This dissertation explores the role of top-down projections in shaping perceptual learning within the olfactory system. The olfactory bulb integrates bottom-up sensory inputs with top-down modulatory signals, creating dynamic representations essential for adaptive perception. Experimental findings presented here demonstrate that cortical feedback from regions such as the piriform cortex drives context-dependent structural and functional plasticity in local olfactory bulb neurons, particularly adult-born granule cells. Moreover, this research identifies distinct neuromodulatory mechanisms through which cholinergic projections selectively enhance sensory representations of behaviorally relevant odors, effectively increasing the signal-to-noise ratio in a context-dependent and modality-specific manner. Parallel studies reveal that noradrenergic projections similarly modulate olfactory processing in a context-dependent manner but differ in temporal dynamics. By synthesizing these findings, the dissertation proposes an integrated model wherein converging top-down pathways—guided by context, attention, and experience—collectively refine olfactory perception. Together, this work provides novel insights into the neural underpinnings of perceptual learning, highlighting not only potential therapeutic targets for disorders associated with perception dysfunction but also biological principles of top-down regulation and experience-dependent plasticity that could inspire advances in artificial intelligence architectures capable of more adaptive and context-sensitive learning.