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Zinke, I.

Publications and source records attributed to Zinke, I..

2 recordsLinked to original sources

Serotonergic reinforcement of a complete swallowing circuit

How the body interacts with the brain to perform vital life functions such as feeding is one of the fundamental questions in physiology and neuroscience. Here, we use a whole-animal scanning transmission electron microscopy dataset of Drosophila to map out the neuronal circuits that connect the entire enteric nervous system to the brain via the insect vagus nerve at synaptic resolution. This revealed a periphery-brain feedback loop in which Piezo-expressing mechanosensory neurons sense food intake and convey that information onto serotonergic neurons within the brain. These serotonergic neurons integrate the interoceptive information with external and central inputs, and in turn stabilize rhythmic activity of serotonin receptor 7 expressing peripheral motor neurons that drive swallowing. Strikingly, the very same motor neurons also share an efference copy of their activity with the aforementioned mechanosensory neurons, thereby closing the motor-sensory-modulatory loop. Our analysis elucidates an elemental, albeit surprisingly complex reinforcement circuit in which rhythmic motor patterns are stabilized through afferent signaling to central serotonergic neurons upon completion of a rewarding action. The circuit motif is constructed to allow the distinction between self-generated action and those in response to the environment.

neuroscience↗

Unveiling the sensory and interneuronal pathways of the neuroendocrine system in Drosophila

Neuroendocrine systems in animals maintain organismal homeostasis and regulate stress response. Although a great deal of work has been done on the neuropeptides and hormones that are released and act on target organs in the periphery, the synaptic inputs onto these neuroendocrine outputs in the brain are less well understood. Here, we use the transmission electron microscopy reconstruction of a whole central nervous system in the Drosophila larva to elucidate the sensory pathways and the interneurons that provide synaptic input to the neurosecretory cells projecting to the endocrine organs. Predicted by network modeling, we also identify a new carbon dioxide responsive network that acts on a specific set of neurosecretory cells and which include those expressing Corazonin (Crz) and Diuretic hormone 44 (DH44) neuropeptides. Our analysis reveals a neuronal network architecture for combinatorial action based on sensory and interneuronal pathways that converge onto distinct combinations of neuroendocrine outputs.

neuroscience↗