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Nicotine modifies cocaine responding in a concurrent self-administration model
被引:2
|作者:
Dawes, Monica H.
[1
]
Estave, Paige M.
[1
,2
]
Albertson, Steven E.
[1
]
Wallace, Conner W.
[1
]
Holleran, Katherine M.
[1
]
Jones, Sara R.
[1
]
机构:
[1] Wake Forest Univ, Bowman Gray Sch Med, Dept Physiol & Pharmacol, Winston Salem, NC 27101 USA
[2] Wake Forest Univ, Bowman Gray Sch Med, Dept Pediat, Winston Salem, NC 27101 USA
关键词:
Cocaine;
Nicotine;
Self-administration;
Polysubstance use;
PROGRESSIVE RATIO SCHEDULES;
CIGARETTE-SMOKING;
NONCONTINGENT NICOTINE;
SEEKING BEHAVIOR;
DOPAMINE;
REINFORCEMENT;
STIMULI;
HUMANS;
SENSITIZATION;
REINSTATEMENT;
D O I:
10.1016/j.drugalcdep.2023.110960
中图分类号:
R194 [卫生标准、卫生检查、医药管理];
学科分类号:
摘要:
Background: Preclinical models of cocaine use disorder (CUD) have not yielded any FDA-approved pharmacotherapies, potentially due to a focus on cocaine use in isolation, which may not fully translate to real-world drug taking patterns. Cocaine and nicotine are commonly used together, and clinical research suggests that nicotine may increase the potency and reinforcing strength of cocaine. In this study, we sought to determine whether and how the addition of nicotine would alter ongoing intravenous cocaine self-administration and motivation to take cocaine in rats. Methods: Male Sprague-Dawley rats self-administered cocaine alone on a long access, Fixed Ratio one (FR1) schedule, and then switched to a combination of cocaine and nicotine. Finally, rats responded on a Progressive Ratio (PR) schedule for several doses of cocaine alone and in combination with a single dose of nicotine. Results: Under long access conditions, rats co-self-administering cocaine and nicotine responded less and with decreased response rates than for cocaine alone and did not escalate responding. However, under PR conditions that test motivation to take drugs, the dose response curve for the combination was shifted upwards relative to cocaine alone. Conclusions: Together, these results suggest that nicotine may enhance the reinforcing strength of cocaine, increasing PR responding for cocaine across the dose response curve.
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