课题基金 / 基金详情

OPIOID CONTROL MECHANISMS OF SIGNAL TRANSDUCTION

OPIOID CONTROL MECHANISMS OF SIGNAL TRANSDUCTION
阿片类药物的信号传导控制机制
批准号:
6489483
负责人:
Paul L Prather
金额:
$9.81万
依托单位国家:
美国
项目类别:
财政年份:
1998
资助国家:
美国
项目状态:
已结题
起止时间:
1998-01-15 至 2003-12-31

项目摘要

项目成果

Paul L Prather的其他基金

相似基金

相关文献

中文摘要
翻译
点击翻译按钮获取中文摘要
英文摘要
DESCRIPTION (Applicant's Abstract): The long term objective of this project is to determine how activation of mu and delta-opioid receptors leads to distinct intracellular signals. Although mu- and delta-opioid receptors may relay intracellular messages in a similar fashion, a clear distinction in the abuse and dependence producing potential of opioids suggests significant differences are yet to be discovered. For this project, a cellular model has been developed in which cloned mu and delta-opioid receptors in stably transfected GH3 cells interact differently with two intracellular effectors, adenylyl cyclase and Ca++ channels. This unique and important model will be used to identify fundamental differences between mu- and delta-opioid signal transduction cascades. This will be accomplished by the systematic analysis of the interactions between opioid receptors, G proteins and effectors in these unique clones. First, the effect of receptor density on mu- and delta-coupling to effectors will be determined. Second, signal transduction in clones expressing only mu-, only delta, or both mu and delta-opioid receptors will be examined. Third, the association of opioid receptors with G proteins will be determined by purification of agonist-stimulated receptor-G protein complexes. Fourth, the activation of G proteins by opioid receptors will be studied using agonist-induced incorporation of [32P]azidoanilido-GTP into G-alpha subunits. Fifth, the composition of the heterotrimeric G proteins (G-alpha, G-beta- and G-gamma subunits) responsible for coupling mu and delta- receptors to effectors will be confirmed by the use of antisense oligonucleotides targeting specific G protein subunits. Finally, the association of Ca2+ channels with G alpha and/or G-beta,gamma subunits will be assessed after the immunoprecipitation of G protein/Ca2+ channel complexes. Understanding basic differences in the way mu and delta-opioid receptors relay information intracellularly could lead to the development of new methods for the treatment of opioid abuse and pain management.
期刊论文(6)
专著(0)
科研奖励(0)
会议论文
Agonist Activity of the delta-antagonists TIPP and TIPP-psi in cellular models expressing endogenous or transfected delta-opioid receptors.
表达内源性或转染的 δ-阿片受体的细胞模型中 δ-拮抗剂 TIPP 和 TIPP-psi 的激动剂活性。
DOI: --
发表时间: 2001
期刊: The Journal of pharmacology and experimental therapeutics
影响因子: --
作者: [Martin,NA, Terruso,MT, Prather,PL]
通讯作者: Prather,PL
Interaction of co-expressed mu- and delta-opioid receptors in transfected rat pituitary GH(3) cells.
转染的大鼠垂体 GH(3) 细胞中共表达 mu- 和 delta-阿片受体的相互作用。
DOI: 10.1124/mol.59.4.774
发表时间: 2001
期刊: Molecular pharmacology
影响因子: 3.6
作者: [Martin,NA, Prather,PL]
通讯作者: Prather,PL
Training in Systems Pharmacology and Toxicology (T-SPaT)
  • 批准号:
    10714918
  • 项目类别:
  • 资助金额:
    $17.4万
  • 财政年份:
    2023
  • 负责人:
    Paul L Prather
  • 依托单位:
Synthetic Cannabinoid Toxicity: Role of Biotransformation
  • 批准号:
    9520656
  • 项目类别:
  • 资助金额:
    $4.35万
  • 财政年份:
    2016
  • 负责人:
    Paul L Prather
  • 依托单位:
Synthetic Cannabinoid Toxicity: Role of Biotransformation
  • 批准号:
    9914444
  • 项目类别:
  • 资助金额:
    $4.35万
  • 财政年份:
    2016
  • 负责人:
    Paul L Prather
  • 依托单位:
Synthetic Cannabinoid Toxicity: Role of Biotransformation
  • 批准号:
    9037178
  • 项目类别:
  • 资助金额:
    $54.97万
  • 财政年份:
    2016
  • 负责人:
    Paul L Prather
  • 依托单位:
海外基金