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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.
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页码:445 / 456
页数:12
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