Overview

Arginine vasopressin (AVP/ADH) is a 9-amino acid neuropeptide produced in hypothalamic paraventricular and supraoptic nuclei and released from the posterior pituitary in response to increased plasma osmolality or decreased blood volume. It is essential for water homeostasis via antidiuresis, and at higher concentrations acts as a powerful vasoconstrictor (hence 'vasopressin'). In critical care, vasopressin is used as a vasopressor in septic shock and as an adjunct to resuscitation algorithms. Its analogs—desmopressin (antidiuresis-selective) and terlipressin (splanchnic-selective)—are more widely used clinically.

Mechanism of Action

Vasopressin activates three receptors: V1a (vascular smooth muscle → vasoconstriction via Gq/PLC/Ca2+ pathway), V1b/V3 (pituitary corticotrophs → ACTH release), and V2 (renal collecting duct → AQP2-mediated antidiuresis via Gs/cAMP/PKA). In septic shock, V1a activation counteracts the profound vasoplegia of vasodilatory shock, restoring vascular tone. V2 activation in the kidney causes AQP2 membrane translocation and maximal water reabsorption, crucial for plasma osmolality regulation. In the brain, AVP modulates social behavior, stress responses, and circadian rhythms.

Potential Benefits

  • Critical care vasopressor for vasodilatory/septic shock
  • Antidiuresis and plasma osmolality regulation
  • Cardiac arrest vasopressor in ACLS protocols
  • Template for desmopressin and terlipressin development
  • Neuromodulator for social behavior and stress responses

Dosage Protocols

The following reflects doses used in published research studies. This is not medical advice. Consult a qualified healthcare professional.

BeginnerHospital use for acute indications
IntermediateN/A — all uses are medically supervised
AdvancedN/A
Cycle DurationAcute (shock) or chronic (DI)

FDA-approved (Vasostrict) for septic shock vasopressor support. Desmopressin preferred for DI due to V2 selectivity.

Routes of Administration

Intravenous Infusion 100%

Primary use — septic shock vasopressor infusion.

Intramuscular / Subcutaneous High

Historical use for central DI — replaced by desmopressin.

Stacking Protocols

Popular research stacks involving Vasopressin (ADH):

Septic Shock Protocol

VASST-guided second-line vasopressor support in septic shock — add vasopressin 0.03 U/min to norepinephrine.

VasopressinNorepinephrine

Reconstitution

StorageRefrigerate 2-8°C. Diluted solution stable 18 hours at room temperature.

Hospital pharmacy preparation.

Need exact syringe measurements?

Amino Acid Sequence

Cys-Tyr-Phe-Gln-Asn-Cys-Pro-Arg-Gly-NH2 (cyclic via disulfide Cys1-Cys6)

Side Effects & Safety

  • Hypertension and excessive vasoconstriction
  • Peripheral ischemia at high doses
  • Hyponatremia
  • Cardiac arrhythmias
  • Mesenteric ischemia at high doses

Safety & Contraindications

This information is for educational purposes only. Consult a qualified healthcare provider before using any peptide.

Relative

Pregnancy / Lactation

Relative

Bleeding Disorders

Absolute

Active Skin Infection at Injection Site

FDA Safety Information

FDA labeling warns of risk of cardiac/mesenteric/peripheral ischemia, water intoxication, and hypersensitivity reactions.

FDA Source: Bulk Drug Substances Safety Risks

Pharmacokinetics

Half-Life~10-20 minutes
StorageRefrigerate at 2-8°C. Do not freeze. Protect from light.

Synergistic Compounds

The following compounds have been studied alongside Vasopressin (ADH) for potential complementary or synergistic effects:

NorepinephrineHydrocortisone (septic shock)Desmopressin

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References & Further Reading

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