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Cardiovascular Drug MOAs – 30+ Verified Mechanisms for Diuretics, Anticoagulants, Statins – Pharm 2025 –

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This pharmacology quick-reference guide outlines 30+ expert-verified mechanisms of action (MOAs) for high-yield cardiovascular medications, perfectly structured for Pharm 2025 exam preparation. Presented in a clear, flashcard-style Q&A format, it condenses key drug actions across diuretics, antihypertensives, anticoagulants, and lipid-lowering agents. Core drug categories include: Diuretics: CA inhibitors: inhibit HCO₃⁻ reabsorption in the proximal tubule Osmotic agents: increase tubular fluid osmolality in the PCT Loop diuretics: inhibit Na⁺/K⁺/2Cl⁻ transport in the ascending limb Thiazides: block Na⁺/Cl⁻ reabsorption in the distal tubule K⁺-sparing diuretics: block aldosterone or ENaC in the collecting duct Antihypertensives: Beta blockers: inhibit B1 receptors at the SA node → ↓HR, ↓contractility ACE inhibitors: block angiotensin I to II conversion; cause dry cough ARBs: block ANGII receptors; no cough Renin inhibitors, alpha blockers, central alpha-2 agonists, vasodilators, sodium nitroprusside, and reserpine – all with their distinct vasculature or CNS effects Anticoagulants & Antiplatelets: Vitamin K antagonists: inhibit factors II, VII, IX, X Direct & indirect Xa inhibitors, UFH/LMWH, and direct thrombin inhibitors COX inhibitors (aspirin), ADP inhibitors (clopidogrel), GP IIb/IIIa inhibitors Thrombolytics: convert plasminogen to plasmin for fibrinolysis Lipid-lowering agents: Statins: inhibit HMG-CoA reductase Bile acid resins, cholesterol absorption inhibitors (NPC1L1) Niacin: inhibits lipolysis via Gi-coupled GPCR Fibrates: activate PPAR-α Omega-3 fatty acids: reduce hepatic triglyceride synthesis Perfect for: Medical, pharmacy, and nursing students in cardiovascular pharmacology modules USMLE Step 1, NAPLEX, NCLEX, or end-of-semester pharmacology exams Flashcard-based memorization and board review Keywords: pharmacology MOAs, cardiovascular drugs, diuretic mechanisms, beta blockers, ACE inhibitors, ARBs, renin inhibitors, anticoagulants, thrombolytics, aspirin, statins, bile acid resins, fibrates, omega-3, niacin, GPCR, PPAR, Pharm 2025, HMG-CoA reductase

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Uploaded on
December 22, 2025
Number of pages
5
Written in
2025/2026
Type
Exam (elaborations)
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Questions & answers

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Pharmacology - Cardiovascular MOAs
2025 Expert Verified | Ace the Test



Carbonic anhydrase inhibitors MOA - 🧠 ANSWER ✔✔Inhibits HCO3

reabsorption in *PCT*.


Osmotic diuretics MOA - 🧠 ANSWER ✔✔Increases tubular fluid osmolality;

changes the osmotic gradient in *PCT*.


Loop diuretics MOA - 🧠 ANSWER ✔✔Inhibit Na/K/2Cl co-transporter in

*ALH*.


Thiazides MOA - 🧠 ANSWER ✔✔Inhibit Na/Cl co-transporter in *ALH* and

early *DCT*.

, Potassium sparing diuretics MOA - 🧠 ANSWER ✔✔Block aldosterone or

reduce Na+ absorption, so K+ is conserved in *DCT*.


ADH Antagonists MOA - 🧠 ANSWER ✔✔Prevent ADH induced water

reabsorption in the *CT*.


Aldosterone antagonists MOA - 🧠 ANSWER ✔✔Prevent Na+ reabsorption

in *CT*.


Beta blockers MOA - 🧠 ANSWER ✔✔Block Ca+ channels by inhibiting B1

receptors in SA node. ↓HR, ↓contractility, ↓AV conduction.


ACE Inhibitors MOA - 🧠 ANSWER ✔✔Inhibits conversion of ANGI to ANGII.

Dry cough


ARBs MOA - 🧠 ANSWER ✔✔Blocks ANGII receptors. No dry cough


CCB MOA - 🧠 ANSWER ✔✔Block Ca+ entry in smooth muscle. ↑smooth

muscle relaxation. ↓myocardial force, and ↓HR.


Renin inhibitors MOA - 🧠 ANSWER ✔✔Bind to renin, inhibiting it from

converting angiotensinogen to ANGI.


Peripheral A1 blockers MOA - 🧠 ANSWER ✔✔Block binding of NE to

smooth muscle.

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