Drug intelligence / Profile preview

dobutamine + terlipressin

Development stage
Preclinical
Modality
Peptides, Small Molecules
Administration
Intravenous
01

Overview

Dobutamine + terlipressin is a combination of two intravenous drugs used in critical care settings, particularly for patients with septic shock or advanced liver disease complicated by hepatorenal syndrome. Dobutamine is a synthetic catecholamine and acts as a beta-1 adrenergic agonist, increasing cardiac contractility and output. Terlipressin is a synthetic vasopressin analogue that acts primarily as a vasoconstrictor via V1 receptors, leading to increased vascular tone and improved renal perfusion. The combination has been studied to counteract the reduction in cardiac output caused by terlipressin alone; dobutamine reverses the cardio-suppressive effects of terlipressin while maintaining hemodynamic stability and reducing norepinephrine requirements[1][2][3][9]. This regimen may be considered in select cases where both improved systemic perfusion (via dobutamine) and splanchnic/renal vasoconstriction (via terlipressin) are desired.

02

Targets

AVPR1A (Arginine vasopressin receptor 1A)AVPR1B (Vasopressin V1b Receptor)AVPR2 (Arginine vasopressin V2 receptor)ADRA1A (α1A)ADRB2 (β2)ADRB1 (β1)

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