Dopamine (medication)

Dopamine, sold under the brand name Intropin among others, is a medication most commonly used in the treatment of very low blood pressure, a slow heart rate that is causing symptoms, and, if epinephrine is not available, cardiac arrest. In newborn babies it continues to be the preferred treatment for very low blood pressure. In children epinephrine or norepinephrine is generally preferred while in adults norepinephrine is generally preferred for very low blood pressure. It is given intravenously or intraosseously as a continuous infusion. Effects typically begin within five minutes. Doses are then increased to effect.

Dopamine
Skeletal formula of dopamine
Ball-and-stick model of the zwitterionic form of dopamine found in the crystal structure
Clinical data
Trade namesIntropin, Dopastat, Revimine, others
Other names2-(3,4-Dihydroxyphenyl)ethylamine; 3,4-Dihydroxyphenethylamine; 3-hydroxytyramine; DA; Intropin; Revivan; Oxytyramine; Prolactin inhibiting factor; Prolactin inhibiting hormone
AHFS/Drugs.comMonograph
Routes of
administration
Intravenous injection
ATC code
Physiological data
Source tissuesSubstantia nigra; ventral tegmental area; many others
Target tissuesSystem-wide
ReceptorsD1, D2, D3, D4, D5, TAAR1
AgonistsDirect: apomorphine, bromocriptine
Indirect: cocaine, substituted amphetamine, cathinone, bupropion
AntagonistsNeuroleptics, metoclopramide, domperidone
MetabolismMAO, COMT, ALDH, DBH, MAO-A, MAO-B, COMT
Legal status
Legal status
  • In general: ℞ (Prescription only)
Pharmacokinetic data
MetabolismMAO, COMT, ALDH, DBH, MAO-A, MAO-B, COMT
ExcretionKidney
Identifiers
  • 4-(2-Aminoethyl)benzene-1,2-diol
CAS Number
PubChem CID
IUPHAR/BPS
DrugBank
ChemSpider
UNII
KEGG
ChEBI
ChEMBL
Chemical and physical data
FormulaC8H11NO2
Molar mass153.181 g·mol−1
3D model (JSmol)
Density1.26 g/cm3
Melting point128 °C (262 °F)
Boiling pointdecomposes
SMILES
  • c1cc(c(cc1CCN)O)O
  • InChI=1S/C8H11NO2/c9-4-3-6-1-2-7(10)8(11)5-6/h1-2,5,10-11H,3-4,9H2 Y
  • Key:VYFYYTLLBUKUHU-UHFFFAOYSA-N Y
  (verify)

Common side effects include worsening kidney function, an irregular heartbeat, chest pain, vomiting, headache, or anxiety. If it enters into the soft tissue around the vein local tissue death may occur. The medication phentolamine can be given to try to decrease this risk. It is unclear if dopamine is safe to use during pregnancy or breastfeeding. At low doses dopamine mainly triggers dopamine receptors and β1-adrenergic receptors while at high doses it works via α-adrenergic receptors.

Dopamine was first synthesized in a laboratory in 1910 by George Barger and James Ewens in England. It is on the World Health Organization's List of Essential Medicines. In human physiology dopamine is a neurotransmitter as well as a hormone.

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