteins and increases intracellular cAMP?
- D1-like receptors (D1, D5)
- D2-like receptors (D2, D3, D4)
- NMDA receptors
- Muscarinic receptors
Correct Answer: D1-like receptors (D1, D5)
Q6. The dopamine transporter (DAT) is responsible for:
- Reuptake of dopamine from the synaptic cleft into presynaptic terminals
- Vesicular uptake of dopamine into synaptic vesicles
- Degradation of dopamine in the synapse
- Conversion of dopamine to norepinephrine
Correct Answer: Reuptake of dopamine from the synaptic cleft into presynaptic terminals
Q7. Which drug increases synaptic dopamine by inhibiting vesicular monoamine transporter 2 (VMAT2) causing depletion of vesicular stores?
- Reserpine
- Levodopa
- Bromocriptine
- Selegiline
Correct Answer: Reserpine
Q8. Levodopa is combined with carbidopa in Parkinson’s therapy because carbidopa:
- Inhibits peripheral aromatic L-amino acid decarboxylase, reducing peripheral conversion to dopamine
- Crosses the blood-brain barrier to enhance central dopamine synthesis
- Acts as a dopamine receptor agonist in the striatum
- Inhibits MAO-B centrally
Correct Answer: Inhibits peripheral aromatic L-amino acid decarboxylase, reducing peripheral conversion to dopamine
Q9. Which dopaminergic pathway is most implicated in the positive symptoms of schizophrenia?
- Mesolimbic pathway
- Nigrostriatal pathway
- Tuberoinfundibular pathway
- Mesocortical pathway
Correct Answer: Mesolimbic pathway
Q10. Blockade of D2 receptors in the tuberoinfundibular pathway commonly causes:
- Hyperprolactinemia
- Parkinsonism
- Psychosis exacerbation
- Increased appetite
Correct Answer: Hyperprolactinemia
Q11. Which imaging ligand is commonly used in PET to assess presynaptic dopamine transporter function?
- 11C-raclopride
- 18F-fluorodeoxyglucose
- 123I-FP-CIT (DaTscan)
- 99mTc-HMPAO
Correct Answer: 123I-FP-CIT (DaTscan)
Q12. Selegiline acts in Parkinson’s disease primarily as a:
- Selective MAO-B inhibitor that reduces dopamine breakdown
- COMT inhibitor preventing peripheral L-DOPA metabolism
- Dopamine D2 receptor agonist
- VMAT2 inhibitor
Correct Answer: Selective MAO-B inhibitor that reduces dopamine breakdown
Q13. Which adverse effect is most characteristic of chronic high-dose levodopa therapy?
- Motor fluctuations and dyskinesias
- Hyperprolactinemia
- QT prolongation
- Anticholinergic toxicity
Correct Answer: Motor fluctuations and dyskinesias
Q14. A dopamine agonist commonly used in Parkinson’s disease is:
- Bromocriptine
- Haloperidol
- Reserpine
- Amantadine
Correct Answer: Bromocriptine
Q15. Which statement about D2 receptor signaling is correct?
- D2 receptors are Gi/o-coupled and inhibit adenylate cyclase
- D2 receptors activate adenylate cyclase via Gs
- D2 receptors are ionotropic and allow Na+ influx
- D2 receptors directly phosphorylate tyrosine residues
Correct Answer: D2 receptors are Gi/o-coupled and inhibit adenylate cyclase
Q16. Which metabolite is the main urinary end product of dopamine metabolism?
- Homovanillic acid (HVA)
- Vanillylmandelic acid (VMA)
- 5-Hydroxyindoleacetic acid (5-HIAA)
- Normetanephrine
Correct Answer: Homovanillic acid (HVA)
Q17. Amphetamine increases extracellular dopamine primarily by:
- Reversing DAT and causing dopamine release into the synapse
- Inhibiting MAO-B to reduce dopamine breakdown
- Blocking D2 autoreceptors permanently
- Increasing BH4 synthesis
Correct Answer: Reversing DAT and causing dopamine release into the synapse
Q18. Which antipsychotic has the highest propensity to cause extrapyramidal symptoms due to strong D2 blockade?
