TY - CHAP
T1 - Optogenetic Modulation of the Visceromotor Response to Reveal Visceral Pain Mechanisms
AU - Najjar, Sarah A.
AU - Loeza-Alcocer, Emanuel
AU - Davis, Brian M.
AU - Smith-Edwards, Kristen M.
N1 - Funding Information:
This work was supported by NIH OT2 OD023859 (SAN, KMSE, BMD), F32 DK120115 (KMSE), and R01 DK107966 (ELA).
Publisher Copyright:
© 2022, Springer Science+Business Media, LLC, part of Springer Nature.
PY - 2022
Y1 - 2022
N2 - Visceral pain is a debilitating condition that is common yet lacks effective treatments. In the case of gastrointestinal disorders (e.g., inflammatory bowel disease and irritable bowel syndrome), pain is thought to be conveyed by primary afferent fibers innervating the colon. These fibers differ in their response properties, anatomical structures, and molecular phenotypes; thus, it is unclear which afferents initiate and maintain changes in visceral sensitivity. Additionally, evidence shows that nonneuronal cell types in the colon (e.g., epithelial cells) can initiate colon afferent activity, indicating that they are an integral part of sensory signaling. Measurement of the visceromotor response (VMR) is an established, reliable method to assess visceral sensitivity to mechanical stimuli. In order to determine the relative contribution of specific cell types to the VMR, our lab has developed techniques utilizing optogenetic mouse models. These techniques will enable researchers to define how subtypes of afferent neurons and nonneuronal cell populations contribute to visceral pain in both normal and pathological conditions. This chapter details how optogenetics can be integrated into VMR analysis, for assessment of colon sensitivity in vivo. These methods can be adapted to other visceral organs and also used in disease models.
AB - Visceral pain is a debilitating condition that is common yet lacks effective treatments. In the case of gastrointestinal disorders (e.g., inflammatory bowel disease and irritable bowel syndrome), pain is thought to be conveyed by primary afferent fibers innervating the colon. These fibers differ in their response properties, anatomical structures, and molecular phenotypes; thus, it is unclear which afferents initiate and maintain changes in visceral sensitivity. Additionally, evidence shows that nonneuronal cell types in the colon (e.g., epithelial cells) can initiate colon afferent activity, indicating that they are an integral part of sensory signaling. Measurement of the visceromotor response (VMR) is an established, reliable method to assess visceral sensitivity to mechanical stimuli. In order to determine the relative contribution of specific cell types to the VMR, our lab has developed techniques utilizing optogenetic mouse models. These techniques will enable researchers to define how subtypes of afferent neurons and nonneuronal cell populations contribute to visceral pain in both normal and pathological conditions. This chapter details how optogenetics can be integrated into VMR analysis, for assessment of colon sensitivity in vivo. These methods can be adapted to other visceral organs and also used in disease models.
KW - Colon afferents
KW - Optogenetics
KW - Primary afferent neurons
KW - Visceral hypersensitivity
KW - Visceral pain
KW - Visceromotor response
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U2 - 10.1007/978-1-0716-2039-7_16
DO - 10.1007/978-1-0716-2039-7_16
M3 - Chapter
AN - SCOPUS:85131122886
T3 - Neuromethods
SP - 321
EP - 332
BT - Neuromethods
PB - Humana Press Inc.
ER -