Suppr超能文献

速激肽受体3与酒精和可卡因依赖有关。

The tachykinin receptor 3 is associated with alcohol and cocaine dependence.

作者信息

Foroud Tatiana, Wetherill Leah Flury, Kramer John, Tischfield Jay A, Nurnberger John I, Schuckit Marc A, Xuei Xiaoling, Edenberg Howard J

机构信息

Indiana University School of Medicine, Indianapolis, Indiana 46202-3002, USA.

出版信息

Alcohol Clin Exp Res. 2008 Jun;32(6):1023-30. doi: 10.1111/j.1530-0277.2008.00663.x. Epub 2008 Apr 15.

Abstract

BACKGROUND

A broad region on chromosome 4q was previously linked to the phenotype of alcohol dependence in the Collaborative Study on the Genetics of Alcoholism sample. A strong positional candidate gene was identified within this region: tachykinin receptor 3 gene (TACR3), which encodes tachykinin receptor 3 (NK3R), the receptor for the tachykinin 3 (neurokinin B) peptide. Pharmacological studies have provided evidence that the administration of NK3R agonists attenuates the intake of alcohol and NK3R can also mediate the acute and chronic behavioral effects of cocaine.

METHODS

Thirty SNPs were genotyped throughout TACR3. Family based association analysis was performed in 219 European American families to detect an association with alcohol dependence. Subsequent analyses were performed to evaluate the evidence of association with other definitions of alcohol dependence as well as cocaine dependence.

RESULTS

Seven of the 9 SNPs in the 3' region of TACR3 provided significant evidence of association with alcohol dependence (p <or= 0.05). Further analyses suggest that the evidence of association is strongest among those subjects with more severe alcohol dependence (defined by ICD-10) and those with co-morbid cocaine dependence. Haplotype analyses further strengthen the evidence of association in the 3' region of the gene.

CONCLUSIONS

These results indicate that sequence variations in TACR3 contribute to the variation in more severe alcohol dependent individuals and those who are also cocaine dependent.

摘要

背景

在酒精中毒遗传学合作研究样本中,4号染色体长臂上的一个广泛区域先前被认为与酒精依赖的表型有关。在该区域内鉴定出一个强有力的位置候选基因:速激肽受体3基因(TACR3),它编码速激肽受体3(NK3R),即速激肽3(神经激肽B)肽的受体。药理学研究已提供证据表明,给予NK3R激动剂可减少酒精摄入,且NK3R还可介导可卡因的急性和慢性行为效应。

方法

对整个TACR3基因的30个单核苷酸多态性(SNP)进行基因分型。在219个欧美家庭中进行基于家系的关联分析,以检测与酒精依赖的关联。随后进行分析,以评估与酒精依赖的其他定义以及可卡因依赖的关联证据。

结果

TACR3基因3'区域的9个SNP中的7个提供了与酒精依赖相关的显著证据(p≤0.05)。进一步分析表明,在酒精依赖更严重(根据国际疾病分类第10版定义)以及同时患有可卡因依赖的受试者中,关联证据最强。单倍型分析进一步强化了该基因3'区域的关联证据。

