TY - JOUR
T1 - Circuit Investigation of Social Interaction and Substance Use Disorder Using Miniscopes
AU - Beacher, Nicholas J.
AU - Washington, Kayden A.
AU - Werner, Craig T.
AU - Zhang, Yan
AU - Barbera, Giovanni
AU - Li, Yun
AU - Lin, Da Ting
N1 - Funding Information:
This research was supported by NIH NIDA IRP. NJB, CTW, and YZ were supported by Post-doctoral Fellowship from the Center on Compulsive Behaviors, National Institutes of Health. YL was supported by NIGMS COBRE 5P20GM121310-05. KAW was supported by NIDA IRP Scientific Director’s Fellowship for Diversity in Research.
Publisher Copyright:
© Copyright © 2021 Beacher, Washington, Werner, Zhang, Barbera, Li and Lin.
PY - 2021/10/5
Y1 - 2021/10/5
N2 - Substance use disorder (SUD) is comorbid with devastating health issues, social withdrawal, and isolation. Successful clinical treatments for SUD have used social interventions. Neurons can encode drug cues, and drug cues can trigger relapse. It is important to study how the activity in circuits and embedded cell types that encode drug cues develop in SUD. Exploring shared neurobiology between social interaction (SI) and SUD may explain why humans with access to social treatments still experience relapse. However, circuitry remains poorly characterized due to technical challenges in studying the complicated nature of SI and SUD. To understand the neural correlates of SI and SUD, it is important to: (1) identify cell types and circuits associated with SI and SUD, (2) record and manipulate neural activity encoding drug and social rewards over time, (3) monitor unrestrained animal behavior that allows reliable drug self-administration (SA) and SI. Miniaturized fluorescence microscopes (miniscopes) are ideally suited to meet these requirements. They can be used with gradient index (GRIN) lenses to image from deep brain structures implicated in SUD. Miniscopes can be combined with genetically encoded reporters to extract cell-type specific information. In this mini-review, we explore how miniscopes can be leveraged to uncover neural components of SI and SUD and advance potential therapeutic interventions.
AB - Substance use disorder (SUD) is comorbid with devastating health issues, social withdrawal, and isolation. Successful clinical treatments for SUD have used social interventions. Neurons can encode drug cues, and drug cues can trigger relapse. It is important to study how the activity in circuits and embedded cell types that encode drug cues develop in SUD. Exploring shared neurobiology between social interaction (SI) and SUD may explain why humans with access to social treatments still experience relapse. However, circuitry remains poorly characterized due to technical challenges in studying the complicated nature of SI and SUD. To understand the neural correlates of SI and SUD, it is important to: (1) identify cell types and circuits associated with SI and SUD, (2) record and manipulate neural activity encoding drug and social rewards over time, (3) monitor unrestrained animal behavior that allows reliable drug self-administration (SA) and SI. Miniaturized fluorescence microscopes (miniscopes) are ideally suited to meet these requirements. They can be used with gradient index (GRIN) lenses to image from deep brain structures implicated in SUD. Miniscopes can be combined with genetically encoded reporters to extract cell-type specific information. In this mini-review, we explore how miniscopes can be leveraged to uncover neural components of SI and SUD and advance potential therapeutic interventions.
KW - in vivo calcium imaging
KW - longitudinal imaging
KW - miniature fluorescence microscopy
KW - miniscope
KW - social interaction
KW - substance use disorder
UR - http://www.scopus.com/inward/record.url?scp=85117296000&partnerID=8YFLogxK
U2 - 10.3389/fncir.2021.762441
DO - 10.3389/fncir.2021.762441
M3 - Review article
AN - SCOPUS:85117296000
SN - 1662-5110
VL - 15
JO - Frontiers in Neural Circuits
JF - Frontiers in Neural Circuits
M1 - 762441
ER -