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Propranolol

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Propranolol chemical structure
Propranolol

1-(isopropylamino)-
3-(naphthalen-1-yloxy)propan-2-ol
IUPAC name
CAS number
525-66-6
ATC code

C07AA05

PubChem
4946
DrugBank
APRD00194
Chemical formula {{{chemical_formula}}}
Molecular weight 259.34 g/mol
Bioavailability 30–70%
Metabolism hepatic (extensive)
Elimination half-life 3–4 hours
Excretion renal <1%
Pregnancy category
Legal status {{{legal_status}}}
Routes of administration oral, iv

Propranolol (INN) (IPA: [proˈprænəloʊl]) is a non-selective beta blocker mainly used in the treatment of hypertension. It was the first successful beta blocker developed. Propranolol is commonly marketed by Wyeth under the trade name Inderal.

History and developmentEdit

Scottish scientist James W. Black successfully developed propranolol in the late 1950s. He was awarded the Nobel Prize in Medicine for this discovery in 1988.

Propranolol developed from the early β-adrenergic antagonists dichloroisoprenaline and pronethalol. The key structural modification, which was carried through to essentially all subsequent beta blockers, was the insertion of an oxymethylene bridge into the arylethanolamine structure of pronethalol thus greatly increasing the potency of the compound. This also apparently eliminated the carcinogenicity found with pronethalol in animal models.

Pharmacology Edit

Propranolol is a non-selective beta blocker, that is, it blocks the action of epinephrine on both β1- and β2-adrenergic receptors. It has little intrinsic sympathomimetic activity (ISA) but has strong membrane stabilising activity.

Pharmacokinetics Edit

Propranolol is rapidly and completely absorbed, with peak plasma levels achieved approximately 1–3 hours after ingestion. Co-administration with food appears to enhance bioavailability. Despite complete absorption, propranolol has a variable bioavailability due to extensive first-pass metabolism. Hepatic impairment will therefore increase its bioavailability. The main metabolite 4-hydroxypropranolol, with a longer half-life (5.2–7.5 hours) than the parent compound (3–4 hours), is also pharmacologically active.

Propranolol is a highly lipophilic drug achieving high concentrations in the brain. The duration of action of a single oral dose is longer than the half-life indicates and may be up to 12 hours, if the single dose is high enough (e.g. 80 mg). Effective plasma concentrations are between 10–100 ng/mL.

Clinical use Edit

Indications Edit

Propranolol is indicated for the management of various conditions including (Rossi, 2006):

Whilst once first-line treatment for hypertension, the role for beta-blockers was downgraded in June 2006 in the United Kingdom to fourth-line as they perform less well than other drugs, particularly in the elderly, and there is increasing evidence that the most frequently used beta-blockers at usual doses carry an unacceptable risk of provoking type 2 diabetes.[1]

It is also used to lower portal vein pressure in portal hypertension and prevent oesophageal variceal bleeding.

Propranolol and PTSDEdit

Propranolol is currently being investigated as a potential treatment for post-traumatic stress disorder [1].

Precautions/contraindications Edit

Propranolol should be used with caution in patients with:

(Rossi, 2006)

Propranolol is contraindicated in patients with:

(Rossi, 2006)

Adverse effects Edit

Adverse drug reactions (ADRs) associated with propranolol therapy are similar to other lipophilic beta blockers (see beta blocker).

Pregnancy and Lactation Edit

Propranolol, like other beta blockers, is classified as Pregnancy category C in the United States and ADEC Category C in Australia. Beta-blocking agents in general reduce perfusion of the placenta which may lead to adverse outcomes for the neonate, including pulmonary or cardiac complications, or premature birth. The newborn may experience additional adverse effects such as hypoglycemia and bradycardia.

Most beta-blocking agents appear in the milk of lactating women. This is especially the case for a lipophilic drug like propranolol. Breastfeeding is not recommended in patients receiving propranolol therapy.

Interactions Edit

Beta blockers, including propranolol, have an additive effect with other drugs which decrease blood pressure, or which decrease cardiac contractility or conductivity. Clinically-significant interactions particularly occur with verapamil, epinephrine, β2-adrenergic receptor agonists, clonidine, ergot alkaloids, isoprenaline, non-steroidal anti-inflammatory drugs, quinidine, cimetidine, lidocaine, phenobarbital and rifampicin. (Rossi, 2006)

Dosage Edit

The usual maintenance dose ranges for oral propranolol therapy vary by indication.

  • Hypertension, angina, essential tremor
    • 120–320 mg daily in divided doses.
    • Sustained-release formulations are available in some markets.
  • Tachyarrhythmia, anxiety, hyperthyroidism
    • 10–40 mg 3–4 times daily

Intravenous (IV) propranolol may be used in acute arrhythmia or thyrotoxic crisis (Joint Formulary Committee, 2004).

References Edit


PTSDEdit

  • Fletcher, T. and Cahill, L. (2002). Propranolol for reemergent posttraumatic stress disorder following an event of retraumatization: a case study . Journal of Traumatic Stress 15, 433-37.
  • Pitman, R. K., Sanders, K. M., Zusman, R. M., Healy, A. R., Cheema, F., Lasko, N. B., Cahill, L. and Orr, S. P. (2002). Pilot study of secondary prevention of posttraumatic stress disorder with propanolol , Biological Psychiatry 51, 189-92.
  • Vaiva, G., Ducrocq, F., Jezequel, K., Averland, B., Lestavel, P., Brunet, A., Marmar, C. R. (2002). Peritraumatic prescription of propranolol decreases acute PTSD symptoms , International Society for Traumatic Stress Studies (ISTSS), Baltimore.

External linksEdit


Beta blockers edit
β1 antagonists (cardioselective) edit

{Acebutolol} {Atenolol} {Betaxolol} {Bisoprolol} {Esmolol} {Metoprolol} {Nebivolol}

β2 antagonists (generally Anxiolytic) edit

{Butoxamine}

Non-selective β-blockers edit

{Nadolol} {Oxprenolol} {Propranolol} {Pindolol} {Sotalol} {Timolol}

β2 antagonists (non cardioselective with alpha-blocking activity) edit

{Carvedilol} {Labetalol}

fr:Propranolol

nl:Propranololth:โพรพาโนลอล

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