Resumen
Reduction of nicotine content in tobacco products is a regulatory control strategy intended to decrease smoking dependence, and is hypothesized to produce gradual reductions of nicotine intake. Rats were initially trained to self-administer 0.06 mg/kg/infusion nicotine (Phase 1), which was followed by a threshold procedure to determine nicotine demand via a behavioral economics (BE) paradigm (Phase 2). Rats then either self-administered the training dose (high dose group), or were switched to a low dose of nicotine (0.001 mg/kg/infusion; low dose group) in Phase 3. Both groups then underwent a second threshold procedure and demand curves were re-determined (Phase 4). In Phase 5, responding for nicotine was extinguished over the course of 21 sessions. Cue-induced reinstatement was then evaluated (Phase 6). Rats in the low dose group maintained a steady amount of infusions, and thus, did not compensate for nicotine reduction. Rats in the low dose group also showed similar demand elasticity and nicotine seeking (Phase 6) compared to the high dose group, indicating that nicotine reduction did not decrease nicotine demand or seeking. Further, both groups displayed resistance to extinction, indicating that nicotine reduction did not facilitate extinction learning. These results suggest that although compensation of intake does not occur, decreasing the dose of nicotine does not alter nicotine reinforcement value or relapse vulnerability. Further, these results indicate persistence of nicotine-motivated behavior after self-administration of a low nicotine dose. Translationally, these results suggest that alternative strategies may be needed to achieve positive smoking cessation outcomes.
| Idioma original | English |
|---|---|
| Número de artículo | 108020 |
| Publicación | Drug and Alcohol Dependence |
| Volumen | 212 |
| DOI | |
| Estado | Published - jul 1 2020 |
Nota bibliográfica
Publisher Copyright:© 2020
Financiación
The authors thank Mark Namba, Vincent Carfagno, Paula Overby, Hanaa Ulangkaya, Andrea Sekito, Laura Vesala, Amanda Ariola, Jason Hguyen, Jackie Moreno, Armani Del Franco and Joseph McCallum for their technical assistance with self-administration and intravenous jugular catheter surgery. Additionally, the authors thank Tanya Gupta, MFA, for her assistance with the Bayesian analysis. This work was supported by the National Institutes of Health Grants DA036569, DA044479, and DA045881 (to CDG) and the Arizona Alzheimer's Consortium (to CDG). The authors report no conflicts of interest. The authors thank Mark Namba, Vincent Carfagno, Paula Overby, Hanaa Ulangkaya, Andrea Sekito, Laura Vesala, Amanda Ariola, Jason Hguyen, Jackie Moreno, Armani Del Franco and Joseph McCallum for their technical assistance with self-administration and intravenous jugular catheter surgery. Additionally, the authors thank Tanya Gupta, MFA, for her assistance with the Bayesian analysis. This work was supported by the National Institutes of Health Grants DA036569 , DA044479 , and DA045881 (to CDG) and the Arizona Alzheimer’s Consortium (to CDG). The authors report no conflicts of interest.
| Financiadores | Número del financiador |
|---|---|
| Arizona Alzheimer's Consortium | |
| National Institutes of Health (NIH) | DA036569, DA045881 |
| National Institute on Drug Abuse | R21DA044479 |
| Banner Alzheimer’s Institute and Arizona Alzheimer’s Consortium |
ODS de las Naciones Unidas
Este resultado contribuye a los siguientes Objetivos de Desarrollo Sostenible
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Good health and well being
ASJC Scopus subject areas
- Toxicology
- Pharmacology
- Psychiatry and Mental health
- Pharmacology (medical)
Huella
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