Contrasting effects of leptin on food anticipatory and total locomotor activity

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Abstract

Obese, leptin deficient obob mice have profoundly decreased activity and increased food seeking behavior. The decreased activity has been attributed to obesity. In mice, we tested the hypothesis that leptin increases total locomotor activity but inhibits food anticipatory activity. We also sought to determine if leptin induced increases in total locomotor activity are independent of changes in body weight and obesity. We studied obob mice and also created a novel transgenic mouse where leptin is over-expressed in a tetracycline-off system and can be abruptly and non-invasively suppressed by doxycycline within few hours. The studies were performed using two independent behavioral assays: home cage activity (HCA) and running wheel activity (RWA). Systemic administration of leptin (150 ng/hr) to obob mice produced a 122%±30% (mean ± SEM) increase (p≤0.01) in locomotor activity within 2 days In addition, cerebroventricular administration of leptin (5 ng/hr) also produced an early and progressive increase in total locomotor activity beginning on the 1st day (+28±8%; p≤0.05) and increasing to +69±23% on day 3 without a decrease in body weight during this time. The increase in activity was restricted to the dark phase. Conversely, in a tet-off transgenic obob mouse line, acute leptin suppression reduced spontaneous locomotor activity. To further define activities that are leptin regulated, we assayed food anticipatory activity (FAA) and found that it was markedly augmented in obob mice compared to wild type mice (+38±6.7 in obob vs +20±6.3% in wild type at peak; mean ± SEM; p≤0.001) and abolished by leptin. Although melanocortin-3 receptors (MC3R) reportedly mediate FAA, we found augmented FAA and preserved inhibitory effects of leptin on FAA in MC3R-/-obob mice. In summary, this study demonstrates that total activity and FAA are regulated independently by leptin. Leptin, acting in the central nervous system and at physiologic levels, produces early increases in locomotor activity before substantial weight loss. In contrast, leptin suppresses augmented food anticipatory activity in obob mice. © 2011 Ribeiro et al.

Figures

  • Figure 2. Time course of leptin-induced increases in activity. (A) Representative actogram of RWA in an obob mouse before and during leptin (n = 6). The increase in RWA began by the 2nd day of leptin. (B) Summary data comparing the time course of increases in RWA vs decreases in body weight. Leptin caused significant(p#0.01) and substantial (+122%) increases in RWA by day 2. At this time, there was a significant (p,0.001) but small (25%) decrease in body weight. doi:10.1371/journal.pone.0023364.g002
  • Figure 1. Locomotor responses to leptin in obob mice. (A and B) 24 hour running wheel activity (RWA) and home cage activity (HCA) in obob and wild type (WT) mice. ***p#0.001 (A, WT n = 11 and obob n = 12; B, WT = 9 and obob n = 6). (C) Effect of leptin (150 ng/h) on 24 h RWA in obob mice. RWA decreased (*p#0.05) with time and vehicle (PBS) in the obob mice (n = 6 for each group). In contrast, RWA activity increased (***p#0.001) during leptin. (D) Effect of leptin (150 ng/h) on 24 h HCA in WT and obob mice. Leptin increased HCA in obob mice (**p#0.01), but not in WT mice (n = 6 for each group). doi:10.1371/journal.pone.0023364.g001
  • Figure 3. Activity responses to cerebroventricular (ICV) administration of leptin. (A) ICV leptin (5 ng/h) increased HCA during weeks 1 (*p#0.05) and 2 in obob mice. (**p#0.01) (B) Temporal data showing that ICV leptin produced significant (p#0.05) increases in HCA between days 1 and 4 whereas body weight did not decrease significantly during this time (PBS group n = 3; leptin group n = 4). doi:10.1371/journal.pone.0023364.g003
  • Figure 4. Effects of acute leptin suppression on activity in Tetoff hyperleptinemic transgenic obob mice. (A) Strategy followed to obtain transgenic mice chronically over-expressing hleptin on an obob background. LAP-tTa/TRE-hleptin/obob mice are skinny since hleptin is over-produced until doxycycline (DOX) is administered. (B) In Tg obob mice, plasma hleptin levels were suppressed 1, 3, 6, and 13 days after beginning chronic administration DOX in the food at concentrations of 0.1, 0.5, and 2 g/kg. After DOX suppression, hleptin can be turned on again by switching back to regular chow. The ‘‘recovery’’ time necessary to document detectable hleptin in the plasma (1M = 1 month, 2M = 2 months) is a function of the DOX concentration in the food and the duration of the administration as shown after a 13 days of DOX. (C) Administration of DOX to LAP-tTa/ Tre-hleptin/obob at 8 weeks of age was accompanied by an increase in body weight. (D) The top panel compares an 8 week old LAP-tTa/Trehleptin/obob mouse (left) and a littermate obob control (center) before DOX. The bottom panel shows the same mice 5 weeks after beginning DOX. (E–F) Effect of acute leptin suppression on activity in Tg obob mice. (E) After beginning DOX, a steady decrease in HCA is observed in Tg obob mice (n = 5) as shown by linear regression analysis, becoming significant (p#0.05) after 7 days of DOX and continuing through the end of the experiment (p,0.005),(n = 9 for wild type and n = 7 for obob). (F) Leptin suppression also significantly decreased RWA in Tg obob (n = 5) although at a slower rate becoming significant at day 20 (p,0.05). (n = 11 for wild type and n = 12 for obob mice.) doi:10.1371/journal.pone.0023364.g004
  • Figure 5. Comparison of the effects of leptin vs pair feeding on RWA in obob mice. (A) As shown previously, leptin (150 ng/h) increased RWA (***p#0.001). Pair fed obob mice (not treated with leptin) also displayed striking increases in activity (***p#0.001). However, the temporal pattern of activity during pair feeding was strikingly different from that seen during leptin (n = 6 each group). The leptin-induced increase in activity occurred entirely during the dark phase (B), whereas the increased activity during pair feeding occurred substantially during the light phase and peaked during the early dark phase time at which food was provided (C). doi:10.1371/journal.pone.0023364.g005
  • Figure 7. Role of melanocortin-3 receptors (MC3R) in augmented FAA in obob mice. (A) Leptin deficient, obob mice with deletion of melanocortin-3 receptors (MC3R2/2 obob, n = 12) had increased FAA (p#0.05) compared with that in obob mice (n = 5). (B) FAA in MC3R2/2 obob mice (n = 7) treated with leptin (150 ng/h) vs FAA in control mice treated with PBS (n = 6). Leptin abolished (p#0.01) FAA in the MC3R2/2obob mice. doi:10.1371/journal.pone.0023364.g007
  • Figure 6. Food anticipatory activity (FAA) is augmented in obob mice and suppressed by leptin. (A–B) FAA measured as HCA in obob and wild type (WT) mice (n = 6 each group) treated with vehicle (PBS) or leptin (150 ng/h). FAA was markedly augmented (p#0.001) in obob mice compared with WT mice. Leptin virtually abolished (p#0.001) FAA in obob mice, but did not attenuate FAA in WT mice. (C) FAA measured as RWA was pronounced in obob mice and abolished by leptin administration (150 ng/h). (n = 6 each group). doi:10.1371/journal.pone.0023364.g006

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Ribeiro, A. C., Ceccarini, G., Dupré, C., Friedman, J. M., Pfaff, D. W., & Mark, A. L. (2011). Contrasting effects of leptin on food anticipatory and total locomotor activity. PLoS ONE, 6(8). https://doi.org/10.1371/journal.pone.0023364

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