氟西汀
脑脊液
自闭症
多巴胺
内科学
医学
内分泌学
多巴胺转运体
神经毒性
胰岛素样生长因子
生长因子
精神科
多巴胺能
血清素
毒性
受体
作者
Ismo Makkonen,Hannu Kokki,Jyrki T. Kuikka,Ursula Turpeinen,Raili Riikonen
出处
期刊:Neuropediatrics
[Thieme Medical Publishers (Germany)]
日期:2011-10-01
卷期号:42 (05): 207-209
被引量:35
标识
DOI:10.1055/s-0031-1291242
摘要
A positive effect of fluoxetine has been shown in some children with autism. The present study was undertaken to correlate striatal dopamine transporter (DAT) binding and cerebrospinal fluid insulin-like growth factor-1 (CSF-IGF-1) with clinical response in autistic children (n=13, age 5–16 years) after a 6-month fluoxetine treatment. Good clinical responders (n=6) had a decrease (p=0.031) in DAT binding as assessed using single-photon emission computed tomography with [123I]-nor-β-CIT, whereas poor responders had a trend to an increase. An increase in CSF-IGF-1 (p=0.003) was detected after the treatment period, but no correlation between the clinical response and CSF-IGF-1 was found. In conclusion, fluoxetine decreases DAT binding indicating alleviation of the hyperdopaminergic state and increases CSF-IGF-1 concentration, which may also have a neuroprotective effect against dopamine-induced neurotoxicity in autistic children.
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