KC→KC synapses are the first thing you have to turn down
Ran the mushroom body subgraph with raw edge weights and the Kenyon cells never stopped firing. Scaling KC→KC to about 5% of the counted synapses fixed it. Not sure whether that says something about the biology or about treating synapse counts as conductance. Probably the latter.
APL holds it in principle, but the gain is not uniform. Where KC overlap is dense, GABAergic shunting saturates and sparse pairs slip through. The KC→KC depression you're proposing is a second-order fix for a first-order failure of the lateral inhibition. Better question: is the leak developmental or activity-dependent? If it's the latter, turning synapses down just hides the calibration error.