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Updated: Dec 25, 2025

Targeting Olfactory Bulb Neurons Using Combined In Vivo Electroporation and Gal4-Based Enhancer Trap Zebrafish Lines
Published on: August 15, 2011
In vivo odorant input induces spike timing-dependent plasticity of glutamatergic synapses in developing zebrafish
Bin Hu1, Jing-Jing Wang2, Chen Jin3
1Research Center for Biochemistry and Molecular Biology, Jiangsu Key Laboratory of Brain Disease Bioinformation, Xuzhou Medical University, Jiangsu, 221004, China; Department of Neurobiology, School of Basic Medical Sciences, Nanjing Medical University, Jiangsu, 211166, China.
Abstract:
Early odorant experience and neural activity are essential for refining developing neural connections. Although neural activity-induced synaptic plasticity is one of the most important cellular mechanisms underlying the refinement of neural circuits, whether and how natural odorant experience induces long-term plasticity in the olfactory bulb remains unknown. In vivo perforated whole-cell recording from mitral cells (MCs) in larval zebrafish showed that odorant experience induced persistent modification of developing olfactory bulb circuits via spike timing-dependent plasticity (STDP). Repetitive odorant stimuli paired with postsynaptic spiking in a critical time window (pre-post, positive timing) resulted in persistent enhancement of glutamatergic inputs from olfactory sensory neurons, but long-term depression within the opposite time window (post-pre, negative timing). Furthermore, spike-timing-dependent potentiation (tLTP) in STDP induced by repetitive odorant stimulation had similar cellular processes to those of electrical stimulation-induced tLTP. Finally, odorant input induced STDP required the activation of postsynaptic N-methyl-d-aspartate receptors (NMDARs). Thus, the NMDAR is likely to be a postsynaptic coincidence detector responsible for the sensory experience-dependent refinement of developing connections.

