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Ranner, T.

Publications and source records attributed to Ranner, T..

2 recordsLinked to original sources

Intrinsic and Extrinsic Modulation of C. elegans Locomotion

Animal locomotion describes the coordinated self-propelled movement of a body, subject to the combined effects of internal muscle forcing and external forces. Here we use an integrated neuromechanical computational model to study the combined effects of neural modulation, mechanical modulation and modulation of the external environments on undulatory forward locomotion in the nematode C. elegans. In particular we use a proprioceptively driven neural control circuit to consider the effects of proprioception, body elasticity and environmental drag on the waveform, frequency and speed of undulations. We find qualitative differences in the frequency-wavelength relationship obtained under extrinsic modulation of the environmental fluid or body elasticity versus intrinsic modulation due to changes in the sensorimotor control. We consider possible targets of modulation by the worm and implications of our results for our understanding of the neural control of locomotion in this system.

neuroscience

Neuromechanical phase lag predicts material and neural control properties in Caenorhabditis elegans

In all animals, the successful orchestration of motor programs hinges on appropriate coupling between components of the system, from neural circuit dynamics, through muscles and body properties to the physical environment. We study this coupling in undulatory locomotion, with a view to better understanding the relative roles of central and reflex-driven control. We ask how the coupling between neural control and body mechanics is affected by sensory inputs during undulatory locomotion in C. elegans. To address this question, we use a biomechanical simulation framework, within which we separately model feed forward and feedback controlled undulations. We characterize neuromechanical phase lag and locomotion speed using body stiffness as a control parameter. We show that sensory entrainment can suppress neuromechanical phase lag, that would otherwise emerge under centrally generated feed forward control.

neuroscience