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Nesiritide

  • Direct vasodilatorsDirect vasodilators

Recombinant human B-type natriuretic peptide (BNP) given intravenously in acute heart failure to dilate vessels. Hypotension limits it; now little used.

Updated

Also called: Recombinant human BNP

Quick facts

Group
Direct vasodilators
Target
Natriuretic peptide receptor A (NPR-A)
Used for
Acutely decompensated heart failure
Key effects
Hypotension · Headache · Nausea
Monitor
Urine output · Symptoms of congestion
ATC
C01DX19

No doses: the clinician sets them by the current guideline.

Mechanism of action

The figure shows the extracellular hormone-binding part of rat NPR-A holding a fragment of human ANP; BNP, which nesiritide copies, binds the same receptor.

Target in 3D: Natriuretic peptide receptor A (NPR-A). PDB structure 7BRK (RCSB PDB, public domain). View the structure at RCSB PDB

Nesiritide has the same amino-acid sequence as human BNP, which the ventricles release when they are stretched. It binds natriuretic peptide receptor A on vascular smooth muscle and other cells; activating this receptor raises cGMP inside the cell. Veins and arteries relax, filling pressure (pulmonary capillary wedge pressure) and blood pressure fall, and there is some natriuresis and inhibition of renin-angiotensin-aldosterone and sympathetic activity. It is cleared by cell uptake, breakdown by neutral endopeptidase and the kidneys.

  1. Binds natriuretic peptide receptor A
  2. Receptor activation raises cGMP
  3. Veins and arteries dilate; filling pressure falls
  4. Some natriuresis; RAAS and sympathetic tone fall

Indications

  • Acutely decompensated heart failure with breathlessness at rest or minimal activity Heart failure →

Adverse effects

Common

  • Hypotension (the most common, dose-related)
  • Headache
  • Nausea
  • Rise in blood urea in people with poor kidney function

Contraindications

  • Cardiogenic shock (as primary therapy)
  • Low systolic blood pressure
  • Hypersensitivity to any component

Key interactions

Oral ACE inhibitors
More hypotension.
Heparin, insulin, furosemide, hydralazine (same line)
Physically incompatible: not infused through the same catheter.

What is monitored

  • Blood pressure closely during the infusion
  • Urine output, creatinine and urea
  • Symptoms of congestion and breathlessness

Administration and safety

  • Intravenous infusion in hospital with blood-pressure monitoring.
  • Infused through its own line: incompatible with heparin, insulin, furosemide and hydralazine in the same catheter.
  • If hypotension occurs, the infusion is stopped and restarted only when pressure recovers.

Pregnancy and breastfeeding

Experience in pregnancy is minimal; it is used only if clearly needed.

Nursing care

  • Before: measure blood pressure and check kidney function.
  • During: check blood pressure frequently; lay the patient flat if hypotensive and inform the team.
  • Record urine output and daily weight.
  • Watch for breathlessness, headache and arrhythmias.

Pharmacokinetics

Absorption
Intravenous only.
Elimination
Taken up and broken down by cells, cleaved by neutral endopeptidase, and filtered by the kidneys.
Half-life
Short (about 18 minutes in its terminal phase); the effect on pressure lasts longer.

Test yourself

Think of the answer, then tap the question to see it.

Which natural hormone is nesiritide a copy of?

B-type natriuretic peptide (BNP).

Which second messenger rises when its receptor is activated?

cGMP.

What is the main dose-limiting adverse effect of nesiritide?

Hypotension.

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More Pharmacology questions →

Connections

← Back to the class: Direct vasodilators

Educational content on how drugs work; not a prescribing guide and no substitute for a health professional's advice. No doses are given.

Sources: Nesiritide — A New Agent For Acute Decompensated Heart Failure (Medical Journal Armed Forces India, via PubMed Central, 2005); Atrial Natriuretic Peptide Receptor complexed with deletion mutant of human Atrial Natriuretic Peptide[5-27] (RCSB Protein Data Bank, 2021); ATCDDD - ATC/DDD Index (WHO Collaborating Centre for Drug Statistics Methodology, 2026).

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Representative model, for educational purposes only.