Drug intelligence / Profile preview

vasopressin + methylprednisolone

Development stage
Unknown
Lead developer
Skejby Sygehus
Modality
Orthosteric Ligands → Classical Binding Small Molecules → Small Molecules, Peptides
Administration
Intravenous
01

Overview

**Vasopressin + methylprednisolone** is a combination of two drugs administered together during cardiopulmonary resuscitation for **in-hospital cardiac arrest**. Vasopressin is a nonapeptide hormone acting as a vasoconstrictor via agonism at the vasopressin V1 receptor, increasing systemic vascular resistance and thus arterial blood pressure. Methylprednisolone is a synthetic glucocorticoid corticosteroid with anti-inflammatory and immunosuppressant properties, acting mainly through the glucocorticoid receptor to modulate gene transcription and reduce inflammation. Clinical trials have specifically studied this combination as adjunctive therapy to epinephrine in cardiac arrest. Evidence shows this drug combination significantly increases the probability of return of spontaneous circulation (ROSC) compared to placebo in adults with in-hospital cardiac arrest, although it does not improve long-term survival or neurologic outcomes. The mechanism is presumed to be vasoconstrictive support combined with mitigation of inflammatory injury during resuscitation[1][2][4][8].

Brand names
EmpressinSolu-Medrol
Other names
vasopressin + methylprednisolone
02

Targets

AVPR1B (Vasopressin V1b Receptor)AVPR2 (Arginine vasopressin V2 receptor)GR (Glucocorticoid receptor)

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