Abstract

One of the key approaches for studying neural network function is the simultaneous measurement of the activity of many neurons. Voltage-sensitive dyes (VSDs) simultaneously report the membrane potential of multiple neurons, but often have pharmacological and phototoxic effects on neuronal cells. Yet, to study the homeostatic processes that regulate neural network function long-term recordings of neuronal activities are required. This study aims to test the suitability of the VSDs RH795 and Di-4-ANEPPS for optically recording pattern generating neurons in the stomatogastric nervous system of crustaceans with an emphasis on long-term recordings of the pyloric central pattern generator. We demonstrate that both dyes stain pyloric neurons and determined an optimal concentration and light intensity for optical imaging. Although both dyes provided sufficient signal-to-noise ratio for measuring membrane potentials, Di-4-ANEPPS displayed a higher signal quality indicating an advantage of this dye over RH795 when small neuronal signals need to be recorded. For Di-4-ANEPPS, higher dye concentrations resulted in faster and brighter staining. Signal quality, however, only depended on excitation light strength, but not on dye concentration. RH795 showed weak and slowly developing phototoxic effects on the pyloric motor pattern as well as slow bleaching of the staining and is thus the better choice for long-term experiments. Low concentrations and low excitation intensities can be used as, in contrast to Di-4-ANEPPS, the signal-to-noise ratio was independent of excitation light strength. In summary, RH795 and Di-4-ANEPPS are suitable for optical imaging in the stomatogastric nervous system of crustaceans. They allow simultaneous recording of the membrane potential of multiple neurons with high signal quality. While Di-4-ANEPPS is better suited for short-term experiments that require high signal quality, RH795 is a better candidate for long-term experiments since it has only minor effects on the motor pattern.

Highlights

  • One of the challenges of modern Neuroscience is the simultaneous manipulation and activity measurement of many neurons to uncover how neural circuits and networks deliver their integral functionality [1,2,3,4,5,6,7,8,9]

  • Photos were taken with three different picture exposure times: Since Di-4-ANEPPS typically resulted in a stronger staining than RH795 (Fig. 1C), we chose longer exposure times for RH795 (100, 200 and 300 ms) than for Di-4-ANEPPS (50, 100 and 200 ms)

  • Duration of dye application influenced staining intensity significantly (Two-way ANOVA, p,0.0001, N = 3), indicating that the staining intensity increased in a time-dependent manner for both dyes. This increase was faster for Di-4-ANEPPS than for RH795: After 40 minutes, the Di-4-ANEPPS staining reached 95.563.9% of its maximum value while RH795 staining reached only 47.1621.1% of its maximum intensity (t-test; p,0.05; N = 3)

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Summary

Introduction

One of the challenges of modern Neuroscience is the simultaneous manipulation and activity measurement of many neurons to uncover how neural circuits and networks deliver their integral functionality [1,2,3,4,5,6,7,8,9]. Classical methods such as extracellular field potential recordings or single cell electrophysiology are, insufficient to fulfill the requirements for characterizing more than a few neurons. Dyes need to be evaluated separately for each system regarding their ability to stain neurons, their S/N, their bleaching kinetics and regarding their toxic and phototoxic effects

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