三重再摄取抑制剂
(重定向自5-羟色胺、去甲肾上腺素和多巴胺再摄取抑制剂)
此條目需要擴充。 (2015年9月29日) |
血清素-去甲肾上腺素-多巴胺再摄取抑制剂(英語:serotonin–norepinephrine–dopamine reuptake inhibitor,SNDRI),也称作三重再摄取抑制剂(TRI),是多种单胺类神经递质的再摄取抑制剂,原理为通过抑制5-羟色胺转运体、去甲肾上腺素转运体和多巴胺转运体体来分别抑制5-羟色胺、 去甲肾上腺素和多巴胺的再摄取。这个作用会增加这些神经递质在突触间隙的浓度。
SNDRI作為一系列疾病的藥物候選而被開發,如抗憂鬱劑[1][2][3][4][5] 和治療肥胖、古柯鹼成癮、注意力缺陷/過動症(ADHD)及慢性疼痛的藥物。SNDRI作為選擇性血清素再吸收抑制劑(SSRIs)及血清素-去甲腎上腺素再吸收抑制劑(SNRIs)的延伸,增加了多巴胺的再吸收抑制作用,這被認為具有增加療效的可能,但副作用及藥物濫用的可能也隨之增加。
引用
- ^ Musk, P. Magic shotgun methods for developing drugs for CNS disorders. Discovery medicine. 2004, 4 (23): 299–302. PMID 20704963.
- ^ Millan, MJ. Dual- and triple-acting agents for treating core and co-morbid symptoms of major depression: Novel concepts, new drugs. Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics. 2009, 6 (1): 53–77. PMID 19110199. doi:10.1016/j.nurt.2008.10.039.
- ^ Chen, Z; Skolnick, P. Triple uptake inhibitors: Therapeutic potential in depression and beyond. Expert Opinion on Investigational Drugs. 2007, 16 (9): 1365–77. PMID 17714023. doi:10.1517/13543784.16.9.1365.
- ^ Perona, MT; Waters, S; Hall, FS; Sora, I; Lesch, KP; Murphy, DL; Caron, M; Uhl, GR. Animal models of depression in dopamine, serotonin, and norepinephrine transporter knockout mice: Prominent effects of dopamine transporter deletions. Behavioural Pharmacology. 2008, 19 (5–6): 566–74. PMC 2644662 . PMID 18690111. doi:10.1097/FBP.0b013e32830cd80f.
- ^ Chen, Z; Yang, J; Tobak, A. Designing new treatments for depression and anxiety. IDrugs : the investigational drugs journal. 2008, 11 (3): 189–97. PMID 18311656.