Angiotensin II (medication)
| Clinical data | |
|---|---|
| Trade names | Giapreza |
| Other names | Ang II |
| AHFS/Drugs.com | Monograph |
| License data | |
| Routes of administration | Intravenous injection |
| Drug class | Vasoconstrictor |
| ATC code | |
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| Pharmacokinetic data | |
| Protein binding | None |
| Metabolism | Proteolysis by glutamyl aminopeptidase, angiotensin converting enzyme 2 |
| Metabolites | Angiotensin III, angiotensin-(1-7) |
| Elimination half-life | Less than one minute (IV administration) |
| Identifiers | |
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| CAS Number | |
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| DrugBank | |
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| E number | {{#property:P628}} |
| CompTox Dashboard (EPA) |
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| ECHA InfoCard | {{#property:P2566}}Lua error in Module:EditAtWikidata at line 29: attempt to index field 'wikibase' (a nil value). |
| Chemical and physical data | |
| Formula | C50H71N13O12 |
| Molar mass | 1046.197 g·mol−1 |
| 3D model (JSmol) | |
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Angiotensin II, sold under the brand name Giapreza, is a medication that is used to treat hypotension resulting from septic shock or other distributive shock. It is a synthetic vasoconstrictor peptide that is identical to human hormone angiotensin II.[3] The Food and Drug Administration approved the use of angiotensin II in December 2017 to treat low blood pressure resulting from septic shock.[4]
The US Food and Drug Administration (FDA) considers it to be a first-in-class medication.[5] It is approved as a generic medication.[6]
Medical uses
[edit | edit source]Angiotensin II is a vasoconstrictor used to increase blood pressure in adults with septic or other distributive shock.[1] Angiotensin II is a naturally occurring hormone secreted as part of the renin-angiotensin system that results in powerful systemic vasoconstriction.[7][8] The vasopressor effects of angiotensin have been studied since it was first isolated in the late 1930s.[9]
Adverse effects
[edit | edit source]Angiotensin II treated patients are at an increased risk of thromboembolic events. There was a higher incidence of arterial and venous thrombotic and thromboembolic events in patients who received angiotensin II compared to placebo treated patients in the ATHOS-3 study [13% (21/163 patients) vs. 5% (8/158 patients)].[10] It is recommended that patients be on concurrent venous thromboembolism prophylaxis. Other adverse reactions include thrombocytopenia, tachycardia, fungal infection, delirium, acidosis, hyperglycemia, and peripheral ischemia.[1]
Angiotensin II acts on angiotensin receptor (AT1) on presynaptic adrenergic nerves → release of catecholamine → excessive catecholamine can be harmful as it can cause myocyte necrosis.[11]
References
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