Vasopressin Other names: 3-Isoleucyl vasopressin Arginine oxytocin Arginine vasotocin Argipressin Argiprestocin Pitressin tannate

Molecular mass: 2,140.46 g/mol 

Pharmacodynamic properties

The antidiuretic action of argipressin is ascribed to increase in reabsorption of water by the renal tubules. Argipressin can cause contraction of smooth muscle of the gastrointestinal tract, gall bladder, urinary bladder and all parts of the vascular bed, especially the capillaries, small arterioles and venules with less effect on the smooth musculature of the large veins. The direct effect on the contractile elements is neither antagonised by adrenergic blocking agents nor prevented by vascular denervation.

Pharmacokinetic properties

Absorption

Following subcutaneous or intramuscular administration of argipressin injection, the duration of antidiuretic activity is variable, but effects are usually maintained for 2-8 hours.

Biotransformation

The majority of the dose of argipressin is metabolised and rapidly destroyed in the liver and kidneys. Argipressin has a plasma half-life of about 10 to 20 minutes.

Elimination

Approximately 5% of a subcutaneous dose of argipressin is excreted unchanged in the urine four hours after dosing.

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