TY - JOUR
T1 - Interactions between modafinil and cocaine during the induction of conditioned place preference and locomotor sensitization in mice
T2 - Implications for addiction
AU - Shuman, Tristan
AU - Cai, Denise J.
AU - Sage, Jennifer R.
AU - Anagnostaras, Stephan G.
N1 - Funding Information:
We thank Stephanie Carmack for helpful comments on an earlier version of this manuscript. We also thank Joseph Cheong, and Nicole Garces for excellent technical assistance. This work was supported by grant DA020041 from the National Institute on Drug Abuse and a Hellman Fellowship (SGA) and the UCSD Interdisciplinary Collaboratory Grant (TS, DJC). The authors have no conflicts of interest and did not receive funding from the makers of modafinil.
PY - 2012/12/1
Y1 - 2012/12/1
N2 - Modafinil is a wake-promoting drug effective at enhancing alertness and attention with a variety of approved and off-label applications. The mechanism of modafinil is not well understood but initial studies indicated a limited abuse potential. A number of recent publications, however, have shown that modafinil can be rewarding under certain conditions. The present study assessed the reinforcing properties of modafinil using conditioned place preference and locomotor sensitization in mice. Experiment 1 examined a high dose of modafinil (75 mg/kg) as well as its interactions with cocaine (15 mg/kg). Cocaine alone and modafinil co-administered with cocaine induced sensitization of locomotor activity; modafinil alone showed little or no locomotor sensitization. Animals given modafinil alone, cocaine alone, and modafinil plus cocaine exhibited a strong and roughly equivalent place preference. When tested for sensitization using a low challenge dose of modafinil, cross-sensitization was observed in all cocaine-pretreated mice. Experiment 2 examined a low dose of modafinil that is similar to the dose administered to humans and has been shown to produce cognitive enhancements in mice. Low dose modafinil (0.75 mg/kg) did not produce conditioned place preference or locomotor sensitization. Together, these results suggest that modafinil has the potential to produce reward, particularly in cocaine addicts, and should be used with caution. However, the typical low dose administered likely moderates these effects and may account for lack of addiction seen in humans.
AB - Modafinil is a wake-promoting drug effective at enhancing alertness and attention with a variety of approved and off-label applications. The mechanism of modafinil is not well understood but initial studies indicated a limited abuse potential. A number of recent publications, however, have shown that modafinil can be rewarding under certain conditions. The present study assessed the reinforcing properties of modafinil using conditioned place preference and locomotor sensitization in mice. Experiment 1 examined a high dose of modafinil (75 mg/kg) as well as its interactions with cocaine (15 mg/kg). Cocaine alone and modafinil co-administered with cocaine induced sensitization of locomotor activity; modafinil alone showed little or no locomotor sensitization. Animals given modafinil alone, cocaine alone, and modafinil plus cocaine exhibited a strong and roughly equivalent place preference. When tested for sensitization using a low challenge dose of modafinil, cross-sensitization was observed in all cocaine-pretreated mice. Experiment 2 examined a low dose of modafinil that is similar to the dose administered to humans and has been shown to produce cognitive enhancements in mice. Low dose modafinil (0.75 mg/kg) did not produce conditioned place preference or locomotor sensitization. Together, these results suggest that modafinil has the potential to produce reward, particularly in cocaine addicts, and should be used with caution. However, the typical low dose administered likely moderates these effects and may account for lack of addiction seen in humans.
KW - Activity
KW - Behavior
KW - Dopamine
KW - Provigil
KW - Stimulant
UR - http://www.scopus.com/inward/record.url?scp=84865321195&partnerID=8YFLogxK
U2 - 10.1016/j.bbr.2012.07.039
DO - 10.1016/j.bbr.2012.07.039
M3 - Article
C2 - 22963989
AN - SCOPUS:84865321195
SN - 0166-4328
VL - 235
SP - 105
EP - 112
JO - Behavioural Brain Research
JF - Behavioural Brain Research
IS - 2
ER -