Development of Potential Treatment Medications for Drug Abuse
Development of Potential Treatment Medications for Drug Abuse
批准号:
8445334
负责人:
BRUCE E BLOUGH
金额:
$47.92万
依托单位国家:
美国
项目类别:
财政年份:
1999
资助国家:
美国
项目状态:
已结题
起止时间:
1999-09-30 至 2016-03-31
关键词:
AddressAgonistAmphetamine AddictionAnxietyAppetite DepressantsApplications GrantsBehaviorBehavioralBehavioral AssayBindingBiochemicalBiological AssayCardiacChronicClinicalCocaineDevelopmentDopamineDopamine Uptake InhibitorsDoseDrug abuseEquilibriumFenfluramineFoodGoalsGrantHeartHumanHybridsIn VitroIndividualLeadLinkMacaca mulattaMental DepressionMental disordersMethodsModelingMolecularNational Institute of Drug AbuseNeurotransmittersNorepinephrineNorfenfluraminePharmaceutical PreparationsPhenmetrazinePost-Traumatic Stress DisordersPrimatesPsychological reinforcementPsychostimulant dependencePublishingRattusRelapseResearchRiskRodentSafetySelf AdministrationSeriesSerotoninSerotonin AgonistsSiteStressStructureSymptomsSynapsesSystemTestingTherapeuticTherapeutic UsesToxic effectTriageTryptaminesUnited StatesWithdrawaladdictionanalogbasecombatdesigndrug relapseecstasyexperiencein vivoinhibitor/antagonistneurochemistrynoradrenergicprogramspulmonary arterial hypertensionresearch studyserotonin transportersmall moleculestimulant abusesubstance abuse treatmenttherapeutic targettooluptake
中文摘要
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英文摘要
ABSTRACT
The major goal of this application is to discover and develop medications for the treatment of substance
abuse. Furthermore, we expect that the compounds developed will also serve as biochemical probes useful in
gaining a better understanding of the biochemical and molecular mechanisms of cocaine, and amphetamine
addiction and withdrawal. The initial objective of this proposal is to design, synthesize, and evaluate dopamine
(DA), serotonin (5-HT), and norepinephrine (NE) releasers. To date, most efforts towards an "agonist" therapy
of stimulant addiction have concentrated on the discovery of selective DA uptake blockers. However increasing
evidence shows that dual DA/5-HT selective or non-selective compounds may be required to "correct" the
totality of stimulant-induced deficits during withdrawal. Experimental results published since the original
grant application also suggests that releasers as a class may be effective synaptic agonist treatments. The
optimal balance of activity between these three neurotransmitter systems is not known; however it is assumed
that DAergic activity must be present with some combination of other activity. Thus, the primary objective of
this application is to further develop the dual DA/5HT and non-selective "universal" releaser leads generated
during the initial project period. These compounds may also be useful for treating other psychiatric disorders
such as depression, anxiety, and stress. The target compounds will be small molecules that are expected to
penetrate the CNS and have reasonable stability so that they will be useful medications and can be used as in
vitro and in vivo probes.
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DOI:
10.1016/j.neuropharm.2015.09.004
发表时间:
2016-02
期刊:
Neuropharmacology
影响因子:
4.7
作者:
[Marusich JA, Antonazzo KR, Blough BE, Brandt SD, Kavanagh PV, Partilla JS, Baumann MH]
通讯作者:
Baumann MH
DOI:
10.1111/adb.12399
发表时间:
2017-09
期刊:
Addiction biology
影响因子:
3.4
作者:
[Smith DA, Negus SS, Poklis JL, Blough BE, Banks ML]
通讯作者:
Banks ML
The dopamine, serotonin and norepinephrine releasing activities of a series of methcathinone analogs in male rat brain synaptosomes.
