Rat (Wistar) |
Female and male |
22 weeks unrestricted access |
Food restriction increased wheel running, while increased access to food decreased wheel running |
Finger (1951)
|
Rat (Sprague–Dawley) |
Male |
10 min per day |
Rats lever-pressed for access to running wheels |
Kagan and Berkun (1954)
|
Rat (albino from Holtzman Research) |
Male |
Up to 14 days, unrestricted access |
Food was ignored upon presentation of wheel, resulting in self-starvation |
Routtenberg and Kuznesof (1967)
|
Rat (Sprague–Dawley) |
Male |
Varied |
Rats lever-pressed for access to running wheels |
Collier and Hirsch (1971)
|
Rat (Long Evans) |
Male |
2 h per day, 5 days/week for 8 weeks |
Increased brain catecholamine levels related to running, weight loss, and hyperphagia |
de Castro and Duncan (1985)
|
Rat (Sprague–Dawley) |
Female and male |
Varied |
Food deprivation increased lever pressing for access to a running wheel; acute wheel exposure during food deprivation decreased responding for food reward |
Pierce et al. (1986)
|
Rat (Sprague–Dawley) |
Male |
Up to 70% of starting body-weight, or 20 days unrestricted access |
Activity-induced anorexia (and death) was reduced by propylene glycol but not ethanol |
Spigelman et al. (1991)
|
Rat (Long–Evans) |
Female |
Varied |
Rats lever-pressed for access to running wheels |
Iversen (1993)
|
Rat (Sprague–Dawley) |
Male |
Alternating access |
Wheel access decreased oral amphetamine intake |
Kanarek et al. (1995)
|
Rat (Wistar) |
Male |
Varied |
Rats lever-pressed for access to running wheels; running behavior was dependent on duration of opportunity to run |
Belke (1997)
|
Rat (Lewis and Fischer) |
|
30 days, unrestricted Access |
Addiction-prone rats exhibited higher levels of running compared to non-addiction-prone rats |
Werme et al. (1999)
|
Rat (Sprague–Dawley) |
Male |
2-h controlled access on alternating days, over ~2 weeks |
Wheel running induced conditioned place preference, which was reversible by the opioid antagonist naloxone |
Lett et al. (2001)
|
Rat (Sprague–Dawley) |
Male |
2-h controlled access on alternating days, over ~2 weeks |
Wheel running blocked the ability of morphine to produce conditioned place preference |
Lett et al. (2002)
|
Rat (Long Evans) |
Female |
8 weeks unrestricted access |
Wheel running decreased breakpoint on a progressive ratio schedule for cocaine self-administration |
Cosgrove et al. (2002)
|
Rat (Sprague–Dawley) |
Male |
24 days, 2-h per day or unrestricted access |
Escalated running with unrestricted access |
Lattanzio and Eikelboom (2003)
|
Rat (Wistar) |
Male |
Varied |
Rats developed conditioned place preference to context associated with wheel |
Belke and Wagner (2005)
|
Rat (Sprague–Dawley) |
Male |
25 days |
Wheel access suppressed sucrose and food intake |
Satvat and Eikelboom (2006)
|
Rat (Long Evans) |
Female |
8 weeks unrestricted access |
Wheel running increased conditioned place preference to cocaine |
Smith et al. (2008)
|
Rat (Fischer 344) |
Male |
2 and 6 weeks |
Increased conditioned place preference after 6 weeks of wheel running |
Greenwood et al. (2011)
|
Mice (BALB-c) |
Male |
90 min |
Wheel running induced c-Fos in nucleus accumbens (core) |
Vargas-Perez et al. (2003)
|
Mice (C57BL/6J) |
Female |
Varied |
Wheel running increased in the absence of ethanol |
Ozburn et al. (2008)
|
Mice (BALB-c-type and D2L receptor-deficient) |
Male |
30 min/day for 20 days |
Wheel running engages dopamine and opioid reward systems; motivational state affects ability of wheel to engage these systems |
Vargas-Perez et al. (2004), Vargas-Perez et al. (2008)
|
Syrian hamster |
Male |
Up to 35 days |
Amount of wheel running was positively correlated with self-administration of testosterone, which has reinforcing properties |
Wood (2002)
|