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Chem Senses. 2009 Jan;34(1):27-35. doi: 10.1093/chemse/bjn049. Epub 2008 Sep 4.
2
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Genetic variance contributes to ingestive processes: a survey of eleven inbred mouse strains for fat (Intralipid) intake.遗传变异对摄食过程有影响:对11种近交系小鼠品系脂肪(英脱利匹特)摄入量的调查。
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Inbred mouse strain differences in alcohol and nicotine addiction-related phenotypes from adolescence to adulthood.近交系小鼠从青春期到成年期在酒精和尼古丁成瘾相关表型上的差异。
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Back-translating GWAS findings to animal models reveals a role for Hgfac and Slc39a8 in alcohol and nicotine consumption.将 GWAS 研究结果反向翻译到动物模型中,揭示了 Hgfac 和 Slc39a8 在酒精和尼古丁消费中的作用。
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Sex Differences in the Nicotinic Acetylcholine Receptor System of Rodents: Impacts on Nicotine and Alcohol Reward Behaviors.啮齿动物烟碱型乙酰胆碱受体系统中的性别差异:对尼古丁和酒精奖赏行为的影响。
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Sensory Effects of Nicotine and Tobacco.尼古丁和烟草的感官效应。
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Flavor-specific enhancement of electronic cigarette liquid consumption and preference in mice.特定口味增强电子烟液的消费和小鼠的偏好。
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Neuropharmacology. 2019 Oct;157:107669. doi: 10.1016/j.neuropharm.2019.107669. Epub 2019 Jun 18.
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Genetic correlations between nicotine reinforcement-related behaviors and propensity toward high or low alcohol preference in two replicate mouse lines.两个重复小鼠品系中尼古丁强化相关行为与高或低酒精偏好倾向之间的遗传相关性。
Genes Brain Behav. 2019 Mar;18(3):e12515. doi: 10.1111/gbb.12515. Epub 2018 Sep 10.
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Pharmacol Biochem Behav. 2016 Sep;148:28-37. doi: 10.1016/j.pbb.2016.05.010. Epub 2016 May 27.
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本文引用的文献

1
Allelic variation of the Tas1r3 taste receptor gene selectively affects taste responses to sweeteners: evidence from 129.B6-Tas1r3 congenic mice.味觉受体基因Tas1r3的等位基因变异选择性地影响对甜味剂的味觉反应:来自129.B6-Tas1r3同源基因小鼠的证据。
Physiol Genomics. 2007 Dec 19;32(1):82-94. doi: 10.1152/physiolgenomics.00161.2007. Epub 2007 Oct 2.
2
Behavioral genetics and taste.行为遗传学与味觉。
BMC Neurosci. 2007 Sep 18;8 Suppl 3(Suppl 3):S3. doi: 10.1186/1471-2202-8-S3-S3.
3
Taste solution preferences of C57BL/6J and 129X1/SvJ mice: influence of age, sex, and diet.C57BL/6J和129X1/SvJ小鼠的味觉溶液偏好:年龄、性别和饮食的影响
Chem Senses. 2007 Sep;32(7):655-71. doi: 10.1093/chemse/bjm034. Epub 2007 Jun 12.
4
Nicotine improves cognitive deficits of dopamine transporter knockout mice without long-term tolerance.尼古丁可改善多巴胺转运体基因敲除小鼠的认知缺陷,且无长期耐受性。
Neuropsychopharmacology. 2007 Dec;32(12):2465-78. doi: 10.1038/sj.npp.1301385. Epub 2007 Mar 21.
5
C57BL/6J and DBA/2J mice vary in lick rate and ingestive microstructure.C57BL/6J和DBA/2J小鼠在舔舐速率和摄食微观结构上存在差异。
Genes Brain Behav. 2007 Oct;6(7):619-27. doi: 10.1111/j.1601-183X.2006.00293.x. Epub 2006 Dec 21.
6
Chromosomal loci that influence oral nicotine consumption in C57BL/6J x C3H/HeJ F2 intercross mice.影响C57BL/6J×C3H/HeJ F2杂交小鼠口服尼古丁摄入量的染色体位点。
Genes Brain Behav. 2007 Jul;6(5):401-10. doi: 10.1111/j.1601-183X.2006.00266.x. Epub 2006 Sep 8.
7
Monoamine oxidase A knockout mice exhibit impaired nicotine preference but normal responses to novel stimuli.单胺氧化酶A基因敲除小鼠表现出对尼古丁的偏好受损,但对新刺激的反应正常。
Hum Mol Genet. 2006 Sep 15;15(18):2721-31. doi: 10.1093/hmg/ddl206. Epub 2006 Aug 7.
8
Effects of chronic nicotine administration and its withdrawal on striatal FosB/DeltaFosB and c-Fos expression in rats and mice.长期给予尼古丁及其戒断对大鼠和小鼠纹状体FosB/DeltaFosB及c-Fos表达的影响。
Neuropharmacology. 2006 Jul;51(1):44-51. doi: 10.1016/j.neuropharm.2006.02.014. Epub 2006 Apr 24.
9
Individual differences in novelty-seeking behavior but not in anxiety response to a new environment can predict nicotine consumption in adolescent C57BL/6 mice.在新奇寻求行为方面存在个体差异,但对新环境的焦虑反应不存在个体差异,这可以预测青春期C57BL/6小鼠的尼古丁摄入量。
Behav Brain Res. 2006 Feb 15;167(1):175-82. doi: 10.1016/j.bbr.2005.09.003. Epub 2005 Oct 7.
10
Initial licking responses of mice to sweeteners: effects of tas1r3 polymorphisms.小鼠对甜味剂的初始舔舐反应:味觉受体1型成员3(Tas1r3)基因多态性的影响
Chem Senses. 2005 Sep;30(7):601-14. doi: 10.1093/chemse/bji054. Epub 2005 Aug 31.

