课题基金 / 基金详情

DOPAMINE TRANSPORTER I--REGULATION BY PHOSPHORYLATION

DOPAMINE TRANSPORTER I--REGULATION BY PHOSPHORYLATION
多巴胺转运蛋白 I——磷酸化调节
批准号:
2571612
负责人:
G R UHL
金额:
$0.0万
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

项目摘要

项目成果

G R UHL的其他基金

相似基金

相关文献

中文摘要
翻译
多巴胺转运体(DAT)已被确定为主要的大脑
英文摘要
The dopamine transporter (DAT) has been identified as the principal brain receptor site best correlated with the rewarding and euphoric properties of cocaine. Euphoric responses to rapid administration of cocaine can be much more prominent than those that follow slower rates of administration. In previous FYs, investigators in this Branch have found that activators of protein kinase C (PKC) modulate dopamine transport in transiently-expressing COS cells (Eur. J. Pharmacol., 268, 115-119). In this FY, we have identified the DAT as a phosphoprotein with evidence for rapid phosphorylation/dephosphorylation cycling in expressing cell lines and in brain synaptosomes. Phosphorylation displays many parallels to functional reductions in DAT Vmax values identified in parallel experiments. These data increase evidnece that PKC activation enhances levels of DAT phosphorylation, and makes phosphorylation an increasingly-strong candidate mechanism for rapid adaptations in dopaminergic systems relevant to cocaine-induced euphoria.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
GENETIC APPROACHES TO CHARACTERIZING DRUG RESPONSES AND VULNERABILITIES
DOPAMINE TRANSPORTER-- CELLULAR AND SUBCELLULAR LOCALIZATIONS
GENES RELATED TO DRUG ABUSE--REGULATION OF OPIOID PEPTIDE GENES
DOPAMINERGIC LESIONS AND SUBJECTIVE EFFECTS OF METHYLPHENIDATE
海外基金