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Pharmacology · Drugs and Prescriptions

Angiotensinamide

Angiotensinamidum

Angiotensinamid is a peptide-structured antihypertensive agent that is a synthetic amide of angiotensin II. The drug belongs to the group of substances that predominantly increase peripheral vascular tone and is characterized by the ability to cause a potent yet uneven arteriolar spasm.

Pharmacological groupAntihypertensive agents (polypeptides)
Site of actionArteriolar angiotensin receptors
Dosage formVials containing 0.001 g of dry substance
Route of administrationIntravenous drip (5–20 mcg/min)
How to write a prescription
Rp.: Angiotensinamidi 0,001
D.t.d. N 5 in flac.
S. Содержимое флакона растворить ex tempore в 1000 мл 0,9% раствора натрия хлорида, вводить в/в капельно со скоростью 5–20 мкг/мин

Alternative notation: Pulv. Angiotensinamidi 0.001; Angiotensinamidi 0.001 in flac.

Dosage form
Vials of 0.001 g
Administration
Dissolve the contents of the vial ex tempore in 1000 mL of 0.9% NaCl or 5% glucose solution, administer intravenously at 5–20 mcg/minute
Group
Agents acting on the cardiovascular system
3 min readFor medical studentsUpdated 09/24/2026
Material prepared by WhiteCoat Pro editorial team based on platform study guidesReviewed by medical editor: Aulov A. A., general practitioner · 09/24/2026

Classification and place in therapy

In pharmacology, antihypertensive agents are traditionally divided into two major groups based on their effect on systemic hemodynamics.

The first group consists of drugs that increase both cardiac output and peripheral vascular tone (a typical representative is the $\alpha, \beta$-adrenomimetic epinephrine).

Angiotensinamidum belongs to the second group — agents that predominantly increase peripheral vascular tone. This hemodynamic group also includes $\alpha$-adrenomimetics (norepinephrine, phenylephrine), but angiotensinamid stands out due to its chemical nature: it is not a catecholamine derivative, but a drug of polypeptide structure.

Mechanism of action and vascular effects

The pharmacological target of the drug is angiotensin receptors located in the walls of arterioles.

Stimulation of these receptors leads to a rapid and extremely pronounced vasoconstrictor effect. Notably, the pressor effect of angiotensinamid significantly exceeds that of epinephrine (adrenaline).

The key feature of the drug is localization of action. Vasospasm occurs unevenly: the most pronounced vasoconstriction is observed in the vascular bed of the internal organs, skin, and kidneys. This feature of blood flow distribution must be taken into account when assessing the risks of tissue ischemia with the use of the drug.

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Effect on water-electrolyte metabolism

In addition to its direct effect on vascular smooth muscle, Angiotensinamidum exhibits a pronounced hormonal effect.

The drug interferes with the endocrine system by stimulating the production of the mineralocorticoid aldosterone. The consequences of this hormonal shift are:

  • Active retention of sodium ions in the body.
  • Secondary water retention.
  • A predictable increase in extracellular fluid volume.

This mechanism provides an additional contribution to maintaining high blood pressure.

Dosage form and rules of administration

The drug is available as a dry substance in vials containing 0.001 g (1 mg).

An infusion solution must be prepared before administration. This must be done strictly ex tempore (immediately before use).

Preparation and administration algorithm:

  1. The contents of one vial are dissolved in a large volume of liquid — 1000 mL of 0.9% sodium chloride solution (normal saline) or 5% glucose solution.
  2. Administration is performed exclusively intravenously.
  3. The infusion rate must be strictly controlled and range from 5 to 20 mcg per minute, depending on the patient's hemodynamic response.

Briefly: answers to topical questions

What are the main clinical indications for the use of angiotensinamid?

The provided sources do not specify particular clinical indications for angiotensinamid. It is noted that angiotensinamid belongs to peptide/polypeptide antihypertensive agents that predominantly increase peripheral vascular tone.

What side effects may occur with the administration of angiotensinamid?

The provided sources do not list the side effects of angiotensinamid. Its pharmacological effects are indicated:

  • pronounced and rapid vasoconstrictor effect, predominantly narrowing of the blood vessels of internal organs, skin, and kidneys;
  • stimulation of aldosterone production;
  • sodium and water retention in the body with an increase in extracellular fluid volume.
How to memorize

The rule of four 'A's: Angiotensinamid — Angiotensin Amide, More Active than Adrenaline, Activates Aldosterone.

Class and exam questions

To which group of antihypertensive agents does angiotensinamid belong?

It belongs to the group of agents that predominantly increase peripheral vascular tone. Structurally, it is a polypeptide drug.

In which organs is vasoconstriction most pronounced upon drug administration?

Maximum vascular spasm is observed in the arterioles of internal organs, skin, and kidneys.

How does the drug affect water-electrolyte balance?

It stimulates aldosterone production, leading to sodium and water retention, which contributes to an increased extracellular fluid volume.

What is the difference between the hemodynamic effects of angiotensinamid and epinephrine?

Epinephrine increases both cardiac output and vascular tone. Angiotensinamid acts primarily on peripheral resistance, while exerting a more potent pressor (vasoconstrictor) effect.

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What else to study on this topic

  • Comparative profile with $\alpha$-adrenomimetics (norepinephrine, phenylephrine).
  • The role of the renin-angiotensin-aldosterone system (RAAS) in blood pressure regulation.
  • Risks of renal and splanchnic ischemia during potent vasoconstriction.
  • Rules for calculating intravenous drip infusion rates (converting mg/mL to mcg/min).

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