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USMLE STEP 1 Pharmacology EXAM –150 ACCURATE QUESTIONS WITH CORRECT ANSWER 2026/2027 LATEST EXAM UPDATE GUARANTEE HIGH PASS MARK

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Prepare for the USMLE Step 1 Pharmacology Exam (2026–2027) with this comprehensive and up-to-date study resource designed to support medical students in mastering high-yield pharmacology concepts and exam readiness. This guide includes structured practice questions with detailed explanations covering essential pharmacology topics commonly assessed on the USMLE Step 1 examination. Areas of focus include autonomic pharmacology, cardiovascular drugs, antimicrobials, endocrine pharmacology, central nervous system agents, chemotherapy, toxicology, pharmacokinetics, pharmacodynamics, adverse drug reactions, and mechanisms of drug action. The content emphasizes clinical reasoning, integration of basic science with clinical application, and high-yield concept retention to help learners strengthen understanding, improve confidence, and prepare effectively for board-style exam scenarios. Ideal for structured review, self-assessment, and comprehensive USMLE Step 1 pharmacology preparation.

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19 May 2026


USMLE STEP 1 Pharmacology EXAM –150
ACCURATE QUESTIONS WITH CORRECT ANSWER
2026/2027 LATEST EXAM UPDATE GUARANTEE
HIGH PASS MARK
1. Which receptor causes vasoconstriction, pupil dilation, and contraction of urinary/GI
sphincters?

A. β1
B. β2
C. α1
D. M3

Answer: C. α1

Rationale:
α1 receptors (Gq) cause smooth muscle contraction, especially:

 Vasoconstriction

 Mydriasis (radial muscle contraction)

 Increased bladder and GI sphincter tone



2. Which receptor decreases sympathetic outflow and reduces insulin release?

A. α2
B. β1
C. H1
D. M2

Answer: A. α2

Rationale:
α2 receptors are Gi-coupled inhibitory receptors that:

 ↓ NE release (presynaptic inhibition)

 ↓ insulin secretion

 ↓ lipolysis



3. Which receptor increases heart rate and renin release?

A. β1
B. β2
C. D1
D. M3

Answer: A. β1

,19 May 2026


Rationale:
β1 (Gs) stimulation leads to:

 ↑ HR and contractility

 ↑ renin release from JG cells

 ↑ cardiac output



4. Which receptor causes bronchodilation and uterine relaxation?

A. α1
B. β2
C. M2
D. H2

Answer: B. β2

Rationale:
β2 activation causes smooth muscle relaxation:

 Bronchodilation

 Uterine relaxation (tocolysis)

 Vasodilation in skeletal muscle



5. Which muscarinic receptor is responsible for decreased heart rate?

A. M1
B. M2
C. M3
D. M4

Answer: B. M2

Rationale:
M2 receptors (Gi) act on the heart to:

 ↓ SA node firing → ↓ HR

 ↓ atrial contractility



6. Which receptor increases gastric acid secretion?

A. H1
B. H2
C. M3
D. D2

Answer: B. H2

,19 May 2026


Rationale:
H2 receptors on parietal cells increase:

 cAMP → ↑ gastric acid secretion



7. Which receptor causes miosis, increased secretions, and GI motility?

A. M3
B. M2
C. β2
D. α1

Answer: A. M3

Rationale:
M3 receptors (Gq) mediate parasympathetic effects:

 ↑ secretions (saliva, tears)

 ↑ GI motility

 Bronchoconstriction

 Miosis + accommodation



8. Which receptor is coupled to Gi protein?

A. β2
B. H2
C. α2
D. D1

Answer: C. α2

Rationale:
Gi receptors inhibit adenylate cyclase:

 α2, M2, D2 → ↓ cAMP



9. Which drug is used for Alzheimer disease and works by increasing acetylcholine via AChE
inhibition?

A. Atropine
B. Donepezil
C. Salmeterol
D. Phenylephrine

Answer: B. Donepezil

, 19 May 2026


Rationale:
Donepezil is a reversible acetylcholinesterase inhibitor, increasing ACh in CNS → improves cognitive
function in Alzheimer disease.



10. Which drug is used in acute asthma due to β2 agonism?

A. Albuterol
B. Propranolol
C. Atropine
D. Neostigmine

Answer: A. Albuterol

Rationale:
Albuterol is a short-acting β2 agonist (SABA):

 Bronchodilation

 First-line for acute asthma attacks



11. Which drug is used to reverse neuromuscular blockade and treat myasthenia gravis?

A. Neostigmine
B. Epinephrine
C. Atropine
D. Dopamine

Answer: A. Neostigmine

Rationale:
Neostigmine is an AChE inhibitor:

 ↑ ACh at neuromuscular junction

 Used in MG and post-op ileus



12. Which toxin blocks voltage-gated sodium channels and prevents depolarization?

A. Ciguatoxin
B. Tetrodotoxin
C. Scombroid toxin
D. Histamine

Answer: B. Tetrodotoxin

Rationale:
Tetrodotoxin (pufferfish toxin):

 Blocks Na⁺ channels

 Prevents action potential initiation

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