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Angiotensin converting enzyme function

Angiotensin converting enzyme function

Angiotensin converting enzyme function

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ACE - The Lung's Workhorse

  • Primary Function: Converts Angiotensin I → Angiotensin II.
  • Location: Primarily on the surface of pulmonary (lung) and renal endothelial cells.
  • Secondary Function: Inactivates bradykinin (a vasodilator).
    • This breakdown is key to understanding ACE inhibitor side effects (e.g., dry cough, angioedema) which result from ↑ bradykinin.

⭐ ACE's dual action is a high-yield concept: it simultaneously generates a potent vasoconstrictor (Angiotensin II) while degrading a vasodilator (bradykinin), robustly increasing blood pressure.

ACE action on angiotensin and bradykinin in RAAS

ACE's Two-Step - Make & Break

  • Dual Function: ACE is a peptidase primarily located on the surface of pulmonary and renal endothelial cells. It plays two major roles in blood pressure regulation.

  • Make (Activation): Converts inactive Angiotensin I to the highly active Angiotensin II.

    • Angiotensin II effects: vasoconstriction, aldosterone release (Na⁺/H₂O retention), ADH release.
  • Break (Inactivation): Degrades bradykinin, a potent vasodilator.

    • Bradykinin also mediates inflammation, pain, and the cough reflex.

High-Yield: ACE inhibitors (e.g., lisinopril) cause accumulation of bradykinin. This contributes to their therapeutic effect but also causes the classic side effects of dry cough and, rarely, angioedema.

RAAS and Bradykinin Pathway with Clinical Manifestations

Inhibiting ACE - The '-prils' Story

  • Dual Function of ACE:

    • Converts Angiotensin I → Angiotensin II (potent vasoconstrictor).
    • Breaks down Bradykinin (a vasodilator).
  • Mechanism of ACE Inhibitors (-pril drugs: Lisinopril, Captopril):

    • Block the conversion of Angiotensin I to Angiotensin II.
    • Result: ↓ Angiotensin II → Vasodilation (↓ TPR) & ↓ Aldosterone secretion.
    • Prevents Bradykinin breakdown → ↑ Bradykinin levels.
  • Key Side Effects & Causes:

    • Dry, non-productive cough: Due to ↑ Bradykinin in the lungs.
    • Angioedema: Swelling of face/airways; also from ↑ Bradykinin.
    • Hyperkalemia: Due to ↓ Aldosterone → ↓ K+ excretion.
    • Hypotension: Especially first-dose effect.

Contraindications: ACE inhibitors are teratogenic and absolutely contraindicated in pregnancy. Also contraindicated in patients with bilateral renal artery stenosis.

📌 Mnemonic (CAPTOPRIL):

  • Cough
  • Angioedema/ Agranulocytosis
  • Proteinuria/ Potassium excess
  • Taste changes
  • Orthostatic hypotension
  • Pregnancy (contraindicated)
  • Renal artery stenosis (contraindicated) / Rash
  • Increased renin
  • Lower GFR

RAAS pathway with ACE inhibitor action and bradykinin

High‑Yield Points - ⚡ Biggest Takeaways

  • ACE converts angiotensin I to angiotensin II (a potent vasoconstrictor), primarily in the lungs.
  • It is a key drug target for controlling hypertension.
  • ACE also inactivates bradykinin, a potent vasodilator.
  • Inhibition of bradykinin breakdown by ACE inhibitors is responsible for side effects like dry cough and angioedema.
  • The enzyme is a dipeptidyl carboxypeptidase found on the surface of endothelial cells.

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