结论

这些结果表明,TACR3基因的序列变异导致了更严重酒精依赖个体以及同时患有可卡因依赖个体的变异。

相似文献

1
The tachykinin receptor 3 is associated with alcohol and cocaine dependence.
Alcohol Clin Exp Res. 2008 Jun;32(6):1023-30. doi: 10.1111/j.1530-0277.2008.00663.x. Epub 2008 Apr 15.
2
Neuropeptide Y receptor genes are associated with alcohol dependence, alcohol withdrawal phenotypes, and cocaine dependence.
Alcohol Clin Exp Res. 2008 Dec;32(12):2031-40. doi: 10.1111/j.1530-0277.2008.00790.x. Epub 2008 Sep 25.
3
Genetic variation in the CHRNA5 gene affects mRNA levels and is associated with risk for alcohol dependence.
Mol Psychiatry. 2009 May;14(5):501-10. doi: 10.1038/mp.2008.42. Epub 2008 Apr 15.
6
Association of the PDYN gene with alcohol dependence and the propensity to drink in negative emotional states.
Int J Neuropsychopharmacol. 2013 Jun;16(5):975-85. doi: 10.1017/S1461145712001137. Epub 2012 Oct 29.
9
Rare missense variants in CHRNB3 and CHRNA3 are associated with risk of alcohol and cocaine dependence.
Hum Mol Genet. 2014 Feb 1;23(3):810-9. doi: 10.1093/hmg/ddt463. Epub 2013 Sep 20.
10
An association study of tachykinin receptor 3 gene with schizophrenia in the Japanese population.
Neuroreport. 2008 Mar 5;19(4):471-3. doi: 10.1097/WNR.0b013e3282f600b4.

引用本文的文献

1
Evolutionary conserved peptide and glycoprotein hormone-like neuroendocrine systems in C. elegans.
Mol Cell Endocrinol. 2024 Apr 15;584:112162. doi: 10.1016/j.mce.2024.112162. Epub 2024 Jan 28.
2
The collaborative study on the genetics of alcoholism: Genetics.
Genes Brain Behav. 2023 Oct;22(5):e12856. doi: 10.1111/gbb.12856. Epub 2023 Jun 30.
4
Arc Regulates Transcription of Genes for Plasticity, Excitability and Alzheimer's Disease.
Biomedicines. 2022 Aug 11;10(8):1946. doi: 10.3390/biomedicines10081946.
5
Neuropeptidergic regulation of compulsive ethanol seeking in C. elegans.
Sci Rep. 2022 Feb 2;12(1):1804. doi: 10.1038/s41598-022-05256-1.
6
Identification of a sex-stratified genetic algorithm for opioid addiction risk.
Pharmacogenomics J. 2021 Jun;21(3):326-335. doi: 10.1038/s41397-021-00212-0. Epub 2021 Feb 15.
7
Neurokinin receptors in drug and alcohol addiction.
Brain Res. 2020 May 1;1734:146729. doi: 10.1016/j.brainres.2020.146729. Epub 2020 Feb 15.
9
Prenatal Exposure to Methamphetamine: Up-Regulation of Brain Receptor Genes.
Front Neurosci. 2019 Aug 1;13:771. doi: 10.3389/fnins.2019.00771. eCollection 2019.
10
Neural and psychological characteristics of college students with alcoholic parents differ depending on current alcohol use.
Prog Neuropsychopharmacol Biol Psychiatry. 2018 Feb 2;81:284-296. doi: 10.1016/j.pnpbp.2017.09.010. Epub 2017 Sep 20.

本文引用的文献

2
Association of alcohol craving with alpha-synuclein (SNCA).
Alcohol Clin Exp Res. 2007 Apr;31(4):537-45. doi: 10.1111/j.1530-0277.2007.00337.x.
4
5
The tachykinin NK3 receptor antagonist SR142801 blocks the behavioral effects of cocaine in marmoset monkeys.
Eur J Pharmacol. 2006 May 1;536(3):269-78. doi: 10.1016/j.ejphar.2006.03.010. Epub 2006 Mar 10.
6
Association of alcohol dehydrogenase genes with alcohol dependence: a comprehensive analysis.
Hum Mol Genet. 2006 May 1;15(9):1539-49. doi: 10.1093/hmg/ddl073. Epub 2006 Mar 28.
7
Confirmation of association of the GABRA2 gene with alcohol dependence by subtype-specific analysis.
Psychiatr Genet. 2006 Feb;16(1):9-17. doi: 10.1097/01.ypg.0000185027.89816.d9.
8
Efficiency and power in genetic association studies.
Nat Genet. 2005 Nov;37(11):1217-23. doi: 10.1038/ng1669. Epub 2005 Oct 23.
10
New challenges in the study of the mammalian tachykinins.
Peptides. 2005 Aug;26(8):1356-68. doi: 10.1016/j.peptides.2005.03.030. Epub 2005 Apr 20.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验