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As both enantiomers compete in binding to an allosteric site of the transporter and S-citalopram binds to both primary and allosteric lexapro 20 mg tablet lexapro dosage lexapro pregnancy is lexapro effective lexapro 5mg what is sites, it has been suggested to classify escitalopram as an ‘allosteric serotonin reuptake inhibitor’ [9,10] .
Selective inhibition of serotonin reuptake was also demonstrated in vivo using single photon emission computer tomography scanning, which has shown highly significant blockade of the serotonin transporter in healthy volunteers after clinically relevant doses lexapro 5 is escitalopram lexapro lexapro mg dosage lexapro generic name escitalopram oxalate what of escitalopram [11] .
Escitalopram and its metabolite demethylescitalopram do not exert significant affinity to any of 140 types of receptors and binding sites, what drug class is lexapro is lexapro effective is 5mg of lexapro effective lexapro side effects with some exception of σ1+2 receptors [4] .
Unlike R-citalopram, escitalopram was not escitalopram a significant antagonist of 5-hydroxytryptamine (serotonin; 5-HT2C) and histamine H1 receptors, and only slightly influences σ1+2 receptors [2,6] .
In this way, escitalopram differs from fluoxetine with its affinity for 5-HT2C receptors, paroxetine with its binding to muscarinic M receptors, and from citalopram with its blockade escitalopram of histamine H1 receptors [2] .
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Neurotherapeutics escitalopram 8(4), (2008) Escitalopram for the treatment of major depression & anxiety disorders Table 1 .
Affinity of escitalopram to human serotonin, noradrenaline and dopamine transporters in comparison lexapro side effects reviews how to take lexapro what doses does lexapro come in lexapro español how to other SSRIs Human monoamine transporters of escitalopram .
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