再摄取

在体内其活性代谢物二级胺M1及一级胺M2可抑制5羟色胺及去甲肾上腺素的再摄取，通过增加饱胀感而抑制食欲，并诱导产热，增加能量消耗。

Its active metabolite M 1 and M 2 , inhibit the reuptake of 5 HT and noradrenaline and induce the anorectic effects .

目的：探讨选择性5羟色胺再摄取抑制剂（SSRI）对体重的影响。

Objective : To explore the effect of selective serotonin reuptake inhibitors ( SSRIs ) on body weight .

经Morris水迷宫对大鼠的空间学习记忆能力及对已存储信息的再摄取能力进行评价。

Spatial learning and memory ability was evaluated by Morris water maze .

PD组患者服用5-羟色胺再摄取抑制剂4周、12周、24周时予以复查。

PD patients were followed up with the same markers after SSRI treatment for 4 weeks , 12 weeks and 24 weeks .

西酞普兰是一种应用广泛的选择性5-HT再摄取抑制剂类抗抑郁药。

Citalopram , a selective serotonin reuptake inhibitor ( SSRI ), is one of the most widely used antidepressants .

本课题尝试应用计算机辅助药物分子设计方法为寻找新型的选择性5-HT再摄取抑制剂提供指导。

In order to search for new selective inhibitors of the 5-HT , the computer-aided drug design ( CADD ) technology was applied .

利用比较分子力场分析法分别建立了可提示具有高活性及高选择性的5-HT再摄取抑制剂分子结构信息的三维定量构效关系模型。

By using the comparative molecular field analysis ( CoMFA ), a3D-QSAR model was established to display the relationship between structure and the potency for inhibition of5-HT uptake .

最常见的抗抑郁药这些药也用于治疗焦虑症是选择性血清素再摄取抑制剂（selectiveserotoninreuptakeinhibitors，简称SSRI），它能强化血清素的输送。

The most common antidepressants , which are also used to treat anxiety , are selective serotonin reuptake inhibitors ( S.S.R.I.s ) that enhance serotonin transmission .

综述选择性5羟色胺再摄取抑制药（SSRIs）与性功能的关系。

This article reviews current evidence regarding sexual adverse reaction of selective serotonin reuptake inhibitors ( SSRIs ) .

目的：研究临床应用5-羟色胺（5-HT）再摄取抑制剂作为辅助药物治疗膀胱活动过度症（OAB）的可行性和安全性。

OBJECTIVE : To study the feasibility and safety of serotonin ( 5-HT ) reuptake inhibitor in the adjunctive therapy of the patients with OAB .

结论TPM对发育期大脑的长期记忆功能及信息再摄取能力均无影响，而且对幼鼠的空间学习能力的影响也是极短暂的。

Conclusion : For developing rat brain , TPM has no impairment on the ability of long-term memory and information retrieval meanwhile its negative effect on spatial learning is temporary .

百忧解是一类名为选择性血清素再摄取抑制剂（SSRI）的新型药物中的明星产品。

It was the star in a class of new pharmaceuticals known as S.S.R.I.s - selective serotonin reuptake inhibitors .

结论异丙酚以非竞争性的方式抑制了DAT的转运功能，降低了多巴胺（DA）的再摄取，导致突触间隙DA浓度升高，从而增强了中枢多巴胺能神经信息的传递。

Conclusion Propofol inhibits the transport ability of DAT in a noncompetitive fashion and reduces the reuptake of dopamine , leading to elevation in DA concentration in the synaptic cleft and potentiation of dopaminergic neurotransmission in central nervous system .

说明两菌株对烷烃具有不同的摄取机制，Pseudomonassp.A是以直接接触烷烃的方式摄取，而Pseudomonassp.B则是通过产生生物表面活性剂对烷烃进行乳化后再摄取。

The above results indicated the different mechanisms of alkane uptake in two Pseudomonas strains , Pseudomonas sp. A uptakes kerosene by the direct contact mechanism , while Pseudomonas sp. B uptakes the kerosene emulsified with the biosurfactant produced by the cells .

目的：氢溴酸西酞普兰（简称西酞普兰）是一种高选择性的5-羟色胺再摄取抑制剂（SSRI），临床广泛用于各种抑郁症的治疗。

Objectives : Citalopram Hydrobromide is a highly selective 5-HT reuptake inhibitor ( SSRI ) which is widely used in a variety of depression treatment in clinics .

