Tools for dissecting neural circuits of interoception and autonomic regulation

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Abstract/Contents

Abstract
Behavioral states and physiological states are often linked, and concurrently perturbed in disease processes such as anxiety and panic disorder, but the bottom-up influence of internal physiological signals on behavior is complex. Physiological theories of emotion were proposed over a century ago, hypothesizing that rapid heartbeats alone could give rise to fear responses and are not merely a consequence of subjective emotional processing, but direct testing of such hypotheses has been infeasible. Investigation of the roles of afferent, interoceptive signaling in behavioral regulation requires spatial and temporal dissection of the interactions between autonomic and central circuits, but to date such studies have been limited, in part due to challenges both in observing multi-organ neural systems in their anatomically intact states, as well as in manipulating relevant physiological signals on rapid time-scales in awake, freely moving animals. To enable further studies of interactions between physiological states and behavior, in my thesis I describe a series of tools addressing these challenges. First, I built upon the hydrogel tissue chemistry technique CLARITY to enable rapid volumetric imaging of cleared peripheral organs in their intact state, enabling direct visualization of autonomic innervation throughout diverse tissue types. Second, I worked collaboratively to develop a computational tool enabling registration of cleared mouse brains to common reference atlases, enabling quantification of brain-wide activity changes under different physiological conditions. Finally, I developed a non-invasive optogenetic pacemaker to precisely control cardiac rhythms in freely-moving mice, utilizing the recently discovered red-shifted and ultra-photosensitive marine opsin, ChRmine, in conjunction with wearable micro-LED optics. Using the optical pacemaker, I directly tested the behavioral impact of cardiac palpitations on anxiety-like and apprehensive behavior, and found that intermittent tachyarrhythmia enhanced anxiety-like behavior and apprehension in stressful settings, but those same cardiac rhythms did not generate such behaviors in the absence of external stressors. Using whole brain activity mapping and tissue clearing, I then mapped regions of the brain that were preferentially activated by aberrant cardiac rhythms, and identified numerous anatomical regions -- including regions well known to be part of a "Central Autonomic Network" -- as potential mediators of bottom-up cardiac signal processing. Simultaneous optogenetic inhibition of posterior insula cortex, but not other regions within the Central Autonomic Network, during optical cardiac pacing was sufficient to reverse the induced behaviors, indicating that this region is one necessary site mediating cardiogenic anxiety-like and apprehensive behavior. Taken together, these findings offer insights into the neural mechanisms by which visceral signals can causally influence complex behaviors, and further present simple and generalizable tools for both volumetric mapping of diverse tissues, as well as non-invasive, temporally precise control of genetically-targeted organs throughout the body.

Description

Type of resource text
Form electronic resource; remote; computer; online resource
Extent 1 online resource.
Place California
Place [Stanford, California]
Publisher [Stanford University]
Copyright date 2021; ©2021
Publication date 2021; 2021
Issuance monographic
Language English

Creators/Contributors

Author Hsueh, Brian
Degree supervisor Deisseroth, Karl
Thesis advisor Deisseroth, Karl
Thesis advisor Chen, Xiaoke
Thesis advisor Kaltschmidt, Julia
Thesis advisor McNab, Jennifer (Jennifer A.)
Degree committee member Chen, Xiaoke
Degree committee member Kaltschmidt, Julia
Degree committee member McNab, Jennifer (Jennifer A.)
Associated with Stanford University, Neurosciences Program

Subjects

Genre Theses
Genre Text

Bibliographic information

Statement of responsibility Brian Hsueh.
Note Submitted to the Neurosciences Program.
Thesis Thesis Ph.D. Stanford University 2021.
Location https://purl.stanford.edu/qh852cy6710

Access conditions

Copyright
© 2021 by Brian Hsueh
License
This work is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported license (CC BY-NC).

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