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Heart & circulationNatriuretic peptide

Nesiritide

Also known as: Natrecor, Recombinant human BNP

By the Peptide Dossier Editorial TeamUpdated How we source

Nesiritide is recombinant human BNP, historically used as an IV treatment for acute decompensated heart failure. Early hemodynamic improvement did not translate into better 30-day outcomes in the larger ASCEND-HF trial.

Quick Facts

Class:Natriuretic peptide
Product status:Natrecor has a historical acute-heart-failure approval; contemporary availability and use are limited.
Research context:FDA approved

A recombinant heart-derived hormone

Nesiritide, marketed as Natrecor, reproduces the 32-amino-acid human B-type natriuretic peptide released when ventricular pressure or volume stretches the heart. It was designed to enhance the natural vessel-relaxing and fluid-excreting signal in acute heart failure. FDA approval dates to 2001; the product has since been largely withdrawn for commercial reasons.

Natriuretic signaling

Binding natriuretic peptide receptor-A raises cyclic GMP in vascular walls and relaxes arteries and veins. This reduces cardiac afterload and filling pressure, reflected in pulmonary capillary wedge pressure. It also promotes renal sodium and water excretion and suppresses the renin–angiotensin–aldosterone system.

Hemodynamics versus clinical outcomes

Nesiritide’s differing trial outcomes
TrialResult
VMACGreater reduction in filling pressure than nitroglycerin or placebo and improved breathing at three hours
ASCEND-HFSmall nonsignificant dyspnea effect; no reduction in 30-day death or rehospitalization; more hypotension

Supporting references: no benefit.

Sources: [1]

Historical approval and current role

The 2001 FDA indication was acute decompensated heart failure with dyspnea at rest or minimal activity, treated intravenously in a monitored hospital setting. Neutral ASCEND-HF outcomes, evolving practice and broad market withdrawal have made contemporary use uncommon. Historical approval should not be interpreted as routine current availability.

Hypotension is the central risk

Blood-pressure lowering can be symptomatic, substantial or prolonged. Headache, nausea and slowed heart rate are other reported effects. Earlier concerns that the drug worsened renal function were not confirmed in ASCEND-HF. Improved short-term pressure measurements do not establish improved survival or rehospitalization outcomes.

References and further reading

This reference draws on Superpower’s Peptide Library and the research linked below. Peptide Dossier’s editorial team adapted and integrated the material on .

  1. 10.1056/NEJMoa1100171Hemodynamics versus clinical outcomesCited in: Hemodynamics versus clinical outcomes

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Disclaimer: This article is for informational and educational purposes only. It is not intended as medical advice. The information presented is based on published research and should not be used as a substitute for professional medical guidance. Always consult a qualified healthcare provider before starting any peptide protocol. Some peptides discussed may not be approved for human use by the FDA or equivalent regulatory bodies.