In the locust's lobula giant movement detector neural pathways, four categories of inhibition, i.e., global inhibition, self-inhibition, lateral inhibition, and feed-forward inhibition, have been functionally explored in the context of looming perception. However, their combined influence on shaping selectivity to looming motion remains unclear. Driven by recent physiological advancements, this paper offers new insights into the roles of these inhibitory mechanisms at multiple levels and scales in simulations, refining the specific selectivity for responding only to objects approaching the eyes while remaining unresponsive to other forms of movement. Within a feed-forward, multi-layer neural network framework, global inhibition, lateral inhibition, self-inhibition, and feed-forward inhibition are integrated. Global inhibition acts as an immediate feedback mechanism, normalising light intensities delivered by ommatidia, particularly addressing low-contrast looming. Self-inhibition, modelled numerically for the first time, suppresses translational motion. Lateral inhibition is formed by delayed local excitation spreading across a larger area. Notably, self-inhibition and lateral inhibition are sequential in time and are combined through feed-forward inhibition, which indicates the angular size subtended by moving objects. Together, these inhibitory processes attenuate motion-induced excitation at multiple levels and scales. This research suggests that self-inhibition may act earlier than lateral inhibition to rapidly reduce excitation in situ, thereby suppressing translational motion, and global inhibition can modulate excitation on a finer scale, enhancing selectivity in higher contrast range.

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