Chemosensory Cue Conditioning With Stimulants in a Caenorhabditis Elegans Animal Model of Addiction

被引:23
作者
Musselman, Heather N. [1 ]
Neal-Beliveau, Bethany [1 ]
Nass, Richard [2 ]
Engleman, Eric A. [3 ]
机构
[1] Indiana Univ Purdue Univ, Dept Psychol, Indianapolis, IN 46202 USA
[2] Indiana Univ Sch Med, Dept Pharmacol & Toxicol, Indianapolis, IN 46202 USA
[3] Indiana Univ Sch Med, Dept Psychiat, Indianapolis, IN 46202 USA
关键词
Caenorhabditis elegans; chemosensory cue conditioning; stimulants; addiction; drug reward; C-ELEGANS; MOLECULAR-MECHANISMS; PLACE PREFERENCE; NEURONS; CHEMOTAXIS; PLASTICITY; DOPAMINE; SEROTONIN; ETHANOL; BEHAVIORS;
D O I
10.1037/a0028303
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
The underlying molecular mechanisms of drug abuse and addiction behaviors are poorly understood. Caenorhabditis elegans (C. elegans) provide a simple, whole animal model with conserved molecular pathways well suited for studying the foundations of complex diseases. Historically, chemotaxis has been a measure used to examine sensory approach and avoidance behavior in worms. Chemotaxis can be modulated by previous experience, and cue-dependent conditioned learning has been demonstrated in C. elegans, but such conditioning with drugs of abuse has not been reported. Here we show that pairing a distinctive salt cue with a drug (cocaine or methamphetamine) results in a concentration-dependent change in preference for the cue that was paired with the drug during conditioning. Further, we demonstrate that pairing of either drug with a distinctive food type can also increase preference for the drug-paired food in the absence of the drug. Dopamine-deficient mutants did not develop drug-paired, cue-conditioned responses. The findings suggest that, like vertebrates, C. elegans display a conditioned preference for environments containing cues previously associated with drugs of abuse, and this response is dependent on dopamine neurotransmission. This model provides a new and powerful method to study the genetic and molecular mechanisms that mediate drug preference.
引用
收藏
页码:445 / 456
页数:12
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