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For research use only — not for human consumption
Desmopressin original Regena research vial

Hormone · Synthetic peptide analog

Desmopressin

Also known as DDAVP

A selective V2 receptor agonist and synthetic vasopressin analog used to investigate renal water transport and aquaporin-2 trafficking in vitro.

Length
9 amino acids
Half-life
1.5 to 2.5 hours in plasma
Mechanism
Desmopressin is a synthetic analog of vasopressin that acts as a selective agonist for the vasopressin V2 receptor, with minimal activity at the V1 receptor.
Studied in
It is utilized in laboratory models to study renal water reabsorption, V2 receptor signaling, and cellular pathways involving adenylyl cyclase and aquaporin-2.

About Desmopressin

Desmopressin is a synthetic structural analog of the natural pituitary hormone arginine vasopressin. Its structure has two key modifications: deamination of cysteine at position 1 and substitution of L-arginine with D-arginine at position 8. These changes increase its half-life and enhance its selectivity for the V2 receptor over the V1 receptor.

Activation of the Gs-protein coupled V2 receptor, primarily in renal collecting duct cells, stimulates the adenylyl cyclase pathway, leading to increased intracellular cAMP. This cascade promotes the translocation of aquaporin-2 (AQP2) water channels to the apical membrane, increasing water reabsorption. As a reference compound with a clinical history, desmopressin is a standard tool for studying these cellular mechanisms in renal physiology research.

Laboratory notes

  • For cell-based assays, desmopressin is typically dissolved in sterile water or buffered saline.
  • Phosphodiesterase inhibitors like IBMX are often co-administered in vitro to potentiate the cAMP-mediated response.
  • The trafficking of AQP2 to the cell membrane can be visualized using immunofluorescence microscopy in cultured collecting duct cells.

Storage and reconstitution basics: storage guide.

Questions about Desmopressin

What makes Desmopressin selective for the V2 receptor?

The deamination at position 1 and the D-arginine at position 8 reduce its affinity for the V1 (vasopressor) receptor while maintaining high affinity for the V2 (antidiuretic) receptor.

What is the downstream effect of V2 receptor activation by Desmopressin?

It initiates a signaling cascade that results in the insertion of aquaporin-2 water channels into the apical membrane of renal collecting duct cells.

What is a common use for Desmopressin in a research lab?

It is used as a specific agonist to stimulate V2 receptors in cultured renal cells to study cAMP signaling and water channel regulation.

Is Desmopressin for human use?

No. It is supplied strictly for in-vitro laboratory research and is not for human or animal consumption.

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All products are sold for laboratory research use only. Not for human consumption, not a medicine, not for diagnosing, treating or preventing any condition.