Abstract

Temperature affects the conductances and kinetics of the ionic channels that underlie neuronal activity. Each membrane conductance has a different characteristic temperature sensitivity, which raises the question of how neurons and neuronal circuits can operate robustly over wide temperature ranges. To address this, we employed computational models of the pyloric network of crabs and lobsters. We produced multiple different models that exhibit a triphasic pyloric rhythm over a range of temperatures and explored the dynamics of their currents and how they change with temperature. Temperature can produce smooth changes in the relative contributions of the currents to neural activity so that neurons and networks undergo graceful transitions in the mechanisms that give rise to their activity patterns. Moreover, responses of the models to deletions of a current can be different at high and low temperatures, indicating that even a well-defined genetic or pharmacological manipulation may produce qualitatively distinct effects depending on the temperature.

Highlights

  • Biological systems depend on many interacting nonlinear processes that together produce complex outputs

  • Temperature influences all biological processes, to a greater or lesser degree. This poses an inherent difficulty for neuronal signaling: if the currents involved in neuronal and network dynamics are differentially temperature-dependent a system that is well-tuned to work at one temperature may not function at a different temperature (Caplan et al, 2014; O’Leary and Marder, 2016; Tang et al, 2010; Tang et al, 2012)

  • The triphasic pyloric rhythm is produced by the periodic sequential activation of the pyloric dilator (PD) neurons, which are electrically coupled to the anterior burster (AB) neuron forming a pacemaking kernel, the lateral pyloric (LP) neuron and five to eight pyloric (PY) neurons

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Summary

Introduction

Biological systems depend on many interacting nonlinear processes that together produce complex outputs. Neuronal activity requires the coordinated activation and inactivation of many inward and outward currents. Temperature influences all biological processes, to a greater or lesser degree. This poses an inherent difficulty for neuronal signaling: if the currents involved in neuronal and network dynamics are differentially temperature-dependent a system that is well-tuned to work at one temperature may not function at a different temperature (Caplan et al, 2014; O’Leary and Marder, 2016; Tang et al, 2010; Tang et al, 2012). Many ectothermic animals have neurons and circuits that function well over an extended temperature range (Robertson and Money, 2012). It becomes important to understand how and to what extent this can occur

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