Angiotensin II (Giapreza)
Overview
A synthetic form of the endogenous octapeptide angiotensin II, the primary effector of the renin-angiotensin system. Angiotensin II acts on AT1 receptors on vascular smooth muscle to produce potent vasoconstriction, and on the adrenal cortex to stimulate aldosterone release. Exogenous administration raises blood pressure in vasodilatory shock refractory to conventional vasopressors by restoring vascular tone through a mechanism complementary to catecholamine vasopressors.
Key Research Findings
FDA-approved in 2017 as a vasopressor for adults with septic or other distributory shock. ATHOS-3 trial demonstrated significant blood pressure improvement (MAP increase of 12.5 mmHg vs. placebo) in patients with catecholamine-resistant vasodilatory shock (Khanna et al., NEJM, 2017). Post-hoc analyses suggest particular benefit in patients with elevated renin and those on renal replacement therapy.
Intravenous
FDA Approved
Interested in Angiotensin II (Giapreza)?
Find a verified provider experienced with Angiotensin II (Giapreza) protocols in your area. All providers are credentialed and use compliant sourcing.
Find a Angiotensin II (Giapreza) ProviderRelated Peptides
Eptifibatide (Integrilin)
FDA ApprovedA synthetic cyclic heptapeptide modeled after the KGD (Lys-Gly-Asp) disintegrin sequence found in the venom of the southeastern pygmy rattlesnake (Sistrurus miliarius barbouri). Eptifibatide is a potent, reversible glycoprotein IIb/IIIa receptor antagonist that blocks the final common pathway of platelet aggregation by preventing fibrinogen and von Willebrand factor binding to activated platelets.
Nesiritide (Natrecor)
FDA ApprovedA recombinant form of human B-type natriuretic peptide (BNP), a 32-amino acid peptide naturally produced by ventricular cardiomyocytes in response to volume overload and wall stress. Nesiritide binds natriuretic peptide receptor A (NPR-A), activating guanylyl cyclase and increasing intracellular cGMP to produce venous, arterial, and coronary vasodilation, natriuresis, and suppression of the renin-angiotensin-aldosterone and sympathetic nervous systems.