近交系小鼠尼古丁摄入量的差异与口面部感觉能力无关。

Variation in nicotine consumption in inbred mice is not linked to orosensory ability.

作者信息

Glatt A Rebecca, Denton Kelley, Boughter John D

机构信息

Department of Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, TN 38163, USA.

出版信息

Chem Senses. 2009 Jan;34(1):27-35. doi: 10.1093/chemse/bjn049. Epub 2008 Sep 4.

DOI:10.1093/chemse/bjn049
PMID:18775876
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2639451/
Abstract

Genetic studies of nicotine addiction in mice have utilized the oral self-administration model. However, it is unclear if strain differences in nicotine consumption are influenced by variation in bitter taste sensitivity. We measured both nicotine consumption and nicotine brief-access licking behavior in several commonly used inbred strains of mice that were previously shown to differ in nicotine consumption. A/J (A), C57BL/6J (B6), and DBA/2J (D2) mice were given a 2-bottle choice test with a single concentration of nicotine (75 microg/ml; nicotine vs. water). Mice of these strains were also tested with a range of nicotine concentrations (5-400 microg/ml) using a brief-access test, which measures orosensory response and minimizes postingestive effects. Although B6 mice consumed more 75-microg/ml nicotine than A or D2 mice in the 2-bottle test, these strains did not differ in level of aversion to nicotine when tested with the brief-access procedure. Strain differences in orosensory response to nicotine were not found; yet, differences emerged during the 2-bottle tests. This study provides evidence that variation in intake level of nicotine is likely not due to differences in taste or trigeminal sensitivity but likely due to postingestive factors.

摘要

对小鼠尼古丁成瘾的遗传学研究采用了口服自我给药模型。然而,尚不清楚尼古丁摄入量的品系差异是否受苦味敏感性变化的影响。我们测量了几种常用近交系小鼠的尼古丁摄入量和尼古丁短暂接触舔舐行为,这些品系先前已被证明在尼古丁摄入量上存在差异。给A/J(A)、C57BL/6J(B6)和DBA/2J(D2)小鼠进行单浓度尼古丁(75微克/毫升;尼古丁与水)的双瓶选择试验。还使用短暂接触试验对这些品系的小鼠进行一系列尼古丁浓度(5 - 400微克/毫升)的测试,该试验测量口腔感觉反应并将摄入后效应降至最低。尽管在双瓶试验中B6小鼠比A或D2小鼠摄入更多75微克/毫升的尼古丁,但在用短暂接触程序测试时,这些品系对尼古丁的厌恶程度并无差异。未发现品系对尼古丁的口腔感觉反应存在差异;然而,在双瓶试验中出现了差异。这项研究提供了证据,表明尼古丁摄入水平的变化可能不是由于味觉或三叉神经敏感性的差异,而是可能由于摄入后因素。