ETHANOL AND PHOSPHORYLATION OF THE 5-HT3 RECEPTOR
ETHANOL AND PHOSPHORYLATION OF THE 5-HT3 RECEPTOR
批准号:
2894093
负责人:
TINA K MACHU
金额:
$10.87万
依托单位国家:
美国
项目类别:
财政年份:
1995
资助国家:
美国
项目状态:
已结题
起止时间:
1995-05-01 至 2000-04-30
中文摘要
点击翻译按钮获取中文摘要
英文摘要
The function of the 5-hydroxytryptamine3 (5-HT3) receptor is enhanced by
alcohols, but the mechanism(s) of action remains unknown. In addition,
regulation of the 5-HT3 receptor by post-translational modification events,
such as phosphorylation, has not been well characterized. To date, one
subunit of the 5-HT3 receptor has been cloned, and it possesses multiple
consensus sequence sites for protein kinase dependent phosphorylaiton.
Previous work with other ligand-gated ion channels, namely the GABA A and
NMDA receptors, has suggested that protein kinase C may be involved in
mediating these receptors' responsiveness to ethanol. Therefore, it is
reasonable to speculate that kinases may modulate the responsiveness of the
5-HT 3 receptor to alcohols. In the present proposal, functional studies
of the 5-HT3 receptor will be performed using Xenopus laevis oocytes as an
expression system. Two-electrode voltage clamp electrophysiological
recordings of expressed wild-type or mutagenized 5-HT3 receptors will be
made. First, the sensitivity of the 5-HT3 receptor to alcohols will be
measured. Next, the ability of serine/threonine kinases to alter 5-HT3
receptor function will be addressed. To determine which amino acid(s) are
substrates for these kinases, candidate serines in consensus sequences for
protein kinase dependent phosphorylation in the receptor will be mutated to
nonphosphorylatable residues. Kinases which alter 5-HT3 receptor function
will be examined for their ability to change the sensitivity of this
receptor to alcohols. The alternative hypothesis, that tonic kinase
activity underlies the 5-HT3 receptor's sensitivity to alcohols, will be
tested by measuring alcohol modulation of 5-HT3 receptors with mutagenized
consensus sequence sites for phosphorylation. Thus, the ultimate goal of
the proposal is to determine if phosphorylation events alter the function
of the 5-HT3 receptor and its modulation by alcohols. A better
understanding of the regulation of the 5-HT3 receptor is important, given
that this receptor may be involved in mediating the rewarding actions of
drugs of abuse such as ethanol.
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Selective actions of a detergent on ligand-gated ion channels expressed in Xenopus oocytes.
去垢剂对非洲爪蟾卵母细胞中表达的配体门控离子通道的选择性作用。
DOI:
--
发表时间:
1998
期刊:
The Journal of pharmacology and experimental therapeutics.
影响因子:
--
作者:
[Machu,TK, Mihic,SJ, Dildy-Mayfield,JE]
通讯作者:
Dildy-Mayfield,JE
Characterization of interaction of 3,4,5-trimethoxybenzoic acid 8-(diethylamino)octyl ester with Torpedo californica nicotinic acetylcholine receptor and 5-hydroxytryptamine3 receptor.
3,4,5-三甲氧基苯甲酸 8-(二乙氨基)辛酯与加州鱼雷烟碱乙酰胆碱受体和 5-羟色胺 3 受体相互作用的表征。
DOI:
--
发表时间:
1999
期刊:
The Journal of pharmacology and experimental therapeutics.
影响因子:
--
作者:
[Sun,H, McCardy,EA, Machu,TK, Blanton,MP]
通讯作者:
Blanton,MP
Bicuculline antagonizes 5-HT(3A) and alpha2 glycine receptors expressed in Xenopus oocytes.
Bicuculline 拮抗非洲爪蟾卵母细胞中表达的 5-HT(3A) 和 α2 甘氨酸受体。
DOI:
10.1016/s0014-2999(00)00083-2
发表时间:
2000
期刊:
European journal of pharmacology
影响因子:
5
作者:
[Sun,H, Machu,TK]
通讯作者:
Machu,TK
Mutation of putative phosphorylation sites in the 5-hydroxytryptamine3 receptor does not eliminate its modulation by ethanol.