目的：了解选择性5羟色胺再摄取抑制剂（SSRIs）氟西汀、舍曲林、帕罗西汀的不良反应特点，增强对5羟色胺（5HT）综合征的认识。

AIM : To study the characteristic of adverse reactions of SSRIs such as fluoxetine , sertraline , paroxetine and to enhance the realization of the serotonin syndrome .

在常规治疗的基础上随机予IBS患者选择性5鄄羟色胺再摄取抑制剂（SSRI）类抗抑郁药治疗，20例患者使用盐酸帕罗西汀，16例患者使用盐酸氟西汀，疗程均为12周。

On the basis of routine treatment , selective serotonin reuptake inhibitor ( SSRI ) antidepressants were randomly given to IBS patients for 12 weeks , among them , 20 received paroxetine hydrochloride , 16 received fluoxetine hydrochloride .

方法采用99mTc植酸钠胶体肝再摄取和首次通过斜率原理，运用自编程序，检测20例肝癌和10例正常健康人的HBF、HAF、PVF。

Methods HBF , HAF and PVF were determined in 20 patients with primary liver cancer and 10 normal individuals by detecting colloid re-uptake by liver cells and the method of slope in the first pass after injecting 99m Tc-phytate .

二十世纪七十年代，人们发现氟西汀可以作为一种选择性血清再摄取抑制剂。但是，整整十年，美国食品药品管理局都没有批准施用此药物。二十世纪七十年代，美国礼来公司（EliLilly）发现氟西汀，并获得了它的专利。

Fluoxetine 's potential as a selective serotonin reuptake inhibitor was actually discovered in the 1970s , but the FDA didn 't give the drug the go-ahead for an entire decade.Fluoxetine was discovered and patented by Eli Lilly and Company in the 1970s ;

百忧解是一类名为选择性血清素再摄取抑制剂（SSRI）的新型药物中的明星产品。其作用基于的观念为，抑郁症是由一种名叫血清素的神经递质不足引起的。

It was the star in a class of new pharmaceuticals known as S.S.R.I.s & selective serotonin reuptake inhibitors . Underlying their use is a belief that depression is caused by a shortage of the neurotransmitter serotonin .

三环类药物（TCAs）使用频率为419%，五羟色胺再摄取抑制剂（SSRIs）治疗者占全部病人的445%，其他新型抗抑郁药占216%。

The frequency of each drug in five economic level regions were different significantly . TCAs account for 41 9 % ( vs 44 5 % for SSRIs and 21 6 % for other novel drugs ) among the patients with pharmacological treatment .

心理治疗与5-羟色胺再摄取抑制剂对脑卒中后抑郁患者神经功能康复的影响

Psychotherapy and serotonin reuptake inhibitor for rehabilitating nerve function after stroke

这些抗抑郁的药物都是选择性5-羟色胺再摄取抑制剂。

These antidepressants are known as selective serotonin reuptake inhibitors .

5-羟色胺再摄取抑制剂和其它类新型药物有较好发展前景。

5-serotonin re-intake inhibitor and other new drugs have a better future .

5-羟色胺再摄取抑制剂治疗孤独症的临床机制研究

Research on clinical mechanism of selective serotonin reuptake inhibitor in treatment of autism

2月龄婴儿出生前后暴露于选择性5-羟色胺再摄取抑制剂药物后的疼痛反应

Pain reactivity in 2-month-old infants after prenatal and postnatal selective serotonin reuptake inhibitor medication exposure

上文结果提示，普鲁卡因胺降低凝血酶诱导的血小板游离Ca2+升高，对Ca2+的再摄取没有影响。

These results indicate that procainamide decrease platelet free-Ca2 + induced by thrombin without affecting the rate of Ca2 + uptake .

目的调查心血管疾病患者中抑郁症的患病率及应用选择性5羟色胺再摄取抑制剂帕罗西汀（赛乐特）的疗效。

Objective To investigate the prevalence of depression in patients with cardiovascular diseases and the effect of Selective Serotonin Reuptake Inhibitor ( Seroxat ) .

目的研究抑郁症的注意网络状况及抑制神经递质再摄取的药物万拉法新对其的影响，探索神经递质与注意网络的关系。

To estimate attention networks in patients with depression and the effects of venlafaxine ( selective noradrenergic and serotonin reuptake inhibition ) on them .

青风藤对单胺类转运蛋白再摄取功能的抑制目的提取分离青风藤不同极性部位，研究它们对单胺类神经递质转运蛋白再摄取功能的影响。

Inhibition of Sinomenium Acutum Extract on Monoamine Transmitters Reuptake Objective To study the effects of Sinomenium acutum on monoamine transmitters reuptake by their transporters .