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Escitalopram

艾司西酞普蘭
Mechanism of action:
Escitalopram 是一種選擇性血清素再回收抑制劑(selective serotonin reuptake inhibitor),為西酞普蘭(citalopram)的 S-對映異構物(S-enantiomer)。Escitalopram 會高親和力結合突觸前神經元膜上的血清素轉運蛋白(serotonin transporter),阻斷血清素(5-HT)由突觸間隙回收至神經元內。血清素在突觸間隙停留時間延長、濃度上升,增強突觸後 5-HT 受體的活化,進而調節與情緒、焦慮及強迫相關的神經路徑活動。
Reference(s):
1. Moore N et al. (2005). Prospective, multicentre, randomized, double-blind study of the efficacy of escitalopram versus citalopram in outpatient treatment of major depressive disorder. Int Clin Psychopharmacol.
2. Boulenger JP et al. (2006). A comparative study of the efficacy of long-term treatment with escitalopram and paroxetine in severely depressed patients. Curr Med Res Opin.
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