M-Hydroxyphenylpropanolamine
M-Hydroxyphenylpropanolamine Uses, Dosage, Side Effects, Food Interaction and all others data.
An adrenergic agonist that acts predominantly at alpha adrenergic receptors and also stimulates the release of norepinephrine. It has been used primarily as a vasoconstrictor in the treatment of hypotension.
M-Hydroxyphenylpropanolamine is a potent sympathomimetic amine that increases both systolic and diastolic blood pressure. M-Hydroxyphenylpropanolamine is indicated for prevention and treatment of the acute hypotensive state occurring with spinal anesthesia. It is also indicated as adjunctive treatment of hypotension due to hemorrhage, reactions to medications, surgical complications, and shock associated with brain damage due to trauma or tumor. M-Hydroxyphenylpropanolamine acts on both α1-adrenergic receptors but appears to have no effect on β-adrenergic receptors. It acts by increasing the force of the heart's pumping action as well as constricting peripheral blood vessels.
Trade Name | M-Hydroxyphenylpropanolamine |
Availability | Discontinued |
Generic | Metaraminol |
Metaraminol Other Names | 1-Metaraminol, Hydroxynorephedrine, L-Metaraminol, m-Hydroxy norephedrine, m-Hydroxyphenylpropanolamine, m-Hydroxypropadrine, Metaraminol, Métaraminol, Metaraminolum |
Type | |
Formula | C9H13NO2 |
Weight | Average: 167.205 Monoisotopic: 167.094628665 |
Protein binding | Approximately 45% |
Groups | Approved, Investigational |
Therapeutic Class | |
Manufacturer | |
Available Country | |
Last Updated: | September 19, 2023 at 7:00 am |
Uses
For the treatment and prevention of hypotension due to hemorrhage, spinal anesthesia, and shock associated with brain damage
How M-Hydroxyphenylpropanolamine works
M-Hydroxyphenylpropanolamine acts through peripheral vasoconstriction by acting as a pure alpha-1 adrenergic receptor agonist, consequently increasing systemic blood pressure (both systolic & diastolic). Its effect is thought to be associated with the inhibition of adenyl cyclase which leads to an inhibition of the production of cAMP. Another effect of M-Hydroxyphenylpropanolamine is that it releases norepinephrine from its storage sites indirectly.
Toxicity
LD50=240 mg/kg (rat, oral); LD50=99 mg/kg (mouse, oral)
M-Hydroxyphenylpropanolamine Drug Interaction
Moderate: digoxin, digoxin, levothyroxine, levothyroxineUnknown: aspirin, aspirin, charcoal, charcoal, epinephrine, epinephrine, amoxicillin / clavulanate, amoxicillin / clavulanate, multivitamin, multivitamin, chloramphenicol, chloramphenicol, hydrocortisone, hydrocortisone, acetaminophen, acetaminophen
M-Hydroxyphenylpropanolamine Disease Interaction
Elimination Route
The effect starts 1-2 min after IV injection, 10 min after IM injection, 5-20 min after subcutaneous injection.
Innovators Monograph
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