PUBLICATION
Neuromodulatory Selection of Motor Neuron Recruitment Patterns in a Visuomotor Behavior Increases Speed
- Authors
- Jha, U., Thirumalai, V.
- ID
- ZDB-PUB-200225-25
- Date
- 2020
- Source
- Current biology : CB 30(5): 788-801.e3 (Journal)
- Registered Authors
- Jha, Urvashi, Thirumalai, Vatsala
- Keywords
- D1-like receptor, central pattern generator, dopamine, excitability, locomotion, optomotor response, spinal cord, swimming, synaptic, zebrafish
- MeSH Terms
-
- Animals
- Biomechanical Phenomena
- Dopamine/pharmacology*
- Instinct
- Motor Neurons/drug effects
- Motor Neurons/physiology*
- Neurotransmitter Agents/pharmacology*
- Swimming/physiology*
- Tail/physiology*
- Zebrafish/physiology*
- PubMed
- 32084402 Full text @ Curr. Biol.
Citation
Jha, U., Thirumalai, V. (2020) Neuromodulatory Selection of Motor Neuron Recruitment Patterns in a Visuomotor Behavior Increases Speed. Current biology : CB. 30(5):788-801.e3.
Abstract
Animals generate locomotion at different speeds to suit their behavioral needs. Spinal circuits generate locomotion at these varying speeds by sequential activation of different spinal interneurons and motor neurons. Larval zebrafish can generate slow swims for prey capture and exploration by activation of secondary motor neurons and much faster and vigorous swims during escape and struggle via additional activation of primary motor neurons. Neuromodulators are known to alter the motor output of spinal circuits, but their precise role in speed regulation is not well understood. Here, in the context of optomotor response (OMR), an innate evoked locomotor behavior, we show that dopamine (DA) provides an additional layer to regulation of swim speed in larval zebrafish. Activation of D1-like receptors increases swim speed during OMR in free-swimming larvae. By analyzing tail bend kinematics in head-restrained larvae, we show that the increase in speed is actuated by larger tail bends. Whole-cell patch-clamp recordings from motor neurons reveal that, during OMR, typically only secondary motor neurons are active, whereas primary motor neurons are quiescent. Activation of D1-like receptors increases intrinsic excitability and excitatory synaptic drive in primary and secondary motor neurons. These actions result in greater recruitment of motor neurons during OMR. Our findings provide an example of neuromodulatory reconfiguration of spinal motor neuron speed modules where members are selectively recruited and motor drive is increased to effect changes in locomotor speed.
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping