Project 1 - Chemistry & In Vitro Studies of Chinese Herbal Remedies
Project 1 - Chemistry & In Vitro Studies of Chinese Herbal Remedies
批准号:
7667980
负责人:
DAVID Yue-Wei LEE
金额:
$39.31万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
--
资助国家:
美国
项目状态:
未结题
起止时间:
至
关键词:
AbstinenceAdenylate CyclaseAdverse effectsAffinityAgonistAlcoholsAttenuatedBehavioralBindingChemicalsChemistryChinaChinese HerbsClinical ProtocolsClinical ResearchCocaineCocaine DependenceDataDiscriminationDopamineDopamine D1 ReceptorDopamine D2 ReceptorDrug abuseEatingEconomicsFingerprintFractionationGTP gamma SHerbal MedicineHigh Pressure Liquid ChromatographyIn VitroLaboratoriesMediatingMediationMedicalMedicineMethodsModificationMolecularMotor ActivityNarcotic AntagonistsNucleus AccumbensOpioidOpioid ReceptorPersonal SatisfactionPharmaceutical PreparationsPharmacotherapyPrincipal InvestigatorRattusRelapseResearch Project GrantsScreening procedureSedation procedureSelf AdministrationStandards of Weights and MeasuresSubstance abuse problemSystemTestingTherapeuticUnited StatesUnited States Food and Drug AdministrationWithdrawalclinically significantcravingextracellularin vivoin vivo Modelkappa opioid receptorsnociceptinnociceptin receptornorbinaltorphimineopium dependencepreventprogramsreceptor functionremediationresearch clinical testingsocialtool
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Alcohol and drug abuse pose serious medical, social, and economic problems in the United States and around the world. A great deal of effort has been directed toward developing effective therapies. Unfortunately, in the last 40 years, only three medications with limited efficacy have been approved by the U.S. Food and Drug Administration. The complexity of cocaine dependence and the lack of effective remediation, especially for relapse, which is often
precipitated by withdrawal and/or intense craving even after prolonged abstinence, poses a serious therapeutic challenge. One possible mechanism of action underlying the modification of cocaine's behavioral effects by herbal remedies is through kappa opioid receptors. Because many herbal remedies that were originally developed during the 18th and 19th centuries in China were targeted at opium addiction, chemical fractions that will be screened in Project 1
for kappa receptor activity may be found to have kappa agonist or antagonist actions. It is well established that some abuse related effects of cocaine can be modified through kappa opioid receptors, and these effects have been related to kappa opioid modulation of dopamine levels in the nucleus accumbens. For example, in rats, kappa opioid agonists have been shown to attenuate cocaine-stimulated locomotor activity, cocaine discrimination and cocaine self-administration. Moreover, kappa opioid agonists have also been shown to attenuate cocaine-induced increases in extracellular levels of dopamine in the nucleus accumbens. In addition, recent studies also indicate that kappa antagonists may be useful in preventing relapse to opioid and cocaine use. Therefore, a consortium effort focusing on alternative pharmacotherapies would have important clinical significance, especially in preventing relapse.
We selected two Chinese herbal medicines, YGT (NPI-025) and XJL (NPI-028), for this project because of their proven efficacy in the treatment of substance abuse in China and encouraging scientific data obtained in recent years in our laboratories. The specific aims of this Research Project 1 are (1) to procure and standardize these two herbal medicines by HPLC fingerprinting; (2) to provide purified components by fractionation as internal standards and as molecular
tools to elucidate the mechanism of action; (3) to distribute these standardized herbal medicines and fractions to Research Projects 1, 2, and 4 for in vitro, in vivo, and clinical evaluations respectively; and (4) to conduct in vitro screening of Chinese herbal remedies and fractions for their affinity at the mu, delta and kappa opioid receptors, the nociceptin / orphanin FQ (N/OFQ) receptor and D1 and D2 dopamine receptors and for their receptor functions by [35S]GTPgammaS binding and adenylyl cyclase activity. The herbal medicines or fractions that show positive results in vitro will be examined in Project 2 using various in vivo models. Only those with the best in vivo activity will be subiect to clinical evaluation in Project 4.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Mechanism of Action of L THP as an Alternative Therapy for Cocaine Addiction
-
批准号:8369115
-
项目类别:
-
资助金额:$45.72万
-
财政年份:2012
-
负责人:DAVID Yue-Wei LEE
-
依托单位:
Mechanism of Action of L THP as an Alternative Therapy for Cocaine Addiction
-
批准号:8858518
-
项目类别:
-
资助金额:$41.59万
-
财政年份:2012
-
负责人:DAVID Yue-Wei LEE
-
依托单位:
Mechanism of Action of L THP as an Alternative Therapy for Cocaine Addiction
-
批准号:8686757
-
项目类别:
-
资助金额:$42.56万
-
财政年份:2012
-
负责人:DAVID Yue-Wei LEE
-
依托单位:
Mechanism of Action of L THP as an Alternative Therapy for Cocaine Addiction
-
批准号:8537821
-
项目类别:
-
资助金额:$42.1万
-
财政年份:2012
-
负责人:DAVID Yue-Wei LEE
-
依托单位:
Pharmacology and Metabolism of Salvia divinorum
-
批准号:7615517
-
项目类别:
-
资助金额:$27.68万
-
财政年份:2006
-
负责人:DAVID Yue-Wei LEE
-
依托单位:
Pharmacology and Metabolism of Salvia divinorum
-
批准号:7808820
-
项目类别:
-
资助金额:$27.41万
-
财政年份:2006
-
负责人:DAVID Yue-Wei LEE
-
依托单位:
Pharmacology and Metabolism of Salvia divinorum
-
批准号:7407483
-
项目类别:
-
资助金额:$27.68万
-
财政年份:2006
-
负责人:DAVID Yue-Wei LEE
-
依托单位:
Pharmacology and Metabolism of Salvia divinorum
-
批准号:7148534
-
项目类别:
-
资助金额:$21.72万
-
财政年份:2006
-
负责人:DAVID Yue-Wei LEE
-
依托单位:
Pharmacology and Metabolism of Salvia divinorum
-
批准号:7287300
-
项目类别:
-
资助金额:$28.47万
-
财政年份:2006
-
负责人:DAVID Yue-Wei LEE
-
依托单位:
Alternative Therapies for Alcohol and Drug Abuse
-
批准号:6861518
-
项目类别:
-
资助金额:$121.4万
-
财政年份:2004
-
负责人:DAVID Yue-Wei LEE
-
依托单位:
Administrative Core
-
批准号:6883599
-
项目类别:
-
资助金额:$14.88万
-
财政年份:2004
-
负责人:DAVID Yue-Wei LEE
-
依托单位:
Alternative Therapies for Alcohol and Drug Abuse
-
批准号:6952268
-
项目类别:
-
资助金额:$113.84万
-
财政年份:2004
-
负责人:DAVID Yue-Wei LEE
-
依托单位:
Alternative Therapies for Alcohol and Drug Abuse
-
批准号:7115879
-
项目类别:
-
资助金额:$114.29万
-
财政年份:2004
-
负责人:DAVID Yue-Wei LEE
-
依托单位:
Alternative Therapies for Alcohol and Drug Abuse
-
批准号:7237832
-
项目类别:
-
资助金额:$117.2万
-
财政年份:2004
-
负责人:DAVID Yue-Wei LEE
-
依托单位:
Project 1 - Chemistry & In Vitro Studies of Chinese Herbal Remedies
-
批准号:6883593
-
项目类别:
-
资助金额:$29.42万
-
财政年份:2004
-
负责人:DAVID Yue-Wei LEE
-
依托单位:
Naturally Occurring Agent for Alcohol Liver Diseases
-
批准号:6703343
-
项目类别:
-
资助金额:$22.27万
-
财政年份:2003
-
负责人:DAVID Yue-Wei LEE
-
依托单位:
Development of Standardized Milk Thistle Product
-
批准号:6399638
-
项目类别:
-
资助金额:$22.12万
-
财政年份:2001
-
负责人:DAVID Yue-Wei LEE
-
依托单位:
Development of Standardized Milk Thistle Product
-
批准号:6949210
-
项目类别:
-
资助金额:$28.8万
-
财政年份:2001
-
负责人:DAVID Yue-Wei LEE
-
依托单位:
Development of Standardized Milk Thistle Product
-
批准号:6682780
-
项目类别:
-
资助金额:$59.27万
-
财政年份:2001
-
负责人:DAVID Yue-Wei LEE
-
依托单位:
Development of Standardized Milk Thistle Product
-
批准号:6603554
-
项目类别:
-
资助金额:$69.83万
-
财政年份:2001
-
负责人:DAVID Yue-Wei LEE
-
依托单位:
海外基金