- Haloperidol
- Clozapine
- Quetiapine
- Aripiprazole
Correct Answer: Haloperidol
Q19. The nigrostriatal pathway primarily modulates:
- Motor control and coordination
- Endocrine secretion from pituitary
- Cognitive executive functions
- Reward and reinforcement
Correct Answer: Motor control and coordination
Q20. Which drug class is used to inhibit peripheral COMT to prolong levodopa half-life?
- Entacapone and tolcapone (COMT inhibitors)
- MAO inhibitors
- Dopamine agonists
- Muscarinic antagonists
Correct Answer: Entacapone and tolcapone (COMT inhibitors)
Q21. Dopamine’s role in the hypothalamus includes:
- Inhibition of prolactin release via tuberoinfundibular pathway
- Stimulation of growth hormone release directly
- Activation of aldosterone secretion
- Enhancement of insulin secretion from pancreas
Correct Answer: Inhibition of prolactin release via tuberoinfundibular pathway
Q22. Which feature helps distinguish central from peripheral causes of dopamine deficiency on imaging?
- Reduced striatal DAT binding on SPECT or PET indicates presynaptic degeneration (central)
- Elevated urinary HVA indicates peripheral deficiency
- Normal DAT binding with low CSF dopamine indicates central cause
- Increased cardiac sympathetic innervation rules out central causes
Correct Answer: Reduced striatal DAT binding on SPECT or PET indicates presynaptic degeneration (central)
Q23. A partial agonist at D2 receptors used as an antipsychotic is:
- Aripiprazole
- Risperidone
- Haloperidol
- Chlorpromazine
Correct Answer: Aripiprazole
Q24. In Parkinson’s disease, neuronal loss is most pronounced in which structure?
- Substantia nigra pars compacta
- Ventral tegmental area
- Nucleus accumbens
- Locus coeruleus
Correct Answer: Substantia nigra pars compacta
Q25. Which adverse effect is commonly associated with dopamine agonists like bromocriptine and pramipexole?
- Impulse control disorders (e.g., gambling, hypersexuality)
- Severe anticholinergic delirium
- Marked weight loss in all patients
- Profound bradycardia as first-line effect
Correct Answer: Impulse control disorders (e.g., gambling, hypersexuality)
Q26. Which drug reduces dopamine catabolism by inhibiting MAO-B selectively at therapeutic doses?
- Selegiline
- Imipramine
- Propranolol
- Fluoxetine
Correct Answer: Selegiline
Q27. Dopamine D1 receptor activation in the renal system primarily causes:
- Renal vasodilation and natriuresis
- Sodium retention and hypertension
- Glomerular filtration rate decrease
- Antidiuretic hormone release
Correct Answer: Renal vasodilation and natriuresis
Q28. Which test sample is most useful to measure central dopamine turnover clinically or in research?
- Cerebrospinal fluid levels of homovanillic acid (HVA)
- Serum dopamine concentration
- Urinary VMA concentration
- Salivary dopamine levels
Correct Answer: Cerebrospinal fluid levels of homovanillic acid (HVA)
Q29. Which pharmacologic strategy is appropriate for a Parkinson’s patient experiencing wearing-off between levodopa doses?
- Add a COMT inhibitor or increase dosing frequency
- Stop levodopa and start haloperidol
- Introduce an antimuscarinic agent only
- Switch to a selective serotonin reuptake inhibitor
Correct Answer: Add a COMT inhibitor or increase dosing frequency
Q30. Which statement about dopamine and reward pathways is correct?
- Mesolimbic dopamine release reinforces motivated behaviors and drug reward
- Dopamine inhibits all reward processing in the nucleus accumbens
- Mesocortical dopamine exclusively controls motor function
- Tuberoinfundibular pathway mediates reward and reinforcement
Correct Answer: Mesolimbic dopamine release reinforces motivated behaviors and drug reward

I am a Registered Pharmacist under the Pharmacy Act, 1948, and the founder of PharmacyFreak.com. I hold a Bachelor of Pharmacy degree from Rungta College of Pharmaceutical Science and Research. With a strong academic foundation and practical knowledge, I am committed to providing accurate, easy-to-understand content to support pharmacy students and professionals. My aim is to make complex pharmaceutical concepts accessible and useful for real-world application.
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