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APPETITE, OBESITY, DIGESTION, AND METABOLISM
Department of Biology, Neurobiology and Behavior Program, and Center for Behavioral Neuroscience, Georgia State University, Atlanta, Georgia
Submitted 20 December 2004 ; accepted in final form 7 February 2005
Fasting has widespread physiological and behavioral effects such as increases in arcuate nucleus neuropeptide Y (NPY) gene expression in rodents, including Siberian hamsters. Fasting also stimulates foraging and food hoarding (appetitive ingestive behaviors) by Siberian hamsters but does relatively little to change food intake (consummatory ingestive behavior). Therefore, we tested the effects of third ventricular NPY Y1 ([Pro34]NPY) or Y5 ([D-Trp34]NPY) receptor agonists on these ingestive behaviors using a wheel running-based food delivery system coupled with simulated burrow housing. Siberian hamsters had 1) no running wheel access and free food, 2) running wheel access and free food, or 3) foraging requirements (10 or 50 revolutions/pellet). NPY (1.76 nmol) stimulated food intake only during the first 4 h postinjection (
2001,000%) and mostly in hamsters with a foraging requirement. The Y1 receptor agonist markedly increased food hoarding (2501,000%), increased foraging as well as wheel running per se, and had relatively little effect on food intake (<250%). Unlike NPY, the Y5 agonist significantly increased food intake, especially in foraging animals (
225800%), marginally increased food hoarding (250500%), and stimulated foraging and wheel running 424 h postinjection, with the distribution of earned pellets favoring eating versus hoarding across time. Across treatments, food hoarding predominated early postinjection, whereas food intake tended to do so later. Collectively, NPY stimulated both appetitive and consummatory ingestive behaviors in Siberian hamsters involving Y1/Y5 receptors, with food hoarding and foraging/wheel running (appetitive) more involved with Y1 receptors and food intake (consummatory) with Y5 receptors.
appetitive; consummatory; wheel running; neuropeptide Y; Y1 and Y5 receptors
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