Synaptic Modulation in Drosophila After Exposure to Prolonged Light

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Begin with freshly eclosed Drosophila melanogaster flies in a collection vial containing nutrients.

Place these vials in a transparent acrylic rack.

Position the rack inside an incubator equipped with an internal light source at a precise distance to provide uniform and desired light exposure.

Rear the flies under these light conditions for a prolonged period.

In Drosophila eyes, the photoreceptor cells act as sensory neurons, detecting the light and converting it into electrical signals.

These signals travel along the axon and reach the synaptic terminals, where they connect with other neurons.

These terminals possess the Bruchpilot proteins, which facilitate the fusion of neurotransmitter-carrying vesicles to the cell membrane, allowing neurotransmitter release.

The released neurotransmitters bind to the receptors on the postsynaptic neurons to transmit the electrical signal, leading to synaptic activity.

With continuous exposure to light, the Bruchpilot protein level decreases, reducing neurotransmitter release and resulting in the plasticity or modulation of synaptic activity.

For this experiment, collect the flies into normal vials within six hours of occlusion. Load the collection vials into a transparent acrylic rack. In a small incubator, set to 25 degrees Celsius, position the rack at a precise distance from an LED panel where the light exposure is at an average of 1,000 lux. Then, rear flies for one to three days, using one of the following conditions, either constant darkness, 12 hours of light followed by 12 hours of darkness, or constant light.

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Last updated: 27 June 2026