5-羟色胺3受体中假定的磷酸化位点的突变并不能消除乙醇对其的调节。
DOI:
--
发表时间:
1999
期刊:
Alcoholism, clinical and experimental research.
影响因子:
--
作者:
[Machu,TK, Coultrap,SJ, Waugh,MD, Hamilton,ME]
通讯作者:
Hamilton,ME
Ligand Binding Domains in the 5-HT3 Receptor
-
批准号:6822013
-
项目类别:
-
资助金额:$23.37万
-
财政年份:2002
-
负责人:TINA K MACHU
-
依托单位:
Ligand Binding Domains in the 5-HT3 Receptor
-
批准号:6685216
-
项目类别:
-
资助金额:$25.6万
-
财政年份:2002
-
负责人:TINA K MACHU
-
依托单位:
Ligand Binding Domains in the 5-HT3 Receptor
-
批准号:6571504
-
项目类别:
-
资助金额:$26.29万
-
财政年份:2002
-
负责人:TINA K MACHU
-
依托单位:
Ligand Binding Domains in the 5-HT3 Receptor
-
批准号:6984758
-
项目类别:
-
资助金额:$22.71万
-
财政年份:2002
-
负责人:TINA K MACHU
-
依托单位:
ALCOHOL MODULATORY SITES IN THE 5HT3A RECEPTOR
-
批准号:6867385
-
项目类别:
-
资助金额:$28.4万
-
财政年份:2001
-
负责人:TINA K MACHU
-
依托单位:
ALCOHOL MODULATORY SITES IN THE 5HT3A RECEPTOR
-
批准号:6509376
-
项目类别:
-
资助金额:$27.01万
-
财政年份:2001
-
负责人:TINA K MACHU
-
依托单位:
ALCOHOL MODULATORY SITES IN THE 5HT3A RECEPTOR
-
批准号:6284859
-
项目类别:
-
资助金额:$27.68万
-
财政年份:2001
-
负责人:TINA K MACHU
-
依托单位:
ALCOHOL MODULATORY SITES IN THE 5HT3A RECEPTOR
-
批准号:6629671
-
项目类别:
-
资助金额:$7.53万
-
财政年份:2001
-
负责人:TINA K MACHU
-
依托单位:
ALCOHOL MODULATORY SITES IN THE 5HT3A RECEPTOR
-
批准号:6806405
-
项目类别:
-
资助金额:$19.48万
-
财政年份:2001
-
负责人:TINA K MACHU
-
依托单位:
ALCOHOL MODULATORY SITES IN THE 5HT3A RECEPTOR
-
批准号:6710013
-
项目类别:
-
资助金额:$28.4万
-
财政年份:2001
-
负责人:TINA K MACHU
-
依托单位:
ETHANOL AND PHOSPHORYLATION OF THE 5-HT3 RECEPTOR
-
批准号:2047214
-
项目类别:
-
资助金额:$10.45万
-
财政年份:1995
-
负责人:TINA K MACHU
-
依托单位:
ETHANOL AND PHOSPHORYLATION OF THE 5-HT3 RECEPTOR
-
批准号:2699676
-
项目类别:
-
资助金额:$10.47万
-
财政年份:1995
-
负责人:TINA K MACHU
-
依托单位:
ETHANOL AND PHOSPHORYLATION OF THE 5-HT3 RECEPTOR
-
批准号:2047215
-
项目类别:
-
资助金额:$9.71万
-
财政年份:1995
-
负责人:TINA K MACHU
-
依托单位:
ETHANOL AND PHOSPHORYLATION OF THE 5-HT3 RECEPTOR
-
批准号:2413263
-
项目类别:
-
资助金额:$10.1万
-
财政年份:1995
-
负责人:TINA K MACHU
-
依托单位:
ETHANOL AND PHOSPHORYLATION OF THE GABAA RECEPTOR
-
批准号:3028466
-
项目类别:
-
资助金额:$2.86万
-
财政年份:1992
-
负责人:TINA K MACHU
-
依托单位:
ETHANOL AND PHOSPHORYLATION OF THE GABAA RECEPTOR
-
批准号:3028465
-
项目类别:
-
资助金额:$2.27万
-
财政年份:1991
-
负责人:TINA K MACHU
-
依托单位:
海外基金