雄性大鼠脑突触体中一系列甲性苯他酮类似物的多巴胺,5-羟色胺和去甲肾上腺素释放活性。
DOI:
10.1007/s00213-018-5063-9
发表时间:
2019-03
期刊:
Psychopharmacology
影响因子:
3.4
作者:
[Blough BE, Decker AM, Landavazo A, Namjoshi OA, Partilla JS, Baumann MH, Rothman RB]
通讯作者:
Rothman RB
DOI:
10.1097/fbp.0b013e32834d63ac
发表时间:
2011-12
期刊:
Behavioural pharmacology
影响因子:
1.6
作者:
[Banks ML, Blough BE, Negus SS]
通讯作者:
Negus SS
Dopamine/serotonin releasers as medications for stimulant addictions.
多巴胺/血清素释放剂作为兴奋剂成瘾的药物。
DOI:
10.1016/s0079-6123(08)00919-9
发表时间:
2008
期刊:
Progress in brain research
影响因子:
--
作者:
[Rothman,RichardB, Blough,BruceE, Baumann,MichaelH]
通讯作者:
Baumann,MichaelH
共 25 条
Development of Potential Treatment Medications for Drug Abuse
-
批准号:7812821
-
项目类别:
-
资助金额:$60.36万
-
财政年份:2009
-
负责人:BRUCE E BLOUGH
-
依托单位:
Potential Treatment Medications for Drug Abuse
-
批准号:6913389
-
项目类别:
-
资助金额:$42.97万
-
财政年份:1999
-
负责人:BRUCE E BLOUGH
-
依托单位:
Development of Potential Treatment Medications for Drug Abuse
-
批准号:7789588
-
项目类别:
-
资助金额:$47.45万
-
财政年份:1999
-
负责人:BRUCE E BLOUGH
-
依托单位:
Development of Potential Treatment Medications for Drug Abuse
-
批准号:7654884
-
项目类别:
-
资助金额:$47.76万
-
财政年份:1999
-
负责人:BRUCE E BLOUGH
-
依托单位:
Potential Treatment Medications for Drug Abuse
-
批准号:7060959
-
项目类别:
-
资助金额:$42.38万
-
财政年份:1999
-
负责人:BRUCE E BLOUGH
-
依托单位:
Potential Treatment Medications for Drug Abuse
-
批准号:6680600
-
项目类别:
-
资助金额:$42.14万
-
财政年份:1999
-
负责人:BRUCE E BLOUGH
-
依托单位:
Potential Treatment Medications for Drug Abuse
-
批准号:7229518
-
项目类别:
-
资助金额:$41.57万
-
财政年份:1999
-
负责人:BRUCE E BLOUGH
-
依托单位:
POTENTIAL TREATMENT MEDICATIONS FOR DRUG ABUSE
-
批准号:6038948
-
项目类别:
-
资助金额:$19.95万
-
财政年份:1999
-
负责人:BRUCE E BLOUGH
-
依托单位:
POTENTIAL TREATMENT MEDICATIONS FOR DRUG ABUSE
-
批准号:6175448
-
项目类别:
-
资助金额:$20.55万
-
财政年份:1999
-
负责人:BRUCE E BLOUGH
-
依托单位:
POTENTIAL TREATMENT MEDICATIONS FOR DRUG ABUSE
-
批准号:6378971
-
项目类别:
-
资助金额:$21.17万
-
财政年份:1999
-
负责人:BRUCE E BLOUGH
-
依托单位:
Development of Potential Treatment Medications for Drug Abuse
-
批准号:8253789
-
项目类别:
-
资助金额:$44.85万
-
财政年份:1999
-
负责人:BRUCE E BLOUGH
-
依托单位:
Development of Potential Treatment Medications for Drug Abuse
-
批准号:8049625
-
项目类别:
-
资助金额:$44.87万
-
财政年份:1999
-
负责人:BRUCE E BLOUGH
-
依托单位:
Potential Treatment Medications for Drug Abuse
-
批准号:6785450
-
项目类别:
-
资助金额:$41.32万
-
财政年份:1999
-
负责人:BRUCE E BLOUGH
-
依托单位:
国内基金
海外基金
Agonist-GPR119-Gs复合物的结构生物学研究
-
批准号:32000851
-
项目类别:青年科学基金项目
-
资助金额:24.0万元
-
批准年份:2020
-
负责人:乔安娜
-
依托单位: