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Venlafaxine is a bicyclic antidepressant, and is usually categorized
as a serotonin-norepinephrine reuptake inhibitor (SNRI), but it
has been referred to as a serotonin-norepinephrine-dopamine reuptake
inhibitor. It works by blocking the transporter "reuptake"
proteins for key neurotransmitters affecting mood, thereby leaving
more active neurotransmitters in the synapse. The neurotransmitters
affected are serotonin (5-hydroxytryptamine) and norepinephrine
(noradrenaline). Additionally, in high doses it weakly inhibits
the reuptake of dopamine, with recent evidence showing that the
norepinephrine transporter also transports some dopamine as well,
implying that SNRIs may also increase dopamine transmission. This
is because SNRIs work by inhibiting reuptake, i.e. preventing
the serotonin and norepinephrine transporters from taking their
respective neurotransmitters back to their storage vesicles for
later use. If the norepinephrine transporter normally recycles
some dopamine too, then SNRIs will also enhance dopaminergic transmission.
Therefore, the antidepressant effects associated with increasing
norepinephrine levels may also be partly or largely due to the
concurrent increase in dopamine (particularly in the prefrontal
cortex).
Pharmacokinetics
Venlafaxine is well absorbed with at least 92% of an oral dose
being absorbed into systemic circulation. It is extensively metabolized
in the liver via the CYP2D6 isoenzyme to O-desmethylvenlafaxine,
which is just as potent a serotonin-norepinephrine reuptake inhibitor
as the parent compound, meaning that the differences in metabolism
between extensive and poor metabolizers are not clinically important.
Steady-state concentrations of venlafaxine and its metabolite
are attained in the blood within 3 days. Therapeutic effects are
usually achieved within 3 to 4 weeks. No accumulation of venlafaxine
has been observed during chronic administration in healthy subjects.
The primary route of excretion of venlafaxine and its metabolites
is via the kidneys. The half-life of venlafaxine is relatively
short, therefore patients are directed to adhere to a strict medication
routine, avoiding missing a dose. Even a single missed dose can
result in the withdrawal symptoms.
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