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Methyldopa, also known as α-methyl-L-DOPA and sold under the brand name Aldomet among others, is a medication used for high blood pressure.<ref name="AHFS2016" /> It is one of the preferred treatments for high blood pressure in pregnancy.<ref name="AHFS2016" /> For other types of high blood pressure including very high blood pressure resulting in symptoms other medications are typically preferred.<ref name="AHFS2016" /> It can be given by mouth or injection into a vein.<ref name=AHFS2016/> Onset of effects is around 5 hours and they last about a day.<ref name="AHFS2016">{{#invoke:citation/CS1|citation |CitationClass=web }}</ref>

Common side effects include sleepiness.<ref name=AHFS2016/> More severe side effects include red blood cell breakdown, liver problems, and allergic reactions.<ref name=AHFS2016/> Methyldopa is in the alpha-2 adrenergic receptor agonist family of medication. It works by stimulating the brain to decrease the activity of the sympathetic nervous system.<ref name=AHFS2016/>

Methyldopa was discovered in 1960.<ref name=Wal2012>Template:Cite book</ref> It is on the World Health Organization's List of Essential Medicines.<ref name="WHO21st">Template:Cite book</ref>

Medical usesEdit

Methyldopa is used in the clinical treatment of the following disorders:

Side effectsEdit

Methyldopa is capable of inducing a number of adverse side effects, which range from mild to severe. Nevertheless, they are generally mild when the dose is less than 1 gram per day.<ref>Template:Cite book</ref> Side effects may include:

WithdrawalEdit

Rebound hypertension via withdrawal on account of tolerance upon the abrupt discontinuation of methyldopa has been reported.<ref>Methyldopa (PIM 342) Template:Webarchive</ref>

Mechanism of actionEdit

The mechanism of action of methyldopa is not fully clear. It may reduce the dopaminergic and serotonergic transmission in the central and peripheral nervous system and it indirectly affects norepinephrine (noradrenaline) synthesis by way of inhibiting dopamine synthesis. Methyldopa acts on alpha-2 adrenergic receptors, which are found on the pre synaptic nerve terminal.<ref name="AHFS2016" /> This inhibits the release of norepinephrine from the presynaptic neuron.

The S-enantiomer of methyldopa is a competitive inhibitor of the enzyme aromatic L-amino acid decarboxylase (LAAD), which converts L-DOPA into dopamine. L-DOPA can cross the blood–brain barrier and thus methyldopa may have similar effects. LAAD converts it into alpha-methyldopamine, a false prescursor to norepinephrine, which in turn reduces synthesis of norepinephrine in the vesicles. Dopamine beta hydroxylase (DBH) converts alpha-methyldopamine into alpha-methylnorepinephrine, which is an agonist of the presynaptic α2-adrenergic receptor causing inhibition of neurotransmitter release.

Methyldopa has been found to be a monoamine depleting agent.<ref name="TungGoldbergHollister1988">Template:Cite journal</ref>

PharmacokineticsEdit

Maximum decrease in blood pressure occurs 4–6 hours after oral dosage. The half-life of methyldopa is 105 minutes.<ref>{{#invoke:citation/CS1|citation |CitationClass=web }}</ref> Methyldopa exhibits variable absorption from the gastrointestinal tract. It is metabolized in the liver and intestines and is excreted in urine.Template:Citation needed

HistoryEdit

When methyldopa was first introduced, it was the mainstay of antihypertensive treatment, but its use has declined on account of relatively severe adverse side effects, with increased use of other safer and more tolerable agents such as alpha blockers, beta blockers, and calcium channel blockers. Additionally, it has yet to be associated with reducing adverse cardiovascular events including myocardial infarction and stroke, or overall all-cause mortality reduction in clinical trials.<ref name="pmid19821316">Template:Cite journal</ref> Nonetheless, one of methyldopa's still current indications is in the management of pregnancy-induced hypertension (PIH), as it is relatively safe in pregnancy compared to many other antihypertensives which may affect the fetus.Template:Citation needed

See alsoEdit

ReferencesEdit

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External linksEdit

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