Stomatogastric Ganglion

The stomatogastric ganglion is a compact neural circuit in the foregut of crustaceans that controls rhythmic movements required for feeding and digestion, making it a powerful model for studying nervous system function. Its identified neurons interact through electrical and chemical synapses, while sensory signals and neuromodulators adjust the timing and strength of patterned motor activity in response to physiological conditions. Because its neurons, connections, and outputs can be examined in detail, the stomatogastric ganglion helps researchers investigate neural circuits, motor control, synaptic plasticity, and neuromodulation. Findings from this system also inform broader principles of biological rhythm generation and network resilience.

Stomatogastric Ganglion - Related Videos

Research

JoVE Journal - Neuroscience
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Optical Imaging of Neurons in the Crab Stomatogastric Ganglion with Voltage-sensitive Dyes

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Cited by 4 •

2011

Here we present the methodology for fast and high resolution fluorescent voltage-sensitive dye imaging of detailed activity of neurons in the crab stomatogastric ganglion.

Research

JoVE Journal - Biology
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Homarus Americanus Stomatogastric Nervous System Dissection

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Cited by 3 •

2009

We describe the fine dissection of the stomatogastric nervous system from the stomach of the American lobster (Homarus americanus).

Research

JoVE Journal - Biology

Cancer Borealis Stomatogastric Nervous System Dissection

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Cited by 103 •

2009

The stomatogastric nervous system (STNS) of the Jonah crab (C. borealis) can be used for electrophysiology, immunohistochemistry, and cell culture studies. The STNS extraction is done in two parts: the gross and fine dissection.

Isolating Vestibular Ganglion Neurons From a Mouse Inner Ear

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2025

This video showcases a method for isolating vestibular neurons from a mouse pup's inner ear. It meticulously outlines the steps involved in dissecting the inner ear, harvesting the vestibular ganglion, and subsequently dissociating the ganglion into single cells. These cells are then cultured on glass-bottom dishes to establish a vestibular neuron culture.

Transfection of Mouse Retinal Ganglion Cells by in vivo Electroporation

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Cited by 5 •

2011

We demonstrate an in vivo electroporation protocol for transfecting single or small clusters of retinal ganglion cells (RGCs) and other retinal cell types in postnatal mice over a wide range of ages. The ability to label and genetically manipulate postnatal RGCs in vivo is a powerful tool for developmental studies.

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