Identification of Functional nAChR Variants in Mice

小鼠功能性 nAChR 变异体的鉴定

基本信息

  • 批准号:
    6763143
  • 负责人:
  • 金额:
    $ 20.8万
  • 依托单位:
  • 依托单位国家:
    美国
  • 项目类别:
  • 财政年份:
    2001
  • 资助国家:
    美国
  • 起止时间:
    2001-08-01 至 2007-01-31
  • 项目状态:
    已结题

项目摘要

DESCRIPTION (Provided by applicant): It is the long-term objective of this proposal to identify inbred mouse strains that express functionally distinct isoforms of the neuronal nicotinic receptor subunits alpha3, alpha4, alpha6, alpha7, and beta2. These subunits were chosen based on their potential roles in mediating the dependence-causing actions of nicotine. Identification of functionally distinct nicotinic receptor isoforms will be initiated by mutation analysis of the exons of the genes that encode these receptor subunits. Approximately forty inbred mouse strains of distinct genetic origins will be evaluated in the mutation screen. Once the mutation screen identifies nicotinic receptor subunit isoforms in mice with amnino acid differences, the appropriate cDNAs will be generated. Subsequently, the variant nicotinic receptor subunit isoforms will be evaluated in vitro for their pharmacological and functional properties. These experiments will lead to the establishment of a catalogue of mouse strains with known variations in nicotinic receptor subtype functional properties. This catalogue of mouse strains will serve as an important additional resource to evaluate the role of the various nicotinic receptor subunits in modulating the dependence-causing actions of nicotine. It has been estimated that 25 percent of all premature deaths in the United States are due to tobacco use. Despite the widespread knowledge of the health risks of smoking, approximately 25 percent of adults in the United States continue to smoke. Among smokers, nearly 80 percent say that they would like to quit although less than 5 percent successfully do so. It is well established that nicotine is the major dependence-causing agent in tobacco and that the initial actions of nicotine in the brain are mediated by nicotinic acetyicholine receptors. However, which nicotinic receptor subtypes mediate the dependence-causing actions of nicotine is poorly understood. To date, only modest success, at best, has been achieved in resolving this issue. The mouse strain nicotinic receptor "function" catalogue that will result from the studies outlined in this proposal will add a valuable resource for addressing this issue. By elucidating which nicotinic receptor subtypes are critical for the establishment of nicotine dependence, more effective pharmacological strategies for smoking cessation may be developed.
描述(由申请人提供):

项目成果

期刊论文数量(7)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
Naturally occurring genetic variability in the nicotinic acetylcholine receptor alpha4 and alpha7 subunit genes and phenotypic diversity in humans and mice.
烟碱乙酰胆碱受体 α4 和 α7 亚基基因自然发生的遗传变异以及人类和小鼠的表型多样性。
{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

数据更新时间:{{ journalArticles.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ monograph.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ sciAawards.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ conferencePapers.updateTime }}

{{ item.title }}
  • 作者:
    {{ item.author }}

数据更新时间:{{ patent.updateTime }}

JERRY A STITZEL其他文献

JERRY A STITZEL的其他文献

{{ item.title }}
{{ item.translation_title }}
  • DOI:
    {{ item.doi }}
  • 发表时间:
    {{ item.publish_year }}
  • 期刊:
  • 影响因子:
    {{ item.factor }}
  • 作者:
    {{ item.authors }}
  • 通讯作者:
    {{ item.author }}

{{ truncateString('JERRY A STITZEL', 18)}}的其他基金

Role of Chrna5 genotype on outcomes of developmental nicotine exposure
Chrna5 基因型对发育期尼古丁暴露结果的作用
  • 批准号:
    8950029
  • 财政年份:
    2015
  • 资助金额:
    $ 20.8万
  • 项目类别:
Role of Chrna5 genotype on outcomes of developmental nicotine exposure
Chrna5 基因型对发育期尼古丁暴露结果的作用
  • 批准号:
    9086317
  • 财政年份:
    2015
  • 资助金额:
    $ 20.8万
  • 项目类别:
Function of the CHRNA5 D398N SNP: implications for addiction and lung cancer ris
CHRNA5 D398N SNP 的功能:对成瘾和肺癌的影响
  • 批准号:
    7707167
  • 财政年份:
    2009
  • 资助金额:
    $ 20.8万
  • 项目类别:
Circadian Variations in Nicotine Sensitivity in Mice
小鼠尼古丁敏感性的昼夜节律变化
  • 批准号:
    7477295
  • 财政年份:
    2007
  • 资助金额:
    $ 20.8万
  • 项目类别:
Circadian Variations in Nicotine Sensitivity in Mice
小鼠尼古丁敏感性的昼夜节律变化
  • 批准号:
    7305834
  • 财政年份:
    2007
  • 资助金额:
    $ 20.8万
  • 项目类别:
Research Training - Genetics of Substance Abuse
研究培训 - 药物滥用的遗传学
  • 批准号:
    10618400
  • 财政年份:
    2004
  • 资助金额:
    $ 20.8万
  • 项目类别:
Research Training - Genetics of Substance Abuse
研究培训 - 药物滥用的遗传学
  • 批准号:
    10381506
  • 财政年份:
    2004
  • 资助金额:
    $ 20.8万
  • 项目类别:
Identification of Functional nAChR Variants in Mice
小鼠功能性 nAChR 变异体的鉴定
  • 批准号:
    6946535
  • 财政年份:
    2001
  • 资助金额:
    $ 20.8万
  • 项目类别:
ROLE OF CHRNA5 IN MODULATING SENSITIVITY TO NICOTINE IN MICE
CHRNA5 在调节小鼠尼古丁敏感性中的作用
  • 批准号:
    7874635
  • 财政年份:
    2001
  • 资助金额:
    $ 20.8万
  • 项目类别:
Identification of Functional nAChR Variants in Mice
小鼠功能性 nAChR 变异体的鉴定
  • 批准号:
    6365366
  • 财政年份:
    2001
  • 资助金额:
    $ 20.8万
  • 项目类别:

相似海外基金

Pharmacogenomic study for optimizing dosage of antipsychotic drugs based on individual genetic polymorphism
基于个体遗传多态性优化抗精神病药物剂量的药物基因组学研究
  • 批准号:
    21K07490
  • 财政年份:
    2021
  • 资助金额:
    $ 20.8万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Association between the clinical effect of DPP-4 inhibitors and the genetic polymorphism of BDNF gene
DPP-4抑制剂临床疗效与BDNF基因多态性的关系
  • 批准号:
    20K07855
  • 财政年份:
    2020
  • 资助金额:
    $ 20.8万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
An association between serum uric acid and genetic polymorphism among pre- and post-menoposal women
绝经前后女性血清尿酸与遗传多态性的相关性
  • 批准号:
    20K10522
  • 财政年份:
    2020
  • 资助金额:
    $ 20.8万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Atypical odontalgia and genetic polymorphism of pain sensitivity
非典型牙痛与疼痛敏感性基因多态性
  • 批准号:
    20K10044
  • 财政年份:
    2020
  • 资助金额:
    $ 20.8万
  • 项目类别:
    Grant-in-Aid for Scientific Research (C)
Association between non-alcoholic fatty liver diseases related genetic polymorphism, lipid metabolism, and atherosclerosis
非酒精性脂肪肝相关基因多态性、脂质代谢和动脉粥样硬化的关联
  • 批准号:
    20K17155
  • 财政年份:
    2020
  • 资助金额:
    $ 20.8万
  • 项目类别:
    Grant-in-Aid for Early-Career Scientists
Characterizing the Impact of Genetic Polymorphism on Fentanyl Efficacy and Tolerance in Pediatrics
表征遗传多态性对儿科芬太尼疗效和耐受性的影响
  • 批准号:
    10246970
  • 财政年份:
    2019
  • 资助金额:
    $ 20.8万
  • 项目类别:
Impacts of environmental chemical substance exposure to pregnant woman on sexual differentiation of the child and its modification by genetic polymorphism.
孕妇环境化学物质暴露对胎儿性别分化的影响及其遗传多态性的改变。
  • 批准号:
    19K18601
  • 财政年份:
    2019
  • 资助金额:
    $ 20.8万
  • 项目类别:
    Grant-in-Aid for Early-Career Scientists
Characterizing the Impact of Genetic Polymorphism on Fentanyl Efficacy and Tolerance in Pediatrics
表征遗传多态性对儿科芬太尼疗效和耐受性的影响
  • 批准号:
    10475268
  • 财政年份:
    2019
  • 资助金额:
    $ 20.8万
  • 项目类别:
Characterizing the Impact of Genetic Polymorphism on Fentanyl Efficacy and Tolerance in Pediatrics
表征遗传多态性对儿科芬太尼疗效和耐受性的影响
  • 批准号:
    10015364
  • 财政年份:
    2019
  • 资助金额:
    $ 20.8万
  • 项目类别:
Verification of novel methods to identify migraines using genetic polymorphism analysis and spectral analysis of heart rate variability
使用遗传多态性分析和心率变异性频谱分析验证识别偏头痛的新方法
  • 批准号:
    18K15413
  • 财政年份:
    2018
  • 资助金额:
    $ 20.8万
  • 项目类别:
    Grant-in-Aid for Early-Career Scientists
{{ showInfoDetail.title }}

作者:{{ showInfoDetail.author }}

知道了